define genotype
the genetic constitution of an organism
- defined in relation to a particular gene or gene combinations
- eg Aa, Bb
define phenotype
feature of the organism as observed
- used when discussing a trait of an organism that varies
- eg size, fur colour, mRNA expression level
define genome
the entirety of an organism’s DNA
- includes genes and non-coding regions
state 3 sources of genetic variation
define a mutation
a stable change in the DNA sequence
how often do mutations occur?
at a low rate
- mutation rate varies in ways that are partially predictable
what are the different possible effects of mutations on fitness?
state the 4 main characteristics of mutation
what are the 4 types of mutation?
describe a mutation involving a change in repeat number
describe an example of a chromosomal rearrangement
inversions:
- flipping of the nucleotide sequence
- occurs when there is a double break in DNA strand; when enzymes try to put the two strands back together, it is hard to know which one was forward and which one was backwards
give an example of a method that can be used to identify a new mutation?
a trio study:
- two parents (reproducing organisms) are selected
- their genome and the genome of their offspring is sequenced
what is the rate of new mutation in humans?
per base pair of DNA: 16 in every billion nucleotides each generation
per individual genome (two copies of our 3 billion base pair genome): approx. 96 new mutations per zygote
for the entire human population (8 billion): every base pair in the genome mutated about 126 times over per generation
why do some mutations not lead to amino acid changes?
we have more codons than amino acids - so sometimes mutations don’t make a difference to the amino acid sequence (= silent substitution)
give an animal example of how single mutations can cause profound effects on traits
describe G6DP deficiency in humans?
Glucose-6-phosphate dehydrogenase
most common enzyme deficiency in humans
- causes severe anemia
- also protects against malaria
- 2 amino acid replacement mutations in the coding sequence of G6PD are associated with disease allele (A-)
what are polymorphisms?
what are allozymes?
Alloenzymes are variant forms of an enzyme which differ structurally but not functionally from other allozymes coded for by different alleles at the same locus.
give a flow chart for how mutations in G6PD lead to genetic variation
DNA (polymorphisms) -> proteins (allozymes) -> phenotype (polyphenisms)
define independent assortment
the alleles of two (or more) different genes get sorted into gametes independently of one another.
how does independent assortment in segregation during meiosis generate diversity?
how can we tell if a mutation has increased or decreased fitness from a fitness distribution bar chart?
if the mutation leads to a fitness less than 1 (which is the fitness of the ancestor) then they are detrimental
describe how recombination during meiosis (metaphase) further contributes to variation
there is synapsis of bivalents, leading to crossing over at chiasmata and recombinant chromosomes.