Baumberger N, Baulcombe D C
Sainsbury Laboratory, Norwich Research Park, Norwich NR4 7UH, United Kingdom.
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11928-33. doi: 10.1073/pnas.0505461102. Epub 2005 Aug 4.
ARGONAUTE (AGO) RNA-binding proteins are involved in RNA silencing. They bind to short interfering RNAs (siRNAs) and microRNAs (miRNAs) through a conserved PAZ domain, and, in animals, they assemble into a multisubunit RNA-induced silencing complex (RISC). The mammalian AGO2, termed Slicer, directs siRNA- and miRNA-mediated cleavage of a target RNA. In Arabidopsis, there are 10 members of the AGO family, and the AGO1 protein is potentially the Slicer component in different RNA-silencing pathways. Here, we show that AGO1 selectively recruits certain classes of short silencing-related RNA. AGO1 is physically associated with miRNAs, transacting siRNAs, and transgene-derived siRNAs but excludes virus-derived siRNAs and 24-nt siRNAs involved in chromatin silencing. We also show that AGO1 has Slicer activity. It mediates the in vitro cleavage of a mir165 target RNA in a manner that depends on the sequence identity of amino acid residues in the PIWI domain that are predicted by homology with animal Slicer-competent AGO proteins to constitute the RNase catalytic center. However, unlike animals, we find no evidence that AGO1 Slicer is in a high molecular weight RNA-induced silencing complex. The Slicer activity fractionates as a complex of approximately 150 kDa that likely constitutes the AGO1 protein and associated RNA without any other proteins. Based on sequence similarity, we predict that other Arabidopsis AGOs might have a similar catalytic activity but recruit different subsets of siRNAs or miRNAs.
AGO(Argonaute)RNA结合蛋白参与RNA沉默。它们通过保守的PAZ结构域与小干扰RNA(siRNA)和微小RNA(miRNA)结合,并且在动物中,它们组装成多亚基RNA诱导沉默复合体(RISC)。哺乳动物的AGO2,也称为Slicer,指导siRNA和miRNA介导的靶RNA切割。在拟南芥中,AGO家族有10个成员,AGO1蛋白可能是不同RNA沉默途径中的Slicer组分。在这里,我们表明AGO1选择性地招募某些类别的短沉默相关RNA。AGO1与miRNA、反式作用siRNA和转基因衍生的siRNA在物理上相关联,但排除病毒衍生的siRNA和参与染色质沉默的24核苷酸siRNA。我们还表明AGO1具有Slicer活性。它以一种依赖于PIWI结构域中氨基酸残基序列同一性的方式介导mir165靶RNA的体外切割,这些氨基酸残基通过与具有Slicer活性的动物AGO蛋白的同源性预测构成RNase催化中心。然而,与动物不同,我们没有发现证据表明AGO1 Slicer存在于高分子量RNA诱导沉默复合体中。Slicer活性分离为一个约150 kDa的复合体,该复合体可能由AGO1蛋白和相关RNA组成,没有任何其他蛋白质。基于序列相似性,我们预测拟南芥中的其他AGO可能具有类似的催化活性,但招募不同的siRNA或miRNA子集。