4.8 Article

The CSRP2BP histone acetyltransferase drives smooth muscle gene expression

期刊

NUCLEIC ACIDS RESEARCH
卷 45, 期 6, 页码 3046-3058

出版社

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkw1227

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资金

  1. International Science & Technology Cooperation Program of China [2014DFA30180]
  2. State Key Development Programs of China [2012CB966502]
  3. National Institutes of Health [HL-089902]
  4. National Science Foundation of China [81060016, 81260032, 81660433, 31140021, 81460034]
  5. Hainan Provincial Department of Science and Technology [ZDZX2013003, KJHZ2014-11]

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The expression of nearly all smooth muscle genes are controlled by serum response factor binding sites in their promoter regions. However, SRF alone is not sufficient for regulating smooth muscle cell development. It associates with other cardiovascular specific cofactors to regulate smooth muscle gene expression. Previously, we showed that the transcription co-factor CRP2 was a regulator of smooth muscle gene expression. Here, we report that CSRP2BP, a coactivator for CRP2, is a histone acetyltransferase and a driver of smooth muscle gene expression. CSRP2BP directly interacted with SRF, CRP2 andmyocardin. CSRP2BP synergistically activated smooth muscle gene promoters in an SRF-dependent manner. A combination of SRF, GATA6 and CRP2 required CSRP2BP for robust smooth muscle gene promoter activity. Knockdown of Csrp2bp in smooth muscle cells resulted in reduced smooth muscle gene expression. We conclude that the CSRP2BP histone acetyltransferase is a coactivator for CRP2 thatworks synergistically with SRF and myocardin to regulate smooth muscle gene expression.

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