Section 4 - Chapter 9 : Diversity Flashcards
What is a mutation
- Any change to the quantity or the base sequence of the DNA of an organism is known as a mutations
- Mutations occuring during the formation of gametes can be inherited
- Any change to one or more nucleotide bases, or a change in the sequence of the bases, in DNA is known as a gene mutation - this can happen spontaneously during DNA replication and include base substitution and base deletion.
What are the 3 types of mutation
- Deletion
- Substitution
- Addition (Insertion)
What is a base substitution
- The type of gene mutation in which a nucleotide in a DNA molecule is replaced by another nucleotide that has a different base
- Less impact than deletions and additions: will differ in an amino acid.
- The significance of the difference will depend on the precise role - may not form the same bonds - different shape, non-functional.
- No change if the new triplet codes for the same amino acid - degenerative
What are examples of mutagenic agents
- UV radiation, ionizing radiation, chemicals some viruses
- These mutagenic agents increase the probability of a mutation occuring
What are the 2 types of chromosome mutation
- Changes in whole sets of chromosomes - organism have 3 or more sets of chromosomes rather than 2 - polyploidy (occurs mostly in plants)
- Changes in the number of individual chromosomes - sometimes individual homologous pairs fail to separate in meiosis. The offspring have fewer or more chromosomes than normal. Down Syndrome
EXAM QUESTION: A mutation can lead to the production of a non-functional enzyme. Explain how
- Change/mutation in base/ nucleotide sequence (of DNA/gene)
- Change in amino acid sequence (primary structure)
- Change in hydrogen/ ionic/ disulfide bonds
- Change in tertiary structure
- Change in active site
- Substrate not complementary/ can’t bind no enzyme-substrate complexes form.
What is the importance of meiosis
- During sexual reproduction gametes give rise to a new offspring. If each gamete had a “full” set (diploid) then the offspring would have 92 (this doubling would continue) To maintain chromosome numbers the number must be halved haploid - occurs in meiosis
- Every diploid cell has 2 complete sets of chromosomes (parents). During meiosis homologous pairs separate so that only one chromosome from each pair enter the daughter cell (haploid number)
- When 2 haploid cells fuse, diploid number is restored
What does diploid and haploid mean
- Haploid: When a cell contains one copy of each chromosome
- Diplod: When a cell contains 2 copies of each chromosome (1 from each parent)
What are the 2 types of cell division
- Mitosis: Produces 2 daughter cells with the same number of chromosomes as the parent cell
- Meiosis: Usually produces 4 daughter cells, each with half the number of chromosomes as the parent cell
What is the process of meiosis of the first division (also including interphase)
- Interphase - DNA replicating, cell growth, organelles increase. Replicated chromosome is an x of 2 sister chromatids
- Prophase I: Nuclear envelope disintegrates, spindles form, homologous chromosomes pair up (bivalent) and crossing over occurs creating new combinations of alleles
- Metaphase I: Homologous chromosomes line up along the equator via spindle fibres. Independent assortment and segregation = creates unique combination of maternal and paternal chromosomes in gametes
- Anaphase I: HC pairs pulled apart, spindle fibres contract pulled to opposite poles of the cell
- Telophase I: Nuclear envelope reform
- Cytokinesis: 2 daughter cells with 1/2 chromosome number. Cytoplasm divides
What is the process of meiosis (meiosis 2)
- Prophase II: Nuclear envelope disintegrates, spindle fibres reform
- Metaphase II: chromosomes line up in the equator by spindle fibres
- Anaphase II: Separation of sister chromatids
- Telophase II: Nuclear envelope reforms
- Cytokinesis: Half chromosome - ends eith 4 genetically different gametes
How does meiosis bring genetic variation
- Independent segregation of homologous chromosomes
- New combinations of maternal and paternal alleles by crossing over
EXAM QUESTION: Meiosis results in cells that have the hapoid number of chromosomes and show gentic variation. Explain how. (6)
- Homologous chromosomes pair up/ bivalent form
- Crossing over/ chiasmata form
- Produces new combination of alleles
- Chromosomes separate (segregate)
- At random (random segregation)
- Produces varying combinations of chromosomes/ genes/ alleles
- Chromatids separated at meiosis 2 later
What is independent segregation of homologous chromosomes
- One of each pair of chromosomes will pass to each daughter cell. Which one goes into the daughter cell and any other pair depends on how the pairs are lined up in the parent cell.
- Since the pairs are lined up at random, the combination of chromosomes of maternal and paternal origin that go into the daughter cell is chance - independent segregation
The chromosomes line up alongside its homologous partner What is genetic recombination by crossing over and what are the events
- The chromatids of each pair become twisted around one another
- During the twisting process tensions are created and portions of the chromatids break off
- These broken portion might then rejoin with the chromatids of its homologous partner
- Usually it is equivalent portions of homologous chromosomes that are exchanged
- In this way new genetic combinations of maternal and paternal alleles are produced
- The chromatids cross over one another many times - crossing over
- The broken off portions recombine wiyth another chromatid - recombination