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Gene expression is circular: Factors for mRNA degradation also foster mRNA synthesis

机译:基因表达是循环的:mRNA降解的因素也促进了mRNA的合成

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摘要

Maintaining proper mRNA levels is a key aspect in the regulation of gene expression. The balance between mRNA synthesis and decay determines these levels. We demonstrate that most yeast mRNAs are degraded by the cytoplasmic 5′-to-3′ pathway (the "decaysome"), as proposed previously. Unexpectedly, the level of these mRNAs is highly robust to perturbations in this major pathway because defects in various decaysome components lead to transcription downregulation. Moreover, these components shuttle between the cytoplasm and the nucleus, in a manner dependent on proper mRNA degradation. In the nucleus, they associate with chromatin - preferentially ~30 bp upstream of transcription start-sites - and directly stimulate transcription initiation and elongation. The nuclear role of the decaysome in transcription is linked to its cytoplasmic role in mRNA decay; linkage, in turn, seems to depend on proper shuttling of its components. The gene expression process is therefore circular, whereby the hitherto first and last stages are interconnected.
机译:维持适当的mRNA水平是调节基因表达的关键方面。 mRNA合成与衰变之间的平衡决定了这些水平。我们证明,大多数酵母mRNA通过细胞质5'到3'途径(“衰变体”)降解,如前所述。出乎意料的是,这些mRNA的水平对这种主要途径的干扰高度鲁棒,因为各种衰变成分的缺陷会导致转录下调。而且,这些成分以依赖于适当的mRNA降解的方式在细胞质和细胞核之间穿梭。在细胞核中,它们与染色质结合-优先在转录起始位点上游〜30 bp处结合-并直接刺激转录的起始和延长。衰变体在转录中的核作用与其在mRNA衰变中的细胞质作用有关。反过来,链接似乎取决于其组件的正确穿梭。因此,基因表达过程是循环的,从而迄今为止的第一阶段和最后阶段是相互联系的。

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