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Non-Mendelian Genetics: Genetics that don’t follow Mendel’s laws. 93. Pedigree 94. Sex-linked trait 95. Polygenic trait 96. Incomplete dominance 97. Codominance 98. Multiple alleles 99. Mutation. Vocabulary Terms…. Read 171-180. Chromosomes and Human Genetics.
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Non-Mendelian Genetics:Genetics that don’t follow Mendel’s laws
93. Pedigree 94. Sex-linked trait 95. Polygenic trait 96. Incomplete dominance 97. Codominance 98. Multiple alleles 99. Mutation Vocabulary Terms… Read 171-180
Chromosomes and Human Genetics 2 Types of Human Chromosomes: • Sex Chromosomes- Determine the sex of the individual as well as other traits. Diploid cells have 1 pair of these. • Male- XY (not the same size but are homologous partners during meiosis). • Female- XX • Autosomes- Contain genes unrelated to the sex of the individual. Diploid cells have 22 pairs of these.
Determining Sex MOM X X X X X X X DAD X Y X Y Y
Sex-Linked TraitsGenes on the Sex Chromosomes • Expression of certain genes often appears more in one sex than the other • Males have 1 x sex chromosome; therefore, it only takes that one x to be affected to make the male have a x-linked disease • X linked disorders show up in males whose mothers were carriers (heterozygotes) • X-linked disorders show up rarely in females • See Royal Families of Europe Pedigree • Ex. Eye color in fruit flies, hemophilia, color-blindness
Practice Sex-linked Problems • Hemophilia is a recessive trait linked to the x sex chromosome. What will the result be of mating between a carrier female and a normal male?
Red-green colorblindness is a recessive trait linked to the x sex chromosome. A colorblind female and a normal male have a child. What is the probability that it will be colorblind?
4. Muscular Dystrophy is an X-linked recessive trait. A carrier female and a normal male have children. Will any of their children have a chance of having this disorder? If so, who? Show your work.
NOT IN YOUR NOTES BUT GIVE IT A TRY! • Hemophilia is inherited as an X-linked recessive. A woman has a brother with this defect and a mother and father who are phenotypically normal. What is the probability that this woman will be a carrier if she herself is phenotypically normal?
Pedigree Analysis • Method of tracking a trait through generations within a family. • Good method of tracking sex-linked traits as well as autosomal traits.
X-Sex-Linked Pedigree • Shows gender bias with males exhibiting the trait more often than females
Autosomal Dominant Pedigree • Autosomal dominant traits do not skip a generation • Autosomal dominant traits do not show gender bias
Autosomal Recessive Pedigree • Autosomal recessive traits skip a generation • Autosomal recessive traits do not show gender bias
Gene Location • Linked – Linkage Groups – genes located so close together on a chromosome that the traits always seem to appear together Ex. Red hair and freckles Ex. Colorblindness and Hemophilia X X
Gene Interactions • Polygenetic trait – many genes influence a single trait (ex. Height, intelligence) • Pleiotropic effect – one gene having many effects (ex. Gene to make testosterone)
Pleiotropy ? • Expression of a single gene which has multiple phenotypic effects • Marfan Syndrome – abnormal gene that makes fibrillin (important in connective tissues)
Non-Mendelian Genetics • Incomplete Dominance – blended inheritance • Neither form of the gene is able to mask the other • Ex. Snap dragon petal color • R1R1 – RED • R1R2 – PINK • R2R2 - WHITE
Try these • In a plant species, if the B1allele (blue flowers) and the B2 allele (white flowers) are incompletely dominant (B1 B2is light blue), what offspring ratio is expected in a cross between a blue-flowered plant and a white-flowered plant?
What would be the phenotypic ratio of the flowers produced by a cross between two light blue flowers?
2. Oompas can have red (H1H1), blue (H2H2), or purple hair (H1H2). The allele that controls this is incompletely dominant. A purple haired Oompa marries a blue haired Oompa. What will their children be like? Give phenotypic and genotypic ratios.
Codominance • No dominance and both alleles are completely expressed • Ex. Cat color • C1C1 – Tan • C1C2 – Tabby (black and tan spotted) • C2C2 - Black
Try These • Cattle can be red (RR = all red hairs), white (WW = all white hairs), or roan (RW = red & white hairs together. • Predict the phenotypic ratios of offspring when a homozygous white cow is crossed with a roan bull.
What should the genotypes & phenotypes for parent cattle be if a farmer wanted only cattle with roan fur?
A cross between a black cat & a tan cat produces a tabby pattern (black & tan fur together). • What pattern of inheritance does this illustrate? • What percent of kittens would have tan fur if a tabby cat is crossed with a black cat?
Multiple Alleles • More than 2 alleles for one trait • Ex. Eye color, hair color, blood type, guinea pig fur color • ABO blood groups • Each individual is A, B, AB, or O phenotype • Phenotype controlled by marker on RBC • IA and IB alleles are dominant to the i allele • IA and IB alleles are codominant to each other
Blood Type: A B AB O Genotype IAIA, IAi IBIB, IBi IAIB ii Blood Types
Human hair color follows a similar pattern: Alleles: HBn = brown HBd = blonde hR = red hbk = black HBnHBn = dark brown HBnHBd = sandy brown HBnhR = auburn HBnhbk = dark brown HBdHBd = blonde HBdhR = strawberry blonde HBdhbk = blonde hRhR = red hRhbk = red hbkhbk = black Recessive can be common! Dominant does NOT mean frequent!
Try These • If a male is homozygous for blood type B and a female is heterozygous for blood type A, what are the possible blood types in the offspring?
Is it possible for a child with Type O blood to be born to a mother who is type AB? Why or why not?
A child is type AB. His biological mother is also type AB. What are the possible phenotypes of his biological father?
V. Genetic Conditions • Genetic Abnormality – rare condition with little or no ill effects - Ex. Six fingers, albino, colorblindness
2. Genetic Disorders • Inherited condition that results in a medical problem - Ex. Huntington’s Disease, Sickle Cell Anemia, Hemophilia, Muscular Dystrophy
3. Genetic Disease • A genetic condition that makes the individual susceptible to infection (bacterial or viral) - Ex. Cystic fibrosis, Down syndrome, SCID (severe combined immunodeficiency disease = bubble boy)
VI. Mutations • Definition – any change in the DNA • Possible outcomes: good, bad, or no effect • Location: • Somatic Cell (body cell) – can lead to cancer • Sex Cell – reproductive organ affecting gametes
Observed vs. Expected Ratios • Observed Ratio – what you actually get from two organisms having offspring – ex. having all girls • Expected Ratio – based on your Punnett square results – what you would expect to get – ex. half girls and half boys • Another Example – using dice
Human Genetics Test Topics • Sex-linked Traits • Incomplete Dominance/ Codominance • Multiple Alleles (blood typing problems) • Genetic Conditions • Sex Chromosomes vs. Autosomes • Pedigrees/Karyotypes • Observed vs. Expected Ratios • LOTS OF GENETICS PROBLEMS – SHOW WORK!!!
Human Genetics Test Review Questions: My daughter is type A, my grandson is type B. What are the blood type(s) that the father would have to be in order for my grandson to be type B?
Red-green color blindness is X-linked in humans. If a male is red-green color blind, and both parents have normal color vision, which of the male's grandparents is most likely to be red-green color blind? • A. maternal grandmother B. maternal grandfather C. paternal grandmother D. paternal grandfather E. either grandfather is equally likely
Suppose a child is of blood type A and the mother is of type 0. What type or types may the father belong to?