Welcome

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Welcome What is a dihybrid cross?

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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 - PowerPoint PPT Presentation

Transcript of Welcome

Page 1: Welcome

Welcome

What is a dihybrid cross?

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Agenda

• Quiz• Sex Linked Traits• Mutations

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Sex Determination

• Thomas Hunt Morgan – studied fruit flies in the early 1900’s

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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

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XY XX

X Y X X

X X

X

Y

XX

FemaleXX

Female

XY

Male

XY

Male

50% Female; 50% Male

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Sex Linkage

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

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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

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Fruit Fly Eye Color

• Fruit flies normally have red eyes

• A few males have white eyes

• Red is dominant; white is recessive

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Morgan’s Fruit Fly Experiments

• Red-eyed female (XRXR) x White-eyed male (XrY)

XR XR

Xr

Y

XRXr XRXr

XRY XRY

RESULTS:

F1 generation – all red-eyed

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Morgan’s Fruit Fly Experiments

• Red-eyed female (XRXr) x Red-eyed male (XRY)

XR Xr

XR

Y

XRXR XRXr

XRY XrY

RESULTS:

F2 generation – 3 red-eyed and 1 white-eyed

** all white-eyed where males…why?

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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

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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.

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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?

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Worksheet

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Linkage Groups

• 2 or more genes that are on the same chromosome are “linked”

• Linked genes tend to be inherited together

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More Fruit Fly Experiment

• Gray, long-winged (GGLL) x black, short-winged (ggll)

• F1 generation = all heterozygous gray, long-winged (GgLl)

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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

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Morgan’s Fruit Fly Experiment

• Unexpected results– Some gray, short-winged (Ggll)– Some black, long-winged (ggLl)

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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

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Chromosome Mapping

• Chromosome Map: diagram that shows the possible genes on a chromosome

• Made using crossing-over data

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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

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MUTATIONS

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Mutations

• Mutation: change in DNA

VIDEO

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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

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Possible Effects of Mutations

• Lethal mutations: cause death, often before birth

• Beneficial mutations: provide variation needed for evolution

• No effect

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Chromosome Mutations

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

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Chromosome Mutations

• Deletion: loss of piece of chromosome due to breakage

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Chromosome Mutations

• Deletion: loss of piece of chromosome due to breakage

– Example – Cri du chat; deletion of part of chromosome 5

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Chromosome Mutations

• Duplication: part of chromosome is duplicated/copied

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Chromosome Mutations

• Duplication: part of chromosome is duplicated/copied

– Example – Charcot-Marie Tooth Disease

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Chromosome Mutations• Inversion: piece breaks off and reattaches to

SAME chromosome in wrong order

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Chromosome Mutations

• Inversion: piece breaks off and reattaches to SAME chromosome in wrong order

– Example – Hemophilia (this disorder is also X linked)

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Chromosome Mutations

• Translocation: piece breaks off and reattaches to DIFFERENT chromosome

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Chromosome Mutations

• Translocation: piece breaks off and reattaches to DIFFERENT chromosome

– Example – Cancer

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Chromosome Mutations

• Nondisjunction: chromosomes do not separate during meiosis

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Chromosome Mutations

• Nondisjunction: chromosomes do not separate during meiosis

– Example – trisomy, monosomy

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Gene Mutations

• Gene Mutations: involve large segments of DNA (genes) or a single nucleotide

– Causes possible changes in the amino acid sequence

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Gene Mutations

• Point Mutation: substitution, addition, or deletion of a single nucleotide

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Gene Mutations

• Point Mutation: substitution, addition, or deletion of a single nucleotide

– Example – sickle cell anemia

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Gene Mutations

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