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Sex-Linked Inheritance
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Two copies of each autosomal gene affect phenotype
Mendel studied autosomal gene traits (these genes are on autosomes), like hair texture. The “either-or” traits that were seen in your tutorial. Genes found on autosomes (1-22 for humans) = autosomal traits Genes found on sex chromosomes (pair 23 for humans) = sex-linked traits
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There is a 50/50 chance of child being a boy/girl
Sex Determination Sex determined by genes found on the X and Y chromosome Females: egg produced with an X chromosome X chromosome genes in mammals affect many traits. Males: ½ sperm cells contain X; and the other ½ contain Y Chromosome genes in mammals are responsible for male characteristics. X X X Y X X X X X Y X Y There is a 50/50 chance of child being a boy/girl
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Males & Females have Different
Inheritance Patterns ALL of a male’s sex-linked genes are expressed. Males have no second copies of sex-linked genes. Because of this, males can NEVER be “carriers” of sex-linked traits or disorders. Ex: Colorblindness, Hemophilia, Muscular dystrophy
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Sex-Linked Disorders Defined: Inherited conditions found on X chromosome Usually recessive Females: XX chromosomes XH XH = healthy XH Xh = healthy carrier Xh Xh = disease Males: XY chromosomes XHY = healthy XhY = disease Rare in women (back-up X chromosome) Ex: Colorblindness, Hemophilia, Muscular dystrophy
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Sample Colorblind Tests
4 Sex-Linked Traits: 1. Normal Color Vision: A: 29, B: 45, C: --, D: 26 2. Red-Green Color-Blind: A: 70, B: --, C: 5, D: -- 3. Red Color-blind: A: 70, B: --, C: 5, D: 6 4. Green Color-Blind: A: 70, B: --, C: 5, D: 2
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Sex-Linked Punnett Squares
Let’s take a look at… Sex-Linked Punnett Squares
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Jen is a healthy carrier (XH Xh) of hemophilia and Adam has no history in his family (XH Y).
What is the probability of getting: Daughter with hemophilia? 0% Carrier child? 25% Child with hemophilia? Two healthy children? ¾ x ¾ = 9/16 (56%) Healthy girl Healthy boy Healthy girl (carrier) Disease boy
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Kelly is a healthy carrier of hemophilia, but Jim suffers from the disease.
What is the probability of getting a: Healthy son? 25% Healthy daughter? Child with hemophilia? 50% Carrier child? Healthy girl (carrier) Healthy boy Disease girl Disease boy
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If the phenotype is more common in males, the gene is likely sex-linked.
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Let’s try a sex-linked problem:
A man and a woman marry. The woman is a carrier of colorblindness, an X-linked disorder. They have 4 children, 3 boys and one girl. Two of the boys are colorblind, and the girl is a carrier. The carrier daughter marries a healthy man. a)What is the probability they will have a carrier? b)What is the probability they will have a child that is colorblind? XD Xd XD Y Xd Y Xd Y XD Y XD Xd XD Y ? XD Xd XD XD XD Xd XD Y 25% XD Y Xd Y 25%
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REVIEW How are sex-linked disorders different from autosome disorders?
Why are sex-linked disorders more common in males? Write the genotype of a heterozygous dominant female. Write the genotype of a carrier female. Examine Kelly and Jim’s Punnett square. What are the chances they would have three children, all of whom are healthy?
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