| Literature DB >> 20603076 |
Jason S Lee1, Yunho Kim, Ik Soo Kim, Bogyou Kim, Hee June Choi, Ji Min Lee, Hi-Jai R Shin, Jung Hwa Kim, Ji-Young Kim, Sang-Beom Seo, Ho Lee, Olivier Binda, Or Gozani, Gregg L Semenza, Minhyung Kim, Keun Il Kim, Daehee Hwang, Sung Hee Baek.
Abstract
Lysine methylation within histones is crucial for transcriptional regulation and thus links chromatin states to biological outcomes. Although recent studies have extended lysine methylation to nonhistone proteins, underlying molecular mechanisms such as the upstream signaling cascade that induces lysine methylation and downstream target genes modulated by this modification have not been elucidated. Here, we show that Reptin, a chromatin-remodeling factor, is methylated at lysine 67 in hypoxic conditions by the methyltransferase G9a. Methylated Reptin binds to the promoters of a subset of hypoxia-responsive genes and negatively regulates transcription of these genes to modulate cellular responses to hypoxia. 2010 Elsevier Inc. All rights reserved.Entities:
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Year: 2010 PMID: 20603076 PMCID: PMC4651011 DOI: 10.1016/j.molcel.2010.06.008
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970