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急性坏死性脑病相关突变 Nup358 损害 Nup358 与 TNRC6/GW182 的相互作用及 miRNA 功能。

Acute necrotizing encephalopathy-linked mutations in Nup358 impair interaction of Nup358 with TNRC6/GW182 and miRNA function.

机构信息

National Centre for Cell Science, S.P. Pune University Campus, Pune, 411007, India.

National Centre for Cell Science, S.P. Pune University Campus, Pune, 411007, India.

出版信息

Biochem Biophys Res Commun. 2021 Jun 25;559:230-237. doi: 10.1016/j.bbrc.2021.04.027. Epub 2021 May 4.

Abstract

MicroRNA (miRNA)-mediated translational suppression of mRNAs is involved in the regulation of multiple cellular processes. A recent study showed that Nup358, a protein mutated in a neurological disorder called acute necrotizing encephalopathy 1 (ANE1), helps in the coupling of miRNA-induced silencing complex (miRISC) - consisting of miRNA, AGO and GW182/TNRC6 proteins - with the target mRNA. Here we provide a detailed characterization of the interaction between Nup358 and GW182. We identified that the N-terminal region of Nup358 directly interacts with the C-terminal silencing domain of GW182. Interestingly, ANE1-associated Nup358 mutants display reduced interaction with GW182. Consistent with this, one of the prevalent ANE1 mutations, 585th threonine (T) residue changed to methionine (M) [T585M] compromised Nup358's ability to function in the miRNA pathway. Collectively, these results suggest that the ANE1-associated mutations in Nup358 might affect the miRNA pathway and contribute to the development of ANE1.

摘要

微小 RNA(miRNA)介导的 mRNA 翻译抑制参与了多种细胞过程的调节。最近的一项研究表明,在一种称为急性坏死性脑病 1(ANE1)的神经紊乱中发生突变的核孔蛋白 358(Nup358)有助于将 miRNA 诱导的沉默复合物(miRISC)与靶 mRNA 偶联,miRISC 由 miRNA、AGO 和 GW182/TNRC6 蛋白组成。在这里,我们详细描述了 Nup358 与 GW182 之间的相互作用。我们发现 Nup358 的 N 端区域直接与 GW182 的 C 端沉默结构域相互作用。有趣的是,与 ANE1 相关的 Nup358 突变体与 GW182 的相互作用减少。与此一致的是,ANE1 中常见的突变之一,第 585 个苏氨酸(T)残基变为蛋氨酸(M)[T585M],削弱了 Nup358 在 miRNA 途径中的功能。总之,这些结果表明,Nup358 中的 ANE1 相关突变可能会影响 miRNA 途径,并导致 ANE1 的发生。

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