| Literature DB >> 17272723 |
Junhong Han1, Hui Zhou, Bruce Horazdovsky, Kangling Zhang, Rui-Ming Xu, Zhiguo Zhang.
Abstract
Acetylation of histone H3 lysine 56 (H3-K56) occurs in S phase, and cells lacking H3-K56 acetylation are sensitive to DNA-damaging agents. However, the histone acetyltransferase (HAT) that catalyzes global H3-K56 acetylation has not been found. Here we show that regulation of Ty1 transposition gene product 109 (Rtt109) is an H3-K56 HAT. Cells lacking Rtt109 or expressing rtt109 mutants with alterations at a conserved aspartate residue lose H3-K56 acetylation and exhibit increased sensitivity toward genotoxic agents, as well as elevated levels of spontaneous chromosome breaks. Thus, Rtt109, which shares no sequence homology with any other known HATs, is a unique HAT that acetylates H3-K56.Entities:
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Year: 2007 PMID: 17272723 DOI: 10.1126/science.1133234
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728