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where are genes located?
on chromosomes
when do chromosomes duplicate?
before cell division
how many versions of a gene does each chromosome have?
one (one allele)
law of segregation
two alleles for each gene separate
law of independent assortment
alleles of genes on nonhomologous chromosomes assort independently
why did morgan choose to use fruit flies for his experiment?
many offspring
short generation time (every two weeks)
only 4 pairs of chromosomes
what did morgan find?
all of the white eyed flies were males
how many types of sex chromosomes do humans have?
two: a larger X chromosome and a smaller Y chromosome
(XX→ typically female, XY → typically male)
SRY gene
sex-determining region on the Y gene: triggers testis development in an embryo; located on the Y chromosome
how do X and Y chromosomes pair during meiosis?
they share small homologous regions that allow for pairing
sex-linked gene
gene located on a sex chromosome
x-linked gene
gene located on the x-chromosome
y-linked gene
gene located on the y-chromosome
x-linked recessive traits - female (XX)
usually needs two recessive alleles to express the trait; heterozygous female = carrier
x-linked recessive traits - male (XY)
needs only one recessive allele on X; hemizygous
who are x-linked recessive traits more common in?
males
who do fathers pass their X chromosome to?
daughters (NOT sons)
what happens to an inactive X chromosome?
condenses into a barr body
XX cell → random X inactivation (one active X + one inactive X) → barr body → mosaic expression
which chromosome does NOT have hundreds/thousands of genes?
the Y chromosome
linked genes
genes located on the same chromosome; inherited together (the closer, the more likely of inheritance together)
how does linkage affect inheritance?
genes do not assort independently
they are linked on the same chromosome
crossing over can produce recombinant offpring
how can linked genes be separated?
by crossing over (between homologous chromosomes during prophase I)
recombination of linked genes - crossing over
linked genes usually stay together → crossing over can separate them → recombinant gametes → recombinant offspring
genetic recombination
produces new combos of alleles in offspring
parental type
allele combos found in parents
recombinant types
new allele combos
unlinked genes
50% recombinant offspring
what can chromosomal alterations involve?
chromosome number
chromosome structure
nondisjunction
chromosomes fail to separate normally during meiosis → one gamete receives two of the same type of chromosome while the other receives no copy
when can nondisjunction happen?
meiosis I: homologous chromosomes fail to separate → all 4 gametes = abnormal
meiosis II: sister chromatids fail to separate → 2 abnormal + 2 normal
aneuploidy
abnormal number of a particular chromosome; nondisjunction → abnormal gametes (n+1 or n-1) → aneuploid zygote
what are some examples of aneuploidy?
trisomy (2n+1) = three copies
monosomy (2n-1) = one copy
polyploidy
more than two complete sets of chromosomes; common in plants, rare in animals; “normal” appearance
what are some examples of polyploidy?
triploidy (3n) = three sets of chromosomes
tetraploidy (4n) = four sets of chromosomes
chromosome structural change: deletion
a chromosomal segment is removed/lost
chromosome structural change: duplication
a segment is repeated
chromosome structural change: inversion
a segment is reversed within a chromosome
chromosome structural change: translocation
a segment from one chromosome is moved to a nonhomologous chromosome
what are some examples of when the parent that contributes the allele matters?
genomic imprinting and organelle inheritance
genetic imprinting
same allele → different effect depending on parent of origin; one parental allele is silenced while the other is expressed
inheritance of organelle genes
mitochondria and chloroplasts contain their own DNA located outside the nucleus
in most animals, who is the mitochondrial DNA primarily inherited from?
the mother