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脊髓灰质炎病毒感染细胞提取物中蛋白质合成的控制。I. 粗起始因子对mRNA的识别

Control of protein synthesis in extracts from poliovirus-infected cells. I. mRNA discrimination by crude initiation factors.

作者信息

Helentjaris T, Ehrenfeld E

出版信息

J Virol. 1978 May;26(2):510-21. doi: 10.1128/JVI.26.2.510-521.1978.

Abstract

By using cell-free systems prepared from uninfected and poliovirus-infected cells, we have been able to demonstrate that crude preparations of initiation factors from infected cells do not stimulate the initiation of translation by polyribosomes containing endogenous host cell mRNA. When tested with polysomes containing endogenous viral mRNA, however, they were able to stimulate initiation of translation nearly as well as uninfected cell initiation factors. The uninfected cell initiation factor preparations were able to stimulate initiation of translation of both cell and viral mRNA. The results indicate an mRNA-specific activity present in crude initiation factor preparations from infected cells. Furthermore, the ability of eIF2 from infected cells to form a ternary complex with GTP and formyl [35S]methionine-tRNAfmet, an mRNA-independent step in initiation, was found not to be deficient. Implications of these data for proposed mechanisms of poliovirus-induced host cell shutoff are discussed.

摘要

通过使用从未感染和脊髓灰质炎病毒感染细胞制备的无细胞系统,我们已经能够证明,来自感染细胞的起始因子粗制品不会刺激含有内源性宿主细胞mRNA的多核糖体的翻译起始。然而,当用含有内源性病毒mRNA的多核糖体进行测试时,它们几乎能够像未感染细胞的起始因子一样有效地刺激翻译起始。未感染细胞的起始因子制剂能够刺激细胞和病毒mRNA的翻译起始。结果表明,感染细胞的起始因子粗制品中存在一种mRNA特异性活性。此外,发现来自感染细胞的eIF2与GTP和甲酰基[35S]蛋氨酸-tRNAfmet形成三元复合物的能力,这是起始过程中一个不依赖mRNA的步骤,并未受损。讨论了这些数据对脊髓灰质炎病毒诱导宿主细胞关闭的拟议机制的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bfcd/354088/075a11f18233/jvirol00197-0316-a.jpg

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