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绿豆黄花叶印度病毒编码的AC2蛋白通过抑制拟南芥RDR6和AGO1的活性来抑制RNA沉默。

Mungbean yellow mosaic Indian virus encoded AC2 protein suppresses RNA silencing by inhibiting Arabidopsis RDR6 and AGO1 activities.

作者信息

Kumar Vikash, Mishra Sumona Karjee, Rahman Jamilur, Taneja Jyoti, Sundaresan Geethaa, Mishra Neeti Sanan, Mukherjee Sunil K

机构信息

Plant Molecular Biology, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110067, India; Department of Physiology, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee 53226, USA.

Plant Molecular Biology, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi 110067, India.

出版信息

Virology. 2015 Dec;486:158-72. doi: 10.1016/j.virol.2015.08.015. Epub 2015 Oct 1.

Abstract

RNA silencing refers to a conserved RNA-directed gene regulatory mechanism in a wide range of eukaryotes. It plays an important role in many processes including growth, development, genome stability, and antiviral defense in the plants. Geminivirus encoded AC2 is identified as an RNA silencing suppressor protein, however, the mechanism of action has not been characterized. In this paper, we elucidate another mechanism of AC2-mediated suppression activity of Mungbean Yellow Mosaic India Virus (MYMIV). The AC2 protein, unlike many other suppressors, does not bind to siRNA or dsRNA species and its suppression activity is mediated through interaction with key components of the RNA silencing pathway, viz., RDR6 and AGO1. AC2 interaction inhibits the RDR6 activity, an essential component of siRNA and tasi-RNA biogenesis and AGO1, the major slicing factor of RISC. Thus the study identifies dual sites of MYMIV-AC2 interference and probably accounts for its strong RNA silencing suppression activity.

摘要

RNA沉默是指在广泛的真核生物中一种保守的RNA指导的基因调控机制。它在植物的许多过程中发挥重要作用,包括生长、发育、基因组稳定性和抗病毒防御。双生病毒编码的AC2被鉴定为一种RNA沉默抑制蛋白,然而,其作用机制尚未明确。在本文中,我们阐明了AC2介导的对印度绿豆黄花叶病毒(MYMIV)抑制活性的另一种机制。与许多其他抑制蛋白不同,AC2蛋白不与siRNA或dsRNA结合,其抑制活性是通过与RNA沉默途径的关键组分,即RDR6和AGO1相互作用介导的。AC2的相互作用抑制了RDR6的活性,RDR6是siRNA和tasi-RNA生物合成的必需组分,以及AGO1,RISC的主要切割因子。因此,该研究确定了MYMIV-AC2干扰的两个位点,这可能解释了其强大的RNA沉默抑制活性。

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