Department of Biological Sciences and Biotechnology, Minnan Normal University, Zhangzhou 363000, China;
Chin J Cancer Res. 2013 Aug;25(4):430-41. doi: 10.3978/j.issn.1000-9604.2013.08.13.
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.
微小 RNA(miRNA)通过与靶 mRNA 完全或不完全互补结合来转录后调控基因表达,招募 Argonaute(AGO)蛋白复合物,通常导致靶 mRNA 的降解或翻译抑制。AGO 蛋白在 miRNA 和小干扰 RNA(siRNA)途径中作为 Slicer 酶发挥作用,参与人类生理和病理生理过程,如抗病毒反应和疾病形成。尽管过去十年见证了 AGO 蛋白功能研究的快速进展,但进一步阐明 AGO 蛋白在细胞功能和生化过程中的分子机制确实是研究人员面临的一个具有挑战性的领域。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、功能域、亚细胞定位、翻译后修饰和蛋白质-蛋白质相互作用。我们的讨论强调了它们在早期诊断、疾病预防、药物靶点识别、药物反应等方面的作用。