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Detalle de: Resolution of R-loops by INO80 promotes DNA replication and maintains cancer cell proliferation and viability

Title Resolution of R-loops by INO80 promotes DNA replication and maintains cancer cell proliferation and viability
Abstract

Collisions between the DNA replication machinery and co-transcriptional R-loops can impede DNA synthesis and are a major source of genomic instability in cancer cells. How cancer cells deal with R-loops to proliferate is poorly understood. Here we show that the ATP-dependent chromatin remodelling INO80 complex promotes resolution of R-loops to prevent replication-associated DNA damage in cancer cells. Depletion of INO80 in prostate cancer PC3 cells leads to increased R-loops. Overexpression of the RNA:DNA endonuclease RNAse H1 rescues the DNA synthesis defects and suppresses DNA damage caused by INO80 depletion. R-loops co-localize with and promote recruitment of INO80 to chromatin. Artificial tethering of INO80 to a LacO locus enabled turnover of R-loops in cis . Finally, counteracting R-loops by INO80 promotes proliferation and averts DNA damage-induced death in cancer cells. Our work suggests that INO80-dependent resolution of R-loops promotes DNA replication in the presence of transcription, thus enabling unlimited proliferation in cancers.

Apa Reference Prendergast, L., McClurg, U.L., Hristova, R., Berlinguer-Palmini, R., Greener, S., Veitch, K., Hernandez, I., Pasero, P., Rico, D., Higgins, J.M.G., Gospodinov, A. & Papamichos-Chronakis, M. (2020). Resolution of R-loops by INO80 promotes DNA replication and maintains cancer cell proliferation and viability. Nature Communications, 11(1). 10.1038/s41467-020-18306-x
Doi 10.1038/s41467-020-18306-x
Publication Date 10 Sep 2020
Publication Type Article
Researcher Daniel Rico
Ontology Genomics
Research Groups
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