Aberrant mRNA Transcripts and the Nonsense-Mediated Decay Proteins UPF2 and UPF3 Are Enriched in the Arabidopsis Nucleolus
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Aberrant mRNA Transcripts and the Nonsense-Mediated Decay Proteins UPF2 and UPF3 Are Enriched in the Arabidopsis Nucleolus

机译:异常的mRNA转录本和无义介导的衰变蛋白UPF2和UPF3富含拟南芥核仁。

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nnnThe eukaryotic nucleolus is multifunctional and involved in the metabolism and assembly of many different RNAs and ribonucleoprotein particles as well as in cellular functions, such as cell division and transcriptional silencing in plants. We previously showed that Arabidopsis thaliana exon junction complex proteins associate with the nucleolus, suggesting a role for the nucleolus in mRNA production. Here, we report that the plant nucleolus contains mRNAs, including fully spliced, aberrantly spliced, and single exon gene transcripts. Aberrant mRNAs are much more abundant in nucleolar fractions, while fully spliced products are more abundant in nucleoplasmic fractions. The majority of the aberrant transcripts contain premature termination codons and have characteristics of nonsense-mediated decay (NMD) substrates. A direct link between NMD and the nucleolus is shown by increased levels of the same aberrant transcripts in both the nucleolus and in Up-frameshift (upf) mutants impaired in NMD. In addition, the NMD factors UPF3 and UPF2 localize to the nucleolus, suggesting that the Arabidopsis nucleolus is therefore involved in identifying aberrant mRNAs and NMD.
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nnn,真核细胞核是多功能的,并参与 元许多不同的RNA和核糖蛋白 颗粒的代谢和组装以及细胞功能,例如植物的细胞分裂 和转录沉默。我们先前显示了 拟南芥外显子连接复合蛋白将 与核仁相关,暗示了核仁在mRNA 生产。在这里,我们报道植物核仁包含 mRNA,包括完全剪接,异常剪接和单个 外显子基因转录本。异常的mRNAs在核仁级分中含量丰富得多,而完全剪接的产物在核质级分中含量更高 。大多数异常的 转录本都含有过早的终止密码子,并且具有无义介导的衰变(NMD)底物的特征 NMD和核仁之间的直接联系通过核仁和上移框 异常转录本水平的提高来表明> upf )突变体在NMD中受损。此外,NMD因子 UPF3和UPF2定位于核仁,这表明 拟南芥核仁因此参与了异常 < / SUP> mRNA和NMD。

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    《THE PLANT CELL》 |2009年第7期|2045-2057|共13页
  • 作者单位

    Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom;

    Department of Cell and Developmental Biology, John Innes Centre, Colney, Norwich NR4 7UH, United Kingdom;

    Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom;

    Department of Cell and Developmental Biology, John Innes Centre, Colney, Norwich NR4 7UH, United Kingdom;

    Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom;

    Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom;

    Department of Cell and Developmental Biology, John Innes Centre, Colney, Norwich NR4 7UH, United Kingdom;

    Genetics Programme, Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom|Division of Plant Sciences, University of Dundee at Scottish Crop Research Institute, Invergowrie, Dundee DD2 5DA, Scotland, United Kingdom;

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