Albert Thomas K, Grote Korbinian, Boeing Stefan, Stelzer Gertraud, Schepers Aloys, Meisterernst Michael
Department of Gene Expression and Gene Vectors, GSF-National Research Center for Environment and Health, Marchioninistrasse 25, 81377 Munich, Germany.
Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10000-5. doi: 10.1073/pnas.0703490104. Epub 2007 Jun 4.
Negative cofactor 2 (NC2) forms a stable complex with TATA-binding protein (TBP) on promoters in vitro. Its association with TBP prevents the binding of TFIIB and leads to inhibition of preinitiation complex formation. Here, we investigate the association of NC2 subunit-alpha with human RNA polymerase II promoter regions by using gene-specific ChIP and genome-wide promoter ChIPchip analyses. We find NC2alpha associated with a large number of human promoters, where it peaks close to the core regions. NC2 occupancy in vivo positively correlates with mRNA levels, which perhaps reflects its capacity to stabilize TBP on promoter regions. In single gene analyses, we confirm core promoter binding and in addition map the NC2 complex to enhancer proximal regions. High-occupancy histone genes display a stable NC2/TFIIB ratio during the cell cycle, which otherwise varies markedly from one gene to another. The latter is at least in part explained by an observed negative correlation of NC2 occupancy with the presence of the TFIIB recognition element in core promoter regions. Our data establish the genome-wide basis for general and gene-specific functions of NC2 in mammalian cells.
负辅因子2(NC2)在体外可与启动子上的TATA结合蛋白(TBP)形成稳定的复合物。它与TBP的结合会阻止TFIIB的结合,并导致起始前复合物形成的抑制。在此,我们通过基因特异性染色质免疫沉淀(ChIP)和全基因组启动子芯片分析来研究NC2亚基α与人RNA聚合酶II启动子区域的关联。我们发现NC2α与大量人类启动子相关联,其峰值出现在靠近核心区域的位置。体内NC2的占据情况与mRNA水平呈正相关,这可能反映了其在启动子区域稳定TBP的能力。在单基因分析中,我们证实了核心启动子结合,并进一步将NC2复合物定位到增强子近端区域。高占据率的组蛋白基因在细胞周期中显示出稳定的NC2/TFIIB比例,而其他基因的这一比例则在不同基因间有显著差异。后者至少部分是由观察到的NC2占据情况与核心启动子区域中TFIIB识别元件的存在呈负相关所解释的。我们的数据为NC2在哺乳动物细胞中的普遍和基因特异性功能建立了全基因组基础。