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Published byLewis George Modified over 9 years ago
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Recall that the 23 rd chromosome in humans dictates the gender of the individual The Y chromosome is much smaller, and carries much less genetic info
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X chromosome Y chromosome Colourblindness Hemophilia 900-1600 genes 70-200 genes
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Genes found on the either chromosome are called sex-linked traits Far more are found on the X, and not found on the Y What does this mean for males?? They are more susceptible to conditions found on the Y chromosome All X-linked conditions are expressed more so in males
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Can result from a defect in one of three genes found on X chromosome
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Possible Inheritance of Colorblindness Allele
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Hemophilia Genes for clotting found on X chromosome Defects lead to deficiencies in expression of coagulation factors Patients blood does not clot as easily ◦ Cuts can be fatal
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Duchenne Muscular Dystrophy Another X-linked condition Sufferers lack a muscle protein, skeletal muscle degrades
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One of the X chromosomes is inactivated in females (randomly) Chromosome forms a dense region that attaches to nuclear envelope Stains darker, visible under light microscope Called a Barr Body Discovered by a Canadian cytogeneticist Dr Murray L. Barr
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Other dark spots are nucleoli
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Used in 1966 Olympics to test for males attempting to pass as females Resulted in the stripping of medals from individuals because of ambiguous genital sex ◦ Genetic defect that allows males to appear as females Also successfully indentified a number of cases of testicular feminization syndrome (androgen insensitivity syndrome) ◦ Error in androgen receptors resulting in XY individual developing phenotypically as females
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