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拟南芥FIERY1、XRN2和XRN3是内源性RNA沉默抑制因子。

Arabidopsis FIERY1, XRN2, and XRN3 are endogenous RNA silencing suppressors.

作者信息

Gy Isabelle, Gasciolli Virginie, Lauressergues Dominique, Morel Jean-Benoit, Gombert Julie, Proux Florence, Proux Caroline, Vaucheret Hervé, Mallory Allison C

机构信息

Laboratoire de Biologie Cellulaire, Institut Jean-Pierre Bourgin, Institut National de la Recherche Agronomique (INRA), 78026 Versailles Cedex, France.

出版信息

Plant Cell. 2007 Nov;19(11):3451-61. doi: 10.1105/tpc.107.055319. Epub 2007 Nov 9.

Abstract

The eukaryotic defense response posttranscriptional gene silencing (PTGS) is directed by short-interfering RNAs and thwarts invading nucleic acids via the RNA slicing activity of conserved ARGONAUTE (AGO) proteins. PTGS can be counteracted by exogenous or endogenous suppressors, including the cytoplasmic exoribonuclease XRN4, which also degrades microRNA (miRNA)-guided mRNA cleavage products but does not play an obvious role in development. Here, we show that the nuclear exoribonucleases XRN2 and XRN3 are endogenous PTGS suppressors. We also identify excised MIRNA loops as templates for XRN2 and XRN3 and show that XRN3 is critical for proper development. Independently, we identified the nucleotidase/phosphatase FIERY1 (FRY1) as an endogenous PTGS suppressor through a suppressor screen in a hypomorphic ago1 genetic background. FRY1 is one of six Arabidopsis thaliana orthologs of yeast Hal2. Yeast hal2 mutants overaccumulate 3'-phosphoadenosine 5'-phosphate, which suppresses the 5'-->3' exoribonucleases Xrn1 and Rat1. fry1 mutant plants recapitulate developmental and molecular characteristics of xrn mutants and likely restore PTGS in ago1 hypomorphic mutants by corepressing XRN2, XRN3, and XRN4, thus increasing RNA silencing triggers. We anticipate that screens incorporating partially compromised silencing components will uncover additional PTGS suppressors that may not be revealed using robust silencing systems.

摘要

真核生物的转录后基因沉默(PTGS)防御反应由短干扰RNA引导,并通过保守的AGO(ARGONAUTE)蛋白的RNA切割活性来抵御入侵的核酸。PTGS可被外源性或内源性抑制因子抵消,包括细胞质外切核糖核酸酶XRN4,它也会降解miRNA(微小RNA)引导的mRNA切割产物,但在发育过程中不发挥明显作用。在此,我们表明核外切核糖核酸酶XRN2和XRN3是内源性PTGS抑制因子。我们还确定切除的miRNA环是XRN2和XRN3的模板,并表明XRN3对正常发育至关重要。另外,我们通过在功能减弱的ago1基因背景下进行抑制因子筛选,确定核苷酸酶/磷酸酶FIERY1(FRY1)为内源性PTGS抑制因子。FRY1是酵母Hal2在拟南芥中的六个直系同源物之一。酵母hal2突变体中3'-磷酸腺苷5'-磷酸过度积累,抑制了5'→3'外切核糖核酸酶Xrn1和Rat1。fry1突变体植株重现了xrn突变体的发育和分子特征,并且可能通过共抑制XRN2、XRN3和XRN4来恢复ago1功能减弱突变体中的PTGS,从而增加RNA沉默触发因子。我们预计,包含部分受损沉默成分的筛选将发现更多使用强大沉默系统可能无法揭示的PTGS抑制因子。

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