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新型环状 RNA 分子 circzip-2 及其在帕金森病线虫模型中合成基因 zip-2 的功能特征。

Functional Characterization of Novel Circular RNA Molecule, circzip-2 and Its Synthesizing Gene zip-2 in C. elegans Model of Parkinson's Disease.

机构信息

Laboratory of Functional Genomics and Molecular Toxicology, Division of Toxicology and Experimental Medicine, CSIR-Central Drug Research Institute, Lucknow, UP, 226 031, India.

出版信息

Mol Neurobiol. 2018 Aug;55(8):6914-6926. doi: 10.1007/s12035-018-0903-5. Epub 2018 Jan 23.

Abstract

Circular RNAs (circRNAs) are peculiar non-coding RNA molecules which are known to be present across taxa. Considering the body of evidence that establishes critical functions of non-coding RNA molecules, we endeavored to study circRNAs in the context of Parkinson's disease (PD). Employing transgenic C. elegans model of PD, we used RNase R-mediated cleavage of linear RNA followed by divergent primer-based amplifications towards identifying circzip-2, a novel circRNA molecule. We went on to sequence circzip-2 which is synthesized from functionally important gene zip-2. Studying RNAi-induced knockdown conditions of zip-2, we observed a reduced aggregation of α-synuclein protein along with an enhanced lifespan of the worms. We further carried out transcriptome analysis of zip-2 silenced worms, which suggested that zip-2 might be functioning via Daf-16 pathway. Further interaction studies revealed that circzip-2 possibly sponges microRNA molecule miR-60 towards asserting an important role in various processes associated with PD.

摘要

环状 RNA(circRNAs)是一类具有特殊结构的非编码 RNA 分子,广泛存在于各种生物中。鉴于非编码 RNA 分子具有重要功能的大量证据,我们致力于研究环状 RNA 在帕金森病(PD)中的作用。我们使用 PD 的转基因秀丽隐杆线虫模型,通过 RNase R 介导的线性 RNA 切割,以及基于分歧引物的扩增,鉴定出一种新型环状 RNA 分子 circzip-2。我们对 circzip-2 进行了测序,它是由功能重要的基因 zip-2 合成的。研究 zip-2 的 RNAi 诱导敲低条件,我们观察到α-突触核蛋白的聚集减少,同时线虫的寿命延长。我们进一步对 zip-2 沉默的线虫进行了转录组分析,表明 zip-2 可能通过 Daf-16 途径发挥作用。进一步的相互作用研究表明,circzip-2 可能通过海绵 microRNA 分子 miR-60 发挥作用,在与 PD 相关的各种过程中发挥重要作用。

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