Hartzog Grant A
Department of MCD Biology, University of California, Santa Cruz, California 95064, USA.
Curr Opin Genet Dev. 2003 Apr;13(2):119-26. doi: 10.1016/s0959-437x(03)00024-8.
The elongation of transcripts by RNA polymerase II (RNAPII) is subject to regulation and requires the services of a host of accessory proteins. Although the biochemical mechanisms underlying elongation and its regulation remain obscure, recent progress sets the stage for rapid advancement in our understanding of this phase of transcription. High-resolution crystal structures will allow focused analyses of RNAPII in all its functional states. Several recent studies suggest specific roles for the C-terminal heptad repeats of the largest subunit of RNAPII in elongation. Proteomic approaches are being used to identify new transcription-elongation factors and to define interactions between elongation factors and RNAPII. Finally, a combination of genetic analysis and the localization of factors on transcribed chromatin is being used to confirm a role for factors in elongation.
RNA聚合酶II(RNAPII)介导的转录本延伸受到调控,并且需要许多辅助蛋白的参与。尽管延伸及其调控背后的生化机制仍不清楚,但最近的进展为我们快速深入理解转录的这一阶段奠定了基础。高分辨率晶体结构将有助于对处于所有功能状态的RNAPII进行重点分析。最近的几项研究表明,RNAPII最大亚基的C端七肽重复序列在延伸过程中具有特定作用。蛋白质组学方法正被用于鉴定新的转录延伸因子,并确定延伸因子与RNAPII之间的相互作用。最后,遗传分析与因子在转录染色质上的定位相结合,正被用于证实因子在延伸过程中的作用。