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Chapter 12

Chapter 12. Patterns of Heredity and Human Genetics. Making a Pedigree. A pedigree is a graphic representation of the genetic inheritance of ONE trait Symbols Circle - female Square - male Shaded in - shows the trait

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Chapter 12

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  1. Chapter 12 Patterns of Heredity and Human Genetics

  2. Making a Pedigree • A pedigree is a graphic representation of the genetic inheritance of ONE trait • Symbols • Circle - female • Square - male • Shaded in - shows the trait • Half shaded in - is a carrier, heterozygous individual that does not show the trait • Each horizontal row is a generation - represented by roman numerals • Parents are connected horizontally • Children are connected to parents with a vertical line

  3. Pedigree Example

  4. Simple Recessive Heredity • Most genetic disorders are recessive • Cystic Fibrosis • 1/25 white Americans is a carrier • 1/2500 white Americans inherits the disorder • Defective protein in the plasma membrane • Formation and accumulation of thick mucus in the lungs and digestive tract

  5. Simple Recessive Heredity • Tay-Sachs Disease • Results in the absence of an enzyme that normally breaks down a lipid produced and stored in the central nervous system(CNS) • The lipid accumulates • Common among Ashkanazic Jews - Eastern Europe • Blue stained areas are swollen neurons

  6. Simple Recessive Heredity • Phenylketonuria (PKU) • Absence of an enzyme that converts the amino acid, phenyalanine, to tyrosine. • Phenylalanine accumulates and damages the CNS (in milk, diet foods) • Can also damage a heterozygous fetus with blood from homozygous recessive mother • Common in those with ancestry from Norway, Sweden, or Iceland

  7. Simple Dominant Heredity • Cleft chin, widow’s peak, unattached earlobes, hitchhiker’s thumb (back more than 30 degrees), almond-shaped eyes, thick lips, mid-digital hair

  8. Simple Dominant Heredity • Huntington’s Disease • Breakdown of certain areas of the brain • Usually, dominant disorders like this disappear, because it kills before the individual can reproduce • In this disease, onset happens between 30 and 50

  9. Section 1 Review • What do these symbols represent in a pedigree: square, circle, unshaded circle, shaded square, horizontal line, vertical line? • Describe a genetic disorder that is inherited as a recessive trait. • How are the cause and onset of symptoms of Huntington’s disease different from those of PKU and Tay-Sachs disease? • Describe one trait that you inherited by simple dominance.Will you pass it on to your offspring? • Suppose that a child with unattached earlobes has a mother with attached earlobes. Can a man with attached earlobes be the child’s father?

  10. Incomplete Dominance • The phenotype of heterozygous individuals is intermediate between those of the two homozygotes • Snap Dragon • Red Flowered (RR) x White Flowered (R’R’) • All F1 will be pink(RR’) • What will the F2 generation look like?

  11. Codominance • The phenotypes of both homozygotes is expressed in heterozygous individuals • Chickens • Black-feathered (BB) x White-feathered (WW) • All F1 will have both black feathers and white feathers (BW) • What will F2 look like?

  12. Multiple Phenotypes from Multiple Alleles • For many traits, though you only have two alleles, many can exist in a population • The trait is said to have multiple alleles • Pigeons • Three alleles govern feather color • BA is dominant - ash red feathers • B allele is dominant to b, but recesive to BA - blue feathers • b is recessive to both - chocolate-colored feathers

  13. Sex Determination • There are 22 pairs of homologous chromosomes called autosomes • The 23rd pair of chromosomes are called the sex chromosomes • Male XY • Female XX

  14. Sex-Linked Traits • Traits controlled by genes located on sex chromosomes are called sex-linked traits • The alleles are written as superscripts of the X or Y chromosome • Alleles on Y chromosomes don’t have a corresponding allele on an X chromosome • In males, if they have a recessive allele on their X chromosomes, there isn’t another allele to cover it up Virtual Fruit Fly Lab

  15. Fruit Flies • Thomas Hunt Morgan (1910) experimented with fruit fly eye color • Red Eyed Female (XRXR) x White-Eyed Male (XrY) • Assume two females and two males, what will the kids look like? • Females - all red (XRXr) • Males - all red (XRY)

  16. Polygenic Inheritance • The inheritance pattern of a trait is controlled by two or more genes • Skin color, height, corn cob length • Genes may be on the same chromosome or different chromosomes • Each gene may have two or more alleles • Each allele represented by an uppercase letter contributes a small, but equal, portion to the trait being expressed • The result is that phenotypes show a continuous range of variability back

  17. Polygenic Inheritance • Hypothetical Example • Stem length in a plant is controlled by 3 different genes: A, B, D. • Each gene is on a different chromosome and has two alleles (A & a, B & b, D & d) • Each plant will have 6 alleles for stem length • Each tall allele contributes 2 cm (4 cm base minimum) • What would a plant with a genotype of AaBbDd look like? • A population will follow a normal curve. back

