130 likes | 394 Views
Sex-Linked Inheritance. 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
E N D
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
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. Sex Determination X X X Y X X X X X Y X Y There is a 50/50 chance of child being a boy/girl
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 NEVERbe “carriers” of sex-linked traits or disorders. • Ex: Colorblindness, Hemophilia, Muscular dystrophy
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 Sex-Linked Disorders
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
Let’s take a look at… Sex-Linked Punnett Squares
What is the probability of getting: Daughter with hemophilia? 0% Carrier child? 25% Child with hemophilia? 25% Two healthy children? ¾ x ¾ = 9/16 (56%) Jen is a healthy carrier (XH Xh) of hemophilia and Adam has no history in his family (XH Y). Healthy girl Healthy boy Healthy girl (carrier) Disease boy
What is the probability of getting a: Healthy son? 25% Healthy daughter? 25% Child with hemophilia? 50% Carrier child? 25% Kelly is a healthy carrier of hemophilia, but Jim suffers from the disease. Healthy girl (carrier) Healthy boy Disease girl Disease boy
If the phenotype is more common in males, the gene is likely sex-linked.
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? XDXd XDY Xd Y Xd Y XDXd XDY XDY ? XD Xd XDXDXDXd XD Y 25% XD YXdY 25%
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?