Wang Z, Luo T, Roeder R G
Laboratory of Biochemistry and Molecular Biology, The Rockefeller University, New York, New York 10021, USA.
Genes Dev. 1997 Sep 15;11(18):2371-82. doi: 10.1101/gad.11.18.2371.
Transcription by RNA polymerase III (Pol III) requires multiple general initiation factors that, in isolated form, assemble onto the promoter in an ordered fashion. Here, it is shown that all components required for transcription of the VA1 and tRNA genes, including TFIIIB, TFIIIC, and RNA Pol III, can be coimmunopurified from a HeLa cell line that constantly expresses a FLAG epitope-tagged subunit of human RNA Pol III. This finding of an RNA Pol III "holoenzyme" suggests similarities between transcription initiation by RNA Pol II and RNA Pol III and has led to the identification of a novel general initiation factor (TDF, translation dependent factor) that is present within the holoenzyme. TDF is selectively inactivated during protein synthesis inhibition by cycloheximide and at a late stage of adenovirus infection, thus accounting for the loss of RNA Pol III-mediated transcription of the tRNA and VA RNA genes under these conditions. On the basis of these observations, possible mechanisms for the global regulation of transcription by RNA Pol III and for disassembly of RNA Pol III initiation complexes are proposed.
RNA聚合酶III(Pol III)的转录需要多种通用起始因子,这些因子以分离的形式有序地组装到启动子上。本文表明,VA1和tRNA基因转录所需的所有组分,包括TFIIIB、TFIIIC和RNA Pol III,都可以从一个持续表达人RNA Pol III的FLAG表位标签亚基的HeLa细胞系中通过共免疫纯化得到。这种RNA Pol III“全酶”的发现表明RNA Pol II和RNA Pol III的转录起始之间存在相似性,并导致了一种存在于全酶中的新型通用起始因子(TDF,翻译依赖性因子)的鉴定。TDF在环己酰亚胺抑制蛋白质合成期间以及腺病毒感染后期被选择性失活,因此解释了在这些条件下tRNA和VA RNA基因的RNA Pol III介导的转录缺失。基于这些观察结果,提出了RNA Pol III转录全局调控以及RNA Pol III起始复合物解离的可能机制。