跳到主要导航 跳到搜索 跳到主要内容

ICBP90, a novel methyl K9 H3 binding protein linking protein ubiquitination with heterochromatin formation

  • Panagiota Karagianni*
  • , Larbi Amazit
  • , Jun Qin
  • , Jiemin Wong
  • *此作品的通讯作者
  • Baylor College of Medicine
  • Massachusetts General Hospital Cancer Center
  • Institut national de la santé et de la recherche médicale

科研成果: 期刊稿件 › 文章 › 同行评审

摘要

Methylation of histone H3 on lysine 9 is critical for diverse biological processes including transcriptional repression, heterochromatin formation, and X inactivation. The biological effects of histone methylation are thought to be mediated by effector proteins that recognize and bind to specific patterns of methylation. Using an unbiased in vitro biochemical approach, we have identified ICBP90, a transcription and cell cycle regulator, as a novel methyl K9 H3-specific binding protein. ICBP90 and its murine homologue Np95 are enriched in pericentric heterochromatin of interphase nuclei, and this localization is dependent on H3K9 methylation. Specific binding of ICBP90 to methyl K9 H3 depends on two functional domains, a PHD (plant homeodomain) finger that defines the binding specificity and an SRA (SET- and RING-associated) domain that promotes binding activity. Furthermore, we present evidence that ICBP90 is required for proper heterochromatin formation in mammalian cells.

源语言英语
页(从-至)705-717
页数13
期刊Molecular and Cellular Biology
卷28
期2
DOI
出版状态已出版 - 1月 2008

学术指纹

探究 'ICBP90, a novel methyl K9 H3 binding protein linking protein ubiquitination with heterochromatin formation' 的科研主题。它们共同构成独一无二的学术指纹。

引用此