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利用温度敏感突变体研究水疱性口炎病毒的转录和复制

Study of the transcription and the replication of vesicular stomatitis virus by using temperature-sensitive mutants.

作者信息

Printz-Ané C, Combard A, Martinet C

出版信息

J Virol. 1972 Nov;10(5):889-95. doi: 10.1128/JVI.10.5.889-895.1972.

Abstract

The viral ribonucleic acids (RNA species) synthesized in HeLa cells infected with temperature-sensitive (ts) mutants and with the wild type of vesicular stomatitis virus at permissive (30 C) and nonpermissive (39.2 C) temperatures were compared by sucrose gradient centrifugation. Two ts mutants (ts 5 and ts 100) representing two separate complementation groups (respectively, groups I and IV), each concerned with viral RNA synthesis, were chosen. Mutant ts 5 failed to synthesize any RNA at 39.2 C. Under the same conditions, mutant ts 100 showed a low, but easily detectable, synthesis of RNA without characteristic peaks. The in vitro transcriptase activity was tested with mutants ts 5 and ts 100 at 39.2 C: normal activity, compared with wild-type virus, was detected with purified ts 100, but no activity was detected with purified ts 5. From all our data we conclude that mutant ts 5 is defective in transcription. The defect could be in the structural transcriptase enzyme or at the level of template for transcription. Results with mutant ts 100 were not so clear-cut. However, we suggest that this mutant is concerned with some aspect of transcription in vivo. In addition, our results lead us to postulate some linkage between transcription and replication.

摘要

通过蔗糖梯度离心法,比较了在允许温度(30℃)和非允许温度(39.2℃)下,感染温度敏感(ts)突变体和水疱性口炎病毒野生型的HeLa细胞中合成的病毒核糖核酸(RNA种类)。选择了两个ts突变体(ts 5和ts 100),它们代表两个独立的互补组(分别为I组和IV组),每组都与病毒RNA合成有关。突变体ts 5在39.2℃时无法合成任何RNA。在相同条件下,突变体ts 100显示出低水平但易于检测到的RNA合成,且无特征峰。在39.2℃下对突变体ts 5和ts 100的体外转录酶活性进行了测试:与野生型病毒相比,纯化的ts 100检测到正常活性,但纯化的ts 5未检测到活性。根据我们所有的数据,我们得出结论,突变体ts 5在转录方面存在缺陷。缺陷可能在于结构转录酶或转录模板水平。突变体ts 100的结果不那么明确。然而,我们认为该突变体与体内转录的某些方面有关。此外,我们的结果使我们推测转录与复制之间存在某种联系。

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Temperature-sensitive mutants of vesicular stomatitis virus. II. Evidence of defective polymerase.
Virology. 1971 Sep;45(3):824-6. doi: 10.1016/0042-6822(71)90205-4.

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