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Year 10 Biology

Cells and Organelle

  • All living organisms are made up of cells

  • Cells are the building blocks for life

Organelle Name

Function

Cell Membrane

  • Barrier/gatekeeper

  • Controls what enters and exits

Cell Wall

  • Gives plant structure and shape

  • Only in plants/fungi

Cytoplasm

Jelly like material that other organelle are suspended in

Mitochondria

For cellular respiration and energy production

Chloroplast

  • Where photosynthesis happens

  • Only in plant cells

Vacuole

Stores waste

Ribosomes

Where amino acids combine creating proteins

Endoplasmic Reticulum

  • Provides surface for chemical reactions

  • Channels for transporting molecules

Golgi Body/Apparatus

Modifies proteins in ribosomes and packages before sending them to secretion cell

Nucleus

Contains DNA

Lysosomes

Contains digestive enzymes, able to break down large molecules

Centrioles

Very important for cell division

Plant Cells vs Animal Cells

  • Different Shapes

  • Plant cells contain:

    • Cell walls

    • Chloroplasts

    • Larger Vacuoles

DNA (Deoxyribonucleic Acid)

  • Carries genetic information determining the structure of cells and the way if functions

  • Chemical code that the cell uses to produce proteins enzymes

  • Found in both the mitochondria and the nucleus

  • A polymer - a substance made up of a large number of small substances joined together

  • Nucleotides

    • Make up DNA

    • Monomers - the smallest base units of a substance

    • Made up of a phosphate group, a sugar and a nitrogen base

  • 4 Nitrogenous Bases

    • Adenine (A)

    • Thymine (T)

    • Guanine (G)

    • Cytosine (C)

      • A and T can only bond

      • C and G can only bond

  • Protein Synthesis

    • Order of base pairing represents a code for making proteins

  • Nucleotides form a ladder (double helix structure)

    • Sugar and Phosphate form the uprights

    • Nitrogenous bases form the rungs

  • Watson and Crick were the two scientists who finalised this model

  • Replication

  • Chromosomes consist of DNA coiled around a protein (Histone)

  • Chromosomes can consist of 1 or 2 strands of DNA

  • The strand is called a chromatid

  • Cells divide to replace old/dead/damaged cells and create new ones so organisms can grow

  • Cell Division

    • New cells created are called Daughter cells and they need to have an exact copy of DNA from the Parent cell

      • DNA Replication is the first step of cell division and it ensures inherited information is passed on unchanged when new cells are formed

  • The 2 linked chains of DNA molecules separate or unzip and this is controlled by an enzyme called DNA helicase

  • Unzipped DNA molecule now has the bases exposed and they serve as a template for the nucleotides that will form the new half

  • DNA polymerase move along the exposed strands and adds complementary nucleotides to each nucleotide in each existing strand

Mitosis

  • the process of division of the nucleus of a cell in which the two daughter nuclei have the same number and type of chromosome as the parent nucleus

  • makes daughter cells, which have identical copies of parent cell DNA

  • imperative for growth and repair of the body

  • happens for the first 22 pairs of chromosomes

    • before mitosis happens DNA replication takes place

    • interphase happens next, which is also not apart of Mitosis, the replicated DNA coils up forming chromosomes

4 Stages of Mitosis

  • Prophase

  • Metaphase

  • Anaphase

  • Telophase

Prophase

  • centrioles become visible and migrate to opposite poles, producing spindles which grow towards the chromosome

  • the nuclear membrane breaks down and the chromosomes become visible and they move to the centre of the cell

Metaphase

  • the chromosomes create a line on the cell equator and the spindle fibres attach to the centromere of each chromosomes

Anaphase

  • the spindle fibres retract back to the centrioles, separating the chromosomes into chromatids, pulling them to the poles of the cell

Telophase

  • nuclear membrane reforms and spindle fibres breakdown

Cytokinesis

  • the cell membrane and cytoplasm splits into two new cells

This leaves you with 2 exact replicas of the parent cell

Meiosis

  • Diploid cells

    • a body cell contains 2(set/pair) of chromosomes

    • referred as 2n with n= number of different chromosomes

  • Haploid cells (half)

    • in a gamete (sperm/egg cell) there is a haploid number of chromosomes

    • referred as n

    • amount of sets

  • Process of cell division that produces gametes (sperm/ova)

  • Gametes have half the amount on chromosomes that a body cell has

  • Homologous Chromosomes

    • pairs of chromosomes that are identical in size/shape/genes

    • each member influences the same characteristics

  • Aim of Meiosis

    • to produce haploid cells from diploid body cells

DNA Replication happens making 4 strands of DNA instead of 2 and then Interphase happen.

