segregation
alleles at the same locus on two homologous chromosomes separate in meiosis
independent assortment
alleles at one locus act independently of alleles at another locus due to recombination
independent assortment recomination is __________
interchromosomal
linked genes
genes close enough to one another on the same chromosome that crossover reshuffles them <50% of the time
crossover generates _______ variation
intrachromosomal
the closer two genes are on a chromosome, the _______ crossover occurs between them
less often
coupling
dominant allels reside on one chromosome and recessives on the other
repulsion
each chromosome carries one dominant and one recessive allele
what is the two-point testcross?
double heterozygous x homozygous recessive
the farther apart two genes are, the more likely we are to _____________ between them and underestimate their genetic distance as a result
miss double crossovers
recombination frequency
(# single recombinants + double recombinants) /( total offspring ) x 100
chromosomal rearrangements are due to
incorrect repair of double-strand breaks (each person has up to about 1000)
duplication
doubling of base pair sequence
tandem duplication
go right next to the original loci (this can cause unequal crossing over when similar genes are next to each other)
reverse duplication
duplication in reverse orientation but ends up right next to the original loci
displaced duplication
duplicated region ends up elsewhere in the genome
segmental duplication
> 1000 base pairs in length and can belong to any category (tandem, reverse, or displaced)
deletion
segment of gene is gone (can be very harmful)
inversion
can break up genes and/or change their expression due to position effect
paracentric inversion
does NOT involve a centromere
-crossover in inverted region leads to acentric and dicentric chromosomes
acentric chromosomes
no centromere, get lost
dicentric chromosome
two centromeres instead of one, usually break
pericentric inversion
-involves a centromere
-crossover in the inverted region leads to chromosomes with incorrect sets/numbers of genes
translocation
part of a gene moved elsewhere