Gilfillan Siv, Stelzer Gertraud, Piaia Elisa, Hofmann Markus G, Meisterernst Michael
Gene Expression, Institute of Molecular Immunology, GSF-National Research Center for Environment and Health, Marchionini-Strasse 25, D-81377 Munich, Germany.
J Biol Chem. 2005 Feb 18;280(7):6222-30. doi: 10.1074/jbc.M406343200. Epub 2004 Nov 30.
Negative cofactor 2 (NC2) forms a stable complex with TATA-binding protein (TBP) on promoters. This prevents the assembly of transcription factor (TF) IIA and TFIIB and leads to repression of RNA polymerase II transcription. Here we have revisited the interactions of NC2.TBP with DNA. We show that NC2.TBP complexes exhibit a significantly reduced preference for TATA box sequences compared with TBP and TBP.TFIIA complexes. In chromatin immunoprecipitations, NC2 is found on a variety of human TATA-containing and TATA-less promoters. Substantial amounts of NC2 are present in a complex with TBP in bulk chromatin. A complex of NC2.TBP displays a K(D) for DNA of approximately 2 x 10(-9) m for a 35-bp major late promoter oligonucleotide. While preferentially recognizing promoter-bound TBP, NC2 also accelerates TBP binding to promoters and stabilizes TBP.DNA complexes. Our data suggest that NC2 controls TBP binding and maintenance on DNA that is largely independent of a canonical TATA sequence.
负辅因子2(NC2)在启动子上与TATA结合蛋白(TBP)形成稳定复合物。这会阻止转录因子(TF)IIA和TFIIB的组装,并导致RNA聚合酶II转录受到抑制。在此,我们重新研究了NC2·TBP与DNA的相互作用。我们发现,与TBP和TBP·TFIIA复合物相比,NC2·TBP复合物对TATA框序列的偏好性显著降低。在染色质免疫沉淀实验中,在多种含TATA和不含TATA的人类启动子上都发现了NC2。在大量染色质中,大量的NC2与TBP形成复合物存在。对于一个35 bp的主要晚期启动子寡核苷酸,NC2·TBP复合物对DNA的解离常数(K(D))约为2×10^(-9) m。NC2虽然优先识别与启动子结合的TBP,但也会加速TBP与启动子的结合,并稳定TBP·DNA复合物。我们的数据表明,NC2在很大程度上独立于典型的TATA序列来控制TBP与DNA的结合及维持。