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首页> 外文期刊>Nucleic Acids Research >AGO-unbound cytosolic pool of mature miRNAs in plant cells reveals a novel regulatory step at AGO1 loading
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AGO-unbound cytosolic pool of mature miRNAs in plant cells reveals a novel regulatory step at AGO1 loading

机译:以前 - 在植物细胞中的成熟miRNAs的未结合细胞溶质池揭示了一个新的监管步骤1

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摘要

RNA interference (RNAi) is mediated by small, 20-24-nt-long, non-coding regulatory (s)RNAs such as micro (mi) and small interfering (si) RNAs via the action of ARGONAUTE (AGO) proteins. High-throughput sequencing of size-separated sRNA pools of plant crude extracts revealed that the majority of the canonical miRNAs were associated with high molecular weight RNA-induced silencing complexes co-migrating with AGO1 (HMW RISC). In contrast, the majority of 24-nt-long siRNAs were found in association with low molecular weight complexes co-migrating with AGO4 (LMW RISC). Intriguingly, we identified a large set of cytoplasmic sRNAs, including mature miRNA sequences, in the low molecular size range corresponding to protein-unbound sRNAs. By comparing the RISC-loaded and protein-unbound pools of miRNAs, we identified miRNAs with highly different loading efficiencies. Expression of selected miRNAs in transient and transgenic systems validated their altered loading abilities implying that this process is controlled by information associated with the diverse miRNA precursors. We also showed that the availability of AGO proteins is a limiting factor determining the loading efficiency of miRNAs. Our data reveal the existence of a regulatory checkpoint determining the RISC-loading efficiencies of various miRNAs by sorting only a subset of the produced miRNAs into the biologically active RISCs.
机译:RNA干扰(RNAi)由小,20-24-nt-long,非编码调节调节(S)介导,例如Micro(Mi)和小干扰(Si)RNA通过Argonaute(前)蛋白质。植物原油提取物的大小分离SRNA池的高通量测序显示,大多数规范miRNA与高分子量RNA诱导的沉默复合物与前迁移(HMW RISC)相关联。相反,大多数24-nt长的siRNA与与以往4(LMW RISC)共同迁移的低分子量复合物相关联。有趣的是,我们鉴定了大量细胞质SRNA,包括成熟的miRNA序列,在对应于蛋白质 - 未结合的SRNA的低分子大小范围内。通过比较MIRNA的RISC加载和蛋白质 - 未结合池,我们鉴定了具有高度不同的装载效率的​​MIRNA。瞬态和转基因系统中所选miRNA的表达验证了它们改变的加载能力,这意味着该过程通过与多样性miRNA前体相关的信息来控制。我们还表明,前一蛋白质的可用性是确定miRNA的负载效率的限制因素。我们的数据揭示了监管检查点,通过仅将产生的miRNA的子集分类到生物活性RISC中,确定各种miRNA的RISS效率。

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  • 来源
    《Nucleic Acids Research》 |2019年第18期|共15页
  • 作者单位

    Natl Agr Res &

    Innovat Ctr Agr Biotechnol Inst Dept Plant Biotechnol Szent Gyorgyi Albert Str 4 H-2100 Godollo Hungary;

    Natl Agr Res &

    Innovat Ctr Agr Biotechnol Inst Dept Plant Biotechnol Szent Gyorgyi Albert Str 4 H-2100 Godollo Hungary;

    Natl Agr Res &

    Innovat Ctr Agr Biotechnol Inst Dept Plant Biotechnol Szent Gyorgyi Albert Str 4 H-2100 Godollo Hungary;

    Natl Agr Res &

    Innovat Ctr Agr Biotechnol Inst Dept Plant Biotechnol Szent Gyorgyi Albert Str 4 H-2100 Godollo Hungary;

    Natl Agr Res &

    Innovat Ctr Agr Biotechnol Inst Dept Plant Biotechnol Szent Gyorgyi Albert Str 4 H-2100 Godollo Hungary;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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