RNA is a labile molecule due to the presence of the 2’-OH group. The 2'-OH group on the ribose sugar in RNA makes the molecule more susceptible to hydrolysis, especially under alkaline conditions. This makes RNA more unstable compared to DNA, which lacks the 2’-OH group (replaced by a 2’-H in deoxyribose).
(1) 3’-OH group: The 3’-OH group is necessary for RNA strand elongation during transcription but does not contribute to its instability.
(2) 5’-OH group: The 5’-OH group is involved in the attachment of nucleotides during transcription but does not significantly contribute to the instability of RNA.
(3) 4’-OH group: This does not exist in the context of the ribose sugar structure of RNA or DNA.
(4) 2’-OH group: The 2’-OH group makes RNA highly reactive and more prone to degradation, especially under alkaline conditions.
Thus, the correct answer is (4) 2’-OH group.
RNA is unstable due to the 2’-OH group, which makes it more prone to hydrolysis in cellular environments. The 2’-OH in RNA, compared to DNA’s absence of this hydroxyl group, contributes to its higher reactivity and lability, leading to faster degradation.
List-I (Scientist) | List-II (Contribution) |
(A) A. Jeffreys | (I) Nuclein |
(B) Miescher | (II) Amino acid formation |
(C) J. Monod | (III) DNA fingerprinting |
(D) S.L. Miller | (IV) Transcriptionally regulated system |