AP Biology
UNIT 1: Chemistry of Life
1.1 Structure of Water and Hydrogen Bonding
Properties of Water
Adhesion
Water molecules are attacted to other polar/charged molecules
Contributes to capillary action
Cohesion
Water molecules are attracted to each other → surface tension
Contributed to capillary action
Neutral pH (7)
Universal Solvent
Can dissolve other polar molecules and charged substances
High Specific Heat (4.18 J/g℃)
Specific Heat → amount of energy required to change 1g of substance by 1℃
Temperature regulator (acts as a buffer to temperature changes)
Due to H-bonds (help it absorb and release heat energy slowly)
High Heat of Vaporization (2260 J/g)
Heat of Vaporization → amount of energy required to change 1g of substance from a liquid to a gas
Due to H-bonds (must overcome IMFs to change from liquid to gas)
Polar Molecule
Due to H-bonds
Large END (EN of O → 3.4, EN of H → 2.2)
Higher e- density at O (due to stronger pull from nucleus)
Attracted to other polar/charged molecules
Repelled by nonpolar molecules
Intramolecular Bonds and Intermolcular Forces
Intramolecular Bonds → ionic and covalent
Within a molcule
Stronger than intermolecular forces
Covalent Bonds → when atoms bond by sharing electrons
Ionic Bonds → when atoms bond by transferring electrons (stay bonding due to electronegative forces)
Intermolecular Forces → H-bonds, London Dispersion Forces
Between atoms of different molecules
Weaker than intramolecular bonds
Hydrogen Bonds → IMF between H and F,O, or N
Strongest IMF due to high E.N.D.
London Dispersion Forces (Van der Waals Forces) → IMF due to temporary dipoles that are formed
1.2 Elements of Life
Atoms → Building blocks of matter
Made up of protons, electrons and neutrons
Ions → Atoms with a charge (postive or negative)
Carbon is the foundation element for molecules in living things
Due to bonding properties
4 electrons in outer shell → can form 4 covalent bonds with other atoms/molecules
Can form long and branching chains of carbon atoms
Can form rings which bonds to other rings
Organic → contains Carbon
Inorganic → does not contain Carbon
1.3 Properties of Biological Macromolecules
Polar Molcules (hydrophilic)
Several highly EN elements (ex: O, N)
High END → asymmetry
pH → logarithmic scale used to measure of acidity/basicity
Acidic, Neutral or Basic
Acidic: pH < 7, H+ donor, procduced H3O+ ions in solution
Neutral: pH = 7
Basic: pH > 7 H+ acceptor, produced OH- ions in solution
Nonpolar Molecules (hydrophobic)
Many C + H
Low END → symmetry
Acidic or Neutral
Symmetrical
Nonpolar
Asymmetrical
Polar
1.4 Strucutre and Function of Biological Macromolecules
Water is esential for building and breaking macromolecules
Dehydration Synthesis/ Condensation Reaction → water is removed from two monomers when they bond together
Hydrolysis Reaction → water is added back to separate two monomers
Carbohydrates
Store energy and provide structure to organisms
Ring or chain structures
Monosaccharide (single ring)
Disaccharide (double ring)
Polysaccharide (larger molecule)
Starch (plant energy storage), cellulose, glycogen (animal energy storage)
1:2:1 ratio (C:H:O)
Monomers connected by glycosidic linkage
Lipids
Made up of C,H,O (sometimes P)
Many hydrocarbons → hydrophobic
Fats, phoshpolipids, steroids, waxes, pigments
Steroids → mutliple rings connected
Fatty Acid → long hydrocarbon chains with a carboxyl group at the end
Fats (triglyceride) → 3 fatty acids attatched to a glycerol
Saturated (single bonds only) and unsaturated chains (at least one double bond)
Glycerol → alcohol that is the backbone of lipids
Phospholipid → two fatty cahins and a phosphate attached to a glycerol
Amphipathic → has a hydrophilic and hydrophobic side
Waxes → hydrocarbon chain with an alcohol (-OH) group and a fatty acid
Proteins
Made up of C, H, O, N (sometimes S)
Facilitate chemical reactions, provide structure, carry information between cells
Shape determines function (how they interact with other molecules)
Amine group, carboxyl group and R-group (variable group)
R-group (side chain) can be nonpolar, polar, or charged (basic or acidic)
Central Carbon
Peptides → short chains of amino acids (building blocks of proteins)
Nucleic Acids
Made up of C, H, O, N, P
store, transmit, and help express hereditary information
Monomer: nucleotides
Phosphate, sugar, base
Can have 1-3 phosphate groups
Nitrogenous Bases → single or double ring
Pyrimidines (single ring) → cytosine, thymine, uracil
Purine (double ring) → adenine, guanine
Functional Groups → atoms or groups of atoms with similar chemical properties
1.5 Nucleic Acids
DNA and RNA
Sugar in DNA → deoxyribose (one of the Oxygens is absent)
Phosphodiester Bond → covalent bond between sugar and phosphate (runs along outside of leader and makes uo sugar-phosphate backbone)
Sugar in RNA → ribose (extra O present)
ATP (adenosine triphosphate)
Adenine (nitrogenous base) + ribose (sugar) + 3 phosphates
1.6 Protein Synthesis
Primary Structure
Chain of amino acids (specific sequence is determined by DNA)
Connected by peptide bonds → bond between Nitrogen in amine and Carbon in carboxyl group (condensation reaction)
Amino acids join to form a polypeptide
Only structure maintained after denaturing a protein
Secondary Strucuture
3-D folding
Due to H-bonds (between Oxygen in amine group and Hydrogen in carboxyl group)
Alpha helix or beta-pleated sheet
Tertiary Structure
3-D folding
Due to disulfide bridges, H-bonds, hydrophobic interactions (C and H must be present) and ionic bonds
Interactions are between R-groups
Quanternary Structure
Fooding between multiple polypeptide chains
Due to disulfide bridges, H-bonds, hydrophobic interactions (C and H must be present) and ionic bonds
Many proteins, but not all have the fourth level of structure
Transcription & Translation
Transcription → DNA is used to synthesize mRNA
Takes place in nucleus
DNA → double helix, can’t leave nucleus, thymine
RNA → single helix, leaves nucleus (responsible for communication with rest of the cell), uracil
mRNA (messenger RNA) → codes for proteins
tRNA (transfer RNA) → brings amino acids to ribosome
Translation → mRNA is used to synthesize proteins in the ribosome
Takes place in cytoplasm
Ribosome has two subunits that come together for protein synthesis
Codons → groups of 3 bases that code for amino acids
Multiple cdons code for the same amino acid to protoect aginst errors (becuase it allows for some errors in the DNA without changing the protein)
1.7 Enzymes Structure
Proteins
10, 20, 30, 40 structure
Reusable
End in -ase or -in
Act on substrates (reactants) which bind to the enzyme’s active site
Through weak IMFs (Van der Waals forces)
Lock and Key Model
Induced Fit Model
1.8 Enzyme Catalysis
Enzymes are biological catalysts
Catalysts → Speed up chemical reactions by lowering activation energy (Ea)
Activation Energy → amount of energy required for a reaction to occur
Chemcial Reaction → Process that changes a set of reactants into products
Atoms are rearranged due to an energy change
Reactants → what is put into a reaction
Products → what results from a reaction
ΔG → Free Energy
Energy released during a chemical reaction
Exergonic Reactions
Reactions that have a negative charge in free energy (release energy)
Endergonic Reaction
Reactions where products have more free energy than reactants
Non-spontaneous
1.9 Enviornmental Impacts on Enzyme Function
Factors that Affect Enzymatic Reaction Rate
Temperature/pH
When temperature/pH is too high, protein becomes denatured
Denaturation → when a proteins becomes unfolded (loses shape and therefore function
Enzyme Concentration (with excess substrate concentration)
Substrate concentration (with constant enzyme concentration)
Cofactors/Coenzymes → increase reaction rate
Cofactors → inorganic substances that facilitate substrate binding to active sites
Coenzymes → organic substances that facilitate substrate binding to active sites
Inhibitors → decrease reaction rate
Competitive → molecules that directly lock active site
Noncompetitive → molecules that bind to allosteric site resulting in a chage in the active site (stop active site conformation)
Allosteric Activation → when an allosteric inhibitor binds to a region on an enzyme adn all active sites on the protein subunits are changed
Enzymatic Pathways (relay race)
Feedback inhibition
Don’t want pathways on all the time → want to conserve resources
1.10 Origins of Life on Earth
Three Hypotheses of Life’s Origins
Primordial Soup Hypothesis
Early Earth’s conditions provided inorganic reactants (NH3, H2O, H2, H2S) and enough free energy in the absence of O2 that lead to the spontaneousfromation of roganic compounds → organic compounds assembled to form the first living organisms
Miller and Urey Experiment → Miller and Urey recreated the conditions of early Earth and successfully sunthesize organic molecules via high voaltge electricity
RNA World Hypothesis
RNA was the first organic molecules and genetic material
RNA is self-replicating and has enzyme-like reactions
RNA drives protein synthesis and can reverse transcribe into DNA
Celestial Orign Hypothesis
Organic molecules could’ve been transported to Eath by meteorites or other space materials
Limitation: Where would those organic molecules come from?
