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Xenopus transcription factor IIIA and the 5S nucleosome: development of a useful in vitro system.

机译:非洲爪蟾转录因子IIIA和5S核小体:开发有用的体外系统。

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5S RNA genes in Xenopus are regulated during development via a complex interplay between assembly of repressive chromatin structures and productive transcription complexes. Interestingly, 5S genes have been found to harbor powerful nucleosome positioning elements and therefore have become an important model system for reconstitution of eukaryotic genes into nucleosomes in vitro. Moreover, the structure of the primary factor initiating transcription of 5S DNA, transcription factor IIIA, has been extensively characterized. This has allowed for numerous studies of the effect of nucleosome assembly and histone modifications on the DNA binding activity of a transcription factor in vitro. For example, linker histones bind 5S nucleosomes and repress TFIIIA binding in vitro in a similar manner to that observed in vivo. In addition, TFIIIA binding to nucleosomes assembled with 5S DNA is stimulated by acetylation or removal of the core histone tail domains. Here we review the development of the Xenopus 5S in vitro system and discuss recent results highlighting new aspects of transcription factor - nucleosome interactions,
机译:非洲爪蟾中的5S RNA基因在发育过程中是通过阻抑染色质结构的组装与生产性转录复合物之间的复杂相互作用来调控的。有趣的是,已发现5S基因具有强大的核小体定位元件,因此已成为将真核基因在体外重组为核小体的重要模型系统。此外,已经广泛地表征了引起5S DNA转录的主要因子转录因子IIIA的结构。这已经允许对核小体组装和组蛋白修饰对体外转录因子的DNA结合活性的影响进行大量研究。例如,接头组蛋白以与体内观察到的相似方式在体外结合5S核小体并抑制TFIIIA结合。另外,通过乙酰化或去除核心组蛋白尾部结构域,可刺激TFIIIA与5S DNA组装的核小体结合。在这里,我们回顾了Xenopus 5S体外系统的开发,并讨论了最近的结果,这些结果突出了转录因子的新方面-核小体相互作用,

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