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高尔基器的碎裂为人鼻病毒 1A 提供了复制膜。

Fragmentation of the Golgi apparatus provides replication membranes for human rhinovirus 1A.

机构信息

Department of Microbiology and Molecular Genetics and Center for Infectious Disease Research, Medical College of Wisconsin, Milwaukee, WI, USA.

出版信息

Virology. 2010 Nov 25;407(2):185-95. doi: 10.1016/j.virol.2010.08.012. Epub 2010 Sep 9.

Abstract

All viruses with a positive-stranded RNA genome replicate their genomic RNA in association with membranes from the host cell. Here we demonstrate a novel organelle source of replication membranes for human rhinovirus 1A (HRV-1A). HRV-1A infection induces fragmentation of the Golgi apparatus, and Golgi membranes are rearranged into vesicles of approximately 250-500 nm diameter. The newly distributed Golgi membranes co-localize with viral RNA replication templates, strongly suggesting that the observed vesicles are the sites of viral RNA replication. Expression of the HRV-1A 3A protein induces alterations in the Golgi staining pattern similar to those seen during viral infection, and expressed 3A localizes to the Golgi-derived membranes. Taken together, these data show that in HRV-1A infection, the 3A protein plays a role in fragmenting the Golgi complex and generating vesicles that are used as the site of viral RNA replication.

摘要

所有正链 RNA 基因组的病毒都与宿主细胞膜结合来复制其基因组 RNA。在这里,我们展示了人鼻病毒 1A(HRV-1A)复制膜的一种新型细胞器来源。HRV-1A 感染诱导高尔基体的碎片化,高尔基体膜被重组成大约 250-500nm 直径的囊泡。新分布的高尔基体膜与病毒 RNA 复制模板共定位,强烈表明观察到的囊泡是病毒 RNA 复制的部位。HRV-1A 的 3A 蛋白的表达诱导高尔基体染色模式的改变,类似于在病毒感染期间观察到的改变,并且表达的 3A 定位到高尔基体衍生的膜上。总之,这些数据表明在 HRV-1A 感染中,3A 蛋白在分裂高尔基体复合物和产生用作病毒 RNA 复制部位的囊泡方面发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01fa/7111317/ccd99d3f1571/gr1_lrg.jpg

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