首页> 外文OA文献 >The Xenopus ribosomal DNA 60- and 81-base-pair repeats are position-dependent enhancers that function at the establishment of the preinitiation complex: analysis in vivo and in an enhancer-responsive in vitro system.
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The Xenopus ribosomal DNA 60- and 81-base-pair repeats are position-dependent enhancers that function at the establishment of the preinitiation complex: analysis in vivo and in an enhancer-responsive in vitro system.

机译:非洲爪蟾核糖体DNA 60和81个碱基对的重复序列是位置依赖性增强子,它们在建立预起始复合体时起作用:体内分析和增强子响应性体外系统。

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摘要

Although it is generally believed that the 60- and 81-base-pair (60/81-bp) repeats of the Xenopus laevis ribosomal DNA (rDNA) spacer are position-independent transcriptional enhancers, this has not been shown directly. We have now developed a critical assay which proves that the 60/81-bp repeats do, in fact, stimulate transcription from promoters in cis and that they function in both orientations and when up to 1 kilobase pair from the initiation site. However, contrary to the widely accepted view, these elements are found to be highly position dependent, for they have no net effect when downstream of the initiation site within the transcribed region and they behave as transcriptional silencers of promoters in cis when moved greater than 2 kilobase pairs upstream of the initiation site. The 60/81-bp elements therefore are position-dependent 5' enhancers. We also found that this rDNA enhancer was polymerase I specific and that it was composed of duplicated, individually functional elements. Finally, we report an in vitro system that reproduces both cis enhancement and trans competition by the 60/81-bp repeats. Sequential-addition studies in this system demonstrated that the rDNA enhancer functions in trans at or before establishment of the stable transcription complex, not subsequently at each round of transcription.
机译:尽管通常认为非洲爪蟾核糖体DNA(rDNA)间隔基的60和81个碱基对(60/81 bp)重复是位置无关的转录增强子,但尚未直接显示出来。现在,我们已经开发出一种关键测定法,该测定法证明60 / 81-bp重复确实能刺激顺式启动子的转录,并且它们在两个方向上以及从起始位点起最多1个碱基对都起作用。但是,与广泛接受的观点相反,发现这些元件高度依赖位置,因为它们在转录区域内起始位点的下游时没有净作用,并且当移动大于2时它们在顺式中充当启动子的转录沉默子。起始位点上游的千碱基对。因此,60 / 81-bp元件是位置依赖性5'增强子。我们还发现,这种rDNA增强子是聚合酶I特异的,并且由重复的,单独的功能元件组成。最后,我们报告了一个体外系统,该系统通过60 / 81-bp重复序列再现顺式增强和反式竞争。在该系统中的顺序加法研究表明,rDNA增强子在建立稳定的转录复合体时或之前具有反式功能,而不是在每一轮转录后均具有反式功能。

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