3.4.3 Genetic diversity can arise as a result of mutation or during meiosis Flashcards
What is a gene mutation?
A gene mutation is a change in the base sequence of DNA.
When do gene mutations arise?
Gene mutations arise spontaneously during DNA replication.
Name two types of gene mutations.
Base deletion and base substitution.
Why do not all base substitutions cause a change in the amino acid sequence?
Because of the degenerate nature of the genetic code where more than one codon codes for the same amino acid.
What can increase the rate of gene mutation?
Mutagenic agents increase the rate of gene mutation.
How can mutations in the number of chromosomes arise?
Mutations in chromosome number arise by chromosome non-disjunction during meiosis.
What does meiosis produce?
Meiosis produces daughter cells that are genetically different from each other.
How many divisions occur in meiosis and what is produced?
Two nuclear divisions produce four haploid daughter cells from a single diploid parent cell.
How does independent segregation create genetic variation?
Independent segregation of homologous chromosomes produces genetically different daughter cells.
How does crossing over create further genetic variation?
Crossing over between homologous chromosomes results in further genetic variation among daughter cells.
Explain the different outcome of mitosis and meiosis.
Mitosis produces two genetically identical diploid cells meiosis produces four genetically different haploid cells.
How does random fertilisation increase genetic variation?
Random fertilisation of haploid gametes produces new combinations of alleles increasing genetic variation within a species.
Meiosis – Causes of Variation (6)
- Homologous chromosomes pair up;
- Chiasmata formed
- Independent segregation;
- Maternal and paternal chromosomes are re-shuffled in any combination;
- Crossing over leads to exchange of parts of (non-sister) chromatids/alleles between homologous chromosomes;
- (Both) create new combinations of alleles
Meiosis – Process of Crossing Over (4)
- Homologous pairs of chromosomes associate / form a bivalent;
- Chiasmata(ta) form;
- (Equal) lengths of (non-sister) chromatids / alleles are exchanged;
- Producing new combinations of alleles;
Describe how the process of meiosis results in haploid cells.
- DNA replication (in interphase) creates two identical chromatids;
- (meiosis has) two nuclear divisions;
- (first division) Homologous pairs separated
- (second division) sister chromatids separated
Define mutation
A change in the base sequence of DNA, results in a new allele
Mutation - How does mutation cause change in enzyme function? (3)
- Change in amino acid / (sequence of) amino acids / primary structure;
- Change in hydrogen / ionic / disulphide bonds alters tertiary structure / active site (of enzyme);
- Substrate not complementary / cannot bind (to enzyme / active site) / no enzyme- substrate complexes form;
Mutation - How does mutation cause change in protein (receptor) structure? (4)
- Change in DNA base (sequence);
- Change in amino acid (sequence)/primary structure;
- Alters (position of) hydrogen/ionic/disulfide bonds;
- Change in tertiary structure (of receptor);
Mutation – Mutation leading to evolutionary changes/phylogenetic relationships
- Mutations change base / nucleotide (sequence);
- (Causing) change in amino acid sequence;
- Mutations build up over time;
- Few(er) mutations / differences (in amino acid / base / nucleotide sequence / primary structure) in closely related species;
- Closely related species have recent common ancestor
Define the term mutagenic agent.
(A factor that) increases (the rate of) mutations;
Name ways which increase genetic variation in a population
- Mutation;
- Meiosis – crossing over and independent segregation
- Random fertilisation/random fusion of gametes
Define how a mutation can have a positive effect on an individual and no effect on a individual
No effect because:
- Genetic code is degenerate/codon codes for the same amino acid
- Mutation is in an intron
- Creates a recessive allele which does not affect phenotype
Positive effect because:
- (new allele) increases chance of survival