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Genes on Chromosomes (Linkage & Sex) Recombination • The reassortment of genes or characteristics into different combinations from those of the parents. • happens during crossing over in prophase of meiosis. • Offspring with a new combination of characteristics/genes are called recombinants. Gene Linkage • Genes often move together in crossing over because the are close together on the same chromosome and therefore called a linkage group. • Discovered because typical expected ratios of 1:1:1:1 were coming out 1:1 or 7:1:1:7 – More offspring had parental characteristics and fewer recombinants because genes were linked • How can geneticists make use of these unusual ratios? – find which gene a chromosome is located on – identify all the genes in a linkage group – estimate how far apart the loci of genes are on a chromosome Inheritance and Gender Pedigree analysis/chart • shows the members of a family and how they are related to each other • can be used: – to follow a trait through many generations – see if the trait is dominant or recessive – see if the trait is sex-linked or not • square is male, circle female • affected individuals are darkened in Colorblindness: p = recessive colorblind allele. See Fig. 11.22 & 11.23 in text Given the following blood types, deduce the genotypes of each individual. (A and B are codominant and both are dominant over O) A_ O_ B_ A_ A_ B_ A_ O_ A_ AB AB A_ B_ A_ _ Given the following individuals affected by the “pruple condition”, deduce all phenotypes. A = normal allele (good) a = purple allele (bad) “A” dominant over “a”. Sex Linkage or X-linked • sex linkage - the association of a characteristic with gender because the gene controlling the char. is located on a sex chromosome • male 23rd chromosomes are XY and female XX • X and Y do not carry the same genes • XX, XY, X, XXY, XYY, XXX, and even more are all possible. Males (23rd – XY) • with only one X chromosome, all alleles on the X will be expressed – dominant or recessive Scientists may have saved the reputation of the ‘Y’, or male-determining human chromosome, whose functions were poorly understood. Researchers from the Whitehead Institute for Biomedical Research in Cambridge (USA) and Washington School of Medicine in St Louis (USA) have identified some 78 genes on the chromosome, instead of the 40 or so it was thought to contain. Females (23rd – XX) • females inactivate one of the two X chromosomes in each cell during embryonic development. This is called a Barr body – an inactive and dense stainable structure found in the nucleus. • X carries hundreds of genes but few, if any, of these have anything to do directly with sex. Sex-linked conditions • all are recessive alleles on the X chromosome • examples – hemophiliacs - blood does not clot very well. – colorblindness – difficulty distinguishing between shade of red and green. – muscular dystrophy - defective proteins causing defective muscles. Hemophilia