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Multiple Choice
Which of the following mutations of the ras gene is most likely associated with cancer?
A
A mutation in the non-coding intronic region of the ras gene
B
A mutation that results in premature stop codon and loss of Ras protein
C
A silent mutation that does not change the amino acid sequence
D
A point mutation that leads to constitutive activation of Ras (e.g., G12V)
Verified step by step guidance
1
Understand the role of the Ras protein: Ras is a GTPase that plays a critical role in cell signaling pathways, particularly those regulating cell growth and division. Mutations in Ras can lead to uncontrolled cell proliferation, which is a hallmark of cancer.
Analyze the types of mutations: Mutations can occur in different regions of a gene (coding or non-coding) and can have varying effects on protein function. For example, mutations in non-coding regions often do not affect protein function, while coding region mutations can alter the protein's structure or activity.
Evaluate the options: Consider the impact of each mutation described in the problem. A mutation in the non-coding intronic region is unlikely to affect Ras protein function. A premature stop codon would lead to a truncated, non-functional Ras protein, which is not associated with cancer. A silent mutation does not change the amino acid sequence and thus does not affect protein function.
Focus on the constitutive activation mutation: A point mutation, such as G12V, leads to constitutive activation of Ras. This means Ras remains permanently active, continuously signaling for cell growth and division, even in the absence of external signals. This uncontrolled signaling is strongly associated with cancer development.
Conclude the reasoning: Based on the analysis, the mutation most likely associated with cancer is the point mutation that leads to constitutive activation of Ras, as it directly contributes to the hallmark of cancer: uncontrolled cell proliferation.