Unit 7- Linkage, Recomb, and Eukaryotic Gene Mapping Flashcards
Principle of Segregation
alleles at same locus of homologous pairs separate during meiosis
Indep Assortment
alleles at one locus sort indep from alleles at another locus
recombination
alleles sort into new combinations
complete linkage
leads to nonrecombinants
- genes very close together and no crossing over
crossing over with linked genes
leads to recombinants (at most half: a single crossover only affects 2 of 4 chromatids)
calc recomb freq
of recomb progeny/ total # of progeny x100%
coupling (cis config)
wild-type alleles are found on 1 chromo; mutant alleles are found on the other chromo
*mostly parental pheno
Repulsion (trans config)
wild-type alleles and mutant allele are found on the same chromo
* mostly recomb pheno
INTERchromosomal Recombination
crossing over between genes located on DIFFERENT chromosomes (due to indep assortment. Mendelian)
INTRAchromosomal Recombination
crossing over between genes located on the SAME chromosome
chi-square test of independence
- Set up table of parents and their progeny (like a punnet sq) with row/column totals
- calc expected: row total x column total / grand total)
- sum of (O-E)^2 / E
- d:f (# rows-1) x (# columns -1)
Gene mapping with recomb freqs
- genetic maps determined by recomb freq (1 mu = 1%)
- map units: centiMorgans
(as % goes up, so does distance)
constructing a genetic map with the 3pt testcross
- more efficient mapping technique
- order of the 3 genes can be established in a single set of progeny
- some double crossovers can usually be detected
- provides more accurate map distances
steps in determining gene order in 3pt cross
- identify the nonrecomb progeny (2 most numerous)
- Identify the recomb progeny (2 least numerous)
- compare the pheno of double-crossover progeny with the pheno of nonrecomb progeny. (should be alike in 2 characteristics and differ in 1)
- differing characteristic is encoded by the middle gene
calc recomb freq
sum of all single and double crossovers/ total progeny
coeff of coincidence
of obs double crossovers/ # of expected double crossovers
interference
The degree to which one crossover interferes with
additional crossovers in the same region
1 - coeff of coincidence
Poisson distribution
predicts the probability of multiple rare events
mapping techniques
- mapping with molec markers (RFLPs)(variations in DNA sequence detected by cutting the DNA with
restriction enzymes) - Genome-wide association studies (associations w/in pops, haplotype, and linkage disequilibrium)
genetic markers
variable genes with easily observable phenos for which inheritance could be studied
- ex: lower color, seed shape, blood types, and biochemical difference
Physical-mapping methods are used to determine the physical position of genes on particular chromo
- somatic-cell hybridization
- deletion mapping
- physical mapping through molec anaysis (in situ hybridization)
hetrokaryons
hybrid cells formed during somatic-cell hybridization (look for differing presence of chromo)
Fluorescence in Situ Hybridization (FISH)
uses a single-stranded complementary DNA probe for the gene
Recomb rates exhibit extensive variation
- among species
- among chromos of same species
- among males and females
Walter Sutton’s Chromo Theory of Inheritance
genes are physically located on chromo
Netti Steven’s and Edmund Wilson’s
sex was associated with specific chromo in insects
Calvin Bridges’
nondisjunction of x chromo was related to the inheritance of eye color in Drosophilia
Harriet Creighton and Barbara McClintock
interchromosomal recomb was the result of physical exchange between chromos
linkage analysis
based on the detection of physical linkage between genes,
as measured by the rate of recombination
genomewide association studies
looks for associations between traits and alleles in a POP
haplotype
A specific set of linked alleles
linkage disequilibrium
nonrandom association
between alleles in a haplotype
single-nucleotide polymorphisms
(SNPs)
positions in the genome where people vary in a single nucleotide base
deletion mapping
homo for mutation x hetero for deletion
- if trait in deletion area, 50% recomb
- if trait isnt in area, wild-type