首页> 美国卫生研究院文献>Nucleic Acids Research >Xenopus tropicalis U6 snRNA genes transcribed by Pol III contain the upstream promoter elements used by Pol II dependent U snRNA genes.
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Xenopus tropicalis U6 snRNA genes transcribed by Pol III contain the upstream promoter elements used by Pol II dependent U snRNA genes.

机译:由Pol III转录的热带非洲爪蟾U6 snRNA基因包含由Pol II依赖性U snRNA基因使用的上游启动子元件。

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摘要

We have cloned and sequenced a 977bp DNA fragment, pXTU6-2, that represents the transcription unit for a Xenopus tropicalis U6 RNA gene. This basic repeating unit is reiterated ca.500-fold per haploid genome. Oocyte injections of pXTU6-2 led to the transcription of a mature-sized U6 RNA that, however, lacked internal 2'-O-methylations. These posttranscriptional modifications of U6 RNA might be cytoplasmic and could require its association with U4 RNA to be accomplished. The low alpha- amanitin sensitivity of U6 RNA synthesis in oocytes suggested that U6 RNA is transcribed by RNA polymerase III, consistent with features of the U6 RNA molecule which also contains a Box A- like intragenic control region. Inspection of X. tropicalis, mouse and human U6 DNA upstream sequences revealed the presence of a TATA box as well as of the proximal and enhancer (octamer motif) elements contained in snRNA genes transcribed by RNA polymerase II. We propose that U6 RNAs are synthesized by a specialized transcription complex consisting of RNA polymerase III and transcription factors, some of which are very likely shared with RNA polymerase II promoters.
机译:我们已经克隆并测序了一个977bp的DNA片段pXTU6-2,该片段代表了非洲爪蟾U6 RNA基因的转录单位。每个单倍体基因组重复此基本重复单元约500倍。卵母细胞注射pXTU6-2导致成熟大小的U6 RNA转录,但该RNA缺乏内部2'-O-甲基化。 U6 RNA的这些转录后修饰可能是细胞质的,可能需要与U4 RNA关联才能完成。卵母细胞中U6 RNA合成对α-天冬酰胺的敏感性较低,这表明U6 RNA被RNA聚合酶III转录,这与U6 RNA分子的特征一致,U6 RNA分子也包含Box A型基因内控制区。对热带假单胞菌,小鼠和人U6 DNA上游序列的检查揭示了TATA盒以及RNA聚合酶II转录的snRNA基因中包含的近端和增强子(八聚体基序)元件的存在。我们建议,U6 RNA是由专门的转录复合物合成的,该复合物由RNA聚合酶III和转录因子组成,其中一些很可能与RNA聚合酶II启动子共享。

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