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DNA Double-Strand Break Repair: All Roads Lead to HeterochROMAtin Marks

Overview
Journal Front Genet
Date 2021 Sep 20
PMID 34539757
Citations 13
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Abstract

In response to DNA double-strand breaks (DSBs), chromatin modifications orchestrate DNA repair pathways thus safeguarding genome integrity. Recent studies have uncovered a key role for heterochromatin marks and associated factors in shaping DSB repair within the nucleus. In this review, we present our current knowledge of the interplay between heterochromatin marks and DSB repair. We discuss the impact of heterochromatin features, either pre-existing in heterochromatin domains or established in euchromatin, on DSB repair pathway choice. We emphasize how heterochromatin decompaction and mobility further support DSB repair, focusing on recent mechanistic insights into these processes. Finally, we speculate about potential molecular players involved in the maintenance or the erasure of heterochromatin marks following DSB repair, and their implications for restoring epigenome function and integrity.

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References
1.
Caridi C, DAgostino C, Ryu T, Zapotoczny G, Delabaere L, Li X . Nuclear F-actin and myosins drive relocalization of heterochromatic breaks. Nature. 2018; 559(7712):54-60. PMC: 6051730. DOI: 10.1038/s41586-018-0242-8. View

2.
Gauchier M, Kan S, Barral A, Sauzet S, Agirre E, Bonnell E . SETDB1-dependent heterochromatin stimulates alternative lengthening of telomeres. Sci Adv. 2019; 5(5):eaav3673. PMC: 6506250. DOI: 10.1126/sciadv.aav3673. View

3.
Schep R, Brinkman E, Leemans C, Vergara X, van der Weide R, Morris B . Impact of chromatin context on Cas9-induced DNA double-strand break repair pathway balance. Mol Cell. 2021; 81(10):2216-2230.e10. PMC: 8153251. DOI: 10.1016/j.molcel.2021.03.032. View

4.
Chen C, Feng W, Lim P, Kass E, Jasin M . Homology-Directed Repair and the Role of BRCA1, BRCA2, and Related Proteins in Genome Integrity and Cancer. Annu Rev Cancer Biol. 2018; 2:313-336. PMC: 6193498. DOI: 10.1146/annurev-cancerbio-030617-050502. View

5.
de Krijger I, van der Torre J, Peuscher M, Eder M, Jacobs J . H3K36 dimethylation by MMSET promotes classical non-homologous end-joining at unprotected telomeres. Oncogene. 2020; 39(25):4814-4827. PMC: 7299843. DOI: 10.1038/s41388-020-1334-0. View