Author:
Liu Bei,Shi Honglue,Rangadurai Atul,Nussbaumer Felix,Chu Chia-Chieh,Erharter Kevin Andreas,Case David A.,Kreutz Christoph,Al-Hashimi Hashim M.
Abstract
ABSTRACTN6-methyladenosine (m6A) is a post-transcriptional modification that controls gene expression by recruiting proteins to RNA sites. The modification also slows biochemical processes through mechanisms that are not understood. Using NMR relaxation dispersion, we show that m6A pairs with uridine with the methylamino group in theanticonformation to form a Watson-Crick base pair that transiently exchanges on the millisecond timescale with a singly hydrogen-bonded low-populated (1%) mismatch-like conformation in which the methylamino group issyn.This ability to rapidly interchange between Watson-Crick or mismatch-like forms, combined with differentsyn:antiisomer preferences when paired (~1:100) versus unpaired (~10:1), explains how m6A robustly slows duplex annealing without affecting melting via two pathways in which isomerization occurs before or after duplex annealing. Our model quantitatively predicts how m6A reshapes the kinetic landscape of nucleic acid hybridization and conformational transitions, and provides an explanation for why the modification robustly slows diverse cellular processes.
Publisher
Cold Spring Harbor Laboratory
Cited by
1 articles.
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