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Hypoxia-induced methylation of a pontin chromatin remodeling factor.


ABSTRACT: Pontin is a chromatin remodeling factor that possesses both ATPase and DNA helicase activities. Although Pontin is frequently overexpressed in human cancers of various types and implicated in oncogenic functions, the upstream signaling network leading to the regulation of Pontin that in turn affects transcription of downstream target genes has not been extensively studied. Here, we identify Pontin is methylated by G9a/GLP methyltransferases in hypoxic condition and potentiates HIF-1?-mediated activation by increasing the recruitment of p300 coactivator to a subset of HIF-1? target promoters. Intriguingly, Pontin methylation results in the increased invasive and migratory properties by activating downstream target gene, Ets1. In contrast, inhibition of Pontin methylation results in the suppression of tumorigenic and metastatic properties. Together, our data provide new approaches by targeting Pontin methylation and its downstream targets for the development of therapeutic agents for human cancers.

SUBMITTER: Lee JS 

PROVIDER: S-EPMC3158161 | biostudies-literature | 2011 Aug

REPOSITORIES: biostudies-literature

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Hypoxia-induced methylation of a pontin chromatin remodeling factor.

Lee Jason S JS   Kim Yunho Y   Bhin Jinhyuk J   Shin Hi-Jai R HJ   Nam Hye Jin HJ   Lee Seung Hoon SH   Yoon Jong-Bok JB   Binda Olivier O   Gozani Or O   Hwang Daehee D   Baek Sung Hee SH  

Proceedings of the National Academy of Sciences of the United States of America 20110808 33


Pontin is a chromatin remodeling factor that possesses both ATPase and DNA helicase activities. Although Pontin is frequently overexpressed in human cancers of various types and implicated in oncogenic functions, the upstream signaling network leading to the regulation of Pontin that in turn affects transcription of downstream target genes has not been extensively studied. Here, we identify Pontin is methylated by G9a/GLP methyltransferases in hypoxic condition and potentiates HIF-1α-mediated ac  ...[more]

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