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水泡性口炎病毒复制核糖核蛋白的电子显微镜观察

Electron microscopy of vesicular stomatitis virus replicative ribonucleoproteins.

作者信息

Naeve C W, Summers D F

出版信息

J Virol. 1980 Jun;34(3):764-71. doi: 10.1128/JVI.34.3.764-771.1980.

Abstract

The objective of this investigation was to examine by electron microscopy the replicative ribonucleoprotein (RNP) structures synthesized in vesicular stomatitis virus-infected HeLa cells. Pulse-labeled in vivo products of vesicular stomatitis virus replication and transcription can be separated by centrifugation in Renografin gradients. Transcription complexes are dissociated, allowing nascent messenger RNPs to remain at the top of the gradient, whereas RNPs biochemically consistent with replication complexes sediment to the middle of the gradient. Examination of these structures by electron microscopy revealed that all exist as coiled or helical RNPs having dimensions of approximately 20 by 700 nm. These structures can be further subdivided into three major morphological classes: (i) linear forms (20 by 769 +/- 158 nm), which have both ends free; (ii) circular forms (20 by 679 +/- 95 nm), which appear to have both ends joined; and (iii) complex forms, which include those structures which are branched replicative complexes as well as those which are random. To distinguish random complexes and possible transcriptive complex contaminants from replicative complexes, it was necessary to uncoil the RNP structures with EDTA so that length measurements could be made relating the nascent strand length to its position on the template. After EDTA treatment, the linear RNPs uncoiled (10 by 4,035 +/- 3,802 nm), and the circular morphology virtually disappeared. However, a new form appeared which was one-half the length and double the width (20 by 2,103 +/- 306 nm) of full-length RNPs and contained a loop at one end and two free ends at the other (alpha-form RNP). The distribution and length analysis of these structures, plus and minus EDTA, suggest that the alpha-form RNPs arise by EDTA-induced uncoiling of circular forms held together at the ends. Close scrutiny of uncoiled complex RNPs revealed no single-strand RNP templates with single-strand nascents. However, several complexes were observed which appeared to contain alpha-form templates with single-strand nascent RNPs. Length measurements suggest these complexes are neither random nor transcriptive, but are replicative. These experiments suggest that replication may, in part, occur on circular coiled RNP templates.

摘要

本研究的目的是通过电子显微镜检查水疱性口炎病毒感染的HeLa细胞中合成的复制性核糖核蛋白(RNP)结构。水疱性口炎病毒复制和转录的体内脉冲标记产物可通过在泛影葡胺梯度中离心进行分离。转录复合物被解离,使新生信使核糖核蛋白(mRNP)保留在梯度顶部,而与复制复合物生化性质一致的核糖核蛋白沉淀到梯度中部。通过电子显微镜检查这些结构发现,它们均以盘绕或螺旋状核糖核蛋白的形式存在,尺寸约为20×700nm。这些结构可进一步细分为三大形态类别:(i)线性形式(20×769±158nm),两端游离;(ii)环形形式(20×679±95nm),两端似乎相连;(iii)复杂形式,包括分支复制复合物以及随机结构。为了将随机复合物和可能的转录复合物污染物与复制复合物区分开来,有必要用乙二胺四乙酸(EDTA)使核糖核蛋白结构解旋,以便进行长度测量,从而将新生链长度与其在模板上的位置相关联。EDTA处理后,线性核糖核蛋白解旋(10×4,035±3,802nm),环形形态几乎消失。然而,出现了一种新形式,其长度为全长核糖核蛋白的一半,宽度为全长核糖核蛋白的两倍(20×2,103±306nm),一端有一个环,另一端有两个游离端(α型核糖核蛋白)。这些结构在有无EDTA情况下的分布和长度分析表明,α型核糖核蛋白是由EDTA诱导两端相连的环形结构解旋产生的。对解旋的复杂核糖核蛋白进行仔细检查,未发现带有单链新生链的单链核糖核蛋白模板。然而,观察到几个复合物似乎包含带有单链新生核糖核酸的α型模板。长度测量表明这些复合物既不是随机的也不是转录性的,而是复制性的。这些实验表明,复制可能部分发生在环形盘绕的核糖核蛋白模板上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf50/288764/e52846c15e0b/jvirol00174-0190-a.jpg

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