UNIT 2: Cell Structure and Function
2.1 Cell Structure: Subcellular Components
Nucleus → controls cell’s activities and serves as the blueprint for controlling cell function and building more cells (contains chromatin → uncondensed DNA)
Nuclear Envelope → membrane that separates the nucleus and the cytoplasm
Mitochondria → sites of aerobic respiration and the major energy production center in cells (produce ATP)
Chloroplast → photosynthesis, synthesizes amino acids and lipids
Rough ER → series of interconnecting flattened tubular channels that have ribosomes attached (role in protein synthesis and folding)
Smooth ER → series of interconnecting flattened tubular channels involved in lipid synthesis
Ribosome → synthesizes proteins (found free floating or in the RER)
Golgi Apparatus → protein modification, sorting and packaging (stack of membranous flattened sacs)
Lysosome → contain hydrolytic enzymes needed for digestion of macromolecules
Cell Membrane → controls exchange between the cell and environment
Cell Wall → gives plants structure and protection
Cytoplasm → aqueous material that contains the other organelles
Cytosol → aqueous component of cytoplasm
Vacuole → involved in storage
Vesicle → used to ship materials around the cell
Cytoskeleton → gives cell structure and maintains intracellular organization
Actin and intermediate filaments → cytoskeleton components
Centrioles → organizes spindle fibers in cell division
Peroxisome → responsible for protecting the cell as they ride the body of toxic substances and break down fat (lipids)
Nucleolus → synthesizes ribosomal RNA
Flagella → Similar to cilia but longer
Cilia → hair-like organelles involved in movement of mucus out of the lungs and the egg in the fallopian tube
Microtubules → found in cilia
2.2 Cell Structure and Function
Missing or dysfunctional organelles lead to disease
Cystic Fibrosis → thick mucus in the lungs, frequent lung infections, clogged pancreas and digestive problems
Cell membrane is affected
ALD → build up of fatty acids in the brain and spinal cord
Peroxisome is affected
Pompe → build up of excess glycogen within muscle cells, extreme muscle weakness and floppy appearance
Lysosome is affected
Kartagener → breathing problems, serious anus, ear and/or lung infections, infertility
Cilia is affected
2.3 Compartmentalization and Origins of Cell Compartmentalization
Types of Cells
Eukaryotic Cells → Compartmentalized
Well-defined sections
Organelles with internal fluid have a phospholipid bilayer membrane
More surface area
Membrane-Bound Organelles
Nucleus, mitochondria, chloro[last, RER, SER, Golgi, lysosome, peroxisome, vacuole, vesicle
Non Membrane-Bound Organelles
Ribosomes, cell wall, cytoplasm, cytoskeleton, cell membrane
The Endomembrane System
Group of membrane-bound organelles that work together to synthesize, modify, package and transport lipids and proteins
Specialization
Cells are specialized → java a specific function
A cell’s shape, size mount and type of organelles determines its function
Cell with many mitochondria utilizes a lot of energy (muscle cells)
Cell with many Golgi Apparatuses has a secretory function
Cell with flagella move (sperm)
More compartmentalization → more specialization of cell type
Autogenic Hypothesis → the cell began as a prokaryotic cell and evolve into a eukaryotic cell with membrane bound organelles
Evidence:
Prokaryotic cells do not have membrane-bound organelles while eukaryotic cells do
Eukaryotic cells have the same organelles as prokaryotic cells, and in addition have membrane-bound organelles
Endosymbiotic Hypothesis → prokaryotes engulfed other phagocytic prokaryotes and the ingested organisms survived and continued to live within the predator
Evidence:
membrane -bound organelles are similar to prokaryotes
Mutualistic relationship would allow them to benefit each other
2.4 Cell Size
Cells need enough surface area to maintain homeostasis
Surface area needed for the exchange of materials through the cell membrane
As cells grow the surface area to volume ratio changes (increases) so there is a limit to cell growth
Cell becomes too large → materials not exchanged fast enough and homeostasis is not maintained
When cell reaches critical surface area to volume ratio it stops growing
Cell is signaled to die to divide
2.5 Plasma Membrane
Phospholipid Bilayer: double layer of phospholipids that speerates extracellular and intracellular space
Amphipathic → phospholipids are polar and nonpolar
Polar head is hydrophilic (attracted to water)
Nonpolar tails are hydrophobic (repelled by water)
Flexible (allows for permeability)
Cholesterol (more = less flexible)
Receives external signals and initiates cellular responses
Receptor Proteins
Ligands
Messenger molecules that connect to a receptor to initiate a signal pathway (hormones, neurotransmitters)
Glycolipids and Glycoproteins
Carb chains tag for self-recognition (only on surface)
Intercellular Junctions → direct contact between cells
Plasmodesmata (passage through cell wall in plants)
Gap Junctions (animals)
Adhere to neighboring cells
Glycolipids and glycoproteins (anchors adjacent cells)
Desmosomes (extensions of cytoskeleton that connect cells together in animals)
Proteins
Integral Proteins → span entire lipid bilayer
Ex: transport proteins (channels, gates, carrier proteins)
Peripheral Proteins → one edge of lipid bilayer
Intracellular or extracellular
Cytoskeleton → proteins scaffold
Can spontaneously repair small tears in the lipid bilayer
Eukaryotic cells have membrane-bound organelles that create specialized compartments within a single cell
Membrane proteins can drift across the lipid bilayer
Gap Junctions: allow for the rapid transit of ions and small molecules between adjacent animal cell membranes
Binary Fission: bacterial cells divide when a thin ring of proteins located at the cells midpoints contracts, effectively cleaving the cell in two
2.6 Membrane Permeability
Selective Permeability:
Small and Nonpolar: can diffuse through membrane
Small and Polar: can sometimes diffuse through membrane
Repelled by nonpolar tails
Large and Nonpolar: can sometimes diffuse through membrane
Hard to it between tails
Large and Polar: require transport proteins
Charged: require transport proteins
Aquaporins: channels for water to pass through
2.7 Mechanisms Transport
Diffusion
Passive
No help
Molecules move from higher to lower concentrations (with concentration gradient) until they are at equilibrium
Facilitated Diffusion
Passive
Membrane Proteins
Movies monosaccharides, amino acids, and other monomers down the concentration gradient into cells with the use of proteins that change conformation
Osmosis (Facilitated diffusion through aquaporins)
Passive
Membrane Proteins
Moves water molecules across cell membrane down the concentration gradient
Facilitate Diffusion through Channel Proteins
Passive
Membrane Proteins MOlecules move down the concentration gradient via protein channel
Na+-K+ Pump
Active
Membrane Proteins
Electrogenic pump that moves 3 Na+ out and 2 K+ in
Proton Pump
Active
Membrane Proteins
Electrogenic pump that moves H+ across a membrane creating an electrochemical gradient
Cotransport
Active
Membrane Proteins
Moves a molecules in/out of cells by carrying its transport to the movement of another
Phagocytosis
Active
Vesicles
Cells engulf large molecules or whole cells
Pinocytosis
Active
Vesicles
Cells engulf small solutes or fluids
Receptor Mediated Endocytosis
Active
Vesicles
Specific molecules are taken into cells after building to receptors on the cell
Exocytosis
Transport vesicles fuse to cell membranes and release contents
2.8 Tonicity and Osmoregulation
Osmosis → diffusion of water
Tonicity → ability of an extracellular solution to cause a cell to gain or lose water
Depends on the concentration of solutes that cannot pass through the membrane
Osmoregulation → cells must be able to regulate their solute concentrations and maintain water balance
Water Potential → a physical property that predicts the direction water will flow
Includes the effect of solute concentration and physical pressure
Water flow:
Water Potential: high to low
Solute Concentration: low to high
Increase in solute causes binding to more free water → reduces solute potential
Pressure: high to low
Hypotonic
Animal Cell: swell and lyse
Plant Cell: turgid
Ideal because it helps plants to stay standing
Osmotic Pressure (turgor): increase
Net movement of water: inside
Water Potential inside the cell is less than the outside
Isotonic
Animal Cell: stays the same
Plant Cell: plasmolyzed
Plasmolysis → vacuole shrinks and the plasma membrane pulls away from the cell wall
Osmotic Pressure (turgor): stays the same
Net movement of water: neither
Water Potential inside the cell is equal to the outside
Hypertonic
Animal Cell: shrinks and shrivels
Plant Cell: flaccid
Osmotic Pressure (turgor): decrease
Net movement of water: decrease
Water Potential inside the cell is greater than the outside
Ψ → water potential
ΨS → solute potential (pure, distilled water = 0 mPA)
ΨP → pressure potential (physical pressure on a solution, “open air” = 0)
i → ionization constant (how many ions are made in solution)
C → molar concentration
R → pressure constant (0.0831 bars or 0.0083 mPA)
T → temperature (K)
Unit 3: Cellular Energetics
3.1 Cellular Energy
Bioenergetics → concept of energy flow through living systems
ATP → energy currency of cells
Metabolic Pathways
Anabolic → requires energy and build molecules
Endergonic
Nonspontaneous
Positive Gibbs Free Energy
Ex: cellular respiration
Catabolic → releases energy and builds molecules
Exergonic
Spontaneous
Negative Gibbs Free Energy
Ex: photosynthesis
Free Energy
Gibbs Free Energy → energy that takes place with a chemical reaction
During energy transfer, some becomes as unusable form (heat)
Enthalpy → total energy in a system
Activation Energy → initial amount of energy required for the reaction to occur
Transition State → molecule is contorted prior to breaking chemical bonds
*Most chemical reactions are reversible
The Laws of Thermodynamics
First Law → the total amount of energy in the universe is constant
Heat Energy → energy that transfers without doing work
Second Law → High entropy results in high disorder and low enthalpy (energy)
Entropy → amount of disorder in a system
3.2 Cellular Respiration
3.3 Photosynthesis
3.4 Fitness