  18. Environmental Influences • Genetics only determine potential • External Environmental Influences • Temperature, nutrition, light, chemicals and infectious agents can all influence gene expression • In Siamese cats and arctic foxes, temperature has an effect on coat color • Leaves can have different sizes, thicknesses, and shapes depending on the amount of sunlight they receive

  19. Environmental Influences • Internal environmental influences • Horn size in males and female mountain sheep is different due to differing internal environments • Also applies to baldness in humans and feather color in peacocks • Age can also affect gene expression, though this isn’t completely understood

  20. Section 2 Review • A cross between an purebred animal with red hairs and a purebred animal with white hairs produces an animal that has both red hairs and white hairs. What type of inheritance pattern is involved? • If a white-eyed male fruit fly were crossed with a heterozygous red-eyed female fruit fly, what ratio of genotypes would be expected in the offspring? • A red-flowered plant is crossed with a white-flowered plant. All of the offspring are pink. What inheritance pattern is expressed? • The color of wheat grains shows variability between red and white with multiple phenotypes. What is the inheritance pattern? • Armadillos always have four offspring that have identical genetic makeups. Suppose that, within a litter, each young armadillo is found to have a different phenotype for a particular trait. How could you explain this?

  21. Sickle-Cell Disease • An example of codominance in humans • Common in African Americans and Americans with ancestry near the Mediterranean Sea • Homozygous – hemoglobin differs from normal by 1 amino acid • Changes the shape of the red blood cells (rbc) • Slow blood flow, block small vessels, and result in tissue damage and pain

  22. Sickle-Cell Disease • Heterozygous – produce both normal and sickled hemoglobin (codominance) • Enough that they don’t have major health problems • Show sickle-cell related disorders when oxygen isn’t readily available

  23. Blood Type • There are three alleles for the gene, “I” • IA, IB, and i • IA,IA or IA, i – blood type A • IB, IB or IB, i – blood type B • IA, IB – codominance, blood type AB • ii – blood type O • There are different molecules that are produced on the surface of the rbc – represented by A and B • Your immune system fights against blood cells with different molecules • So who can donate blood to whom? • IA, i x IB, i – What will be produced?

  24. Nondisjunction in Humans • A karyotype, a chart of chromosome pairs during metaphase, is used to detect these disorders

  25. Down Syndrome • Trisomy 21 • The only autosomal trisomy in which affected individuals survive to adulthood • Occurs about 1 in 700 births • A group of symptoms, including some degree of mental retardation, results from trisomy 21

  26. Nondisjunction in Sex Chromosomes • XO – Turner’s Syndrome • XXY – Klinefelter Syndrome • XXX – Trisomy X Syndrome • XYY Syndrome • Most of these individuals have some degree of mental retardation and they cannot have kids.

  27. Sex-Linked Traits in Humans • Red-Green Color Blindness • Recessive allele on the X chromosome • How will a boy get it? A girl?

  28. Sex-Linked Traits in Humans • Hemophilia • Recessive disease that prevents the blood’s ability to clot • In males – 1 in 10,000 • In females – 1 in 100,000,000 • Why the difference?

  29. Skin & Eye Color • Both polygenic traits • What was polygenic inheritance? • How will this work for skin? • How will this work for eye color?

  30. MiniLab (p. 327 in book) • Human eye color, like skin color, is determined by polygenic inheritance. You can detect several shades of eye color, especially if you look closely at the iris with a magnifying glass. Often, the pigment is deposited so that light reflects from the eye, causing the iris to appear blue, green, gray, or hazel (brown-green). In actuality, the pigment may be yellowish or brown, but not blue. • Procedure: • 1. Use a magnifying glass to observe the patterns and colors of pigments in the eyes of 5 classmates. • 2. Use crayons to make drawings of the 5 irises. • 3. Describe your observations. • Analysis • 1. Observe How many different pigments were you able to detect in each eye? • 2. Critique From your data, do you suspect that eye color might not be inherited by simple Mendelian rules? Explain. • 3. Analyze Suppose that two people have brown eyes. They have two children with brown eyes, one with blue eyes, and one with green eyes. What pattern might this suggest?

  31. Section 3 Review • Describe how a zygote with trisomy 21 is likely to occur during fertilization. • In addition to revealing chromosome abnormalities, what other information about an individual would a karyotype show? • What would the genotypes of parents have to be for them to have a color-blind daughter? • Describe a genetic trait in humans that is inherited as codominance. Describe the phenotypes of the two homozygotes and that of the heterozygote. Why is this trait an example of codominance? • A man is accused of fathering two children, one with type O blood and another with type A blood. The mother of the children has type B blood. The man has type AB blood. Could he be the father of both children? Explain your answer.

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