Question

Human adult hemoglobin is a tetramer containing two alpha (α) and two beta (β) polypeptide chains. The α gene cluster on chromosome 16 and the β gene cluster on chromosome 11 share amino acid similarities such that 61 of the amino acids of the α-globin polypeptide (141 amino acids long) are shared in identical sequence with the β-globin polypeptide (146 amino acids long). How might one explain the existence of two polypeptides with partially shared function and structure on two different chromosomes?

Accepted Answer

Step 1: Understand the biological context — human adult hemoglobin is composed of two alpha (α) and two beta (β) polypeptide chains, each encoded by gene clusters located on different chromosomes (α on chromosome 16 and β on chromosome 11). Step 2: Recognize that the α- and β-globin polypeptides share a significant number of identical amino acids (61 out of 141 in α-globin and 146 in β-globin), indicating a degree of sequence similarity and possibly a common evolutionary origin. Step 3: Consider the concept of gene duplication and divergence, where an ancestral globin gene duplicated in the genome, and over time, the copies evolved separately on different chromosomes, leading to related but distinct polypeptides. Step 4: Explain that this evolutionary process can result in paralogous genes—genes related by duplication within a genome—that retain some structural and functional similarities but also acquire unique features to fulfill specialized roles. Step 5: Conclude that the presence of two polypeptides with partially shared function and structure on different chromosomes is best explained by gene duplication followed by divergence, which allows the organism to produce hemoglobin with subunits adapted for cooperative oxygen binding.

비슷한 문제에 대한 검증된 영상 답변:

주요 개념

Gene Duplication and Divergence

Homologous Genes and Protein Families

Chromosomal Localization and Gene Clusters