Genetic Diversity due to Mutation and Meiosis Flashcards
what is a frame shift
change resulting in misreading of all nucleotides downstream, usually resulting in a truncated non-functional protein
what type of mutations cause a frame shift and explain them
deletion - the removal of 1 or more bases resulting in a frame shift
addition - the adding of one or more bases resulting in a frame shift
duplication - where one or more bases is repeated causing a frame shift
what type of mutations don’t cause a frame shift and explain them
inversion - a sequence of bases is reversed e.g. TAGCAGCT becomes TCGACGAT
translocation - a sequence of bases is moved from one location in the DNA molecule to another part of the genome
substitution - the replacement of one or more bases by one or more different bases
why can a functioning protein still be formed after substitution
- the DNA code is degenerate meaning that an amino acid can be coded by more than 1 base triplet
- the mutation could have occured in an intron which doesn’t code for proteins
- the mutation doesn’t affect the shape of the tertiary in a way that affects the function of the protein
difference between mitosis and meiosis (4)
- mitosis has one nuclear division, meiosis does two
- mitosis produces two daughter cells, meiosis produces four
- mitosis produces genetically identical cells, meiosis doesn’t
- mitosis produces cells with the same amount of chromosomes as the parent cell, meiosis produces cells with half
what is crossover during meiosis
- the pair of homologous chromosomes lie side by side forming a bivalent
- the chromatids of the homologous chromosomes then intertwine
- the chromatids break and equivalent portions of the chromatids are exchanged
how is variation (genetic diversity) achieved during meiosis
- independent segregation of homologous chromosomes
- genetic recombination (crossover) within homologous chromosomes
how do you calculate the possible numbers of varied combinations of paternal and maternal chromosomes
2ⁿ
- n = number of homologous pairs
what is independent segregation during meiosis
- during the first meiotic division, hom. chromosomes pair together and then separate so that one member from each pair enters the gamete
what is a chiasma
site of crossing over
what is genetic recombination
the exchange of alleles ,during cross over, producing new combinations of alleles known as recombinants
what is nondisjunction
the failure of the chromosomes to separate during cell division , which produces daughter cells with abnormal numbers of chromosomes.