The substrate for the repair of DNA damage in living cells is not DNA but chromatin. Chromatin bears a range of modifications, which in turn bind ligands that compact or open chromatin structure, and determine its spatial organization within the nucleus. In some cases, RNA in the form of RNA:DNA hybrids or R-loops modulates DNA accessibility. Each of these parameters can favor particular pathways of repair. Chromatin or nucleosome remodelers are key regulators of chromatin structure, and a number of remodeling complexes are implicated in DNA repair. We cover novel insights into the impact of chromatin structure, nuclear organization, R-loop formation, nuclear actin, and nucleosome remodelers in DNA double- strand break repair, focusing on factors that alter repair functional upon ablation.
机构:
Ecole Normale Super, CNRS, IBENS, UMR 8197, F-75005 Paris, France
Columbia Univ, Med Ctr, Dept Genet & Dev, New York, NY 10032 USAEcole Normale Super, CNRS, IBENS, UMR 8197, F-75005 Paris, France
机构:Mayo Clinic,Mayo Clinic Medical Scientist Training Program, Mayo Clinic Alix School of Medicine and Mayo Clinic Graduate School of Biomedical Sciences
Somaira Nowsheen
Min Deng
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机构:Mayo Clinic,Mayo Clinic Medical Scientist Training Program, Mayo Clinic Alix School of Medicine and Mayo Clinic Graduate School of Biomedical Sciences
Min Deng
Zhenkun Lou
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机构:Mayo Clinic,Mayo Clinic Medical Scientist Training Program, Mayo Clinic Alix School of Medicine and Mayo Clinic Graduate School of Biomedical Sciences