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通过无义介导的mRNA降解对转录起始位点选择进行质量控制。

Quality control of transcription start site selection by nonsense-mediated-mRNA decay.

作者信息

Malabat Christophe, Feuerbach Frank, Ma Laurence, Saveanu Cosmin, Jacquier Alain

机构信息

Institut Pasteur, UMR3525, Génétique des Interactions Macromoléculaires, Centre National de la Recherche Scientifique, Paris, France.

Plate-Forme Génomique, Institut Pasteur, Paris, France.

出版信息

Elife. 2015 Apr 23;4:e06722. doi: 10.7554/eLife.06722.

Abstract

Nonsense-mediated mRNA decay (NMD) is a translation-dependent RNA quality-control pathway targeting transcripts such as messenger RNAs harboring premature stop-codons or short upstream open reading frame (uORFs). Our transcription start sites (TSSs) analysis of Saccharomyces cerevisiae cells deficient for RNA degradation pathways revealed that about half of the pervasive transcripts are degraded by NMD, which provides a fail-safe mechanism to remove spurious transcripts that escaped degradation in the nucleus. Moreover, we found that the low specificity of RNA polymerase II TSSs selection generates, for 47% of the expressed genes, NMD-sensitive transcript isoforms carrying uORFs or starting downstream of the ATG START codon. Despite the low abundance of this last category of isoforms, their presence seems to constrain genomic sequences, as suggested by the significant bias against in-frame ATGs specifically found at the beginning of the corresponding genes and reflected by a depletion of methionines in the N-terminus of the encoded proteins.

摘要

无义介导的mRNA降解(NMD)是一种依赖翻译的RNA质量控制途径,其靶向诸如含有提前终止密码子或短上游开放阅读框(uORF)的信使RNA等转录本。我们对缺乏RNA降解途径的酿酒酵母细胞进行的转录起始位点(TSS)分析表明,约一半的广泛转录本被NMD降解,这提供了一种故障安全机制,以去除在细胞核中逃脱降解的假转录本。此外,我们发现RNA聚合酶II选择TSS的低特异性会为47%的表达基因产生携带uORF或在ATG起始密码子下游起始的对NMD敏感的转录本异构体。尽管最后一类异构体的丰度较低,但它们的存在似乎会限制基因组序列,这从相应基因起始处特别发现的针对框内ATG的显著偏差以及编码蛋白质N端甲硫氨酸的消耗中可以看出。

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