Discover answers to your questions with Westonci.ca, the leading Q&A platform that connects you with knowledgeable experts. Join our platform to get reliable answers to your questions from a knowledgeable community of experts. Our platform offers a seamless experience for finding reliable answers from a network of knowledgeable professionals.

Cystic fibrosis is most common in individuals of Northern European descent, affecting 1 in 3200 newborns. Assuming that these alleles are at Hardy-Weinberg equilibrium, what is the frequency of the disease-causing CFTR alleles in this population

Sagot :

Answer:

0.0177

Explanation:

Cystic fibrosis is an autosomal recessive disease, thereby an individual must have both copies of the CFTR mutant alleles to have this disease. The Hardy-Weinberg equilibrium states that p² + 2pq + q² = 1, where p² represents the frequency of the homo-zygous dominant genotype (normal phenotype), q² represents the frequency of the homo-zygous recessive genotype (cystic fibrosis phenotype), and 2pq represents the frequency of the heterozygous genotype (individuals that carry one copy of the CFTR mutant allele). Moreover, under Hardy-Weinberg equilibrium, the sum of the dominant 'p' allele frequency and the recessive 'q' allele frequency is equal to 1. In this case, we can observe that the frequency of the homo-zygous recessive condition for cystic fibrosis (q²) is 1/3200. In consequence, the frequency of the recessive allele for cystic fibrosis can be calculated as follows:

1/3200 = q² (have two CFTR mutant alleles) >>  

q = √ (1/3200) = 1/56.57 >>

- Frequency of the CFTR allele q = 1/56.57 = 0.0177  

- Frequency of the dominant 'normal' allele p = 1 - q = 1 - 0.0177 = 0.9823