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Implication of Ccr4-Not complex function in mRNA quality control in Saccharomyces cerevisiae

机译:Ccr4-Not复杂功能在酿酒酵母mRNA质量控制中的意义。

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摘要

Production of messenger ribonucleoprotein particles (mRNPs) is subjected to quality control (QC). In Saccharomyces cerevisiae, the RNA exosome and its cofactors are part of the nuclear QC machinery that removes, or stalls, aberrant molecules, thereby ensuring that only correctly formed mRNPs are exported to the cytoplasm. The Ccr4-Not complex, which constitutes the major S. cerevisiae cytoplasmic deadenylase, has recently been implied in nuclear exosome–related processes. Consistent with a possible nuclear function of the complex, the deletion or mutation of Ccr4-Not factors also elicits transcription phenotypes. Here we use genetic depletion of the Mft1p protein of the THO transcription/mRNP packaging complex as a model system to link the Ccr4-Not complex to nuclear mRNP QC. We reveal strong genetic interactions between alleles of the Ccr4-Not complex with both the exosomal RRP6 and MFT1 genes. Moreover, Rrp6p-dependent in vivo QC phenotypes of Δmft1 cells can be rescued by codeletion of several Ccr4-Not components. We discuss how the Ccr4-Not complex may connect with the mRNP QC pathway.
机译:信使核糖核蛋白颗粒(mRNPs)的生产经过质量控制(QC)。在酿酒酵母中,RNA外泌体及其辅因子是核QC机制的一部分,该机制去除或使异常分子失速,从而确保只有正确形成的mRNP才能输出到细胞质中。 Ccr4-Not复合物构成了酿酒酵母的主要胞质去烯基化酶,最近被暗示存在于核外泌体相关的过程中。与复合物的可能的核功能一致,Ccr4-Not因子的缺失或突变也引起转录表型。在这里,我们使用THO转录/ mRNP包装复合体的Mft1p蛋白的遗传耗竭作为模型系统,将Ccr4-Not复合体与核mRNP QC连接起来。我们揭示了与外泌体RRP6和MFT1基因的Ccr4-Not复杂等位基因之间的强大的遗传相互作用。此外,Δmft1细胞的Rrp6p依赖的体内QC表型可以通过几个Ccr4-Not组分的编码来挽救。我们讨论了Ccr4-Not复合物如何与mRNP QC途径联系起来。

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