| Literature DB >> 24647359 |
Jad I Belle1, Anastasia Nijnik2.
Abstract
Posttranslational modifications of histone H2A through the attachment of ubiquitin or poly-ubiquitin conjugates are common in mammalian genomes and play an important role in the regulation of chromatin structure, gene expression, and DNA repair. Histone H2A deubiquitinases (H2A-DUBs) are a group of structurally diverse enzymes that catalyze the removal ubiquitin from histone H2A. In this review we provide a concise summary of the mechanisms that mediate histone H2A ubiquitination in mammalian cells, and review our current knowledge of mammalian H2A-DUBs, their biochemical activities, and recent developments in our understanding of their functions in mammalian physiology.Entities:
Keywords: Chromatin; DNA repair; Deubiquitinase; Histone H2A; Transcriptional regulation
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Year: 2014 PMID: 24647359 DOI: 10.1016/j.biocel.2014.03.004
Source DB: PubMed Journal: Int J Biochem Cell Biol ISSN: 1357-2725 Impact factor: 5.085