Kulaeva Olga I, Hsieh Fu-Kai, Chang Han-Wen, Luse Donal S, Studitsky Vasily M
Department of Pharmacology, UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.
Biochim Biophys Acta. 2013 Jan;1829(1):76-83. doi: 10.1016/j.bbagrm.2012.08.015. Epub 2012 Sep 6.
Efficient maintenance of chromatin structure during passage of RNA polymerase II (Pol II) is critical for cell survival and functioning. Moderate-level transcription of eukaryotic genes by Pol II is accompanied by nucleosome survival, extensive exchange of histones H2A/H2B and minimal exchange of histones H3/H4. Complementary in vitro studies have shown that transcription through chromatin by single Pol II complexes is uniquely coupled with nucleosome survival via formation of a small intranucleosomal DNA loop (Ø-loop) containing the transcribing enzyme. In contrast, transient displacement and exchange of all core histones are observed during intense transcription. Indeed, multiple transcribing Pol II complexes can efficiently overcome the high nucleosomal barrier and displace the entire histone octamer in vitro. Thus, various Pol II complexes can remodel chromatin to different extents. The mechanisms of nucleosome survival and displacement during transcription and the role of DNA-histone interactions and various factors during this process are discussed. This article is part of a Special Issue entitled: RNA polymerase II Transcript Elongation.
在RNA聚合酶II(Pol II)转录过程中高效维持染色质结构对细胞存活和功能发挥至关重要。Pol II对真核基因进行中等水平转录时伴随着核小体的存活、组蛋白H2A/H2B的广泛交换以及组蛋白H3/H4的最小程度交换。互补的体外研究表明,单个Pol II复合物通过染色质的转录与核小体存活独特地耦合在一起,这是通过形成一个包含转录酶的小核小体内DNA环(Ø环)实现的。相比之下,在高强度转录过程中会观察到所有核心组蛋白的瞬时置换和交换。实际上,多个正在转录的Pol II复合物能够在体外有效克服高核小体屏障并置换整个组蛋白八聚体。因此,各种Pol II复合物能够在不同程度上重塑染色质。本文讨论了转录过程中核小体存活和置换的机制以及该过程中DNA-组蛋白相互作用和各种因子的作用。本文是名为《RNA聚合酶II转录延伸》的特刊的一部分。