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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.

机译:猿猴病毒40 T抗原的突变分析:通过T抗原基因缺失的突变体刺激细胞DNA合成和激活rRNA基因。

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摘要

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).
机译:测定了克隆在pBR322中的猿猴病毒40的几个缺失突变体的生物活性。研究了猿猴病毒40 A基因的三个功能:(i)表达T抗原的能力; (ii)诱导细胞DNA复制的能力; (iii)重新激活杂合细胞中沉默rRNA基因的能力。通过手动显微注射或转染将重组质粒DNA引入细胞。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猿猴病毒40 A基因上,如下所示:(i)检测T抗原共同抗原决定簇所需的序列从核苷酸4147至核苷酸4001(映射单位0.45至0.42); (ii)对刺激细胞DNA合成至关重要的序列从核苷酸4327延伸至核苷酸4001(图谱单元0.49至0.42); (iii)对rRNA基因的激活至关重要的核苷酸大约从核苷酸3827延伸至核苷酸3526(图单元0.39至0.33)。

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