Nascent RNA folding mitigates transcription-associated mutagenesis

  1. Jianzhi Zhang1
  1. University of Michigan
  1. * Corresponding author; email: jianzhi{at}umich.edu

Abstract

Transcription is mutagenic, in part because the R-loop formed by the binding of the nascent RNA with its DNA template exposes the non-template DNA strand to mutagens and primes unscheduled error-prone DNA synthesis. We hypothesize that strong folding of nascent RNA weakens R-loops and hence decreases mutagenesis. By a yeast forward-mutation assay, we show that strengthening RNA folding and reducing R-loop formation by synonymous changes in a reporter gene can lower mutation rate by >80%. This effect is diminished after the overexpression of the gene encoding RNase H1 that degrades the RNA in a DNA-RNA hybrid, indicating that the effect is R-loop-dependent. Analysis of genomic data of yeast mutation accumulation lines and human neutral polymorphisms confirms the generality of these findings. This mechanism for local protection of genome integrity is of special importance to highly expressed genes because of their frequent transcription and strong RNA folding, the latter also improves translational fidelity. As a result, strengthening RNA folding simultaneously curtail genotypic and phenotypic mutations.

  • Received May 28, 2015.
  • Accepted October 14, 2015.

This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genome.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

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  1. Genome Res. gr.195164.115 Published by Cold Spring Harbor Laboratory Press

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