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长线形病毒属1a多聚蛋白中的一个保守区域驱动内质网膜的广泛重塑,并在本氏烟草细胞中诱导形成移动小球。

A conserved region in the Closterovirus 1a polyprotein drives extensive remodeling of endoplasmic reticulum membranes and induces motile globules in Nicotiana benthamiana cells.

作者信息

Gushchin V A, Karlin D G, Makhotenko A V, Khromov A V, Erokhina T N, Solovyev A G, Morozov S Yu, Agranovsky A A

机构信息

Faculty of Biology, Moscow State University, Moscow 119991, Russia; N.F. Gamaleya Federal Research Centre for Epidemiology and Microbiology, Ministry of Health of the Russian Federation, Russia.

25, rue de Cassis, 13008 Marseille, France.

出版信息

Virology. 2017 Feb;502:106-113. doi: 10.1016/j.virol.2016.12.006. Epub 2016 Dec 25.

Abstract

In infected plant cells, closterovirus replicative polyproteins 1a and 1ab drive membrane remodeling and formation of multivesicular replication platforms. Polyprotein 1a contains a variable Central Region (CR) between the methyltransferase and helicase domains. In a previous study, we have found that transient expression of the Beet yellows virus CR-2 segment (aa 1305-1494) in Nicotiana benthamiana induces the formation of ~1µm mobile globules originating from the ER membranes. In the present study, sequence analysis has shown that a part of the CR named the "Zemlya region" (overlapping the CR-2), is conserved in all members of the Closterovirus genus and contains a predicted amphipathic helix (aa 1368-1385). By deletion analysis, the CR-2 region responsible for the induction of 1-μm globules has been mapped to aa 1368-1432. We suggest that the conserved membrane-modifying region of the BYV 1a may be involved in the biogenesis of closterovirus replication platforms.

摘要

在受感染的植物细胞中,长线形病毒复制多聚蛋白1a和1ab驱动膜重塑以及多泡状复制平台的形成。多聚蛋白1a在甲基转移酶和解旋酶结构域之间包含一个可变的中央区域(CR)。在先前的一项研究中,我们发现甜菜黄化病毒CR - 2片段(氨基酸1305 - 1494)在本氏烟草中的瞬时表达诱导了源自内质网的约1微米移动小球的形成。在本研究中,序列分析表明,CR的一部分被命名为“泽姆利亚区域”(与CR - 2重叠),在长线形病毒属的所有成员中保守,并且包含一个预测的两亲性螺旋(氨基酸1368 - 1385)。通过缺失分析,负责诱导1微米小球的CR - 2区域已被定位到氨基酸1368 - 1432。我们认为BYV 1a的保守膜修饰区域可能参与长线形病毒复制平台的生物发生。

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