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一种与拟南芥中核RNA沉默及沉默信号在细胞间传播相关的SNF2蛋白。

An SNF2 protein associated with nuclear RNA silencing and the spread of a silencing signal between cells in Arabidopsis.

作者信息

Smith Lisa M, Pontes Olga, Searle Iain, Yelina Nataliya, Yousafzai Faridoon K, Herr Alan J, Pikaard Craig S, Baulcombe David C

机构信息

Sainsbury Laboratory, John Ines Centre, Norwich NR4 7UH, United Kingdom.

出版信息

Plant Cell. 2007 May;19(5):1507-21. doi: 10.1105/tpc.107.051540. Epub 2007 May 25.

Abstract

The silencing phenotype in Arabidopsis thaliana lines with an inverted repeat transgene under the control of a phloem-specific promoter was manifested in regions around veins due to a mobile signal of silencing. Genetic analysis implicates RNA-DEPENDENT RNA POLYMERASE2 (RDR2) and an RNA polymerase IVa subunit gene (NRPD1a) in the signaling mechanism. We also identified an SNF2 domain-containing protein (CLASSY1) that acts together with RDR2 and NRPD1a in the spread of transgene silencing and in the production of endogenous 24-nucleotide short interfering RNAs (siRNAs). Cytochemical analysis indicates that CLASSY1 may act in the nucleus with NRPD1a and RDR2 in the upstream part of RNA silencing pathways that generate a double-stranded RNA substrate for Dicer-like (DCL) nucleases. DCL3 and ARGONAUTE4 act in a downstream part of the pathway, leading to endogenous 24-nucleotide siRNA production, but are not required for intercellular signaling. From genetic analysis, we conclude that another downstream part of the pathway associated with intercellular signaling requires DCL4 and at least one other protein required for 21-nucleotide trans-acting siRNAs. We interpret the effect of polymerase IVa and trans-acting siRNA pathway mutations in terms of a modular property of RNA silencing pathways.

摘要

在韧皮部特异性启动子控制下带有反向重复转基因的拟南芥株系中,沉默表型由于沉默的移动信号而在叶脉周围区域显现出来。遗传分析表明,RNA依赖性RNA聚合酶2(RDR2)和RNA聚合酶IVa亚基基因(NRPD1a)参与了信号传导机制。我们还鉴定出一种含SNF2结构域的蛋白(CLASSY1),它与RDR2和NRPD1a共同作用于转基因沉默的传播以及内源性24核苷酸短干扰RNA(siRNA)的产生。细胞化学分析表明,CLASSY1可能在RNA沉默途径上游部分的细胞核中与NRPD1a和RDR2一起发挥作用,该途径为Dicer样(DCL)核酸酶生成双链RNA底物。DCL3和AGO4在该途径的下游部分发挥作用,导致内源性24核苷酸siRNA的产生,但细胞间信号传导并不需要它们。通过遗传分析,我们得出结论,该途径中与细胞间信号传导相关的另一个下游部分需要DCL4和至少一种其他参与21核苷酸反式作用siRNA生成的蛋白。我们根据RNA沉默途径的模块化特性来解释聚合酶IVa和反式作用siRNA途径突变的影响。

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