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48 Cards in this Set

  • Front
  • Back
blending hypothesis
genetic material mixes in a manner like blue and yellow paints blend to make green
-over a period of time there would be uniform individuals
-fails to explain reappearing traits after skipping a generation
gene idea
parents pass on discrete heritable units(genes) that retain their seperate identities in offspring
character
heritable deature that varies among individuals
trait
each variant for a character
why peas was a good choice
-available in many varieties
-short generation time
-large number of offspring
-able to control mating btwn plants
crossing pea plants
crossing pea plants that vary in flower calor allows study of patterns in inheritance
true-breeding
over many generations of self-pollination produced only same bariety as parent plant
hybridization
mating/crossing of two true-breeding varieties
P generation
true-breeding parents
F1 generation
first filial generation, hybrid offspring of P generation
alleles
alternative versions of genes account for variation in inherited characters
mendel's model
-for each character, an organism inherits two alleles, one from each parent
-if two alleles at a locus differ, then one will be the dominant allele which determines organism's appearance and the other will be the recessive
law of segregation
two alleles for a heritable character segregate (separate) during gamete formation and end up in different gametes
punnett square
diagrammatic device for predicting the allele composition of offspring from a cross btwn individuals of known genetic makeup
homozygous
organism that has a pair of identical alleles for a character
heterozygous
organism that has two different alleles for a gene
-not true-breeding because produce gametes with different alleles
phenotype
organism's appearance/observable traits
genotype
genetic makeup
testcross
breeding an organism of unknown genotype with a recessive homozygote
-will reveal genotype of that organism
monohybrids
heterozygous for one character
dihybrids
individuals heterozygous for two characters (ex: YyRr)
law of independent assortment
each pair of lleles segregate independently of eachother pair of alleles during gamete formation
probbility scale
ranges from 0 to 1
multipliction
to determine probability, multiply the probability of one even by the probability of the other event
addition rule
probability that ny one of two or more mutually exclusive events will occur is calculated by adding their individual probabilities
complete dominance
phenotypes of the heterozygote and the dominant homosygote are indistinguishable
incomplete dominance
neither allele is completly dominant, nd F1 hybrids have a phenotype somewhere between those of two parental varieties
codominance
two alleles both affect the phenotype in separate distinguishable ways
-ex: blood type (AB)
tay-sachs disease
inherited siorders in humans where cannot metabolize certain lipids because crucial enyzme does not work properly
-seizures, blindness, degeneration of motor and mental performance and will die with in a few years
-need two copies of Tay-Sachs allele, recessive at organismal level
-however in heterozygotes the lipid-metabolizing enzyme is intermediate
-biochemical level=incomplete dominance (no diseased symptoms)
frequency of dominant alleles
-affected by natural selection
-not necessarily most popular
pleiotropy
multiple phenotypic effects
ex: cycstic fribrosis and sickle-cell disease
epistasis
a gene at one locus alter the phenotypic expression of a gene at a second locus
ex: albino mice
qunititative characters
characters vary in the population along a continuum (in gradations)
polygenic inheritance
additive effect of two or more genes on a single phenotypic character (converse of pleiotropy)
norm of reaction
range of phenotypic possibilities due to environmental influences
multifactual
many factors, both genetic and environmental collectivly influencing phenotype
pedigree analysis
pedigree information about a family's history for a particular trait and aseembled info into a family tree describing traits of parents and children cross generations
behavior of recessive alleles
an allele that causes a genetic disorder codes either for a mlfunctioning protein or for no protein at all
carriers
heterozygotes that transmit recessive allele to their offspring
cystic fibrosis
most common lethal genetic disease in U.S.
-strikes 1 out of every 2,500 ppl of European descent
-chloride transport chains defected
-increase mucous
sickle-cell disease
most common inherited disorder among ppl of African descent
-will clump small blood vessels
-pleitropy->some heterozygotes with symptoms
achondroplasia
form of dawrfism that occurs in one of every 25,000 people
huntington's disease
-lethal dominant allele
-degenertive diease of the nervous system
multifactorial disorders
genetic component plus a significant envrionmental influence
-heart disease, diabetes, cancer, alcoholism, schizophrenia
amniocentesis
sample of fluid taken t 14th week of pregnancy, biochemical tests, centrifuge, fetal cells cultivated
chorionic villus sampling
sample of tissue from placent at 8th week of pregnancy -->karyotyping
ultrsound
sound waves used to produce image of fetus by simple noninvasive procedure
fetoscopy
needle-thin tube containing viewing scope nd fiber optics is inserted into uterus