首页> 外文期刊>Journal of Virology >Synthesis of RNA by mutants of vesicular stomatitis virus (Indiana serotype) and the ability of wild-type VSV New Jersey to complement the VSV Indiana ts G I-114 transcription defect.
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Synthesis of RNA by mutants of vesicular stomatitis virus (Indiana serotype) and the ability of wild-type VSV New Jersey to complement the VSV Indiana ts G I-114 transcription defect.

机译:晶体口炎病毒突变体(印第安纳血清型)的突变体合成RNA,以及野生型VSV新泽西术的能力补充VSV印第安纳TS G I-114转录缺陷。

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The ability of certain vesicular stomatitis virus (VSV; Indiana serotype) temperature-sensitive (ts) mutants to synthesize intracellular viral complementary RNA (vcRNA) at permissive or nonpermissive temperatures for productive infections has been investigated. Mutants belonging to complementation groups II, III, and V synthesize RNA at nonpermissive temperature in amounts essentially equivalent to that obtained at permissive temperatures. Mutant ts G I-114 possesses a thermolabile transcriptase and does not synthesize vcRNA at 40 degrees C; however, mutants ts O I-5, O I-53, O I-78, and O I-80 possess thermostabile transcriptases that are capable of some vcRNA synthesis at 40 degrees C. All five group I mutants are defective in their secondary transcription ability at 40 degrees C. Wild-type VSV New Jersey virus is able to complement the transcription defect of ts G I-114 at 40 degrees C. This complementation is inhibited by puromycin, suggesting that a viral gene product of VSV New Jersey (e.g., its transcriptase or a transcriptase component) is involved. Mokola virus is not able to complement the ts G I-114 defect, although Mokola does synthesize vcRNA in infected cells (in the presence or absence of cycloheximide).
机译:已经研究了某些脉质口炎病毒(VSV;印第安纳血清型)温敏感(TS)突变体在允许或非施用温度下合成细胞内病毒互补RNA(VCRNA)的能力,已经研究过允许或非施用温度。属于互补基团II,III和V的突变体在非智能温度下合成RNA,其量基本上等同于在允许温度下获得的量。突变体TS G I-114具有热量转录酶,并不在40℃下合成VCRNA;然而,突变体TS O I-5,O I-53,O I-78和O I-80具有能够在40℃下进行一些VcRNA合成的热耦合转录酶。所有五组I突变体在其继发性转录中有缺陷40度C.野生型VSV的能力能够在40摄氏度中补充TS G I-114的转录缺陷。嘌呤霉素抑制该互补,表明VSV新泽西州的病毒基因产物(例如,涉及其转录酶或转录酶组分。 Mokola病毒无法补充TS G I-114缺陷,尽管Mokola确实在感染细胞中合成VCRNA(在存在或不存在环己酰亚胺中)。

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