Literature DB >> 15753656

DNA repair in the context of chromatin.

Ashby J Morrison1, Xuetong Shen.   

Abstract

Modulation of chromatin is essential to nuclear processes that utilize DNA, such as transcription, replication, and repair. For example, transcription is assisted by histone post-translational modifications, as well as chromatin-remodeling complexes, which alter the structure of chromatin. Furthermore, recent advancements in the fields of DNA repair and chromatin reveal that both histone modifications and chromatin-remodeling complexes are essential for the repair of DNA lesions. In particular, chromatin-modifying complexes, such as the INO80 chromatin-remodeling complex and the Tip60 histone acetyltransferase complex, associate with the DNA damage-induced phosphorylated H2AX, which is often referred to as gamma-H2AX. In S. cerevisiae, the association of INO80 with gamma-H2AX is required for the recruitment of INO80 to sites of DNA double-strand breaks. Additionally, in Drosophila, Tip60 exchanges gamma-H2AX for unmodified H2A in regions of DNA damage. This report reviews recent studies that emphasize the intimate relationship between evolutionarily-conserved chromatin-modifying complexes and histone post-translational modifications in the repair of DNA damage.

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Year:  2005        PMID: 15753656

Source DB:  PubMed          Journal:  Cell Cycle        ISSN: 1551-4005            Impact factor:   4.534


  21 in total

1.  The INO80 ATP-dependent chromatin remodeling complex is a nucleosome spacing factor.

Authors:  Maheshi Udugama; Abdellah Sabri; Blaine Bartholomew
Journal:  Mol Cell Biol       Date:  2010-12-06       Impact factor: 4.272

Review 2.  Mi-2/NuRD complex making inroads into DNA-damage response pathway.

Authors:  Da-Qiang Li; Rakesh Kumar
Journal:  Cell Cycle       Date:  2010-06-01       Impact factor: 4.534

Review 3.  INO80 subfamily of chromatin remodeling complexes.

Authors:  Yunhe Bao; Xuetong Shen
Journal:  Mutat Res       Date:  2007-01-21       Impact factor: 2.433

4.  DNA damage phenotype and prostate cancer risk.

Authors:  O Kosti; L Goldman; D T Saha; R A Orden; A J Pollock; H L Madej; A W Hsing; L W Chu; J H Lynch; R Goldman
Journal:  Mutat Res       Date:  2010-11-21       Impact factor: 2.433

5.  The cloning and characterization of the histone acetyltransferase human homolog Dmel\TIP60 in Drosophila melanogaster: Dmel\TIP60 is essential for multicellular development.

Authors:  Xianmin Zhu; Neetu Singh; Christopher Donnelly; Pamela Boimel; Felice Elefant
Journal:  Genetics       Date:  2006-12-18       Impact factor: 4.562

Review 6.  Histone variants and epigenetics.

Authors:  Steven Henikoff; M Mitchell Smith
Journal:  Cold Spring Harb Perspect Biol       Date:  2015-01-05       Impact factor: 10.005

7.  Rational design of substrate-based multivalent inhibitors of the histone acetyltransferase Tip60.

Authors:  Chao Yang; Liza Ngo; Y George Zheng
Journal:  ChemMedChem       Date:  2014-01-20       Impact factor: 3.466

8.  Phosphorylation of histone H2A.X by DNA-dependent protein kinase is not affected by core histone acetylation, but it alters nucleosome stability and histone H1 binding.

Authors:  Andra Li; Yaping Yu; Sheng-Chun Lee; Toyotaka Ishibashi; Susan P Lees-Miller; Juan Ausió
Journal:  J Biol Chem       Date:  2010-03-31       Impact factor: 5.157

9.  The multi-copy mouse gene Sycp3-like Y-linked (Sly) encodes an abundant spermatid protein that interacts with a histone acetyltransferase and an acrosomal protein.

Authors:  Louise N Reynard; Julie Cocquet; Paul S Burgoyne
Journal:  Biol Reprod       Date:  2009-01-28       Impact factor: 4.285

10.  Coordinated Regulation of TIP60 and Poly(ADP-Ribose) Polymerase 1 in Damaged-Chromatin Dynamics.

Authors:  Masae Ikura; Kanji Furuya; Atsuhiko Fukuto; Ryo Matsuda; Jun Adachi; Tomonari Matsuda; Akira Kakizuka; Tsuyoshi Ikura
Journal:  Mol Cell Biol       Date:  2016-05-02       Impact factor: 4.272

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