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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Serine/threonine kinase (pk-1) is a component of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) very late gene transcription complex and it phosphorylates a 102 kDa polypeptide of the complex.
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Serine/threonine kinase (pk-1) is a component of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) very late gene transcription complex and it phosphorylates a 102 kDa polypeptide of the complex.

机译:丝氨酸/苏氨酸激酶(pk-1)是加利福尼亚州的Autographa californica多核多角体病毒(AcMNPV)非常晚的基因转录复合物的组成部分,它使该复合物的102 kDa多肽磷酸化。

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摘要

The baculovirus gene, protein kinase-I (pk-1) encodes a serine/threonine kinase that is essential for very late gene expression. Late and very late genes of the baculoviruses are transcribed by an alpha-amanitin resistant RNA polymerase. The very late gene promoter transcription initiation complex was isolated from nuclei of Autographa californica multiple nucleopolyhedrovirus (AcMNPV)-infected Sf9 cells by DNA affinity purification and found to contain 4 major polypeptides of sizes approximately 102, 38, 32, and 18 kDa. The 32 kDa polypeptide was immunoreactive to AcMNPV anti-pk-1 antibody and phosphorylated the 102 kDa polypeptide, earlier reported as late gene expression factor LEF-8. Electrophoretic mobility shift assays with anti-pk-1 antibody indicated the binding of promoter DNA with recombinant AcMNPV-pk-1 and transcription initiation complex proteins. All these results suggested AcMNPV-pk-1 to be a component of the viral very late gene transcription initiation complex.
机译:杆状病毒基因蛋白激酶-I(pk-1)编码丝氨酸/苏氨酸激酶,这对于非常晚的基因表达必不可少。杆状病毒的晚期和极晚期基因通过抗α-阿马尼汀的RNA聚合酶进行转录。通过DNA亲和力纯化,从感染了苜蓿白纹夜蛾多核多角体病毒(AcMNPV)的Sf9细胞核中分离了非常晚的基因启动子转录起始复合物,发现该复合物包含4种主要多肽,大小分别约为102、38、32和18 kDa。 32 kDa多肽对AcMNPV抗pk-1抗体具有免疫反应性,并使102 kDa多肽磷酸化,该多肽先前被报道为晚期基因表达因子LEF-8。用抗-pk-1抗体进行电泳迁移率迁移分析表明,启动子DNA与重组AcMNPV-pk-1和转录起始复合蛋白​​结合。所有这些结果表明AcMNPV-pk-1是病毒极晚期基因转录起始复合体的一个组成部分。

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