Question

In: Biology

Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by...

Cystic fibrosis is a rare disease caused by homozygosity for a recessive allele, and characterized by a build-up of mucus in the lungs and difficulty breathing. A woman whose maternal uncle had the disease is trying to determine the probability she and her husband could have an affected child. Her husband's sister died of the disease. Assuming the uncle and the sister are the only family members who had the disease, what is the chance that the couple's first child will be affected? I'm getting 1/18, but chegg says 1/64? Please verify it is 1/64 for the answer.

Solutions

Expert Solution

The answer will be 1/18.

Explanation: Let, A = dominant normal allele, a = allele for cystic fibrosis

Now, according to the question, the pedigree is drawn below. III-1 is the woman, III-2 is her husband, II-3 is her maternal uncle & III-3 is her sister-in-law. As no information is given regarding frequency of the allele in the population, we assume that woman's father is homozygous dominant, i.e., AA genotype.

As only maternal uncle of woman & sister of her husband develop the disease, I-1, I-2, II-4 & II-5 will have A/a genotype. Now in order to the woman become carrier of the disease, II-2 has to be carrier. The probability that II-2 has A/a genotype is 2/3 (We would ignore a/a genotype as she doesn't develop the disease). Now, the probability that woman will get the disease allele (Allele a) from II-2 is 1/2.

So, probability that woman has genotype A/a = Probability that woman will get the disease allele (Allele a) from II-2 x Probability that II-2 has A/a genotype = 1/2 x 2/3 = 1/3

Probability that woman's husband (III-2) has A/a genotype = 2/3 (Similar to II-2)

Now, probability that she & her husband will have affected child = 1/4 (As both are carrier for the disease)

So, overall probability that they have an affected child = Probability that woman has genotype A/a x Probability that woman's husband (III-2) has A/a genotype x Probability that she & her husband will have affected child = 1/3 x 2/3 x 1/4 = 1/18


Related Solutions

Cystic fibrosis is caused by a recessive allele. (Use "N" to stand for the normal, non-disease...
Cystic fibrosis is caused by a recessive allele. (Use "N" to stand for the normal, non-disease allele). If parents that are both heterozygous for cystic fibrosis have a child, what is the percent chance that the child will have the disease?
Cystic fibrosis is an autosomal recessive disease characterized by two copies of a mutated CFTR gene....
Cystic fibrosis is an autosomal recessive disease characterized by two copies of a mutated CFTR gene. If one in 100 people in the United States have cystic fibrosis and one in 5.0505050505 people are carriers for cystic fibrosis, calculate the number of individuals that are homozygous dominant. In other words, how many people would have two copies of the normal (non-mutated) CFTR gene. Use the Hardy-Weinberg equation and explain how you determined this. 
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive...
Cystic fibrosis is caused by a mutation in a single gene. Homozygotes for this mutant recessive allele (ff) have cystic fibrosis. Within a population, 2% of people have cystic fibrosis. Assuming Hardy-Weinberg equilibrium, the frequency of heterozygotes in the population is 0.24. If inbreeding was common in this population, what would happen to the percentage of people who have cystic fibrosis over time?
Cystic fibrosis is genetic disease caused by mutations in the CFTR gene. The consequence of this...
Cystic fibrosis is genetic disease caused by mutations in the CFTR gene. The consequence of this is production of an abnormal transmembrane protein that is responsible for producing sweat, mucus, and digestive fluids. Explain in depth the correlation between the defective gene and the abnormal protein that is produced. Be sure to mention the process involved in protein production, whether or not those process(s) have occurred, and their end products. Provide details in your explanation and support your answer with...
Cystic Fibrosis is a disease caused by a defect in a Chloride ion transport channel protein....
Cystic Fibrosis is a disease caused by a defect in a Chloride ion transport channel protein. The channel performs a critical function in the lungs; thus, disease sufferers have trouble clearing mucous from their lungs, leaving them susceptible to opportunistic infections. Discuss how this protein may function (normally) in the lung & hypothesize on possible treatment schemes.
1)Cystic fibrosis an autosomal recessive disorder caused by a single gene, affects the lungs, the pancreas,...
1)Cystic fibrosis an autosomal recessive disorder caused by a single gene, affects the lungs, the pancreas, the digestive system, and other organs, resulting in symptoms ranging from breathing difficulties to recurrent infections. Which of the following terms best describes this? A)incomplete dominance B)multiple alleles C)codominance D)epistasis E)pleiotropy 2)What is one function of a signal peptide during peptide translation? A)to terminate translation of the messenger RNA B)to signal the initiation of transcription C)to bind RNA polymerase to DNA and initiate transcription...
Hemophilia is a disease caused by a recessive allele on the X chromosome. Use a Punnett...
Hemophilia is a disease caused by a recessive allele on the X chromosome. Use a Punnett square to help describe the offspring phenotypes from the cross: heterozygous female crossed to male with hemophilia.
Try-Sachs is a disease characterized by progressive neurologic degeneration, and is caused by a recessive mutation....
Try-Sachs is a disease characterized by progressive neurologic degeneration, and is caused by a recessive mutation. In a certain population, the rate of Try-Sachs is 1 in 4000 births. What is the chance of being a carrier in the population? Name three common features of plasmid vectors and what can be accomplished by each. Indicate the features that are absolutely required and why (one clear sentence about why).                     
1. Duchenne muscular dystrophy (DMD) is caused by a relatively rare X-linked recessive allele. It causes...
1. Duchenne muscular dystrophy (DMD) is caused by a relatively rare X-linked recessive allele. It causes progressive muscular wasting, and usually leads to death before age 20. What is the probability that the first son of a woman (who does not have the disease but whose father is affected) will be affected? 2. Hemophilia in humans is inherited as an X linked recessive trait. A woman whose father is hemophiliac marries a man with normal clotting ability. What is the...
A woman who is a carrier for the cystic fibrosis (cf) allele marries a man who...
A woman who is a carrier for the cystic fibrosis (cf) allele marries a man who is also a carrier. What percentage of the woman’s eggs will carry the cf allele?____________ What percentage of the man’s sperm will carry the cf allele?____________ The probability that they will have a child who carries 2 copies of the cf allele is equal to the percentage of eggs that carry the allele times the percentage of sperm that carry the allele. What is...
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT