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40 Cards in this Set

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What are true-breeding individuals?
Individuals that if self-crossed, produce progeny only with parental phenotype
What is Mendel's First Law? What does it state?
Law of Segregation: an organism has 2 alleles for each inherited trait; one from each parent.
What is a monohybrid cross?
Cross in which only one trait is being studied
What is a Fillial Generation?
Progeny
If the F1 generation of a PP x pp cross is self-crossed, what will be the F2 genotypic and phenotypic ratios?
Genotype: 1:2:1 (1PP:2Pp:1pp)
Phenotype: 3:1 (3 purple:1 white)
For the testcross Ax x aa, what would be the genotypic and phenotypic ratios if the unknown genotype were homozygous? Heterozygous?
AA:
Genotype: 100% Aa
Phenotype: 100% Dominant

Aa:
Genotype: 1:1 (Aa:aa)
Phenotype: 1:1 (Dom:Rec)
What is Mendel's 2nd Law? What does it state?
Law of Independent Assortment: alleles of unlinked egnes will assort independently during meiosis.
What is a dihybrid cross?
Cross where parents differ in 2 traits
What possible gametes can a parent of TTPP produce? ttpp?
TP, tp
What is the phenotypic ratio for the F1 progeny of a TTPP x ttpp cross?
TTPP: TP
ttpp: tp
TP x tp -> 100% TtPp
Phenotypically dominant for both traits.
For a TtPp self-cross what will be the phenotypic ratios of the F1 progeny?
9:3:3:1
(DomDom:DomRec:RecDom:RecRec)
For TTPP x ttpp, what is the probability that the total F2 progeny will be TTPP?
TTPP only possible from two TP gametes.
P: TTPP x ttpp
F1: 100% TtPp (possible gametes: TP, Tp, tP, tp)
Need Tp x TP to get TTPP
Only 1/4 of F1 has TP
So need two parents with TP
Thus, 1/4 x 1/4 = 1/16 probability
For TTPP x ttpp, what is the probability that the total F2 progeny will be TtPp?
TtPp possible from:
TP x tp
Tp x tP
tp x TP
tP x Tp

Each cross has 1/16 probability of occuring
Thus:
1/16 + 1/16 + 1/16 + 1/16 =
1/4 probability
What characteristics define a diploid species in Mendelian genetics?
Have chromosome pairs (homologues) such that alleles for a given trait are segragated (one allele on one chromosome, other allele on homologue)
At what point in meiosis does segregation and independent assortment occur?
During first meiotic division when number of chromosomes per cell goes from 2N-->N
How do linked genes behave during assortment?
Linked genes located on same chromosome and are usually inherited and segregated together, which may explain over-representation of parental phenotypes in progeny.
What is genetic recombination? What is one of its possible effects on linked genes? What is its likelihood to occur dependent on?
Physical exchange of DNA between homologous chromosomes paired during meiosis; can unlink linked genes.

Probability of genetic recombination (AKA CROSSING OVER) dep. on distance between the 2 genes
What are the units of recombination frequency?
1 map unit, which = 1% recombinant frequency
If gene X and gene Y have a recombinant frequency of 8%, and gene X and gene Z recombine 12% of the time, what are the possible distances between genes Y & Z?
4 or 20 map units
Define incomplete dominance.
When phenotype of a heterozygote is an intermediate (blend) of phenotypes of homozygotes.
Define codominance.
When multiple alleles exist for a given gene and more than 1 is dominant.

When 2 dominant alleles present, phenotype is result of simultaneous expression of both alleles.
How are blood types an example of codominance?
IaIa or Iai give Type A
IbIb or Ibi give Type B
ii gives Type O
BUT
IaIb gives Type AB, which is a combination (NOT blend) or characteristics of A&B
What is penetrance?
Percentage of individuals in population carrying allele and actually express its associated phenotype.
What is expressivity?
Degree to which phenotype associated with genotype is expressed in individuals who carry the allele
In the case of recessive inherited disorder, which genotype is required for the disorder to be expressed? Carried?
Homozygous = expressed
Heterozygous = carrier
During what periods of life do recessive inherited disorders tend to be lethal?
Early
During what periods of life do dominant inherited disorders tend to be lethal?
Late (Huntington's)
On what chromosome are most sex-linked genes located?
X; seXXX-linked is XXX-linked
Why is it that x-linked genes are more frequently expressed in males?
Because there is no dominant allele to mask the trait in males (only have 1 x chromosome)
If male parents are unable to pass x-linked genes onto their sons, how is it that these genes are passed to their grandsons?
X-linked gene is passed to ALL daughters who then become carriers (unless mother also has x-linked gene); daughters then can pass it to their sons.
In pedigrees, how are affected individuals represented? Carriers?
Shaded, half shaded
What is the general strategy when analyzing a pedigree?
Look for recessive phenotype, must be homozygous! mating b/t them and other serve as testcrosses
When should a sex-linked gene be suspected in a pedigree?
When only males are affected
Define nondisjunction.
Failure of homologous chromosomes to separate during meiosis 1 OR failure of sister chromatids to separate during meiosis 2.
Describe the consequences of a disjunctive event in a secondary spermatocyte.
Would resuls in 1 gamete with 2 copies of chromosome (polyploid), 2 normal haploid gametes, and 1 with no copies (aneuploid)
Define trisomy and monosomy.
Trisomy = zygote with 3 copies of a chromosome

Monosomy = 1 copy of chromosome
XXY results in?
Klinefelter's syndrome: sterile males, small testes
XXX results in?
Metafemales: mentally retarded, sterile
XYY results in?
Normal males that are usually taller and apparently more violent
Define three possible events following chromosomal breakage.
Duplication: Lost fragment may join homologous chromosome.

Translocation: Joins with non-homologous chromosome

Inversion: rejoins with original chromosome in reverse posn.