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12型腺病毒诱导的神经上皮起源大鼠肿瘤细胞:病毒基因组的持久性和表达

Adenovirus type 12-induced rat tumor cells of neuroepithelial origin: persistence and expression of the viral genome.

作者信息

Ibelgaufts H, Doerfler W, Scheidtmann K H, Wechsler W

出版信息

J Virol. 1980 Jan;33(1):423-37. doi: 10.1128/JVI.33.1.423-437.1980.

Abstract

Four cell lines derived from adenovirus type 12-induced rat brain tumors were studied. The polyploid cells displayed neuroepithelial characteristics and were transplantable into syngeneic rats and nude mice. In tissue culture the cells grew in monolayers and multilayers. A very high saturation density was reached, and the cells plated in agar and were easily agglutinated with low concentrations of concanavalin A. Between 2 and 11 copies of the viral genome per diploid cellular genome were detected by reassociation kinetics analysis in the different lines. The patterns of distribution of viral DNA sequences in these lines, as revealed by blot analysis, suggest colinear integration of the intact viral genome into the cellular DNA. The patterns of integration were stable after more than 15 months of prolonged tissue culture and after animal reimplantation. Integration patterns were identical in three of the tumor lines and different in another line. Viral sequences were transcribed. The extent of homology found toward adenovirus type 12 DNA in polyadenylated polysome-associated mRNA isolated from the tumor lines suggests that the early and some of the late genes of adenovirus type 12 DNA are transcribed in these tumor cells. Infectious virus was not rescuable from these lines.

摘要

对源自12型腺病毒诱导的大鼠脑肿瘤的四种细胞系进行了研究。多倍体细胞呈现神经上皮特征,可移植到同基因大鼠和裸鼠体内。在组织培养中,细胞以单层和多层形式生长。达到了非常高的饱和密度,接种在琼脂中的细胞很容易被低浓度的伴刀豆球蛋白A凝集。通过重缔合动力学分析在不同细胞系中检测到每个二倍体细胞基因组中有2到11份病毒基因组拷贝。印迹分析显示,这些细胞系中病毒DNA序列的分布模式表明完整的病毒基因组共线性整合到细胞DNA中。经过超过15个月的长期组织培养和动物再植入后,整合模式保持稳定。三个肿瘤细胞系的整合模式相同,另一个细胞系的整合模式不同。病毒序列被转录。从肿瘤细胞系分离的多聚腺苷酸化多核糖体相关mRNA中发现的与12型腺病毒DNA的同源程度表明,12型腺病毒DNA的早期和一些晚期基因在这些肿瘤细胞中被转录。从这些细胞系中无法拯救出感染性病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7a6/288558/a17f2904fbd4/jvirol00169-0443-a.jpg

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