Metabolism → all chemical reactions that transpire inside cells
Evolutionary Fitness
The ability to survive AND reproduce in a given environment
Variation in traits (ADAPTATIONS) allow for some organisms to be more fit than others
Number and types of molecules within cells (ex: pigments)
Chemical Pathway
C3, C4, CAM photosynthesis (differ in where and how carbon fixation occurs)
Plant Adaptations: Leaf Structure
Spongy Mesophyll → airspaces help with gas exchange
Palisade Mesophyll → cells have high chloroplast density (where majority of photosynthetic activity occurs)
Stomata → pore through which gases can enter and exit
Open Stomata → hot/dry conditions (prevents water loss and leads to buildup of O2 gas)
Closed Stomata → optimal conditions
Cuticle → waxy covering (hydrophobic)
Epidermis
Lower Epidermis
Vein → transports substances
Xylem → H2O from roots
Phloem → sugars from leaves to roots
Photorespiration
Occurs when O2 concentration is high in the spongy mesophyll (Rubisco fixes O2 instead of CO2 during the Calvin Cycle)
Produces CO2, wasting RuBP, NADPH, and ATP
Transpiration
Occurs when water exits the stomata at a faster rate than it is entering the lead
Net water loss, flaccid plant cells (low structural support), possibility of drying out
Unit 4: Cell Communication and Cell Cycle
4.1 Cell Communication
Signaling Pathway → pathway used to send chemical message from cell to cell
Ligand → signaling molecule that fits into the active site of the receptor
Types of Signaling
Autocrine (auto=self)
Ex: cancer cells release their own growth hormone (signal themselves to reproduce)
Juxtacrine (juxta=bsides, next to, touching)
Ex: Plasmodesmata → channels between plant cells (allow ligand to move directly from one cell to another)
Paracrine (para=nearby)
Ex: Quorum Sensing → used by bacteria to determine the population density of their species in a local area (each bacterium produces a ligand and the ligand reaches a critical concentration to indicate a sufficient population)
Ex: Neurotransmitters → ligands released for communication between nerve cells
Endocrine (endo=within)
Ex: Pancreas cells release insulin when blood sugar levels are elevated, signaling to liver cells to being absorbing the glucose
Ex: hormones (pheromones released by egg provide pathway for sperm to travel)
Release of a Ligand due to Stimuli
Over/Underproduction of molecules
Environmental Factors (light, temperature, sensory triggers)
Age of cells
Stress
Signals from other cells (feedback)
4.2 Signal Transduction
Signal Transduction Pathway: signaling Cell releases ligand → message received → response produced by target cell
Signaling → ligand released
Reception → ligand binds to receptor protein
Transduction → signal is transmitted throughout the cell (amplification)
Response → response is produced
*Once response is achieved in a cell, relay protein must be deactivated to stop response
Ligand-Receptor Specificity needed → ligands and receptors have a specific shape so they can only activate certain ligands/receptors (shape determines function)
Phosphorylation Cascade → phosphate groups added to proteins by kinases to activate them (changed shape so protein can function properly), allowing them to activate other relay proteins
*Set off by ligand binding to receptor protein
Amplification is advantageous because increases the chances of transmitting the signal successful (one signal reception lad to a response occurs in several locations in the cell)
Once response is reached, Protein Phosphatases (PP) remove the phosphate groups to deactivate the proteins (otherwise response will happen forever)
Secondary Messengers (ligand → primary messenger)
Amplify a signal with phosphorylation
Types of Receptors:
Intracellular Internal (for hydrophobic ligands)
Cell Surface
Ion Liked Channels (normally closed, but when ligand binds channel opens to let ions in)
G-Protein Linked (when receptor binds to ligand, a G-protein activates and interacts with another integral protein (channel or enzyme))
Types of Ligands
Small Hydrophobic (ex: steroids)
Small and hydrophobic so do not need to bind to a surface receptor
Medium Hydrophilic (ex: protein signal molecules (epinephrine))
Can’t go through membrane → must bind to surface receptor
Small Hydrophilic (ex: nitric oxide (laughing gas) → anesthetic)
Types of Response
Gene Expression (initiate transcription)
Increase Metabolism
Growth (cell division → mitosis)
Cell Death (apoptosis)
4.3 Changes in Signal Transduction Pathways
Mutation in DNA coding for ligand or receptor protein structure
Toxins
Ex: anthrax releases a toxin that changes the shape of adenylyl cyclase so it can no longer convert ATP to cAMP
Diseases
Ex: type 1 Diabetes causes the lack of insulin production (autoimmune)
Type 2 Diabetes causes the lack of target cells “listening” to ligand binding
4.4 Feedback
Feedback Mechanism → regulatory process that adjusts a system to meet a desired result when stimulated
Positive Feedback
Stimulus is INCREASED → used for amplification
Ex: Baby pushes against cervix → hypothalamus releases oxytocin → uterine wall contacts → baby pushes against cervix
Negative Feedback
Stimulus is DECREASED → used to limit something
Ex: Hypothalamus sense temp too low → signal to heat the body sent → blood vessels constrict (limit heat loss), muscles shiver (generate heat) -> body temp increases
4.5 Cell Cycle
Phases:
G0: not dividing/preparing to divide
G1: cell grows by producing more proteins and organelles
S: DNA replication, shootings in sister chromatids
G2: cell prepares for cell division with the appearance of centrosomes, replenishes energy stores, synthesis proteins necessary for chromosome manipulation and mitotic phase
M: mitosis and cytokinesis
Prophase:
Nuclear envelope breaks down
Membrane organelles fragment and disperse
Centrosomes begin to move to opposite poles of cell
Microtubules that form mitotic spindle extend between centrosomes
Sister chromatids begin to coil more tightly
Prometaphase:
Protein structure called the kinetochore forms at each centromeric region
Proteins bind to the mitotic spindle microtubules
Metaphase:
All chromosomes line up in the metaphase plate
Anaphase:
Cohesion proteins that held sister chromatids together degrade
Each chromatid is pulled toward centrosome
Metaphase:
Chromosomes reach opposite poles and begin to condense
Mitotic spindles depolymerize into tubulin monomers (used to build cytoskeletal components of daughter cells
Cytokinesis
Cells physically separated into daughter cells
Animal Cells: contractile ring forms
Plant Cells: vesicles fuse to form phragmoplast vesicular structure that will become the new cell wall
4.6 Regulation of Cell Cycle
Cell cycle tightly regulated → keeps the multicellular organism healthy
Conserving materials
Ensures that new cells receive accurate genetic information
Prevents uncontrolled growth
Checkpoints:
G1: ample supply of energy and raw materials available; adequate environment for cells (density dependent inhibition → rate of division regulated by how crowded it is); regulates weather the cell is in G0 or not
Cell not grown sufficiently → daughter cells would be small and not have enough organelles to store nutrients/complete metabolism
G2: ample supply of energy and raw materials available; DNA has been completely replicated and checked for errors
M: all chromosomes are attached to spindles
Chromosomes not prepared for division → uneven amount of chromosomes in each cell
Growth Factors → released by specialized cells and trigger cell division
Kinases → provide the energy (through phosphorylation) for processes needed for mitosis
Cyclin Dependent Kinase (CDK)
Molecule Concentration Throughout Cell Cycle
Ligand → lowest at start of mitosis, highest at end of interphase
Kinase → constant
Complex (kinase+ligand+phosphate) → based on ligand concentration
Positive Regulators → molecules that promote progress of the cell cycle
Ex: Cdk/cyclin complex → works by phosphorylating other proteins, allowing cells to pass through the next phase
Negative Regulators → molecules that halt progress of the cell
Ex: RB, p53, p21
Cancer
Cancer covers many different diseases involving UNCONTROLLED CELL GROWTH
Begins with a gene mutation → results in a faulty protein that regulates cell division (snowball effect)
Tumors results when division of mutated cells surpasses growth of normal cell
Benign tumor → cell are NOT cancerous (won’t spread)
Malignant Tumor → cells are cancerous (spread to other tissues and organs)
Metastasize
Rapid Angiogenesis (growth of new blood vessels)
Environmental Cues to permit Cell Growth
Cells will cease cell division due to external signals from the environment/other cells
Density Dependent Inhibition → if cells are crowded, cell division stops
Anchorage Dependent → cells must be attached to something else (like another cell) to divide
Proto-oncogenes
Normal genes (non-mutated version) that code for POSITIVE cell cycle regulators
When these genes MUTATE in certain ways, they become oncogenes (dominant)
Ex: genes for
Cyclins → cell cycle receptors
EGFR →receptor for epidermal growth factor
KDR → receptor for vascular endothelial growth factor (angiogenesis)
Tumor Suppressor Genes (recessive)
Genes that code for NEGATIVE regulator proteins
Activated → PREVENT uncontrolled division
Ex: genes for
(t)p53 → protein checks for and repairs DNA damage (active during G1 & G2 checkpoints)
RB protein → retinoblastoma, checks for proper DNA replication (G2 checkpoint)
Unit 5: Gene Expression and Regulation
5.1 DNA and RNA Structure
Genetic Information
Able to store information
Can be consistently replicated through generations
Able to allow for changes and thus evolution to occur
Purine → 2 rings (adenine, guanine) binds to pyrimidine → 1 ring (thymine, cytosine)
Bind through H-bonds
Uniform diameter
Found in nucleoid region of prokaryotes, nucleus of eukaryotes
In eukaryotes, DNA is wrapped around histones (proteins) to form structures called nucleosomes
Antiparallel (3’ end and 5’ end)
3’ end has an OH (hydroxyl group)
5’ end had a phosphate
James Watson & Francis Crick
Bases are complementary (revealed how genes are replicated, stored and mutated)
Double helix with strands running in opposite directions (antiparallel)
Oswald Avery
Transforming Factor (allows bacteria to transfer genetic material)
Maurice Wilkins & Rosalind Franklin
