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首页> 外文期刊>Journal of Molecular Biology >TOP Promoter Elements Control the Relative Ratio of Intron-encoded snoRNA Versus Spliced mRNA Biosynthesis.
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TOP Promoter Elements Control the Relative Ratio of Intron-encoded snoRNA Versus Spliced mRNA Biosynthesis.

机译:TOP启动子元件控制内含子编码的snoRNA与剪接的mRNA生物合成的相对比例。

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摘要

In vertebrates almost all snoRNAs are encoded in introns of a specific subclass of polII transcripts: the TOP genes. The majority of these RNAs originate through debranching of the spliced introns, the rest through endonucleolytic cleavage of the precursor that contains them. In both cases it has been suggested that snoRNP factors associate at early steps during transcription and control snoRNA biogenesis. Here, we analyzed the specific case of the U16 snoRNA that was shown to originate mainly through endonucleolytic cleavage. We show that TOP promoter elements determine a specific ratio of snoRNA and mRNA production. Under the control of these sequences the snoRNA is likely to originate from both splicing and cleavage of the pre-mRNA. Conversely, canonical polII promoter elements seem not to be compatible with snoRNA release through the cleavage reaction and produce a lower snoRNA/mRNA ratio. In addition, we show that the proximal part of the TOP promoter is responsible for this peculiar post-transcriptional process that controls the relative ratio between snoRNA and mRNA.
机译:在脊椎动物中,几乎所有的snoRNA都在polII转录物的特定亚类:TOP基因的内含子中编码。这些RNA的大部分起源于剪接的内含子的脱支,其余的则通过包含它们的前体的内切核酸酶裂解而产生。在这两种情况下,均提示snoRNP因子在转录过程的早期阶段相互关联并控制snoRNA生物发生。在这里,我们分析了U16 snoRNA的特定情况,该情况主要通过内切核酸酶裂解而产生。我们显示,TOP启动子元件决定snoRNA和mRNA产生的特定比例。在这些序列的控制下,snoRNA可能源自前mRNA的剪接和切割。相反,规范的polII启动子元件似乎与通过切割反应释放的snoRNA不兼容,并产生较低的snoRNA / mRNA比。此外,我们表明,TOP启动子的近端部分负责控制snoRNA和mRNA之间相对比例的这种特殊的转录后过程。

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