| Literature DB >> 12011100 |
Robert J Sims1, Elizabeth K Weihe, Li Zhu, Sean O'Malley, June V Harriss, Paul D Gottlieb.
Abstract
The m-Bop protein encoded by the mouse Bop gene is strongly expressed in heart and skeletal muscle, and recent studies with Bop knockout mice have demonstrated that m-Bop is essential for cardiogenesis in vivo and can act as a HDAC-dependent repressor in vitro. In the present studies, m-Bop was observed to interact with skNAC, a reported transcriptional activator specific to heart and skeletal muscle. The amino-terminal S region of the split S-ET domain of m-Bop as well as the MYND domain were required for interaction with skNAC in both the two-hybrid system and in coimmunoprecipitation experiments from cultured mammalian cells. As shown previously for interaction of the MYND domain-containing transcriptional corepressor, BS69, with several viral and cellular oncoproteins, a PXLXP motif in skNAC was required for interaction with m-Bop. Similar kinetics of induction and localization of m-Bop and skNAC during the induction of myogenesis in cultured C2C12 cells suggests a possible associated role for these proteins during this process.Entities:
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Year: 2002 PMID: 12011100 DOI: 10.1074/jbc.M204121200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157