lecture 11 Flashcards
what is inbreeding
a form of non random mating
make new assumptions = modify hardy weinberg
describe inbreeding - context of crosses
same allele being passed down
mating between first cousins
many possibilityes
what is IBD
alleles that are IDENTICAL BY DESCENT (IBD) are one possible outcome
at single locus
what inbreeding increase
Probability that 2 alleles at a locus will be copies of an allele present in an ancestor
such copies = IBD - identical by descent
what is F coeff
probability of IBD
F quantifies the overall probability that the two alleles inherited by a given individual will be identical by descent
how to calculate inbreeding coeff
locate individual and diagram pathway
people in pathway besides final person = n
inbreeding coeff F= (1/2)^n
(if 2 paths = add both coeffs together)
if parent is inbred = modified formula F = (1/2)^n (1+FA), where FA = inbreeding coeff of parent
what changes genotype frequencies
inbreeding
describe frequencies in changed inbreeding frequencies
in pop that switches over from random mating to inbreeding
fA1A1 = p^2 +Fpq
fA1A2 = 2pq (1-F)
fA2A2 = q^2 + Fpq
more homozygotes and LESS heterozygous
as F increases heterozygous decrease and homozygous increase (if more and more gens = further depart from hardy weinberg)
what is inbreeding depression
reduction in viability of inbred individuals
why does inbreeding depression happen
bc most deleterious conditions require 2 copies of mutation to be expressed
so more and more diseases expressed
reduces vigor, variablity and reproductive sucess
decline in fitness of average individual
what is inbreeding mortality in us
more and more inbred (like the more closely related) = increase infant mortality
does inbreeding cause change in allele frequencies
NOOOO
but genotype frequencies do change
name factors influencing allele frequencies
mutation
Migration
genetic drift
natural selection
describe mutation - factors influencing allele frequencies
ex = Mutations at the Cystic Fibrosis Transmembrane Conductance (CFTR)
locus can lead to Cystic Fibrosis
Particular mutation on chrom 7 cftr gene at base pair level
what is a typical rate of mutation per base pair of dna per gen in humans
one in a billion
low rate of mutation depends if talking about gene or nt but still v small