首页> 外文期刊>Journal of Virology >Retrovirus gene expression during the cell cycle. I. Virus production, synthesis, and expression of viral proteins in Rauscher murine leukemia virus-infected mouse cells.
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Retrovirus gene expression during the cell cycle. I. Virus production, synthesis, and expression of viral proteins in Rauscher murine leukemia virus-infected mouse cells.

机译:细胞周期中的逆转录病毒基因表达。 I.病毒生产,合成和病毒蛋白在Rauscher鼠白血病病毒感染的小鼠细胞中的表达。

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Synchronized mouse cells (JLS-V9) chronically infected with Rauscher murine leukemia virus were used to study virus production, the synthesis of gag and env precursor proteins, and the expression of env protein on the cell surface during the cell cycle. The amount of virus released into the medium by synchronized cells during a 30-min interval was determined by using the XC plaque assay and by measuring reverse transcriptase activity. The results show that virus production occurs during mitosis. Labeling of the cell surface of synchronized cells with 125I or with fluorescein-conjugated antiserum shows that the amount of gp 70env on the cell surface parallels cellular growth. Therefore, the cell cycle-dependent release of virus is not accompanied by similar variations in the amount of viral envelope protein on the cell surface. Immunoprecipitation of cells labeled with [35S]methionine, followed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, was used to measure viral protein synthesis during the cell cycle. The rate of synthesis of gag precursor proteins show three maximums corresponding to the G1, middle S, and late S to G2 phases of the cell cycle. The rate of synthesis of env precursor proteins does not change, suggesting that in these cells the synthesis of these two gene products is controlled separately.
机译:使用RauScher鼠白血病病毒慢性感染的同步小鼠细胞(JLS-V9)用于研究病毒生产,GAG和Env前体蛋白的合成,以及在细胞周期期间细胞表面上的Env蛋白的表达。通过使用XC斑块测定和通过测量逆转录酶活性,确定在30分钟间隔内通过同步细胞释放到培养基中的病毒量。结果表明,病毒生产在有丝分裂期间发生。用125i或荧光素缀合的抗血清标记同步细胞的细胞表面表明,GP 70env在细胞表面上的细胞生长的量。因此,病毒的细胞周期依赖性释放不是伴随细胞表面上病毒包膜蛋白质的相似变化。用[35s]甲硫氨酸标记的细胞的免疫沉淀,然后用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳来测量细胞周期中的病毒蛋白合成。 GAG前体蛋白的合成速率显示了对应于细胞周期的G1,中间S和D至G2阶段的三个最大值。 Env前体蛋白的合成率不会改变,表明在这些细胞中,这两个基因产物的合成分别控制。

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