Schild C, Claret F X, Wahli W, Wolffe A P
Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892.
EMBO J. 1993 Feb;12(2):423-33. doi: 10.1002/j.1460-2075.1993.tb05674.x.
We describe the transcriptional potentiation in estrogen responsive transcription extracts of the Xenopus vitellogenin B1 gene promoter through the formation of a positioned nucleosome. Nuclease digestion and hydroxyl radical cleavage indicate that strong, DNA sequence-directed positioning of a nucleosome occurs between -300 and -140 relative to the start site of transcription. Deletion of this DNA sequence abolishes the potentiation of transcription due to nucleosome assembly. The wrapping of DNA around the histone core of the nucleosome positioned between -300 and -140 creates a static loop in which distal estrogen receptor binding sites are brought close to proximal promoter elements. This might facilitate interactions between the trans-acting factors themselves and/or RNA polymerase. Such a nucleosome provides an example of how chromatin structure might have a positive effect on the transcription process.
我们描述了通过形成定位核小体,非洲爪蟾卵黄蛋白原B1基因启动子的雌激素反应性转录提取物中的转录增强作用。核酸酶消化和羟基自由基切割表明,相对于转录起始位点,在-300至-140之间发生了核小体的强DNA序列导向定位。删除该DNA序列会消除由于核小体组装导致的转录增强作用。位于-300至-140之间的核小体组蛋白核心周围的DNA缠绕形成了一个静态环,其中远端雌激素受体结合位点靠近近端启动子元件。这可能促进反式作用因子自身和/或RNA聚合酶之间的相互作用。这样的核小体提供了一个染色质结构如何对转录过程产生积极影响的例子。