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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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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 • Large one named “X” chromosome • Smaller one named “Y” chromosome • XX = female; XY = male
XY XX X Y X X X X XX Female XX Female X XY Male XY Male Y 50% Female; 50% Male
Sex Linkage • Sex Linkage: the presence of a gene on a sex chromosome (X or Y)
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
Fruit Fly Eye Color • Fruit flies normally have red eyes • A few males have white eyes • Red is dominant; white is recessive
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
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
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
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.
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?
Linkage Groups • 2 or more genes that are on the same chromosome are “linked” • Linked genes tend to be inherited together
More Fruit Fly Experiment • Gray, long-winged (GGLL) x black, short-winged (ggll) • F1 generation = all heterozygous gray, long-winged (GgLl)
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
Morgan’s Fruit Fly Experiment • Unexpected results • Some gray, short-winged (Ggll) • Some black, long-winged (ggLl)
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
Chromosome Mapping • Chromosome Map: diagram that shows the possible genes on a chromosome • Made using crossing-over data
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
Mutations • Mutation: change in DNA VIDEO
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
Possible Effects of Mutations • Lethal mutations: cause death, often before birth • Beneficial mutations: provide variation needed for evolution • No effect
Chromosome Mutations • Chromosome Mutations: a change in the chromosome structure or loss/addition of entire chromosome
Chromosome Mutations • Deletion: loss of piece of chromosome due to breakage
Chromosome Mutations • Deletion: loss of piece of chromosome due to breakage • Example – Cri du chat; deletion of part of chromosome 5
Chromosome Mutations • Duplication: part of chromosome is duplicated/copied
Chromosome Mutations • Duplication: part of chromosome is duplicated/copied • Example – Charcot-Marie Tooth Disease
Chromosome Mutations • Inversion: piece breaks off and reattaches to SAME chromosome in wrong order
Chromosome Mutations • Inversion: piece breaks off and reattaches to SAME chromosome in wrong order • Example – Hemophilia (this disorder is also X linked)
Chromosome Mutations • Translocation: piece breaks off and reattaches to DIFFERENT chromosome
Chromosome Mutations • Translocation: piece breaks off and reattaches to DIFFERENT chromosome • Example – Cancer
Chromosome Mutations • Nondisjunction: chromosomes do not separate during meiosis
Chromosome Mutations • Nondisjunction: chromosomes do not separate during meiosis • Example – trisomy, monosomy
Gene Mutations • Gene Mutations: involve large segments of DNA (genes) or a single nucleotide • Causes possible changes in the amino acid sequence
Gene Mutations • Point Mutation: substitution, addition, or deletion of a single nucleotide
Gene Mutations • Point Mutation:substitution, addition, or deletion of a single nucleotide • Example – sickle cell anemia
Gene Mutations • Frame Shift Mutation: occurs when the number of nucleotides inserted or deleted is not a multiple of 3