Meiosis 1:

Practically the same a Mitosis but is different Prophase 1

  • Prophase 1

    • Crossing over between chromatid pairs happens changing the genetic make-up

  • Metaphase 1

  • Anaphase 1

  • Telophase 1

  • Cytokinesis 1

Meiosis 2:

Is the same as Mitosis

Summary:

Meiosis is a type of cell division used to produce the gametes. It has 2 rounds of division used to create 4 haploid cells. The daughter cells are GENETICALLY DIFFERENT.

Meiosis lMeiosis llCrossing Over

Genes and Alleles

  • Karyotype

    • the full set of chromosomes in a cell

    • in humans, the karyotype of a normal cell shows 46 chromosomes in 23 pairs

    • the 1st 22 pairs are autosomal

    • the 23rd pair are sex chromosomes

    • males have an X and a Y chromosomes

    • females have 2 X chromosomes

  • Inherited Traits

    • a trait is a distinguishing quality or characteristic, typically one belonging to a person

  • Gregor Mendel

    • father of genetics

    • worked on pea plants and concluded how genetics work, genes exist in pairs (one from each parent) and they can separate and form pairs again in the next generation

  • Genes

    • a sequence within the DNA which codes for the production of a protein and this determines a trait

    • difference between genes is the order of nitrogenous bases

  • Alleles

    • an alternative form/variation of a gene

    • the different possibilities for a given trait

    • each chromosome contains alleles, or different variations of the same gene

Chromosomes pair up as Homologous Pairs

  • they’re the same shape/size

  • carry genes controlling the same traits

Monohybrid Crosses

  • Dominant and Recessive

    • a dominant allele will mask the trait of a recessive allele (represented by capital letter)

    • a recessive allele will only be expressed if a dominant allele is not present (represented by lower case letter)

    • e.g. T= curly, t= straight

    • Tt or TT = curly

    • tt = straight

  • Genotype

    • genetic make up of an organism; the gene (or allele) combination an organism has

    • e.g. Tt, tt, TT

  • Phenotype

    • physical characteristic of an organism; the way the organism looks

    • e.g. curly hair or straight hair

  • Homozygous

    • 2 identical alleles for a trait (dominant or recessive)

    • e.g. TT or tt

  • Heterozygous

    • has 2 different alleles for trait (dominant)

    • e.g. Tt

2 plants or animals, which differ at only one gene are bred together

  • Punnet square/monohybrid crosses

    • diagram showing the gene combinations that might result from a genetic cross

    • used to calculate the probability of inheriting a particular trait

      • Rules

        • down key identifying alleles letters represent

        • write down parents pheno/genotypes

        • draw punnet square

        • complete cross

Sex Linked Traits/Characteristics

  • The Y chromosome is very small compared to the X chromosome

  • Y chromosomes doesn’t have the same number of genes in it as the X

  • most of the genes in the x chromosome, will not have a matching allele in males

  • the pattern of inheritance is different in males and females

  • characteristics affected by the genes on your x chromosome are called sex-linked characteristics or x-linked characteristics

  • Hemizygous

    • if a gene is only on the x chromosome, then males only have the one allele. this is referred to as being hemizygous for that gene.

  • Red/Green colour blind

    • ability to discriminate controlled by a gene located in the x chromosome

    • individuals unable to distinguish have the recessive allele of this gene

    • more common in males then females

  • A colour blind male mates with a female homozygous for a regular vision kids

Pedigrees

  • Show the pattern of inheritance of a particular trait within a family

    • symbols

    • conventions

      • always included a title which indicates the trait and its made of inheritance

      • roman numerals indicate the generation

      • numbers represent the individuals

Modes of Inheritance

  • what you need to know

    • whether the trait is dominant or recessive

    • whether the trait is autosomal or sex-linked

      • look for 2 parents without the trait that have a child with the trait (recessive)

      • If there is none it is dominant

      • If recessive look at the sexes affected. If prodominantly in males it is probably sex linked if equal between sexes probably autosomal

AUTOSOMAL RECESSIVE:

·      Equal chance of both sexes being affected; this tells you it is autosomal

·      An affected female does not have an affected father; this tells you it is autosomal

·      Each affected individual has normal parents; this tells you it is recessive

·      If both parents have condition, ALL of the offspring will be affected; this tells you it is recessive

·      Affected individuals must be homozygous recessive (eg rr). These are the shaded individuals.