Photo 51 showed DNA is symmetrical and bases are on the inside
Erwin Chargaff
Amount of A bases and T bases are always the same, amount of G bases and C bases are always the same
Base pairing rule (A-T; G-C)
Frederick Griffith
Bacteria are able to transfer genetic material to one another → transformation
Experiment used virulent S cells, heat-killed (nonvirulent) S cells, and nonvirulent R cells
Mixed dead S cells and living R cells and the R cells became virulent
Suggests that heat-killed S cells provided a transforming factor to the R cells that in turn made them virulent
Alfred Hershey and Martha Chase (Alfred-Chase Experiments)
Used phages (a type of virus made of proteins and DNA that infect and reproduce in bacterial hosts) to determine if genetic material was made of proteins or DNA
Tagged sulfur (proteins) and phosphorus (DNA) → bacterial host cells were infected with radioactively tagged phages → samples were blended and centrifuged → wavy bacterial contents in a pellet were separated from phage contents in liquid
Pellet showed phosphorus → genetic material contains phosphorus → DNA is genetic material
DNA vs RNA
5.2 Replication
DNA must always be protected inside the nucleus except during cell division (mitosis)
Gets destroyed by enzymes (nucleases) in cytoplasm
Enzymes and free nucleotides are available for replication in the nucleus
DNA is synthesized from 5’→3’ (DNA Polymerase adds nucleotides to the 3’ end)
Part 1: Initiation
Helicase attaches to DNA and breaks the H-bonds to unwind and separate the complementary strands, creating a replication fork
Attaches at multiple sites fo the strands to speed up the process, creating the appearance of bubbles along the strand (replication bubbles)
Topoisomerase prevents over-twisting of DNA as it is unwound
Single Stranded Binding Proteins (SSBP) stabilize the single strands of DNA so enzymes can access the bases
Part 2: Elongation
DNA Primase places an rNA primer which acts as a bookmark/placeholder for DNA Polymerase
DNA Polymerase III reads the DNA template strand from 3’→5’ an attaches complementary free nucleotides in a 5’→3’ direction
Attaches at multiple sites fo the strands to speed up the process, creating the appearance of bubbles along the strand (replication bubbles)
DNA Polymerase I removes RNA primers and fills in with more free nucleotides and proofreads for mistakes
Attaches at multiple sites fo the strands to speed up the process, creating the appearance of bubbles along the strand (replication bubbles)
Leading and Lagging Strands
DNA Polymerase can only attach new nucleotides to the 3’ end of the new DNA strand
Must backtrack to copy parts of the newly exposed end of the new DNA strand (process takes longer) → lagging strand
Strands hat does not need to back track (process is quicker) → leading stand
Okazaki Fragments → fragments that are created on the lagging strand
Ligase fuses the sugar-phosphate backbone of the Okazaki fragments together
Part 3: Termination
When complete, the result should be 2 perfect copies of the original
Mistakes (mutations) occur
Semiconservative → each new molecules had one original strand and one new strand
Efficient and lowers risk of errors
5.3 Transcription and RNA Processing
Process by which cell makes an mRNA copy of the DNA
RNA Polymerase binds to template strand of DNA (antisense/non-coding strand)
Read from 3’→5’
RNA Polymerase adds nucleotides across from the template strand in the 5’→3’ direction
Uses base pairing rules
Nontemplate DNA → replace T with U
Prokaryotes
Occurs in cytoplasm (don’t have a nucleus)
No exonucleases → mRNA considered mature and ready for translation at end of transcription
Eukaryotes
Occurs in nucleus
Produces pre-mRNA at end of transcription (because it contains introns) → mRNA not mature
RNA Polymerase joins with transcription factor proteins (helpers) at the promoter/TATA box (special sequence of base pairs that singlas beginning of gene)
Transcription factor proteins and RNA Polymerase → Transcription Initiation Complex
Moves along DNA template strand producing pre-mRNA
RNA Polymerase reaches terminator sequence of base pairs → complete production of pre-mRNA and releases it into the nucleoplasm
Must go through post-transcriptional processing before mRNA can leave nucleus (for translation)
Introns (non-coding regions) are removed
Methyl Cap is added to 5’ end (helps mRNA molecule move through the nuclear pore and attach to ribosome)
Poly-A tail is added to 3’ end (helps protect from degradation by exonucleases in the cytoplasm)
mRNA leaves nucleus through nuclear pores
5.4 Translation
mRNA read in sets of three nucleotides (codons) by ribosomes
Found in either cytoplasm or rough endoplasmic reticulum
Proteins produced through dehydration synthesis reactions between amino acids
tRNA carries amino acids to the ribosome
tRNA has an amino acid on one end and an anticodon on the other (anticodon pairs with codon on mRNA so ribosome can makes sure that correct amino acid is being incorporated into the protein)
Translation proceeds until a STOP codon is reached
Chain of amino acids is released from ribosome and H2O is bonded to the end
Exception to Central Dogma: Viruses
Much smaller than bacteria
No membrane-bound organelles (anaerobic respiration)
Requires a host to reproduce
Raises debate of if they are living or not
Structure: protein (capsid, enzyme) and nucleic acid (DNA, RNA)
Classifications based on shape/composition
Bacteriophage
Retroviruses
Retroviruses
Class of RNA viruses that use reverse transcription (synthesis of DNA based on RNA template)
HIV → retrovirus that causes AIDS by using helper T cells (white blood cell that helps with immune response) as a host
Reverse Transcriptase allows viruses to convert their RNA genome (7,000-12,000 base pairs long) into DNA so that it can be inserted into hos’s genome in order to replicate genetic material and reproduce
Converts viral RNA to single stranded cDNA (complementary DNA)
Creates transposons (“jumping genes”) that allow for variation in the genome
Steps of Reverse Transcription
Virus infects a host cell by releasing viral RNA into cytoplasm
Viral RNA is transcribed into single stranded cDNA (SSDNA) by reverse transcriptase (reads 3’ → 5’; synthesizes 5’ → 3’)
cDNA migrates to the nucleus where it is inserted into the host’s genome by integrase
Transcription and translation are carried out by the host’s enzymes as normal, synthesizing viral proteins (process is repeatable)
Eukaryotic
DNA is constantly shortening
Telomeres are non-coding protective DNA sequences at the end of chromosomes
Telomerase uses mRNA to add cDNA to elongate telomeres to prevent aging
5.5 Mutations
Occur due to errors in DNA replication, exposure to mutagens (ex: UV rays, x-rays), or viral infection (ex: HPV)
Point Mutations
Base Substitution
Base Insertion (frameshift)
Upstream → more impactful
Base Deletion (frameshift)
Upstream → more impactful
Chromosomal Mutations
*All chromosomal mutations occur during cell division
Deletion → part of a chromosome is missing/removed
Duplication → part of the chromosome is copied
Inversion → Parts of chromosome are swapped
Translocation → part of chromosome is move to another chromosome
Impact on Protein
Missense Mutation → codes for the wrong amino acid
Silent Mutation → no change in amino acid (uses different codon for that amino acid)
Nonsense Mutation → premature STOP resulting in incomplete protein
Effects
Positive → change in a protein leading to a beneficial trait (passed down to offspring)
Drives genetic variation
Neutral → silent mutations (no change)
Negative → could lead to major changes in protein structure (shortening, misfolding)
Missense and nonsense mutations
5.6 Regulation of Gene Expression
Control of gene expression
Each somatic (body) cell contains the identical genome
Differential gene expression → cell specialization
All genes do not need to be expressed simultaneously in each cell
Saves energy, space and time
Prokaryotes
Regulation occurs at the transcriptional level only (inducible and repressible)
Genes turned on and off based on environmental factors
Operon → group of genes along with sections of DNA that regulate them
Contain promoter operator, repressor and terminator
Positive Control → when actuator protein binds, transcription begins
Negative Control → when repressor protein binds, transcription is inhibited
Inducible Operon
Switched from OFF to ON
OFF: Repressor binds to operator → RNA Polymerase inhibited -> no gene expression → no proteins
ON: Inducer will bind to repressor → changes repressor shape → repressor no longer binds to operator → gene expression → proteins made
Repressible Operon
Switched from ON to OFF
ON: corepressor molecule not present → repressor protein can’t bind to operator → protein synthesis
OFF: corepressor molecule present → binds to repressor → allows repressor to bind to operator → no protein synthesis
Eukaryotes
Regulated at different stages of the central dogma and DNA packaging
Genomic Regulation (“within” genes)
Positive Regulators
Promoter sequences occur upstream of the gene (transcription factor binds here)
Helps RNA Polymerase bind (initiates transcription)
Enhancer Sequences can occur upstream or downstream of a gene
Activator proteins bind to them and interact with transcription factor to promote RNA Polymerase binding
Increases amount of mRNA being made
Negative Regulators
Silencer Sequences can occur upstream or downstream of a gene (repressor proteins bind to the, blocking RNA Polymerase)
Repressor proteins that bind to the promoter sequence prevent transcription
RNA Processing: Alternative Splicing of mRNA
Alternative splicing of pre-mRNA done by spliceosome (RNA and exonuclease)
Different combinations of introns and exons leads to variation in the ame protein (different gene expression eben in the same types of cells)
Translation Activation/Repression
Translation can be activated or repressed by initiation factors (proteins0)
MicroRNA (MiRNA) and small interfering RNAs (RNAi) can bind/degrade to mRNA, stopping translation
Epigenomic Regulation (“on top of” genes)
Epigenome
“Above” the genome
Chemical markers on the genome that affect how it is expressed
Chromatin Structure and Modifications
If DNA is tightly wound, it is less accessible for transcription
Chromatin Modifications
Histone Acetylation ads acetyl groups to histones, which loosens DNA (gene activating)
