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超微结构原位杂交揭示的5型腺病毒感染中细胞和病毒DNA的区室化

Compartmentalization of cellular and viral DNAs in adenovirus type 5 infection as revealed by ultrastructural in situ hybridization.

作者信息

Besse S, Puvion-Dutilleul F

机构信息

Institut de Recherches Scientifiques sur le Cancer CNRS, Biologie et Ultrastructure du Noyau, Villejuif, France.

出版信息

Chromosome Res. 1994 Mar;2(2):123-35. doi: 10.1007/BF01553491.

Abstract

We describe the respective distributions of cellular DNA and viral genomes in adenovirus type 5 (Ad5)-infected HeLa cells by means of electron microscope in situ hybridization using biotinylated Alu DNA and Ad5 DNA probes in a post-embedding technique. When hybridization was performed on sections of formaldehyde-fixed material, Alu elements were restricted to the cellular chromatin, irrespective of the stage of the infectious cycle, without any interpenetration within the virus-induced regions. Viral DNA was confined entirely to the latter. Similar topological distributions of cellular and viral DNA were obtained when in situ hybridizations were performed at the optical level on methanol-acetone fixed cells. Such separation between cellular and viral DNA persisted under experimental conditions which partially loosened the nucleoproteins. In addition, the viral DNA of the different viral structures spread without interpenetration. On the other hand, the procedure did not dissociate the clusters of viruses which remained, as usual, closely surrounded by innumerable viral genomes. It also preserved the shapes, content (viral ssDNA + viral 72 kD protein) and the topological localization of the pleomorphic viral ssDNA accumulation sites. These data, which suggest that all viral DNAs are spatially linked in the infected nuclei, suggest a prominent role for the internal nuclear matrix in virus replication, assembly and maturation.

摘要

我们采用包埋后技术,通过使用生物素化的Alu DNA和腺病毒5型(Ad5)DNA探针进行电子显微镜原位杂交,描述了Ad5感染的HeLa细胞中细胞DNA和病毒基因组的各自分布情况。当在甲醛固定材料的切片上进行杂交时,无论感染周期处于哪个阶段,Alu元件都局限于细胞染色质,在病毒诱导区域内没有任何相互渗透。病毒DNA则完全局限于后者。当在甲醇 - 丙酮固定细胞上进行光学水平的原位杂交时,也获得了细胞DNA和病毒DNA类似的拓扑分布。在部分松开核蛋白的实验条件下,细胞DNA和病毒DNA之间的这种分离仍然存在。此外,不同病毒结构的病毒DNA分布时没有相互渗透。另一方面,该程序并未使病毒簇解离,这些病毒簇像往常一样,仍然被无数病毒基因组紧密包围。它还保留了多形性病毒单链DNA积累位点的形状、内容物(病毒单链DNA + 病毒72 kD蛋白)和拓扑定位。这些数据表明所有病毒DNA在感染的细胞核中在空间上是相连的,这表明核内基质在病毒复制、组装和成熟中起着重要作用。

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