Svejstrup Jesper Q
Cancer Research UK, London Research Institute, Clare Hall Laboratories, South Mimms, Hertfordshire EN6 3LD, UK.
Curr Opin Genet Dev. 2002 Apr;12(2):156-61. doi: 10.1016/s0959-437x(02)00281-2.
As RNA polymerase II leaves a gene promoter to transcribe the coding region, it faces a major obstacle - nucleosomes tightly wrapped into chromatin. Mechanisms to deal with this obstacle clearly exist in cells, as transcription through chromatin is very efficient in vivo, whereas nucleosomal templates pose a considerable problem for polymerase progression in reconstituted in vitro systems. Advances in our understanding of transcriptional elongation through chromatin have been made possible recently by the identification of several accessory factors that assist polymerase in the process. Insights into the function of these factors have been gained by a combination of yeast genetics and biochemical studies in mammalian systems.
当RNA聚合酶II离开基因启动子去转录编码区时,它面临着一个主要障碍——紧密包裹在染色质中的核小体。细胞中显然存在应对这一障碍的机制,因为在体内通过染色质的转录非常高效,而在体外重构系统中,核小体模板对聚合酶的前进构成了相当大的问题。最近,通过鉴定几种在这一过程中协助聚合酶的辅助因子,我们对通过染色质的转录延伸的理解取得了进展。通过酵母遗传学和哺乳动物系统中的生化研究相结合,人们对这些因子的功能有了深入了解。