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杆状病毒晚期表达因子温度敏感突变的遗传分析。

Genetic analyses of temperature-sensitive mutations in baculovirus late expression factors.

作者信息

Carstens E B, Chan H, Yu H, Williams G V, Casselman R

机构信息

Department of Microbiology and Immunology, Queen's University, Kingston, Ontario, Canada.

出版信息

Virology. 1994 Oct;204(1):323-37. doi: 10.1006/viro.1994.1537.

Abstract

Two temperature-sensitive mutants of Autographa californica nuclear polyhedrosis virus were characterized with respect to late and very late gene expression. Cells infected with ts317 or ts538 at the nonpermissive temperature revealed slightly reduced intracellular levels of late structural gene products including gp64 envelope, vp39 capsid, and p6.9 DNA binding proteins. However, with the exception of gp64, there was a dramatic reduction in extracellular levels of the structural proteins, suggesting that assembly or transport of extracellular virions was impaired. Electron microscopy confirmed the dramatic effect the mutations exhibited on viral morphogenesis. The ts538 mutation was physically mapped to the 60-65 mu region and DNA sequence analysis identified a single nucleotide alteration converting Leu to Phe in amino acid 105 of the late expression factor called lef-4. The mutation was positively correlated with the temperature-sensitive phenotype by analysis of DNA from ts+ revertants generated by marker rescue. Transient expression assays confirmed that lef-4 was required for activation of the late vp39 gene in virus infected cells. The defect in activation of the ts317 and ts538 polyhedrin genes could be overcome by coinfection with helper virus indicating that the mutations affected functions involved in activating the very late class of baculovirus genes as well. These results demonstrated a clear functional differentiation between genes regulating viral DNA replication which was normal in the mutant infected cells and those regulating late gene expression and extracellular virus production which were defective in these same infected cells.

摘要

对苜蓿银纹夜蛾核型多角体病毒的两个温度敏感突变体进行了晚期和极晚期基因表达方面的表征。在非允许温度下用ts317或ts538感染的细胞显示,包括gp64包膜、vp39衣壳和p6.9 DNA结合蛋白在内的晚期结构基因产物的细胞内水平略有降低。然而,除gp64外,结构蛋白的细胞外水平显著降低,这表明细胞外病毒粒子的组装或运输受到损害。电子显微镜证实了这些突变对病毒形态发生的显著影响。ts538突变在物理上定位到60 - 65 mu区域,DNA序列分析确定了晚期表达因子lef-4的第105位氨基酸发生了单个核苷酸改变,将亮氨酸转换为苯丙氨酸。通过对标记拯救产生的ts +回复株的DNA分析,该突变与温度敏感表型呈正相关。瞬时表达分析证实,lef-4是病毒感染细胞中晚期vp39基因激活所必需的。ts317和ts538多角体蛋白基因激活的缺陷可以通过与辅助病毒共感染来克服,这表明这些突变也影响了参与激活杆状病毒极晚期基因类别的功能。这些结果表明,在突变感染细胞中正常的调节病毒DNA复制的基因与在这些相同感染细胞中存在缺陷的调节晚期基因表达和细胞外病毒产生的基因之间存在明显的功能分化。

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