4.4 Article

A role for the Saccharomyces cerevisiae Rtt109 histone acetyltransferase in R-loop homeostasis and associated genome instability

Journal

GENETICS
Volume 222, Issue 1, Pages -

Publisher

GENETICS SOCIETY AMERICA
DOI: 10.1093/genetics/iyac108

Keywords

R-loops; DNA-RNA hybrids; histone acetylation; sister-chromatid recombination; genetic instability

Funding

  1. European Research Council [ERC2014 AdG669898 TARLOOP]
  2. Spanish Ministry of Economy and Competitiveness [BFU2016-75058-P]
  3. Agencia Estatal de Investigacio n (AEI) of the Spanish Ministry of Science and Innovation [PID2019-104270GB-I00]
  4. European Union Regional Funds (FEDER) [US-1258654]
  5. Junta de Andalucia [P12-BIO-1238]
  6. Spanish Ministry of Science and Innovation [PID2020-118423GB-I00]

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The chromatin modifier Rtt109 plays a crucial role in the metabolism and repair of DNA-RNA hybrids and R-loops, with histone acetylation helping to prevent DNA damage and promote repair.
The stability of the genome is occasionally challenged by the formation of DNA-RNA hybrids and R-loops, which can be influenced by the chromatin context. This is mainly due to the fact that DNA-RNA hybrids hamper the progression of replication forks, leading to fork stalling and, ultimately, DNA breaks. Through a specific screening of chromatin modifiers performed in the yeast Saccharomyces cerevisiae, we have found that the Rtt109 histone acetyltransferase is involved in several steps of R-loop-metabolism and their associated genetic instability. On the one hand, Rtt109 prevents DNA-RNA hybridization by the acetylation of histone H3 lysines 14 and 23 and, on the other hand, it is involved in the repair of replication-born DNA breaks, such as those that can be caused by R-loops, by acetylating lysines 14 and 56. In addition, Rtt109 loss renders cells highly sensitive to replication stress in combination with R-loop-accumulating THO-complex mutants. Our data evidence that the chromatin context simultaneously influences the occurrence of DNA-RNA hybrid-associated DNA damage and its repair, adding complexity to the source of R-loop-associated genetic instability.

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