What Would Be the Consequences of a Two Nucleotide-Deletion Mutation

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The Answer is A two nucleotide-deletion mutation in the middle of the first exon of a protein-coding gene would likely have significant consequences for the resulting protein. Exons are the coding regions of a gene, and any mutation within these regions can directly impact the structure and function of the protein that is produced.

In this case, a two nucleotide-deletion mutation would cause a frameshift mutation, where the reading frame of the gene is shifted, leading to a completely different amino acid sequence downstream of the mutation. This can result in a non-functional or significantly altered protein.

The consequences of this mutation could include the production of a truncated protein, a protein with altered function, or the complete loss of protein production. Depending on the specific gene and protein involved, this could lead to a variety of potential outcomes, including genetic disorders, developmental abnormalities, or an increased risk of certain diseases.

Overall, a two nucleotide-deletion mutation in the middle of the first exon of a protein-coding gene would likely have detrimental effects on the function of the gene and the resulting protein, with potential implications for the health and development of an organism.

What Would Be the Consequences of a Two Nucleotide-Deletion Mutation

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