| Literature DB >> 31775053 |
Arianna Lockhart1, Vanessa Borges Pires2, Fabio Bento1, Vanessa Kellner3, Sarah Luke-Glaser3, George Yakoub3, Helle D Ulrich3, Brian Luke4.
Abstract
RNA-DNA hybrids are tightly regulated to ensure genome integrity. The RNase H enzymes RNase H1 and H2 contribute to chromosomal stability through the removal of RNA-DNA hybrids. Loss of RNase H2 function is implicated in human diseases of the nervous system and cancer. To better understand RNA-DNA hybrid dynamics, we focused on elucidating the regulation of the RNase H enzymes themselves. Using yeast as a model system, we demonstrate that RNase H1 and H2 are controlled in different manners. RNase H2 has strict cell cycle requirements, in that it has an essential function in G2/M for both R-loop processing and ribonucleotide excision repair. RNase H1, however, can function independently of the cell cycle to remove R-loops and appears to become activated in response to high R-loop loads. These results provide us with a more complete understanding of how and when RNA-DNA hybrids are acted upon by the RNase H enzymes.Entities:
Keywords: R-loop; RNA-DNA hybrid; RNase H1; RNase H2; cell cycle; ribonucleotide excision repair
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Year: 2019 PMID: 31775053 DOI: 10.1016/j.celrep.2019.10.108
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423