Li Q, Wrange O, Eriksson P
Department of Cell and Molecular Biology, Nobel Medical Institute, Karolinska Institute, Stockholm, Sweden.
Int J Biochem Cell Biol. 1997 May;29(5):731-42. doi: 10.1016/s1357-2725(97)00016-2.
Transcriptional activation is mediated by the facilitated binding of the basal transcription complex to the transcription start site of a promoter. The activation procedure involves protein-protein interactions between specific transcription factors and members of the basal transcription complex. However, since eukaryotic DNA is packaged with histones into nucleosomes the accessibility of the transcription factors is limited. In order to activate transcription, some of the specific transcription factors must have the capacity to bind to their binding sites when organized into nucleosomes. As a next step, the chromatin structure of the promoter needs to be decondensed in order to facilitate the binding of the basal transcription machinery. Recent data have addressed these issues and both binding of transcription factors to their chromatin binding site as well as transcription factor-induced chromatin remodelling have been demonstrated. In addition, factors that are candidates to mediate the chromatin remodelling have recently been identified and characterized. The ability of a transcription factor to recognize its cognate element in a nucleosome is an inheret property that differs among different transcription factors. The implications of the rotational and translational positioning of the DNA within a nucleosome on the accessibility of a transcription factor is described in this review. In addition, nucleosome rearrangement and juxtaposing in the context of transcriptional activation is also discussed.
转录激活是由基础转录复合物与启动子转录起始位点的易化结合介导的。激活过程涉及特定转录因子与基础转录复合物成员之间的蛋白质-蛋白质相互作用。然而,由于真核生物DNA与组蛋白包装成核小体,转录因子的可及性受到限制。为了激活转录,一些特定转录因子在组织成核小体时必须有能力结合到它们的结合位点。下一步,启动子的染色质结构需要解聚,以促进基础转录机制的结合。最近的数据已经解决了这些问题,并且已经证明了转录因子与其染色质结合位点的结合以及转录因子诱导的染色质重塑。此外,最近已经鉴定并表征了介导染色质重塑的候选因子。转录因子在核小体中识别其同源元件的能力是一种内在特性,不同转录因子之间存在差异。本文综述了核小体内DNA的旋转和平移定位对转录因子可及性的影响。此外,还讨论了转录激活背景下的核小体重排和并列。