Unit 5: DNA, Protein Synthesis and Cell Division
DNA: a molecule that carries the genetic instructions
Double helix
Composed of nucleotides
Each nucleotides contains a deoxyribose sugar, a phosphate group and a nitrogen base
Nitrogen bases can be adenine (A), thymine (T), cytosine © or guanine (g). Adenine only bonds to Thymine, Cytosine only bonds to Guanine
Bonds
Nucleotides: Covalent bonds
Base pairs: Hydrogen bonds
Chargaff’s rules:
The amount of guanine should be equal to the amount of cytosine and the amount of adenine should be equal to the amount of thymine
Therefore… A binds with T, and C binds with G
Purine: Adenine and Guanine
Pyrimidines: Cytosine and Thymine
Purine only binds with Pyrimidines because the diameter of DNA should be constant (3 rings)
DNA Replication
Why/When?
New cell must have complete genetic informations so DNA must be replicated
Steps
Unwind/unzip/separate ⇒ break H bonds between Nitrogen bases
Add complementary bases to each side ⇒ form H bonds between Nitrogen bases
Connect the backbone ⇒ form covalent bonds between sugars and phosphates
DNA Replication is considered semiconservative because half of the DNA is conserved.
All these steps are possible due to enzymes!
For split/unzip/separating -> Helicase
For adding complementary bases -> DNA Polymerase
For connecting the backbone -> Ligase
Making Proteins
DNA contains genes
Gene: a segment of DNA that code for a particular trait.
Each gene contains the directions to make one protein that gives you a particular trait.
Ex. Melanin: protein that determines your eye color.
DNA is located in the nucleus and cannot leave.
Proteins are assembled by free ribosomes in the cytoplasm or on the endoplasmic reticulum.
Because DNA is too large to go directly to ribosomes for protein production, it must be changed to RNA (Ribonucleic Acid) before it becomes a protein.
DNA vs. RNA
RNA is different from DNA in that:
It has one strand instead of 2
It has nitrogen base Uracil (U) instead of Thymine (T)
It has sugar Ribose instead of Deoxyribose
3 Types of RNA
mRNA (Messenger RNA)
Carries message from nucleus
DNA cannot leave the nucleus so a temporary simplified copy of a gene is made
Codon: 3 base pairs of mRNA
tRNA (transfer RNA)
Transfers an amino acid to growing protein
One end holds an amino acid
One end has the anticodon
rRNA (ribosomal RNA)
Makes up ribosomes
Steps of Protein Synthesis:
Transcription - a gene in DNA is “transcribed” into mRNA in the nucleus
Steps of Transcription
RNA polymerase “unzips” a gene in DNA
RNA polymerase attaches RNA nucleotides to the exposed DNA strand using the base pairing rules
RNA polymerase detaches at the end of the gene.
Translation - the segment of mRNA is “translated” into a amino chain (aka protein) on a ribosome
Steps of Translation
The mRNA (made by transcription) exits the nucleus and binds together with a ribosome.
A tRNA carrying methionine binds to the start codon
Codon: set of 3 mRNA nucleotide bases codes for 1 amino acid
Anticodon: the part of the tRNA that binds to the codon.
AUG = start codon (methionine)
A tRNA carrying the amino acid specified by the next codon binds to the mRNA strand. The amino acids bind together with a peptide bond.
The process continues until one of the three “stop” codons appear.
How is RNA used to make a protein?
Each set of 3 mRNA nucleotides bases (codon) codes for 1 amino acid
To determine which amino acid is coded for, we use the genetic code.
Mutations
Gene Mutations
A problem at the nucleotide level.
One gene involved
One gene = one enzyme/protein
Ex. The boy ate pie
Point Mutations: mutations that occur at ONE point/base pair. Usually only one messed up amino acid.
Substitution
Ex. Substitution: The boy ate pie -> The boy ate pee
Some substitutions are not a big problem because of wobble.
Wobble: several codons code for the same Amnio Acid
Frameshift mutation: usually mutations that result in many incorrect amino acids from point of mutation on.
