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腺病毒-猴病毒40重组体对人成纤维细胞的高效转化

Efficient transformation of human fibroblasts by adenovirus-simian virus 40 recombinants.

作者信息

Van Doren K, Gluzman Y

出版信息

Mol Cell Biol. 1984 Aug;4(8):1653-6. doi: 10.1128/mcb.4.8.1653-1656.1984.

Abstract

The origin-defective simian virus 40 (SV40) mutant 6-1 has been useful in transforming human cells (Small et al., Nature [London] 296:671-672, 1982; Nagata et al., Nature [London] 306:597-599, 1983). However, the low efficiency of transformation achieved by DNA transfection is a major drawback of the system. To increase the efficiency of SV40-induced transformation of human fibroblasts, we used recombinant adenovirus-SV40 virions which contain a complete SV40 early region including either a wild-type or defective (6-1) origin of replication. The SV40 DNA was cloned into the adenovirus vector in place of early region 1. Cell lines transformed by viruses containing a functional origin of replication produced free SV40 DNA. These cell lines were subcloned, and some of the subclones lost the ability to produce free viral DNA. Subclones that failed to produce free viral DNA were found to possess a mutated T antigen. Cell lines transformed by viruses containing origin-defective SV40 mutants did not produce any free DNA. Because of the high efficiency of transformation, we suggest that the origin-defective chimeric virus is a convenient system for establishing SV40-transformed cell lines from any human cell type that is susceptible to infection by adenovirus type 5.

摘要

起源缺陷型猿猴病毒40(SV40)突变体6 - 1在转化人细胞方面很有用(斯莫尔等人,《自然》[伦敦]296:671 - 672,1982;永田等人,《自然》[伦敦]306:597 - 599,1983)。然而,DNA转染实现的低转化效率是该系统的一个主要缺点。为了提高SV40诱导的人成纤维细胞转化效率,我们使用了重组腺病毒 - SV40病毒粒子,其包含完整的SV40早期区域,包括野生型或缺陷型(6 - 1)复制起点。SV40 DNA被克隆到腺病毒载体中取代早期区域1。由含有功能性复制起点的病毒转化的细胞系产生游离的SV40 DNA。这些细胞系被亚克隆,并且一些亚克隆失去了产生游离病毒DNA的能力。未产生游离病毒DNA的亚克隆被发现具有突变的T抗原。由含有起源缺陷型SV40突变体的病毒转化的细胞系不产生任何游离DNA。由于转化效率高,我们认为起源缺陷型嵌合病毒是一种方便的系统,可用于从任何易受5型腺病毒感染的人细胞类型建立SV40转化的细胞系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8cf9/368963/0430e918b108/molcellb00150-0234-a.jpg

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