lecture 12: chromosome mutations: aneuploidy Flashcards
aneuploidy
2n +/- x chromosomes
euploidy
complete haploid sets of chromosomes present
multiples of n
polypolidy
more than two sets of chromosomes present
3n, 4n, 5n
non-disjunction
no division, all chromosomes go to one gamete
monosomy =
2n-1
monosomy from X chromosomes occurs in humans
turner syndrome
haploinsufficiency
diploid organism has lost one copy of a gene and is left with a single functional copy of that gene
trisomy =
2n + 1
familial downs syndrome
translocation of bottom part of chromosome 21 onto another chromosome
down’s syndrome most frequently occurs due to nondisjuction of chromosome
21
75% of down’s syndrome non-disjunction occurs during
meiosis I
polyploidy, n=
> 2
autopolyploidy
addition of one or more sets of chromosomes identical to haploid complement of same species
allopolyploidy
combintaion of chromosome sets from different species - consequence of interspecific matings
autotriploids arise due to
failure of chromosomes to segregate during meiotic division
autotetraploids have
even number of chromosomes (4n)
autotetraploids arise when
chromosomes have replicated, BUT parent cell fails to divide and instead enters interphase
allotetraploid/amphidiplid results from hybridization of
two closely related species