Zawel L, Kumar K P, Reinberg D
Howard Hughes Medical Institute, Department of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854-5635, USA.
Genes Dev. 1995 Jun 15;9(12):1479-90. doi: 10.1101/gad.9.12.1479.
We have analyzed the fate of the RNA polymerase II (RNAPII) general transcription factors during the transition from initiation to elongation using multiple approaches. We demonstrate that all of the basal factors coexist in mature initiation complexes but that following nucleotide addition, this complex becomes disrupted. During this transition, TFIID remains promoter-bound whereas TFIIB, TFIIE, TFIIF, and TFIIH are released. Upon release, TFIIB reassociates with TFIID, reforming the RNAPII docking site, the DB complex. TFIIE is released before formation of the tenth phosphodiester bond. This precedes TFIIH release, which occurrs after the transcription complex reaches +30. TFIIF is unique in that it is the only basal factor detected in the RNAPII elongation complex. Following its release from the initiation complex, TFIIF has the ability to reassociate with a stalled RNAPII.
我们使用多种方法分析了RNA聚合酶II(RNAPII)通用转录因子在从起始到延伸转变过程中的命运。我们证明,所有基础因子在成熟起始复合物中共同存在,但在添加核苷酸后,该复合物会被破坏。在这个转变过程中,TFIID仍与启动子结合,而TFIIB、TFIIE、TFIIF和TFIIH则被释放。释放后,TFIIB与TFIID重新结合,重新形成RNAPII对接位点,即DB复合物。TFIIE在第十个磷酸二酯键形成之前被释放。这先于TFIIH的释放,TFIIH在转录复合物到达+30之后释放。TFIIF的独特之处在于它是在RNAPII延伸复合物中检测到的唯一基础因子。从起始复合物释放后,TFIIF有能力与停滞的RNAPII重新结合。