Literature DB >> 20144732

Higher-order chromatin structure in DSB induction, repair and misrepair.

Martin Falk1, Emilie Lukasova, Stanislav Kozubek.   

Abstract

Double-strand breaks (DSBs), continuously introduced into DNA by cell metabolism, ionizing radiation and some chemicals, are the biologically most deleterious type of genome damage, and must be accurately repaired to protect genomic integrity, ensure cell survival, and prevent carcinogenesis. Although a huge amount of information has been published on the molecular basis and biological significance of DSB repair, our understanding of DSB repair and its spatiotemporal arrangement is still incomplete. In particular, the role of higher-order chromatin structure in DSB induction and repair, movement of DSBs and the mechanism giving rise to chromatin exchanges, and many other currently disputed questions are discussed in this review. Finally, a model explaining the formation of chromosome translocations is proposed. 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20144732     DOI: 10.1016/j.mrrev.2010.01.013

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  42 in total

1.  HDAC5 is required for maintenance of pericentric heterochromatin, and controls cell-cycle progression and survival of human cancer cells.

Authors:  P Peixoto; V Castronovo; N Matheus; C Polese; O Peulen; A Gonzalez; M Boxus; E Verdin; M Thiry; F Dequiedt; D Mottet
Journal:  Cell Death Differ       Date:  2012-02-03       Impact factor: 15.828

2.  Modeling DNA double-strand break repair kinetics as an epiregulated cell-community-wide (epicellcom) response to radiation stress.

Authors:  Bobby R Scott
Journal:  Dose Response       Date:  2011-02-10       Impact factor: 2.658

3.  Preferential localization of γH2AX foci in euchromatin of retina rod cells after DNA damage induction.

Authors:  Laura Lafon-Hughes; María Vittoria Di Tomaso; Pablo Liddle; Andrea Toledo; Ana Laura Reyes-Ábalos; Gustavo A Folle
Journal:  Chromosome Res       Date:  2013-12-10       Impact factor: 5.239

4.  X inactivation plays a major role in the gender bias in somatic expansion in a mouse model of the fragile X-related disorders: implications for the mechanism of repeat expansion.

Authors:  Rachel Adihe Lokanga; Xiao-Nan Zhao; Ali Entezam; Karen Usdin
Journal:  Hum Mol Genet       Date:  2014-05-08       Impact factor: 6.150

5.  KAP-1 phosphorylation regulates CHD3 nucleosome remodeling during the DNA double-strand break response.

Authors:  Aaron A Goodarzi; Thomas Kurka; Penelope A Jeggo
Journal:  Nat Struct Mol Biol       Date:  2011-06-05       Impact factor: 15.369

6.  Unrepaired clustered DNA lesions induce chromosome breakage in human cells.

Authors:  Aroumougame Asaithamby; Burong Hu; David J Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-28       Impact factor: 11.205

Review 7.  Mechanisms and Consequences of Double-Strand DNA Break Formation in Chromatin.

Authors:  Wendy J Cannan; David S Pederson
Journal:  J Cell Physiol       Date:  2016-01       Impact factor: 6.384

8.  Nanodiamonds and nanoparticles as tumor cell radiosensitizers-promising results but an obscure mechanism of action.

Authors:  Martin Falk
Journal:  Ann Transl Med       Date:  2017-01

9.  Nanoscopy and Nanoparticles Hand-in-Hand to Fight Cancer: An Exciting Entrée into the Rising NANOworld.

Authors:  Martin Falk
Journal:  Biophys J       Date:  2016-02-23       Impact factor: 4.033

Review 10.  The molecular basis and disease relevance of non-homologous DNA end joining.

Authors:  Bailin Zhao; Eli Rothenberg; Dale A Ramsden; Michael R Lieber
Journal:  Nat Rev Mol Cell Biol       Date:  2020-10-19       Impact factor: 94.444

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