DNA Methylation adds methyl groups to DNA which causes the chromatin to condense (gene silencing)
Epigenetic Inheritance
Chromatin modifications do not alter the nucleotide sequence of the DNA but they can be heritable to future generations
modification s can be reversed unlike mutations
Explains why a identical twin may inherit a disease while the other does not
5.7 Biotechnology
Process of manipulating organisms or their components for the purpose of making useful products
Genetic Engineering techniques can be used to analyze and manipulate DNA and RNA
Gel Electrophoresis (DNA Fingerprinting)
Separates molecules according to size and charge (used for comparison)
DNA is process with restriction enzymes (molecular scissors) and cut into fragments of differing sizes
Smaller fragments travel faster through gel and larger fragments travel slower
DNA has a negative charge (migrates towards positive end)
Application
DNA Paternity Testing
Analysis of DNA profiles
DNA Profile/DNA “Fingerprint”
Polymerase Chain Reaction (PCR)
DNA fragments are amplified (manipulates DNA replication)
Automated process of denaturation, annealing, and extension in a series of repeated thermal cycles
Requires template DNA, Taq Polymerase (heat-stable DNA Polymerase), DNA primers and free nucleotides
Application
Consumer Genomics
Food and Agriculture
Medicine
Forensic Science
Environmental Microbiology
Genetic Research
Phylogenetics
Bacterial Transformation (Recombinant DNA)
Introducing DNA into bacterial cells
Bacteria can naturally conduct horizontal gene transfer (HGT)
Introduction of new genes from one organism to another
A driver of bacterial evolution and development of antibiotic resistance
Bacteria can naturally uptake foreign DNA from a dead bacterium via plasmid
Use as a Biotechnology (Insulin Production for Type 1 Diabetes)
Step 1: Cutting
Geen of interest is cut out by restriction enzymes
Restriction enzymes act like scissors cutting genes at restriction site (specific sequence)
Same restriction enzyme cuts the same sequence in plasmid
Step 2: Splicing
Gene of interest is inserted into bacterial plasmid
DNA Ligase forms bonds between gene of interest and plasmid, making recombinant DNA
Step 3: Integration and Reproduction
Recombinant DNA is put into bacteria (transgenic)
Bacteria rapidly reproduce with the new ability to express gene of interest
Application
Genetic modification of bacteria
Human insulin production
Human growth hormone production
DNA Sequencing
Determine the order of nucleotides in a DNA molecule
Application
Medical Diagnosis → genetic diseases, drug targets
Evolutionary Biology → relationship between different organisms and how they evolve
Forensics → DNA Profiling
Virology → identify and study viruses
CRISPR/Cas9
Gene editing system
CRISPR → “clustered regularly interspaced short palindromic repeats”
Short Prokaryotic DNA used to detect and destroy viral DNA
Cas9 → endonuclease enzyme that cuts at specific DNA sequences determined by CRISPR
Guide RNA (a short RNA sequence) to target a specific location on a DNA strand
Cas 9 then cuts the DNA which allows gene editing by inserting, deleting or modifying the DNA
Unit 6: Heredity
6.1 Meiosis
Meiosis: process by which haploid gametes are produced
Haploid → one set of chromosomes (n)
Gametes → sex cells (sperm and egg)
Sperm and egg will eventually combine to make a diploid zygote
Diploid → two sets of chromosomes (2n)
Zygote → diploid cell resulting from fusion of sperm and egg
Ploidity: number of sets of chromosomes in an organism
Haploid (n) or Diploid (2n)
Diploid zygote goes through cell division and differentiation
Chromosomes:
Human females have two X chromosomes in each cell
Human males have one X and one Y chromosome in each cell
Chromosomes are sorted in karyotypes in homologous pairs
Karyotype → picture of all chromosomes in a cell
Autosomes → chromosomes that are ot X or Y (humans have 22 pairs)
Homologous Pairs
Same size
Same centromere position
Contains the same genes at the same loci position on chromosome
Each chromosome can have different alleles
Alleles → alternative forms of the same gene
Come together to form a tetrad
How Sex Cells are Created: Meiosis
Cell division is 3D (duplicate, divide, divide)
1 diploid parent cell → 4 haploid daughter cells (all genetically different)
How is sex determined in humans?
SRY (Sex-Determining Region of the Y Chromosome) ← gene
Males: Early in development, the SRY gene on the Y chromosome activates and the gonads develop as testes
Females: With no SRY gene, the gonads develop as ovaries
Meiosis I
Cell growth takes place before meiosis 1 can begin
Homologous chromosomes separated
At the end of telophase I, cells have two copies of half the genetic information of the cell
Meiosis II
Sister chromatids separated
At the end of telophase II, cells have one copy of half the genetic information of the cell
Gametogenesis and Fertilization
6.2 Meiosis and Genetic Diversity
Meiosis creates genetic variation
Independent assortment → homologous chromosomes are randomly distributed to the four daughter cells
Possible combinations = 2n
Crossing-over increases variability, also known as recombination (mix and match)
Errors in Chromosome Distribution: Nondisjunction
Chromatids (or homologs) do NOT separate during the process resulting in daughter cells with either too many or too few
6.3 Mendelian Genetics
Mendel worked with pea plants to show genetics
P Cross (parental cross) → homozygous dominant bred with homozygous recessive
Results in F1 generation
F1 Cross → 2 hybrids
Results in F2 generation
Mendel’s Laws
Law of Segregation → random separation of two alleles (random chance)
Independent Assortment → traits on different chromosomes don’t affect each other (may travel together if on same chromosome)
Genotypic Ratio: ratio of the genotypes of offspring
For F1 cross
1:2:1 (AA, Aa, aa)
Phenotypic Ratio: ratio of phenotypes of offspring
For F1 cross
3:1 (tall:short)
6.4 Non-Mendelian Genetics
Many traits do not follow ratios predicted by Mendel's laws
Varying degrees of dominance (blend of traits)
Many traits are produced through multiple genes acting together
Some traits are produced by big genes on sex chromosomes
Some traits are the results of non-nuclear inheritance (ex: chloroplast and mitochondrial DNA)
Linked Genes
Genes located near each other on the same chromosome that tend to be inherited together
Violates Law of Independent Assortment
Genes for two or more traits are linked when they are expressed both by parents and offspring
Genes are very close on chromosomes and are often not separated when crossing over
Crossing Over/ Recombination Frequency
Frequency of which crossing over occurs between two genes on homologous chromosomes during meiosis
The closer two genes are on the same chromosome, the lower the probability that a crossing over event will occur and the lower the recombination frequency (close to 0 %)
The further apart two genes are on the same chromosome, the higher the probability that a crossing over event will occur and the higher the recombination frequency
Mapping Distance
Linkage map: genetic map that is based on crossover frequencies
The distance between the genes are MAP UNITS
One amp unit is equivalent to 1% recombination frequency
Express the relative distances among chromosomes
50% recombination frequency means that the genes re far apart on the same chromosomes or on two different chromosomes (unlinked genes)
Incomplete Dominance
Compromise (both traits blend to make final object)
Codominance
Both genes expressed equally and separately
Heterozygote Advantage
Heterozygote has an advantage over homozygous dominant and recessive
Ex: sickle cell anemia and malaria (AS is resistant to malaria and no sickle cell)
Multiple Alleles
Multiple alleles code for one trait, resulting in many possible phenotypes
Ex: eye color
Sex-Linked Genes
Genes on sex chromosomes
On Y chromosome
Only males can get it
On X chromosome
Recessive → less chance for females to get because they need 2 copies while males only need one copy
Ex: Red-green colorblindness
Dominant → if dad has disease, daughter will always have it
Polygenic Traits
Bell curve
Ex: flower color
AABB (4 dom) → dark red
AaBB, AABb (3 dom, 1 rec) → red
AaBb, AAbb, aaBB (2 dom, 2 rec) → pink
Aabb, aaBb (1 dom, 3 rec) → light pink
Aabb (4 rec) → white
Pleiotropic Traits
Single gene can influence multiple seemingly unrelated traits
Ex: Marfan’s syndrome
Episatsis
One gene overrides another/modifies another gene
Ex: yellow lab could have genetic potential to be black but this is overrode by another gene)
Ex: summer squash has two genes that code for shape but spherical shape gene overrides the long/round shape gene
6.5 Environmental Effects on Phenotype
Phenotypic plasticity occurs in individuals
Ability to change phenotype to adapt
Ex: Arctic foxes’ fur color
White in winter to camouflage with snow
Brown in summer to camouflage with woods and dirt
Ex: aquatic invertebrates helmets and tail spines
Grow longer when predators are nearby
No predators will result in adults with less armor
Boosts evolutionary fitness
Evolution occurs in populations over multiple generations
Unit 7: Natural Selection
7.1 Microevolution & Population Genetics
Variation → individuals in a population or group differ in some trait of interest
Inheritance → the variation in the trait of interest is at least partially inherited (passed down from parents to offspring). The variation stems from random mutations and the recombination that companies sexual reproduction. The genetic variation may have arisen many generations in the past
Differential survival and Reproduction → more offspring are born than can survive, resulting in competition among individuals within a population. Some individuals with a particular trait are more likely to survive and/or have relatively more offspring compared to individuals that do not have that trait. Selection depends on the specific context of a species. Traits that are beneficial in one environment may cause problems in another environment
Adaptation → the frequency of the trait that helps individuals survive or leave more offspring will increase in the population over time, as will the alleles that affect the trait. This process can take many generations and extend over a very long period of time.
