Jayashree B. answered 06/13/21
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a) Alleles for Hemophilia:
H - Dominant Allele (Normal)
h - Recessive Allele (Diseased)
A female can be:
XHXH (Genotype) - Normal (Phenotype)
XHXh (Genotype) - Normal and Carrier (Phenotype)
XhXh (Genotype) - Diseased (Phenotype)
A male can be:
XHY (Genotype) - Normal (Phenotype)
XhY (Genotype) - Diseased (Phenotype)
In this case,
Father is unaffected; so, the genotype of dad is XHY
Mother is a carrier; so, the genotype of mom is XHXh
Cross: XHY. x. XHXh
XH Y
XH XHXH XHY. <----- 1/2 sons unaffected
Xh XHXh XhY <----- 1/2 sons diseased
The probability of producing an unaffected son by a father who is unaffected and a mother who is a carrier of hemophilia is 1 out 2.
b) Based on the above Punnett square, we can clearly see that a male cannot be a carrier of the hemophilia allele. This is because hemophilia is an X-linked recessive disease. An X-linked recessive disease is a disease when the recessive defective/diseased allele is located on the X-chromosome. Males only have one X-chromosome. Therefore, a male could either carry the normal (H-dominant allele) or the diseased (h-recessive allele). Therefore, a male cannot be a carrier of the hemophilia allele.