Additions or deletions
Cell Cycle
DNA exists in two forms: Chromatin and Chromosomes
Binary Fission: Cell Division in Prokaryotes (Bacteria and Archaea); Asexual Reproduction; Results in 2 genetically identical daughter cells (clones)
For eukaryotes…
Cell Cycle
Cell undergo Interphase where they grow and replicate their DNA.
Mitosis: division of the nucleus or Meiosis
Cytokinesis: division of the cytoplasm
C words:
Chromatin: Not condensed DNA
Chromosome: condensed DNA
Chromatid:
Centromere:
We count # of chromosomes by # of centromere so the number of chromatid doesn’t matter.
The duplicated chromosomes are called sister chromatids.
Body/Somatic Cells
Diploid (2n)
46 Chromosomes
Made by mitosis
Gametes/sex cells
Haploid (n)
23 Chromosomes
Made by meiosis
Autosomes: 22 pairs of chromosomes that are common between egg and sperm producers.
Sex chromosomes: 23rd pair of chromosome that determines the biological sex.
Mitosis steps
Prophase
Chromosomes condense
Spindle fibers form
Nucleus and nucleolus disappear
Metaphase
Chromosomes line up in the middle
Anaphase
Centromeres split
Sister chromatids separate to opposite sides of the cell.
Telophase
New nuclei form
Chromosomes begin to uncoil.
If Cytokinesis happens, it begins here.
After cytokinesis…
We end up with 2 daughter cells that are clones.
Karyotypes: visual display of an organism’s chromosomes
Why does Karyotypes matter?
Chromosome abnormalities (NOT DNA mutations)
Too few, too many, too short, too long
Biological sex
Credit:Matthew Meng
Meiosis: sex cell reproduction
Leads to variety in organisms that can be inherited
Occurs only in sex cells (gametes)
Sperm cell (male) and egg cell (female)
Goes through interphase just like mitosis
DNA replication occurs →Chromosomes become sister chromatids
Contains 2 steps: meiosis I and meiosis II
Meiosis I: leads to a haploid cell
Same steps as mitosis: PMAT
Prophase I
Nuclear membrane disappears
Chromatin → chromosomes
Centrioles go to opposite sides
Synapsis: homologous chromosomes pair up
Same chromosome from mother and father pair up
This combination is a tetrad (XX shaped)
Consists of 4 chromatids (I shaped)
Crossing over: the 1st form of genetic variation
Tetrads exchange sections of genes at the chiasmata
Forms recombinant chromatids
Metaphase I
Tetrads line up on metaphase plate
Independent assortment: the 2nd form of genetic variation
Tetrads line up randomly, so when they get split, end up in different gametes
Anaphase I
Homologous chromosomes of the tetrad split apart (X and X)
Moves to their centrioles
Telophase I
Nuclear membrane reforms
Nucleolus reforms around isolated sister chromatids
Result: 2 cells with 23 replicated chromosomes (X shaped)
Meiosis II: literally just mitosis
Starts with 2 haploid cells
Separates sister chromatids
Maintains the same haploid number of chromosomes
Result: 4 cells 23 unreplicated chromosomes (I shaped)
Result of meiosis: 4 genetically different haploid daughter cells
Haploid is half the number of a diploid cell (2n)
Human cells usually have 46 chromosomes diploid
Becomes 23 after meiosis
Diploid is usually what the normal cells are (chromosomes from both dad and mom)
Haploid is either dad or mom
When haploid gametes combine into a zygote (fertilized egg) their chromosomes will combine to make diploid again
Random fertilization: the 3rd form of genetic variation
Any random sperm can fertilize any random egg
Crossing over and independent assortment leads to variety of gametes, random fertilization creates a random offspring out of it
4 daughter cells are genetically different due to the 3 forms of genetic variation
Gametogenesis: the production of gametes that uses meiosis
Oogenesis: production of egg cells
Cytoplasm is not evenly split after meiosis
3 polar bodies are nonfunctional, leaving 1 functional egg
Spermatogenesis: production of sperm cells