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点突变改变脊髓灰质炎病毒RNA对翻译起始因子的反应:神经毒力株与减毒株的比较

Point mutations modify the response of poliovirus RNA to a translation initiation factor: a comparison of neurovirulent and attenuated strains.

作者信息

Svitkin Y V, Pestova T V, Maslova S V, Agol V I

机构信息

Institute of Poliomyelitis and Viral Encephalitides, USSR Academy of Medical Sciences, Moscow Region.

出版信息

Virology. 1988 Oct;166(2):394-404. doi: 10.1016/0042-6822(88)90510-7.

Abstract

Upon translation of poliovirus RNA in reticulocyte lysates, initiation occurs largely "incorrectly," that is, at sites in the middle of the viral genome rather than at the beginning of the polyprotein reading frame; the anomaly appears to be due to an initiation factor deficiency. Here, a fraction which stimulated initiation at the correct site, provisionally called "initiation correcting factor" (ICF), was partially purified from Krebs-2 cells. The ICF activity appeared to copurify with a complex of initiation factors eIF-2 and eIF-2B. The ability of ICF to stimulate, in reticulocyte lysates, the correct initiation of translation on the RNAs from neurovirulent and attenuated type 1 and type 3 poliovirus strains was investigated. Like crude initiation factor preparations, ICF appeared to be relatively less active with the RNAs from attenuated strains, the difference being especially pronounced for the type 3 strains. For the latter strains, the data suggested an important role of the nucleotide at, and perhaps around, position 472 in determining a response to the addition of ICF. It is proposed that interaction of a specific segment of the viral RNA with one or more of initiation factors plays an important part in the mechanism of translation of the picornavirus genomes, poliovirus attenuation, and, possibly, pathogenesis of poliomyelitis.

摘要

在网织红细胞裂解物中对脊髓灰质炎病毒RNA进行翻译时,起始过程大多“不正确”,也就是说,起始发生在病毒基因组中部的位点,而非多聚蛋白阅读框的起始处;这种异常现象似乎是由于起始因子缺乏所致。在此,从克雷布斯2细胞中部分纯化出一种能在正确位点刺激起始的组分,暂称为“起始校正因子”(ICF)。ICF活性似乎与起始因子eIF - 2和eIF - 2B的复合物共同纯化。研究了ICF在网织红细胞裂解物中刺激神经毒力型和减毒型1型及3型脊髓灰质炎病毒株RNA正确起始翻译的能力。与粗制起始因子制剂一样,ICF对减毒株RNA的活性似乎相对较低,这种差异在3型毒株中尤为明显。对于后一种毒株,数据表明472位及可能其周围的核苷酸在决定对添加ICF的反应中起重要作用。有人提出,病毒RNA的特定片段与一种或多种起始因子的相互作用在微小核糖核酸病毒基因组的翻译机制、脊髓灰质炎病毒减毒以及可能的脊髓灰质炎发病机制中起重要作用。

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