Evolution in the change in the allele frequency of gene pool in a population over time
Microevolution
Small changes in allele frequency in a SINGLE POPULATION over time
5 mechanics of evolution
Macroevolution
Larger changes in multiple populations an explores COMMON ANCESTRY of different species
Ingredients for Evolution
Variation in heritable traits
Overproduction
Competition for limited resources
*Organisms with the greatest fitness will survive and reproduce → shift in allele frequency
Mechanisms of Evolution (the HOW)
Genetic Drift
Random chance event that equally affects all member of the population
Lowers genetic diversity and makes survivability more difficult
Founder Effect → a small group of an existing population leaves to colonize a new area
Consequences → if the alleles for rare, recessive traits are presented in high frequency in the new population, there can be a higher incidence of rare, recessive disease
Bottleneck Effect → sharp reduction in the population due to natural disaster
Ex: lancaster Amish Community and microcephaly
All families in an area are descended from one couple approximately 10 years ago that carried the genetic predisposition for microcephaly
Sexual Selection (Non-Random Mating)
Allele frequency shifts due to selection of mates based on physical characteristics/behaviors
Mutations
Random changes in allele frequency caused by changes in DNA sequence
Gene Flow (migration)
Natural Selection
Alleles that boost evolutionary fitness are selected for by an environmental factor
These processes change allele frequency non-selectively (random) or selectively for an allele
Population Genetics
Darin and Wallace developed natural selection
Endel helped improve understanding of genetic inheritance
Modern synthesis blends genetic and evolution
Connects to microevolution (population changing over time)
Macroevolution (new species and taxonomic groups)
Population Genetics
Polymorphisms are differences in phenotypes displayed, this distribution is known as population variation
Natural Selection, genetic drift, gene flow, mutation, nonrandom mating all leads to evolution of populations
Studied microevolution
Measures changes in how selective forces change population through changes in allele and genotype frequencies
Mutation → introduces new alleles/traits through random errors/changes in a DNA sequence
Non Random Mating occurs when embers of a population select their mating partner based on the presence of specific desirable traits
Genetic Drift → is the movement of alleles in or out of a population through migration
Gene flow describes how the fittest members of a population pass on their inheritable advantageous traits to their offspring
Natural Selection occurs when a random chance event (like a natural disaster)affects the allele frequency of small populations)
7.2 Natural Selection
Natural Selection → the improved fitness of certain individuals in the population that allows for survival and reproduction (primary mechanism by which populations change over time)
*The world “selects” (although not as a conscious decision) when environmental conditions allow organisms with a particular genetic trait to live healthier lives than other organisms. Populations of most living organisms exhibit genetic diversity among individuals. Certain traits in a population give some organisms a greater cache of survival than individuals that lack these traits. Because these traits tend to increase the chance of survival, these individuals within the population possessing the favorable trait increases while the number of offspring with the favorable trait decreases.
Adaptive Evolution
Natural selection is adaptive evolution, selects stabilizing phenotypes
Frequency-dependent selection selects for common or rare traits
Secual selection mans one sex has more variability in reproductive success
Stabilizing selection, directional selection and disruptive selection
Patterns of Evolution
Divergent evolution → same ancestor, becoming more different
Convergent Evolution → different ancestor, becoming more similar
Parallel Evolution → same ancestor
Coevolution → different ancestor
7.3 Artificial Selection
Artificial Selection → the effect of humans purposefully breeding animals to select fo desirable traits
Ex: breeding domestic animals (choose more tame traits)
7.4 Hardy-Weinberg Equilibrium
A population is in EQUILIBRIUM (and therefore not evolving) when all of the following are assumed
The population is large and diverse
There is no migration
There are no mutations
Mating is random
There is no natural selection
To determine whether a population’s gene pool is changing, allele frequencies must be calculated.
Two equations are used to calculate the frequency of alleles (presented as decimals) in a population:
p represents the frequency of the dominant allele
q represents the frequency of the excessive allele
Allele Frequencies (gene pool): p + q = 1
Says that if there are only two alleles for a gene, one dominant and one recessive, then 100% of the alleles are either dominant (p) or recessive (q)
Genotype Frequencies (population/individuals): p2 + 2pq + q2 = 1
Says that 100% of the individuals in the population will have one of these genotypes: AA, Aa, aa
7.5 Evidence of Evolution
How do we evaluate if a population is evolving?
The genetic definition of evolution is a change to a population’s gene pool
Gene pool is defined as “the total number of alleles present in populations at any given time
Homologous and Analogous Structures
Homologous Structures → occur in organisms that have the same shared ancestor and the structures are similar but have different functions
Analogous Structures → serve similar functions but arise in organisms that are not closely related and don’t share the same ancestor
Theory of Evolution
Analogous Homologies
Morphology (physical structures)
Vestigial Structures → no longer have a purpose in current-day organisms but did in the past
Fossil Record
Relative Dating → older at the bottom, younger at the top
Radioactive Dating → Carbon dating, half-lives
Embryological Homologies
Sonic Hedgehog Protein → found in vertebrate and invertebrates involved in a signal transduction pathway for embryological development
Molecular Homologies
Cytochrome C → a protein involved in the electron transport chain
7.6 Continuing Evolution
Changes in fossil record
Changes in Genome (mutation, jumping genes, transposons, alternative splicing,. “Extinction” of deleterious genes)
Development of genetic resistances
7.7 Phylogeny & Common Ancestry
Cladograms
Evolutionary tree that depicts relationships between species based on physical and biochemical similarities (shows macroevolution)
Macroevolution → overtime, evolution can lead to SPECIATION
Formation of a new species from a common ancestor
Occurs when 2 populations become REPRODUCTIVELY ISOLATED from each other (can’t reproduce and make viable offspring)
Macroevolution observed speciation/extinction events and common ancestry
What is a common ancestor?
A species of organism, from which one or more new species evolves
ALL living organisms share a distant common ancestor as they all share the same fundamental molecular and cellular features (ex: central dogma, anaerobic respiration, fermentation, DNA, glycolysis)
All living EUKARYOTES share distant common ancestor as evidence by the fact that they all
Have membrane-bound organelles
Contain linear chromosomes
Have genes that contain introns
How closely 2 species are related depends on how recently they shared a common ancestor
More recent common ancestor → more related to each other
Less recent common ancestor → less related to each other
Common ancestry is illustrated in diagrams called CLADOGRAMS
Phylogeny
Study of history of evolution in a group of organisms
Cladograms
Illustrated common ancestry
DOES NOT take into account time
Phylogenetic Tree
Illustrated common ancestry
DOES take into account time
Shows the traits that separate one group of organisms from another
Constructing Cladograms
Each line represents a lineage
Each branch point is a node
Nodes represent common ancestors
Nodes and all branches from it are called CLADES
Species in a clade have derived features
The ROOT is the common ancestor of ALL the species
Parsimony
Can be SEVERAL arrangements in a cladogram that are all supported by the data
Use the SIMPLEST cladogram with the least amount of evolutionary changes/forks in the road
Outgroup vs Ingroup
Ingroup → set of organisms under study
Outgroup → more distantly related group of organisms that serves as a companion group when determining the evolutionary relationship of the ingroup
*RELATIVE
7.8 Speciation
Species → individual organisms can interbreed AND produce fertile offspring
Speciation → formation of two species from one original species due to REPRODUCTIVE ORGANIZATION
Allopatric
“Other homeland”
Occurs when a geographic barrier forms, splitting 2 populations
Sympatric
“Same homeland”
Individuals of a single population develop a genetic polymorphism (difference) WITHOUT geographic isolation
Adaptive Radiation
One ancestral species branches into many, each occupying a different NICHE (ecological role or habitat)
Reproductive Isolation (What prevents species from interbreeding?)
Prezygotic Barriers (blocks reproduction from taking place at all)
Temporal Isolation → breeding at different times
Mechanical & Gamete Barriers → anatomy and sperm/egg problems
Habitat Isolation → living in different place
Behavioral Isolation → mating and courtship behavior
Post Zygotic Barriers
Egg and sperm produce offspring that don’t survive or are sterile
Hybrid → cross between two species (often results in infertile offspring → result of post-zygotic barrier)
Rates of Speciation
Gradual speciation → slow change, small steps, relatively stable environment
Punctuated Equilibrium → rapid change, due to major environmental disruption
7.9 Extinction
Extinction → permanent loss of species
Causes
Habitat Loss/Destruction → Deforestation, urbanization, pollution
Invasive Species → Non-native species outcompete or prey on native ones
Overexploitation → Overhunting, overfishing, poaching
Climate Change → Alters ecosystems; species can’t adapt quickly
Natural Disasters → Volcanoes, asteroid impacts, etc.
