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Argonaute protein as a linker to command center of physiological processes

机译:Argonaute蛋白作为生理过程指挥中心的连接物

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摘要

MicroRNAs (miRNAs) post-transcriptionally regulate gene expression by binding to target mRNAs with perfect or imperfect complementarity, recruiting an Argonaute (AGO) protein complex that usually results in degradation or translational repression of the target mRNA. AGO proteins function as the Slicer enzyme in miRNA and small interfering RNA (siRNA) pathways involved in human physiological and pathophysiological processes, such as antiviral responses and disease formation. Although the past decade has witnessed rapid advancement in studies of AGO protein functions, to further elucidate the molecular mechanism of AGO proteins in cellular function and biochemical process is really a challenging area for researchers. In order to understand the molecular causes underlying the pathological processes, we mainly focus on five fundamental problems of AGO proteins, including evolution, functional domain, subcellular location, post-translational modification and protein-protein interactions. Our discussion highlight their roles in early diagnosis, disease prevention, drug target identification, drug response, etc.
机译:MicroRNA(miRNA)转录后通过以完美或不完美的互补性结合靶mRNA来调节基因表达,募集通常导致靶mRNA降解或翻译受阻的Argonaute(AGO)蛋白复合物。 AGO蛋白在miRNA和参与人类生理和病理生理过程(例如抗病毒反应和疾病形成)的小干扰RNA(siRNA)途径中充当切片机酶。尽管过去十年见证了AGO蛋白质功能研究的快速发展,但进一步阐明AGO蛋白质在细胞功能和生化过程中的分子机制对研究人员而言确实是一个充满挑战的领域。为了了解病理过程的分子原因,我们主要关注AGO蛋白的五个基本问题,包括进化,功能结构域,亚细胞定位,翻译后修饰和蛋白-蛋白相互作用。我们的讨论着重介绍了它们在早期诊断,疾病预防,药物靶标识别,药物反应等方面的作用。

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