In a molecular genetics analysis of a patient, a single nucleotide substitution is detected where adenine is replaced by thymine in the sixth codon of the -globin gene, causing glutamic acid to be replaced by valine. Which of the following correctly classifies this genetic change and the pattern of variation its resulting phenotype displays in human populations?
- A gene mutation resulting in discontinuous variationAnswer
- BA gene mutation resulting in continuous variation
- CA sex-linked chromosomal aberration resulting in discontinuous variation
- DA somatic chromosomal aberration inherited via environmental adaptation
Answer
The genetic change is classified as a gene mutation and the resulting phenotype displays discontinuous variation.
The substitution of a single nitrogenous base in a codon alters the amino acid sequence of a specific polypeptide without altering the macroscopic structure or number of chromosomes, defining it as a gene (point) mutation. Because the resulting sickle-cell condition produces distinct, clear-cut phenotypic classes (normal, carrier, affected) without intermediate continuum states, it represents discontinuous variation.
Step-by-Step Solution
Key Concept
Gene mutation vs chromosomal aberration and its phenotypic expression as discontinuous variation
Estimated Time:2m 0s