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猿猴病毒40 T抗原的突变分析:T抗原基因缺失突变体对细胞DNA合成的刺激及rRNA基因的激活

Mutational analysis of simian virus 40 T antigen: stimulation of cellular DNA synthesis and activation of rRNA genes by mutants with deletions in the T-antigen gene.

作者信息

Soprano K J, Galanti N, Jonak G J, McKercher S, Pipas J M, Peden K W, Baserga R

出版信息

Mol Cell Biol. 1983 Feb;3(2):214-9. doi: 10.1128/mcb.3.2.214-219.1983.

Abstract

The biological activity of several deletion mutants of simian virus 40, cloned in pBR322, was determined. Three functions of the simian virus 40 A gene were studied: (i) the ability to express T antigen; (ii) the ability to induce cell DNA replication; and (iii) the ability to reactivate silent rRNA genes in hybrid cells. Recombinant plasmid DNA was introduced into cells by manual microinjection or by transfection. The results (together with previous reports) indicate that the critical sequences for these three functions are located separately on the simian virus 40 A gene, as follows: (i) the sequences necessary for the detection of the common antigenic determinant of T antigen extend from nucleotide 4147 to nucleotide 4001 (map units 0.45 to 0.42); (ii) the sequences critical for the stimulation of cell DNA synthesis extend from nucleotide 4327 to nucleotide 4001 (map units 0.49 to 0.42); and (iii) those critical for the reactivation of rRNA genes extend approximately from nucleotide 3827 to nucleotide 3526 (map units 0.39 to 0.33).

摘要

测定了克隆于pBR322的猴病毒40几种缺失突变体的生物学活性。研究了猴病毒40 A基因的三种功能:(i)表达T抗原的能力;(ii)诱导细胞DNA复制的能力;以及(iii)在杂种细胞中重新激活沉默rRNA基因的能力。通过手工显微注射或转染将重组质粒DNA导入细胞。结果(连同以前的报告)表明,这三种功能的关键序列分别位于猴病毒40 A基因上,如下:(i)检测T抗原共同抗原决定簇所需的序列从核苷酸4147延伸至核苷酸4001(图谱单位0.45至0.42);(ii)刺激细胞DNA合成的关键序列从核苷酸4327延伸至核苷酸4001(图谱单位0.49至0.42);以及(iii)rRNA基因重新激活的关键序列大约从核苷酸3827延伸至核苷酸3526(图谱单位0.39至0.33)。

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