AUTOSOMAL DOMINANT:

·      Equal chance of both sexes being affected; this tells you it is autosomal

·      Each affected individual has at least one affected parent; this tells you it is dominant

·      About ½ of the offspring of affected individuals have the condition; this tells you it is dominant

·      An unaffected individual cannot transmit an affected allele.

Unaffected individuals must be homozygous recessive (eg. rr). These are the unshaded individuals.

 SEX-LINKED RECESSIVE:

·      Affected individuals are usually male; this tells you it is most likely sex-linked

·      An affected female MUST have an affected father; this tells you it is sex-linked

·      Sons of the affected male (XrY) and normal female (XRXR) are normal

·      Two parents that do not show the condition can have affected offspring; this tells you it is recessive

·      Females are generally carriers (XRXr) and thus do not show symptoms of the condition.

SEX-LINKED DOMINANT:

·      Affected individuals are usually female; this tells you it is most likely sex-linked

·      An affected male will pass it on to all his daughters and none of his sons. this tells you it is sex-linked dominant

·      A female with the trait may pass it on to both her sons and daughters.

·      Every affected person has at least one affected parent. this tells you it is dominant

·      Females are generally carriers (XRXr) and thus do show symptoms of the condition.

Mutations

A change in the nucleotide sequence of the DNA of the organism.

It’s random

Can be influenced by mutagens (environmental or external factor that causes a mutation):

  • radiation

  • UV light

  • some chemicals (asbestos, tobacco)

  • viruses

More likely to happen in DNA replication or meiosis.

  • Types of Mutation

    • Gene Mutation: involves an error in a singular nucleotide base and can disrupt a gene or a sequence

    • Chromosomal Mutations: involve an error in a group of nucleotide bases, disrupting gene/gene sequence

  • Gene Mutation Types

    • Substitution/Point: A pair is substituted for another

    • Frameshift: A base pair is added or deleted. This is more impactful as it’s changing the whole code by moving it up or down by one.

  • Chromosomal Abnormality: different amount of chromosomes due to more or less

Natural Selection

Species - a group of organisms in which its members can produce fertile offspring

Population - a group of the same species in a location. all the different types of genes in the population is known as the gene pool

  • Changes in gene pools

    • An allele is an alternative form of a gene (e.g. allele for black hair or allele for blonde hair)

    • Mutations, migration pressure, environmental factors are all reasons the frequency of an allele can change over time

    • E.g. allele frequency for the dark skin will increase in the frog population if it helps with camouflage on the logs.

Evolution - the genetic change in characteristics of a species over generations

Natural selection - the change in proportion of a particular genotype of a species over many generations due to environmental selection of a particular phenotype

  • Natural Selection

    • Driving force behind evolution

    • Process where an environmental factor acts on a population and results in some organisms in one species having more off spring than others

  • Selective agents/pressures'

    • The environmental factor that acts on the population

    • Biotic Factors (living)

      • Predation

      • Bacterial Infection

      • Competition

    • Abiotic Factors (non-living)

      • Temperature

      • Water

      • Soil nutrients

      • Fire

  • Survival of the Fittest

    • in every population there is variation (natural differences) due to individuals having different genes

    • the fittest or most well adapted individuals have a better chance at survival and therefore reproduce

    • these individuals have a survival advantage

Speciation

The process where one species is separated into two different species or more different species

  • Steps to Speciation

    • Variation

    • Isolation

    • Selection

Evidence for Evolution

  • Fossil Record

    • shows intermediate species in an evolutionary lineage

    • shows how more complex species developed from simpler ones over time

  • Comparative Embryonic Analysis

    • embryos of different species look similar to each other due to a shared common ancestor

  • Comparative Anatomy

    • different species show similar structural organisation because they share a common ancestor (e.g. pentadactyl limb)

  • DNA and Protein Evidence

    • species have similar genes or amino acids sequences because they share common ancestors

    • the closer related a species is the more amino acids sequences/genes they have in common