Masson Patrick, Leimgruber Elisa, Creton Sandrine, Collart Martine A
Department of Microbiology and Molecular Medicine, CMU, 1 rue Michel Servet 1211, Geneva 4, Switzerland.
Nucleic Acids Res. 2008 Feb;36(2):539-49. doi: 10.1093/nar/gkm1078. Epub 2007 Nov 29.
Negative co-factor 2 (NC2) is a conserved eukaryotic complex composed of two subunits, NC2alpha (Drap1) and NC2beta (Dr1) that associate through a histone-fold motif. In this work, we generated mutants of NC2, characterized target genes for these mutants and studied the assembly of NC2 and general transcription factors on target promoters. We determined that the two NC2 subunits mostly function together to be recruited to DNA and regulate gene expression. We found that NC2 strongly controls promoter association of TFIIB, both negatively and positively. We could attribute the gene-specific repressor effect of NC2 on TFIIB to the C-terminal domain of NC2beta, and define that it requires ORF sequences of the target gene. In contrast, the positive function of NC2 on TFIIB targets is more general and requires adequate levels of the NC2 histone-fold heterodimer on promoters. Finally, we determined that NC2 becomes limiting for TATA-binding protein (TBP) association with a heat inducible promoter under heat stress. This study demonstrates an important positive role of NC2 for formation of the pre-initiation complex on promoters, under normal conditions through control of TFIIB, or upon activation by stress via control of TBP.
负辅因子2(NC2)是一种保守的真核复合物,由两个亚基组成,即通过组蛋白折叠基序相互关联的NC2α(Drap1)和NC2β(Dr1)。在这项工作中,我们构建了NC2突变体,对这些突变体的靶基因进行了表征,并研究了NC2和通用转录因子在靶启动子上的组装。我们确定,两个NC2亚基大多共同发挥作用,被招募到DNA上并调节基因表达。我们发现,NC2对TFIIB与启动子的结合具有强烈的正负调控作用。我们可以将NC2对TFIIB的基因特异性抑制作用归因于NC2β的C末端结构域,并确定这需要靶基因的开放阅读框序列。相比之下,NC2对TFIIB靶标的正向作用更为普遍,并且需要启动子上有足够水平的NC2组蛋白折叠异二聚体。最后,我们确定在热应激下,NC2成为TATA结合蛋白(TBP)与热诱导启动子结合的限制因素。这项研究表明,在正常条件下,NC2通过控制TFIIB,或在应激激活时通过控制TBP,对启动子上预起始复合物的形成具有重要的正向作用。