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BAV-3的致癌基因作为一种诱变剂。

The oncogene of BAV-3 as a mutagen.

作者信息

Lukash L L, Varshaver N B, Buzhiyevskaya T I, Shapiro N I

出版信息

J Cell Sci. 1985 Oct;78:97-103. doi: 10.1242/jcs.78.1.97.

Abstract

We studied the mutagenic and carcinogenic effects on mammalian cells of two EcoRI DNA fragments of bovine adenovirus type3 (BAV-3) integrated into the pBR325 plasmid. Fragment D located between 3.6 and 19.7 map units, contains the viral oncogene, fragment C, located between 44.3 and 63.7 map units, has no oncogenic activity. The BAV-3 oncogene was shown to increase significantly the frequency of 6-mercaptopurine (6MP)-resistant mutants in Chinese hamster calls. Fragment C, pBR325 without viral sequences and DNA from normal Syrian hamster cells did not have any mutagenic effect. We also looked at the combined action of the viral DNA fragments and the tumour promoter 12-O-tetradecanoylphorbol-13-acetate (TPA), which enhances the transforming effect of carcinogens. TPA was shown to increase the mutant yield on exposure to the viral oncogene but not to induce mutagenic activity in those types of DNA that are unable to transform cells. Probably TPA does not affect the initiation of the mutation process, but acts on later stages just as it affects carcinogenic activity. Thus the results obtained confirm the existence of parallelism between the mutagenic and transforming effects of viral DNA and show that both activities are mapped in the same region of viral DNA - its oncogene.

摘要

我们研究了整合到pBR325质粒中的牛腺病毒3型(BAV - 3)的两个EcoRI DNA片段对哺乳动物细胞的诱变和致癌作用。位于3.6至19.7图谱单位之间的片段D含有病毒癌基因,位于44.3至63.7图谱单位之间的片段C没有致癌活性。结果表明,BAV - 3癌基因可显著提高中国仓鼠细胞中对6 - 巯基嘌呤(6MP)耐药突变体的频率。片段C、不含病毒序列的pBR325以及正常叙利亚仓鼠细胞的DNA均无任何诱变作用。我们还研究了病毒DNA片段与肿瘤启动子12 - O - 十四酰佛波醇 - 13 - 乙酸酯(TPA)的联合作用,TPA可增强致癌物的转化作用。结果表明,TPA在暴露于病毒癌基因时可提高突变体产量,但在那些无法转化细胞的DNA类型中不会诱导诱变活性。TPA可能不影响突变过程的起始,但作用于后期阶段,就如同它影响致癌活性一样。因此,所获得的结果证实了病毒DNA的诱变作用与转化作用之间存在平行关系,并表明这两种活性都定位在病毒DNA的同一区域——其癌基因上。

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