Studitsky V M, Clark D J, Felsenfeld G
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892-0540, USA.
Cell. 1995 Oct 6;83(1):19-27. doi: 10.1016/0092-8674(95)90230-9.
We have studied the kinetics of transcription through a nucleosome core. RNA polymerase transcribes the first approximately 25 bp of nucleosomal DNA rapidly, but then hits a barrier and continues slowly to the nucleosomal dyad region. Here, the barrier disappears and the transcript is completed at a rapid rate, as if on free DNA, indicating that histone octamer transfer is completed as polymerase reaches the dyad. If DNA behind the polymerase is removed during transcription, the barrier does not appear until the polymerase has penetrated up to 15 bp farther into the nucleosome. On a longer template, the barrier is almost eliminated. We have shown previously that the octamer is transferred around the transcribing polymerase via an intermediate containing an intranucleosomal DNA loop. Our results exclude the possibility that polymerase has difficulty breaking histone-DNA contacts and suggest instead that polymerase pauses because it has difficulty transcribing DNA in the loop.
我们研究了RNA聚合酶通过核小体核心进行转录的动力学过程。RNA聚合酶能快速转录核小体DNA的前约25个碱基对,但随后遇到障碍,然后缓慢延伸至核小体二分体区域。在此处,障碍消失,转录以快速速率完成,就好像在游离DNA上一样,这表明当聚合酶到达二分体时,组蛋白八聚体转移已完成。如果在转录过程中去除聚合酶后方的DNA,直到聚合酶进一步深入核小体15个碱基对时,障碍才会出现。在更长的模板上,障碍几乎被消除。我们之前已经表明,八聚体通过包含核小体内DNA环的中间体围绕转录中的聚合酶进行转移。我们的结果排除了聚合酶难以打破组蛋白 - DNA接触的可能性,相反,表明聚合酶暂停是因为它难以转录环中的DNA。