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Negative Regulation of Hypoxic Responses via Induced Reptin Methylation

Authors
Lee, Jason S.Kim, YunhoKim, Ik SooKim, BogyouChoi, Hee JuneLee, Ji MinShin, Hi-Jai R.Kim, Jung HwaKim, Ji-YoungSeo, Sang-BeomLee, HoBinda, OlivierGozani, OrSemenza, Gregg L.Kim, MinhyungKim, Keun IlHwang, DaeheeBaek, Sung Hee
Issue Date
Jul-2010
Publisher
CELL PRESS
Keywords
DNA; Humdisease; Proteins
Citation
MOLECULAR CELL, v.39, no.1, pp 71 - 85
Pages
15
Journal Title
MOLECULAR CELL
Volume
39
Number
1
Start Page
71
End Page
85
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/13170
DOI
10.1016/j.molcel.2010.06.008
ISSN
1097-2765
1097-4164
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.
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