Genetic Bottlenecks → Loss of genetic variation casuing reduced adaptability
Ecology
8.1 Responses to the Environment
Ecology → the study of the relationship between living organisms and their environment
Biotic Factor → any LIVING factor in an organism’s environment (ex: producers, consumers, decomposers)
Abiotic Factor → any NON LIVING factor in an organism's environment (ex: temperature, water, sunlight, soil oxygen, pH levels, CO2 levels)
Levels of Organization
Organism → individual living and responding to their environment
Population → group of interbreeding individuals living in the same location
Community → different species interacting with abiotic factors
Ecosystem → biotic factors interacting with abiotic factors
Biome → a group of ecosystems that share the same climate and have similar types of communities
Biosphere → global sums of all ecosystems and living things
Habitat vs Niche
Habitat = address, Niche = occupation
*Niche reflects an organism’s ROLE in the ecosystem (how the organism uses or interacts with different biotic and abiotic factors in its environment)
Ethology → study of animal behavior
Behavior → actions performed in response to a stimulus
Both genetic and environmental factors
Essential for survival and reproduction
Subject to natural selection over time
How do organisms sense changes in the environment?
Cues that are visual (sight), auditory (hearing), physical (movement/touch), chemical (pheromones), phototrophic (circadian rhythm)
Overlap of Niches
Results in competition over resources
Competitive Exclusion Principle → suggests that species with identical niches cannot coexist indefinitely an competition will result in natural selection
Results in a displacement of one species (NICHE PARTITIONING) → species occupy different niches to avoid competition (usually RESOURCE PARTITIONING → To not compete over one resource)
How do organisms respond to their environment?
Organisms are in constant interaction with their environment and each other
They can respond behaviorally or physiologically (via internal mechanisms)
Responses to Environment
Responses to One Another
Types of Communication
Animal-Specific Communication
Innate, Learned and Cooperative Behaviors
Innate → developmental fices and closely controlled by genes (littke to no environmental influence)
All members of the species perform the behavior in the same way
Usually involve basic life functions (finding food, caring for offspring)
Learned Behaviors → result of experience
Learned behaviors are adaptive because they are flexible and can change if environment changes
Specific behavior may not be passed onto the next generation but ability to learn is passed down
Many complex ways that animals can learn (spatial learning, associative learning (conditioning), observation, insight learning)
Cooperative Behaviors → increase fitness of the individual and increase survival of the population
Pack behvior in animals
Herd, flock and schooling behaviors in animals
Colony and swarming behavior in insects
Kin Selection → Favors altruistic behavior (that reduces the individual organism’ fitness) by enhancing the reproductive success of relatives
Lowers fitness of individual but increases fitness of another individual
Kin selection allows for the fitness of a family member to increase
8.2 Population Ecology — Population Dynamics
Populations are composed of individual organisms of the same species
Population Growth
Depends on
Birth rate (B)
Death rate (D)
Population Size (n)
Birth rate greater than death rate → population increases
Birth rate less than death rate → population decreases
Birth rate equal to death rate → population stays stable
8.3 Population Ecology — Effect of Density of Populations
Exponential growth
No constraints on the population
Creates huge populations
Only possible when infinite natural resources are available
Biotic Potential → highest rate of natural increase for a population when resources are unlimited
Logistic Growth
Shows that there is something that limits the populations size
Seen in real life
Limiting Factor → biotic or abiotic factor that restricts the number, distribution or reproduction of a population within a community
Density-dependent Factors → impact of the factors depends on how dense the population is (ex: space, resources, disease predation, competition)
Density-independent factors → affect populations in the same way, regardless of density (ex: natural disasters, extreme temperatures, rainfall, seasonal cycles)
Tolerance → an organism’s ability to survive biotic and abiotic factors
Carrying Capacity → sustainable abundance of a species that can eb supported by the ecosystem’s total available resources
Determined by limiting factors
Prevents true exponential growth
Population growth generally overshoots carrying capacity and then settle around carrying
8.4 Community Ecology and Biodiversity
Biodiversity
Genetic diversity within a population
Species diversity within a community
Ecosystem diversity (number of different habitats and ecosystems in a given area)
Genetic Diversity in Populations
Population’s ability to respond to changes in the environment is affected by genetic diversity (species and populations with little genetic diversity are at risk of decline or extinction)
Low genetic diversity
Similar susceptibility to hereditary health problems, potential pathogens or environmental changes (may lead to population collapse)
Often genetically similar as sibling or cousins
Genetic diversity allows individuals in a population to respond differently to the same changes in environmental conditions
More likely to contain individuals that can withstand environmental pressure
Species Diversity
Variety of different species within a specific area and has two components
Species richness → measures the total number of species in the community. High richness leads to high diversity
Species evenness → measures the relative abundance of each species. More evenly represented species make up a more diverse ecosystem
Simpson’s Diversity Index
Gives the probability that two individuals randomly selected from a community will be different
The higher the value, the more diverse the community
1 represents high diversity: all individuals in this community are from different species
0 represents no diversity: all individuals in this community are the same species
Community Interactions
How species and populations interact with each other affect the distributions and abundance of populations
Types of Interactions
Niche Partitioning
Competing species use the environment differently in a way that helps them coexist
When species shift niches, they no longer directly compete
Competitive Exclusion → no two species can indefinitely occupy the same niche at the same time
Over time, either one population replaces the other or the two species evolve to occupy different niches
If it appears two species occupy the same niche, there must be slight differences
Specifically called resource partitioning when they use different resources
Keystone Species
An organism that plays a unique and crucial role in the way an ecosystem functions
Without a keystone species, the ecosystem would be dramatically different or cease to exist altogether
The effects of keystone species on the ecosystem are disproportionate relative to their abundance in the ecosystem
A small number of keystone species can have a large impact on the environment
When they are removed from the ecosystem, the ecosystem often collapses
Predator/Prey Population Changes
Reasons for peaks and valleys with the predator population lagging slightly behind the prey:
The biotic potential of the predator may be great enough to over consume the prey, the prey population declines and the predator population then follows
The biotic potential of the prey is unable to keep pace and the prey population overshoots the carrying capacity and suffers a crash
Trophic cascades can also occur, where the impact of a predator on its prey’s ecology trickles down one more feeding level to affect the density and/or behavior of the prey’s food source
8.5 Ecosystem Ecology — Energy Flow and Nutrient Cycling
All organisms require free energy and matter to organize grow, reproduce and maintain homeostasis
*Energy FLOWS, matter CYCLES
Energy
To offset entropy, energy input has to exceed energy lost from and used by an organism to maintain order (laws of thermodynamics)
Energy converted from one type to another
Energy deficiencies are detrimental to individual organisms and cause disruptions to populations and ecosystems
Matter
Matter cycles between various inorganic and organic forms within the environment but DO NOT leave the ecosystem
Organisms need matter (nutrients/mass) to build their macromolecules and maintain systems within their cells
Main elements needed to make organic compounds → Carbon, Hydrogen, Oxygen, Nitrogen, Phosphorus, Sulfur
Organisms lose matter to environment through cellular respiration
Matter moves between environment and organisms through BIOGEOCHEMICAL CUES
Importance of Energy in Organisms
Growth, reproduction, and the maintenance of homeostasis all require a constant input of energy
\Many reactions inside of the organism and their cells require energy (endergonic processes)
Protein synthesis
Active transport
Muscle contraction (in animals)
Maintaining concentration gradients
Cell division
Cell signaling
Gene expression
Changes in energy levels over time determine the fate of the organism
Net Gain of Energy → energy is stored (as fat, glycogen o starch) and growth of the organism
Net Loss of Energy → loss of mass and ul;timatly the death of the organisms
Classifying Organisms by Role in Energy Flow
Organisms have different roles in cycling matter and transferring energy
Reproductive Strategies in response to Energy Availability
Different organisms use various reproductive strategies in response to energy availability
LIFE HISTORY STRATEGY → describes the series of events over and organism's lifetime, such as how resources are allocated for growth, maintenance and reproduction
A species’ life history is genetically determined and shaped by the environment and natural selection
The amount of energy available to the organism and the stability of the environment heavily influence its life history and fitness
*Spectrum that differs in how much ENERGY a parent devotes to each offspring
Alternating between Asexual Reproduction and Sexual Reproduction
Some orgnaisms can rpedice both asexaulyl and sexually
Sexual reproduction requires a mate and organisms often invest energy in order to acquire a mate
Ex: jellyfish and sponges
Plant Life Cycles: Annuals, Biennials, Perennials
Flowering plants are generally split into three reproductive categories based on their lifespan and the energy they devote to each part of their life cycle
Annual Plants
Favored when adult mortality is higher than seed or seedling mortality
Plants invest all their energy into the production of offspring
Dominate environments with disturbances that reduce adult survival (climates with dry summers and regions with high variability year to year)
