Biology 135A Chromosomal Basis for Inheritance PDF
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This document provides an introduction to the chromosomal basis of inheritance, covering key concepts such as recombination frequency, genetic mapping and chromosomal behavior during meiosis. It also features examples and diagrams, all within a biology context.
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Biology 135A Chromosomal Basis for Inheritance (Ch. 15) Rajab Introduction Chromosome theory – Thomas Morgan – Linkage – Recombination Mapping genes on chromosomes-Alfred Sturtevant – Recombination frequency Autosomes vs. sex chromosomes Chromosome theory:...
Biology 135A Chromosomal Basis for Inheritance (Ch. 15) Rajab Introduction Chromosome theory – Thomas Morgan – Linkage – Recombination Mapping genes on chromosomes-Alfred Sturtevant – Recombination frequency Autosomes vs. sex chromosomes Chromosome theory: Mendelian anchromosome address on a genes have loci 1000s per chrom. Chromosomes undergo segregation & independent during meiosis assortment. diploid carriotype Chromosomes can be autosomes or sex chromosomes Thomas Morgan: Morgan’s first question: where are genes located? 1st to associate a gene with a specific chromosome – white eye of fruit fly on X chromosome Morgan’s Experiment In a cross between a wild-type female fruit fly and a mutant white-eyed male, what color eyes will the F1 and F2 offspring have? XEXe or XEy, wont be any homos? this shows that its on the x chromosome XEXe x XEy = XEXE , XExe , XEy , xey white eyes = partially lethal genes so not exactly 25% 4252 flies; 782 white-eyed all male w+ = dominant Xw+ Xw+ = homo dom? Results Xwy = hemizygous recessive Xw+y= hemi dom Morgan’s symbol system differed from Mendel’s 1. All F1 red → white recessive 2. B/C white eyes expressed only in F2 males, then eye-color gene on the X chromosome [with no corresponding locus on the Y chromosome] Next Question: Are the genes for body color and wing size in fruit flies located on the same chromosome or different chromosomes? autosomal (not sex) vestigial: doesnt have a function Morgan did a testcross: b+bvg+vg x bbvgvg His expected result w/o linkage (i.e. independent assortment [this is what Mendel would have predicted]): b+bvg+vg / bbvgvg / b+bvgvg / bbvg+vg in a 1:1:1:1 ratio His expected result w/ linkage: b+bvg+vg / bbvgvg in a 1:1 ratio His actual result: Most were as expected with linkage, but got some that were not expected b+bvg+vg / bbvgvg / b+bvgvg / bbvg+vg in a 5:5:1:1 ratio (965:944:206:185) wait what??? (Morgan was first to use that term) How can this be explained? Crossing over This only happened in 17% of the gametes ****** need to know how to do Genetic Recombination: – recombination is the production of offspring with new combinations of traits inherited from two parents – results from: 1. Independent assortment: – in a dihybrid cross, there are parental and recombinant offspring → show example of pea seed color and shape cross 2. Recombination of linked genes by crossing over: – cross over breaks linkages in parental chromosomes to form recombinant chromosomes with new allele combinations 3. Random fertilization Genes are arranged linearly on a chromosome and we can map them → Morgan…again! (Actually…Sturtevant) – Recombination frequency can be used to map the relative positions of loci → genetic mapping = linkage map Alfred Sturtevant’s hypothesis: recombination frequencies reflect distances between genes on a chromosome – the farther apart two genes are, the higher the probability of a cross-over event. – one map unit = 1% recombination frequency = 1 centimorgan Use the following recombination data (same as what Sturtevant had) to map these genes Gene pair Recombination frequency b and vg 17 mu b and cn 9 mu vg and cn 9.5 mu The b−vg recombination frequency is slightly less than the sum of the b−cn and cn−vg frequencies because double crossovers are fairly likely to occur between b and vg in matings tracking these two genes. A second crossover would “cancel out” the first and thus reduce the observed b−vg recombination frequency. Figure 15.8 A partial genetic (linkage) map of a Drosophila chromosome Linkage maps only show the linear sequence of genes along a chromosome, not precise physical locations precise = DNA sequencing THE TWO GIANTS OF GENETICS Mendel postulated three laws: (1) Alleles segregate (meiosis happens) (2) Dominance (3) Independent assortment Morgan discovered the following: (1) Genes live on chromosomes (2) Chromosomes recombine (cross over) (3) Genes are arranged linearly on chromosomes Autosomes vs. Sex Chromosomes Figure 15.5 Human Sex Chromosomes: – females are XX and males are XY – X and Y behave like homologues during 1,100 genes meiosis but not true homologues – SRY gene on Y determines testes formation w/out SRY, gonads develop as ovaries – males are hemizygous for their sex Y chromosomes – other organisms? 78 genes The transmission of X-linked recessive traits. Sex-Linked Genetic Disorders X-linked disorders in humans: Color-blindness –recessive: 1 in12 men and 1 in 200 women Duchenne muscular dystrophy-recessive Hemophilia-recessive Hypertrichosis-dominant Y-linked disorders: Hairy pinnae (is it dominant or recessive?) Color blindness test. Can you see the number? Just Kidding!! Haha Go to https://colormax.org/color-blind-test/ Hypertrichosis: werewolf syndrome X-linked dominant Hairy ears: a phenotype proposed to be Y linked