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28 Cards in this Set

  • Front
  • Back
binary fission
cell division in prokaryotes
chromosomes attach to plasma membrane at origin of replication
two attachment sites move apart after two copies are made
two daughter cells
mitosis
interphase - longest phase, G1, S (synthesis), G2 (spindle forms, gets ready to divide)
prophase - chromosomes condense, become visible
prometaphase - only fragments of nuclear membrane
metaphase - centrosomes at opposite poles, centromeres line up at center
anaphase - sister chromatids (exact copies) pulled to opposite poles, karyokinesis: splitting of nuclear content
telophase & cytokinesis - nuclear envelope forms, cleavage furrow, nucleolus forming, splitting of cytoplasm
checkpoints
G1: cell decides whether or not to divide NO GOING BACK
G2: is the spindle ready for mitosis to happen
M: (metaphase) are the chromosomes lined up properly
tumors (3 types)
benign - stays contained
malignant - spreads to surrounding areas
metastatic - spreads throughout the body
oncogenes vs. proto-oncogenes
oncogenes are genes that cause cancer
proto-oncogenes are genes that perform normal cellular function but become oncogenes when something goes wrong
SRY gene
makes males male
on y chromosome
XX (SRY+) = male
XY (SRY-) = female
test cross
can distinguish between a homo dominant and a hetero by crossing it with homo recessive
dihybrid cross
follows two traits simultaneously
9:3:3:1
codominance
when two alleles are expressed simultaneously, black & white feathers
incomplete dominance
black + white = gray
pleiotropy
a change in one gene locus results in multiple changes in the phenotype
epistasis
when alleles at one locus affect expression of genes at another locus (labs)
polygenic traits
many traits are the result of the additive effects of many genes
continuous variation (height)
ratio in mendelian mono-hybrid crosses
3:1
ratio in mendelian di-hybrid crosses
9:3:3:1
mendelian ratios found b/c
one allele always fully dominant
trait governed by single locus
no genotypes were lethal
all autosomal
assorted independently
hemizygous
only one gene
i.e. males are hemizygous for most of the genes found on the x chromosome
barr bodies
one x chromosome in each female cell shuts off and becomes forms a tight ball
law of independent assortment
alleles of a gene on nonhomologous chromosomes
test cross
YyRr x yyrr
to determine things b/c you know one parent will only contribute recessive alleles
allele mapping
the closer together two genes are on the same chromosome, the less likely there will be crossing over between them
highest recombinant frequency (map distance), further they are apart
assumes crossing over is completely random
nondisjunction
homologous chromosomes dont separate in meiosis I
OR sister chromatids don't separate in meiosis II
**most often fatal
trisome 21
downsyndrome = 3 copies of chr 21
XXX
female
two barr bodies
XXY
male
1 barr body
XO
alive
female
b/c x chr is very large
YO
dead
y chr relatively small
can't survive w/o x
other genes
located in mitochondria and chloroplasts
-carry their own DNA
inherited from mother only
mutations not lethal b/c so many copies