4.5 Article

Hepatitis B virus-X protein recruits histone deacetylase 1 to repress insulin-like growth factor binding protein 3 transcription

期刊

VIRUS RESEARCH
卷 139, 期 1, 页码 14-21

出版社

ELSEVIER
DOI: 10.1016/j.virusres.2008.09.006

关键词

Insulin-like growth factor binding protein-3; Histone deacetylase 1; Immunoprecipitation; Chromatin immunoprecipitation; Trichostatin A; Insulin-like growth factor type 1

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资金

  1. Korea Science and Engineering Foundation [MTR00-1]
  2. [RO2-2004-000-10070-0]

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Hepatitis B virus (HBV), a major causative agent of hepatocelluar carcinoma (HCC), encodes an oncogenic X-protein (HBx) which has been known as a transcriptional transactivator on multiple viral and celluar promoters. In the report, we verified that HBx transcriptionally repress insulin-like growth factor binding protein-3 (IGFBP-3) by promoting HBx/histone deacetylase 1 (HDAC1) complex formation. HBx recruited HDAC1 forms complex with Sp1 in a p53-independent manner) and deacetylates Sp1 which resulted in the diminished binding of Sp1 on targeted DNA during transcriptional repression. Deacetylation of Sp1 by HBx recruited HDAC1 likely to be a part of the mechanism that controls HBx induced IGFBP-3 repression and the modification of chromatin structure. (C) 2008 Elsevier B.V. All rights reserved.

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