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Welcome. What is a dihybrid cross?. Agenda. Quiz Sex Linked Traits Mutations. Sex Determination. Thomas Hunt Morgan – studied fruit flies in the early 1900’s. Sex Determination. Observed that one pair of chromosomes was different between males and females

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  1. Welcome What is a dihybrid cross?

  2. Agenda • Quiz • Sex Linked Traits • Mutations

  3. Sex Determination • Thomas Hunt Morgan – studied fruit flies in the early 1900’s

  4. Sex Determination • Observed that one pair of chromosomes was different between males and females • Large one named “X” chromosome • Smaller one named “Y” chromosome • XX = female; XY = male

  5. XY XX X Y X X X X XX Female XX Female X XY Male XY Male Y 50% Female; 50% Male

  6. Sex Linkage • Sex Linkage: the presence of a gene on a sex chromosome (X or Y)

  7. Sex Linkage • X-linked genes: genes found on the X chromosome • X chromosome carries more genes • Y-linked genes: genes found on the Y chromosome

  8. Fruit Fly Eye Color • Fruit flies normally have red eyes • A few males have white eyes • Red is dominant; white is recessive

  9. Morgan’s Fruit Fly Experiments • Red-eyed female (XRXR) x White-eyed male (XrY) XR XR XRXr XRXr RESULTS: F1 generation – all red-eyed Xr XRY XRY Y

  10. Morgan’s Fruit Fly Experiments • Red-eyed female (XRXr) x Red-eyed male (XRY) XR Xr RESULTS: F2 generation – 3 red-eyed and 1 white-eyed ** all white-eyed where males…why? XRXR XRXr XR XRY XrY Y

  11. Morgan’s Conclusions • Gene for eye color is carried on the X chromosome = eye color is an X-linked trait • Y chromosome does not carry a gene for eye color • Red-eyed = XRXR, XRXr , XRY • White-eyed = XrXr, XrY

  12. In humans colorblindness (b) is an example of a sex-linked recessive trait. A male with colorblindness marries a female who is not colorblind but carries the (b) allele. Using a Punnett square, determine the genotypic and phenotypic probabilities for their potential offspring.

  13. In fruit flies red eye color (R) is dominant to white eyes (r). In a cross between two flies, 50% of the male and 50% of the female offspring had red eyes. The other half of the males and females had white eyes. What are the phenotype, and all possible genotypes, of the offspring?

  14. Worksheet

  15. Linkage Groups • 2 or more genes that are on the same chromosome are “linked” • Linked genes tend to be inherited together

  16. More Fruit Fly Experiment • Gray, long-winged (GGLL) x black, short-winged (ggll) • F1 generation = all heterozygous gray, long-winged (GgLl)

  17. Morgan’s Fruit Fly Experiment • Cross F1 flies: GgLl x GgLl • F2 generation • If alleles on different chromosomes, they assort independently and get a 9:3:3:1 ratio • If alleles on same chromosome, get 3 gray, long-winged: 1 black, short-winged ratio • Morgan saw roughly the 3:1 ratio

  18. Morgan’s Fruit Fly Experiment • Unexpected results • Some gray, short-winged (Ggll) • Some black, long-winged (ggLl)

  19. Morgan’s Fruit Fly Experiment • How were these alleles separated? • Alleles were rearranged through crossing-over during meiosis • Genes that are farther apart are more likely to be separated by crossovers

  20. Chromosome Mapping • Chromosome Map: diagram that shows the possible genes on a chromosome • Made using crossing-over data

  21. Chromosome Mapping • The percentage of crossing-over between the genes for 2 traits is equal to the distance between them on a chromosome • This distance is measured in map units

  22. MUTATIONS

  23. Mutations • Mutation: change in DNA VIDEO

  24. Mutations • Germ-cell mutation: occurs in sex cells • Affect the offspring • Example – Down Syndrome • Somatic mutation: occurs in body cells • Affect the individual • Example - Cancer

  25. Possible Effects of Mutations • Lethal mutations: cause death, often before birth • Beneficial mutations: provide variation needed for evolution • No effect

  26. Chromosome Mutations • Chromosome Mutations: a change in the chromosome structure or loss/addition of entire chromosome

  27. Chromosome Mutations • Deletion: loss of piece of chromosome due to breakage

  28. Chromosome Mutations • Deletion: loss of piece of chromosome due to breakage • Example – Cri du chat; deletion of part of chromosome 5

  29. Chromosome Mutations • Duplication: part of chromosome is duplicated/copied

  30. Chromosome Mutations • Duplication: part of chromosome is duplicated/copied • Example – Charcot-Marie Tooth Disease

  31. Chromosome Mutations • Inversion: piece breaks off and reattaches to SAME chromosome in wrong order

  32. Chromosome Mutations • Inversion: piece breaks off and reattaches to SAME chromosome in wrong order • Example – Hemophilia (this disorder is also X linked)

  33. Chromosome Mutations • Translocation: piece breaks off and reattaches to DIFFERENT chromosome

  34. Chromosome Mutations • Translocation: piece breaks off and reattaches to DIFFERENT chromosome • Example – Cancer

  35. Chromosome Mutations • Nondisjunction: chromosomes do not separate during meiosis

  36. Chromosome Mutations • Nondisjunction: chromosomes do not separate during meiosis • Example – trisomy, monosomy

  37. Gene Mutations • Gene Mutations: involve large segments of DNA (genes) or a single nucleotide • Causes possible changes in the amino acid sequence

  38. Gene Mutations • Point Mutation: substitution, addition, or deletion of a single nucleotide

  39. Gene Mutations • Point Mutation:substitution, addition, or deletion of a single nucleotide • Example – sickle cell anemia

  40. Gene Mutations • Frame Shift Mutation: occurs when the number of nucleotides inserted or deleted is not a multiple of 3

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