Common early species in ecological succession
Terrestrial ecosystem is disturbed → pioneer species (lichen, fungi) often followed by annual plants
Grow and spread quickly in disturbed environment
Regulating Body Temperature and Metabolism
Animal can be split into two categories based on how they regulate their body temperature
Regulation directly relates to their energy usage, metabolism and rate of cellular respiration
Metabolism → set of life-sustaining chemical reactions that take place inside cells and bigger structures, requires ENERGY to maintain
Representing Energy Flow
Food Chain → follows a single path of energy flow
Food Web → follows many paths of energy flow
More accurate depiction
Shows how all organisms are interdependent on others
Shows the multiple means by which organisms obtain energy
Shows the dependence on producers
Allow for the prediction of the effect of a change to a system
*Depending on the food chain, organisms have multiple trophic levels, making food webs hard to label by trophic level
Trophic Levels
Indicator of feeding level or position n the food chain
(Primary) producer
Primary consumerSecondary consumer
Tertiary Consumer
Quaternary Consumer, etc
Dependency on Primary Productivity
Food webs and chains dependent on primary productivity
Producers (photosynthetic and chemosynthetic organisms) are the base of food chains and webs
Without the organisms, no new energy would be captured/new energy won’t enter the system
Change in producer level affects the number and size of other trophic levels
Ecological Pyramids
Representations of the flow of energy and matter in an ecosystem
Represent a single food chain and are organized by trophic level
Producers on bottom
Primary consumers 2nd level
Secondary consumers 3rd level…
Energy is lost at each trophic level (lower level will have more energy)
Some energy lost as HEAT due to metabolic processes
Energy also lost due to incomplete digestion of food and excretion of waste products
Each level had 10 PERCENT of the energy form the previous level (10% rule)
Largest population funda the bottom
Fewer and fewer individuals at each level (related to the loss of energy)
Amount of biomass decreases at each trophic level (related to loss of energy and numbers)
Biomass → how much matter is made up by living organisms
Biogeochemical Cycles
Flow of nutrients from lying to non living components p Earth
Chemicals sometimes sequestered for long periods of time and taken out of circulation
Reservoirs → locations where elements are stored for long periods of time
Eac cycle demonstrated the conservation of matter
Cycles are interdependent and connected to each other
Each cycle includes matter cycling between abiotic and biotic reservoirs and the processes that cycle matter between reservoirs
Bio → organisms
Geo → inorganic processes
Chem → reactions
Water Cycle
Major Processes
Precipitation → condensed water vapor falls to earth as rain, now, sleet, hail
Evaporation → transformation of water from liquid gas from the ground or bodies of water into the atmosphere
Transpiration → release of water from plants into the air
Condensation → water from gas to liquid water droplets in air, creating clouds and fog
Major Reservoirs
Oceans
Surface Water
Atmosphere
Living Organisms
Water is Necessary for…
Components of the cell (ex: cytosol)
Photosynthesis
Hydrolysis
Carbon Cycle
Major Processes
Photosynthesis → fixes CO2 into organic carbon compounds (ex: g;ucose and other carbohydrates); removes CO2 from atmosphere and water reservoirs
Cellular Respiration → break down organic compounds and releases CO2 into atmosphere or water reservoirs
Decomposition → the decay of organism by decomposers releases CO2 back into the atmosphere, soil, or water
Combustion → burning of fossil fuels releases stored CO2 into the atmosphere
Major Reservoirs
CO2 in the atmosphere
CO2 dissolved in water
Organic compounds in living organisms (including forests, animals, etc)
Fossil fuels and sedimentary rock (take many years to form)
Molecules that require carbon:
All organic molecules, including carbs, lipids, protein, nucleic acids
Nitrogen Cycle
Major Processes
Nitrogen Fixation → nitrogen gas (N2) is fixed into ammonia (NH3) which ionizes into ammonium (NH4+) by acquiring hydrogen ions from the soil solution
Nitrification → bacteria convert ammonium (NH4+) via nitrite (NO2-) into nitrate (NO3-) by acquiring hydrogen ions from the soil solution
Assimilation → plants absorb nitrate from soil to make organic molecules
Ammonification → bacteria/fungi convert organic nitrogen from organisms into ammonia
Denitrification → bacteria convert nitrate (NO3-) back into nitrogen gas (N2)
*Steps performed by microorganisms in the soil
Major Reservoirs
Atmosphere (largest → 78% nitrogen)
Soil
Living Organisms
Molecules that require nitrogen
Proteins
Nucleic Acids
Phosphorus Cycle
Major Process
Rock Weathering → the weathering of rocks release phosphate (PO4>3-) into soil and groundwater
Producers take in phosphate
Consumers eat producers and/or each other
Excretion → returns phosphates back to soil ia the release of waste by organisms
Decomposition → returns phosphates back to soil
*Phosphorus is often the LIMITING NUTRIENT in ecosystems (nutrient in shortest supply due to the slow weathering of rocks)
Major Reservoirs
Rocks, ocean sediments
Soil
Groundwater
Ocean
Living Organisms
*Only cycle without an atmospheric reservoir
*Most phosphorus is recycled within a community
Molecules that require phosphorus
Nucleic acids
Phospholipids
8.6 Disruptions to Ecosystems
Natural Changes in Ecosystems
Geological and meteorological events affect habitat change and ecosystem distribution (biogeographical studies illustrate these changes)
Humans have also cause environmental changes though logging, urbanization and monocropping (practice of growing a single crop on the ame land year after year → lead to soil degradation, pests, disease)
Genetic Variation in Changing Environments
Affects how well population respond to changes in their environment
More genetic variation/diversity → more lilly individuals will survive and reproduce in the new environment
Adaptations that are advantageous in one environment might not be advantageous in another
Ex: Polar Bears well adapted to cold weather and living on the ice in the Arctic → not well adapted as global warming melts the ice
Changes in the environment cannot cause specific mutations, as mutations are not directed b specific environmental pressures
Ex: Global warming will not cause mutations in polar bears (if polar bears have variation that help them survive and reproduce in new environment, then it will have higher fitness than other polar bears)
Heterozygote Advantage → when heterozygous genotype has a higher relative fitness than homozygous genotype (dependent on particular environment)
Human Impact on Ecosystems
Human populations increase → impact on habitats for other species magnified → reduced population size of affected species, resulted in habitat destruction and extinction of species
Biogeochemical Cycles
Humans affect the biogeochemical cycles of ecosystems (especially carbon, nitrogen and phosphorus cycles)
Fertilizers, animal waste, and sewage are adding more nitrogen and phosphates to the water, result in eutrophication
Eutrophication → water pollution from nitrogen-rich and phosphorus-rich substances flowing into waterways, causing algal overgrowth
Algal blooms block sunlight from organisms below and when the algae dies, decomposer suse up O2 as they break down the algae
When fossil fuels are burned, sulfur dioxide and nitrogen dioxide are released into the atmosphere which reacts with water to form acid precipitation
Acid Precipitation → su;fur dioxide and nitrogen dioxide react with water to form sulfuric acid and nitric acid which fall to earth in rain, sleet, snow or fog
Acid Rain weakens tees by dissolving nutrients (like calcium and potassium) in the soil before pants can use them
Trees more susceptible to infections and damage from insects and cold weather
pH of lakes and streams decreases → affect the health of aquatic organisms
Climate Change
Broad range of changes seen in our planet (caused by greenhouse effect)
Naturally live in a greenhouse effect or planet would be much colder
Certain gases block heat from escape (water vapor, carbon dioxide, methane, nitrous oxide, and chlorofluorocarbons)
Burning of fossil fuels increases concentration of greenhouse gasses (block more what from escaping)
Why does it matter?
Temperatures will continue to rise
Frost-free season (and growing season) will legnhten
Changes in precipitation patterns’mroedroughts and heat waves
Hurricanes will become stronger and more intense
Sea level will rise 1-4 feet by 2100
Arctic likely to become ice-free
Pesticides and Chemicals
People use pesticides and chemical everyday
Runoff (movement of land water) usually carries these pesticides from the fields into watershed
Biomagnification
Toxic chemicals and heavy metals flow into ocean when industrial;, agricultura; and human wastes run off or are deliberately discharged inot rivers that then empty inot the sea
Pollutants can cause disease, genetic mutations, birth defect, reproductive difficulties, behavioral changes, and death in many organisms
Severity of damage varies between species
Animals near the top of the food chain usually the most affected due to biomagnification
Toxic compound are digested so they accumulate in the animals that injst them
Become more and more accumulated as they pass along the food chain as animals eat and in turn are eaten
High level predators build up greater and more dangerous amounts of toxic materials than animals lower on the food chain
Invasive Species
Organisms that are introduced (by international or unintentional human action) to an area where they do not naturally live and breed
Often have no competition or predation to control their population (very few limiting factors) and experience exponential growth
Plants and animals in the area have no adaptations to protect themselves from the new species
Often devastated the ecosystems to which they are introduced
No natural predators, parasites, pathogens
Little limitation on resources
No environmental inhibitors (pollutants)
Available nice not occupied by any other species → no successful competitor
Prey lack effective defense mechanism against introduced species
Appropriate environmental conditions (rainfall, temperature)
Human-Caused Extinctions and the Sixth Major Extinction Event
Always background extinction rates (“normal” extinction) but modern extinction raters are exceptionally high and continually increasing
Current extinction rates are 35 time higher than expected background rates prevailing in the last million years under the absence of human impacts
Groups (genera) lost in the last 500 years would have taken some 18,000 years to vanish in the absence of human beings
We have seen 543 land vertebrate species go extinct between the years 1900 and 2000 ecosystems become more fragile when high numbers of animals go extinct