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Chromosomal Genetic. Linked genes Morgan: studied eye color in Drosophila (flies) P1 true breeding white eyed males mated with P1 true breeding red eye.

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Presentation on theme: "Chromosomal Genetic. Linked genes Morgan: studied eye color in Drosophila (flies) P1 true breeding white eyed males mated with P1 true breeding red eye."— Presentation transcript:

1 Chromosomal Genetic

2 Linked genes Morgan: studied eye color in Drosophila (flies) P1 true breeding white eyed males mated with P1 true breeding red eye females F1: all red eyes (expected) F2: 3:1 red eyes to white (expected) BUT, the white eyes showed up only in MALES All females had red eyes: about half the males had red…..the other half of the males had white CONCLUSION: eye color linked to sex of fly

3 Phenotypes In a cross: the offspring will get either:  Parental phenotype: same as 1 of the parents OR  recombinant phenotype NOT same as either parent

4 Genetic Recombination Recombination of unlinked genes:  Independent assortment of chromosomes Recombination of Linked genes:  Crossing over

5 Linkage maps Linkage maps are based on the frequency of recomination. If 50% recombo same as if on separate chromosomes 1% crossing over = 1 map unit

6 Linkage Map Problems Draw a linkage map(s) for the following recombination frequencies: 1. A-B 30%, B-C 20%, B-D 35%, C-D 25%, A-C 50%, A-D 50% 2. A-C 50%, C-D 15%, A-D 50%, A-B 30%, B-C 50%, B-D 50%

7 Sex linked recessive traits are more common in MALES

8 Sex linked disorders (recessive) SEX LINKED DISORDERS Red green color blindness- malfunction in light sensitive cells in the eye Hemophilia- lack one or more proteins needed for blood clotting Duchenne muscular dystrophy- progressive weakening of muscles and loss of coordination

9 Sex linked recessive

10 Common Chromosomal Abnormalities http://anthro.palomar.edu/abnormal/abnormal_ 4.htm Two Main Categories  Structural modification  Irregular number Typically result from nondisjunction during meiosis Polyploidy-complete multiples of sets of chromosomes (23+23+23) Aneulploidy-addition or loss of chromosomes within a set (23+22)

11 Autosomal Defects http://anthro.palomar.edu/abnormal/abnormal_ 4.htm Down’s Syndrome Typically trisomy of chromosome 21 Some have translocation of 21 to 14 or 15 2-4% are genetically mosaic 75-80% of Down syndrome children are born to women under 35 Monosomy Only one set of chromosomes remains after fertilization All fetuses will spontaneously abort

12 Female Abnormalities Male Abnormalities http://anthro.palomar.edu/abnormal/abnormal_ 4.htm Metafemale(XXX)  Unusually tall, low to normal intelligence  Normal sex characteristics, fertile Turner Syndrome (XO)  Ovaries do not develop, and do not ovulate  Lack secondary sex characteristics  Slight mental retardation Klinefelter Syndrome (XXY)  High-pitched voice  Asexual to feminine body type  Low testosterone, sterile  1 in 500 XYY Syndrome  Unusually tall, severe acne  High testosterone levels, possibly leading to violence Sex Chromosome Abnormalities


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