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系统性 RNA 干扰缺陷(SID)基因调节秀丽隐杆线虫多巴胺能神经元退行性变。

Systemic RNA Interference Defective (SID) genes modulate dopaminergic neurodegeneration in C. elegans.

机构信息

Department of Biological Sciences, The University of Alabama, Tuscaloosa, Alabama, United States of America.

Center for Convergent Bioscience and Medicine, The University of Alabama, Tuscaloosa, Alabama, United States of America.

出版信息

PLoS Genet. 2022 Aug 19;18(8):e1010115. doi: 10.1371/journal.pgen.1010115. eCollection 2022 Aug.

Abstract

The fine-tuning of gene expression is critical for all cellular processes; aberrations in this activity can lead to pathology, and conversely, resilience. As their role in coordinating organismal responses to both internal and external factors have increasingly come into focus, small non-coding RNAs have emerged as an essential component to disease etiology. Using Systemic RNA interference Defective (SID) mutants of the nematode Caenorhabditis elegans, deficient in gene silencing, we examined the potential consequences of dysfunctional epigenomic regulation in the context of Parkinson's disease (PD). Specifically, the loss of either the sid-1 or sid-3 genes, which encode a dsRNA transporter and an endocytic regulatory non-receptor tyrosine kinase, respectively, conferred neuroprotection to dopaminergic (DA) neurons in an established transgenic C. elegans strain wherein overexpression of human α-synuclein (α-syn) from a chromosomally integrated multicopy transgene causes neurodegeneration. We further show that knockout of a specific microRNA, mir-2, attenuates α-syn neurotoxicity; suggesting that the native targets of mir-2-dependent gene silencing represent putative neuroprotective modulators. In support of this, we demonstrated that RNAi knockdown of multiple mir-2 targets enhanced α-syn-induced DA neurodegeneration. Moreover, we demonstrate that mir-2 overexpression originating in the intestine can induce neurodegeneration of DA neurons, an effect that was reversed by pharmacological inhibition of SID-3 activity. Interestingly, sid-1 mutants retained mir-2-induced enhancement of neurodegeneration. Transcriptomic analysis of α-syn animals with and without a sid-1 mutation revealed 27 differentially expressed genes with human orthologs related to a variety of diseases, including PD. Among these was pgp-8, encoding a P-glycoprotein-related ABC transporter. Notably, sid-1; pgp-8 double mutants abolished the neurodegeneration resulting from intestinal mir-2 overexpression. This research positions known regulators of small RNA-dependent gene silencing within a framework that facilitates mechanistic evaluation of epigenetic responses to exogenous and endogenous factors influencing DA neurodegeneration, revealing a path toward new targets for therapeutic intervention of PD.

摘要

基因表达的微调对于所有细胞过程都是至关重要的;这种活性的异常会导致病理学,反之亦然。随着它们在协调生物体对内外部因素的反应方面的作用日益受到关注,小非编码 RNA 已成为疾病病因学的一个重要组成部分。我们使用线虫 Caenorhabditis elegans 的系统性 RNA 干扰缺陷(SID)突变体,这些突变体缺乏基因沉默,研究了表观基因组调节功能障碍在帕金森病(PD)背景下的潜在后果。具体来说,分别缺失编码 dsRNA 转运蛋白和内吞调节非受体酪氨酸激酶的 sid-1 或 sid-3 基因,赋予了一种已建立的转基因 C. elegans 菌株中多巴胺能(DA)神经元神经保护作用,该菌株中人类α-突触核蛋白(α-syn)的过表达来自染色体整合的多拷贝转基因导致神经退行性变。我们进一步表明,特定 microRNA,mir-2 的敲除减弱了α-syn 的神经毒性;表明 mir-2 依赖性基因沉默的天然靶标代表潜在的神经保护调节剂。支持这一点,我们证明了多种 mir-2 靶标的 RNAi 敲低增强了α-syn 诱导的 DA 神经退行性变。此外,我们证明源自肠道的 mir-2 过表达可以诱导 DA 神经元的神经退行性变,SID-3 活性的药理学抑制可以逆转这种作用。有趣的是,sid-1 突变体保留了 mir-2 诱导的神经退行性变增强作用。带有和不带有 sid-1 突变的α-syn 动物的转录组分析揭示了 27 个差异表达基因,其具有与多种疾病相关的人类同源物,包括 PD。其中包括编码 P-糖蛋白相关 ABC 转运蛋白的 pgp-8。值得注意的是,sid-1;pgp-8 双突变体消除了肠道 mir-2 过表达引起的神经退行性变。这项研究将已知的小 RNA 依赖性基因沉默调节剂置于一个框架内,该框架有助于对外源性和内源性因素影响 DA 神经退行性变的表观遗传反应进行机制评估,为 PD 的治疗干预提供了新的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a082/9432717/e4a060d42839/pgen.1010115.g001.jpg

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