- In an experiment it was observed that a protein was upregulated in cancer tissues (compared to control tissues) that showed correlation with disease progression. Following are a few possibilities, which can explain the above observation.
A. A mutation could be located in the 3’UTR of the corresponding mRNA at a miRNA binding site.
B. A mutation changes the conformation of the protein, resulting in its better stability.
C. A mutation in the corresponding mRNA promotes ribosome read-through of the termination codon resulting in increased synthesis of the protein.
D. A mutation in the corresponding mRNA increased the stability of the RNA due to change in secondary structure.
Which one of the following combinations represents the most likely explanations?
(1) A, B and C (2) B, C and D
(3) C, D and A (4) A, B and D
The most likely explanations for the observed upregulation of a protein correlated with cancer progression are:
(4) A, B and D
Explanation
-
A. Mutation in the 3’UTR at a miRNA binding site:
Mutations here can disrupt miRNA binding, which normally represses translation or stability of the mRNA, resulting in increased protein expression. -
B. Mutation changes protein conformation leading to better stability:
Altered protein folding or modifications can prevent degradation, increasing protein half-life and accumulation in cancer cells. -
D. Mutation increasing mRNA stability by changing secondary structure:
More stable mRNA leads to increased translation and protein levels, contributing to upregulation. -
C. Mutation causing ribosome read-through of termination codon:
This is a rare and less common mechanism; while it could increase protein synthesis, it is not a frequent or typical cause of upregulation in cancer.
Therefore, combinations involving A, B, and D best explain increased protein expression in cancer tissues.



3 Comments
Shubhi Gargg
November 5, 2025ok done
Kajal
November 6, 2025A, B and D
Sakshi Kanwar
November 18, 2025A, B and D
Mutation increasing mRNA stability by changing secondary structure