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首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >The transcriptional activity of RNA polymerase I is a key determinant for the level of all ribosome components.
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The transcriptional activity of RNA polymerase I is a key determinant for the level of all ribosome components.

机译:RNA聚合酶I的转录活性是所有核糖体组分水平的关键决定因素。

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摘要

Regulation of ribosome biogenesis is a key element of cell biology, not only because ribosomes are directly required for growth, but also because ribosome production monopolizes nearly 80% of the global transcriptional activity in rapidly growing yeast cells. These observations underscore the need for a tight regulation of ribosome synthesis in response to environmental conditions. In eukaryotic cells, ribosome synthesis involves the activities of the three nuclear RNA polymerases (Pol). Although postulated, there is no clear evidence indicating whether the maintenance of an equimolar supply of ribosomal components reflects communication between the nuclear transcriptional machineries. Here, by constructing a yeast strain expressing a Pol I that remains constitutively competent for the initiation of transcription under stress conditions, we demonstrate that derepression of Pol I transcription leads to a derepression of Pol II transcription that is restricted to the genes encoding ribosomal proteins. Furthermore, we show that the level of 5S rRNA, synthesized by Pol III, is deregulated concomitantly with Pol I transcription. Altogether, these results indicate that a partial derepression of Pol I activity drives an abnormal accumulation of all ribosomal components, highlighting the critical role of the regulation of Pol I activity within the control of ribosome biogenesis.
机译:核糖体生物发生的调控是细胞生物学的关键要素,不仅因为核糖体是生长的直接需要,而且还因为核糖体的产生垄断了快速生长的酵母细胞中近80%的全球转录活性。这些观察结果强调了响应环境条件需要严格调节核糖体合成的需要。在真核细胞中,核糖体合成涉及三种核RNA聚合酶(Pol)的活性。尽管是假定的,但没有明确的证据表明维持等摩尔核糖体成分的供应是否反映了核转录机制之间的通讯。在这里,通过构建表达在应激条件下仍具有构成转录起始能力的Pol I的酵母菌株,我们证明了Pol I转录的抑制可导致Pol II转录的抑制,该抑制仅限于编码核糖体蛋白的基因。此外,我们表明由Pol III合成的5S rRNA的水平与Pol I转录同时被解除了调控。总而言之,这些结果表明,Pol I活性的部分降低会导致所有核糖体组分的异常积累,从而突出了调节Pol I活性在核糖体生物发生控制中的关键作用。

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