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Nup358通过其SUMO相互作用基序与AGO蛋白结合,并促进靶mRNA与miRISC的结合。

Nup358 binds to AGO proteins through its SUMO-interacting motifs and promotes the association of target mRNA with miRISC.

作者信息

Sahoo Manas Ranjan, Gaikwad Swati, Khuperkar Deepak, Ashok Maitreyi, Helen Mary, Yadav Santosh Kumar, Singh Aditi, Magre Indrasen, Deshmukh Prachi, Dhanvijay Supriya, Sahoo Pabitra Kumar, Ramtirtha Yogendra, Madhusudhan Mallur Srivatsan, Gayathri Pananghat, Seshadri Vasudevan, Joseph Jomon

机构信息

National Centre for Cell Science, S.P. Pune University Campus, Pune, India.

Division of Biology, Indian Institute of Science Education and Research, Pune, India.

出版信息

EMBO Rep. 2017 Feb;18(2):241-263. doi: 10.15252/embr.201642386. Epub 2016 Dec 30.

Abstract

MicroRNA (miRNA)-guided mRNA repression, mediated by the miRNA-induced silencing complex (miRISC), is an important component of post-transcriptional gene silencing. However, how miRISC identifies the target mRNA in vivo is not well understood. Here, we show that the nucleoporin Nup358 plays an important role in this process. Nup358 localizes to the nuclear pore complex and to the cytoplasmic annulate lamellae (AL), and these structures dynamically associate with two mRNP granules: processing bodies (P bodies) and stress granules (SGs). Nup358 depletion disrupts P bodies and concomitantly impairs the miRNA pathway. Furthermore, Nup358 interacts with AGO and GW182 proteins and promotes the association of target mRNA with miRISC A well-characterized SUMO-interacting motif (SIM) in Nup358 is sufficient for Nup358 to directly bind to AGO proteins. Moreover, AGO and PIWI proteins interact with SIMs derived from other SUMO-binding proteins. Our study indicates that Nup358-AGO interaction is important for miRNA-mediated gene silencing and identifies SIM as a new interacting motif for the AGO family of proteins. The findings also support a model wherein the coupling of miRISC with the target mRNA could occur at AL, specialized domains within the ER, and at the nuclear envelope.

摘要

由微小RNA诱导沉默复合体(miRISC)介导的微小RNA(miRNA)引导的mRNA抑制是转录后基因沉默的重要组成部分。然而,miRISC如何在体内识别靶mRNA尚不清楚。在此,我们表明核孔蛋白Nup358在此过程中起重要作用。Nup358定位于核孔复合体和细胞质环层板(AL),并且这些结构与两种mRNA颗粒动态相关:加工小体(P小体)和应激颗粒(SGs)。Nup358的缺失破坏了P小体,并同时损害了miRNA途径。此外,Nup358与AGO和GW182蛋白相互作用,并促进靶mRNA与miRISC的结合。Nup358中一个特征明确的小泛素样修饰蛋白(SUMO)相互作用基序(SIM)足以使Nup358直接结合AGO蛋白。此外,AGO和PIWI蛋白与源自其他SUMO结合蛋白的SIM相互作用。我们的研究表明,Nup358-AGO相互作用对于miRNA介导的基因沉默很重要,并将SIM鉴定为AGO蛋白家族的新相互作用基序。这些发现还支持了一种模型,其中miRISC与靶mRNA的偶联可能发生在AL、内质网内的特殊结构域以及核膜处。

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