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Translational control mediated by eucaryotic initiation factor-2 is restricted to specific mRNAs in transfected cells.

机译:真核生物起始因子2介导的翻译控制仅限于转染细胞中的特定mRNA。

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摘要

The translational efficiency of mRNA molecules transcribed from plasmid DNA transfected into COS-1 monkey cells can be increased 10- to 20-fold by the coexpression of the adenovirus virus-associated RNAs I and II. Experiments described here demonstrate a similar increase in translational efficiency by the addition of 2-aminopurine, an inhibitor of double-stranded RNA-activated protein kinase, to the culture medium. Both virus-associated RNA and 2-aminopurine presumably exert their effect by alteration of the functional level of eucaryotic initiation factor-2. The translational stimulation mediated by both means is shown to be restricted to the plasmid-derived mRNAs because there is no qualitative or quantitative alteration in host protein synthesis. The results are consistent with models invoking a localized activation of double-stranded RNA-activated kinase leading to a translational block.
机译:通过与腺病毒病毒相关的RNA I和II的共表达,从转染到COS-1猴细胞中的质粒DNA转录的mRNA分子的翻译效率可以提高10到20倍。此处描述的实验表明,通过向培养基中添加双链RNA活化蛋白激酶的抑制剂2-氨基嘌呤,可以有效提高翻译效率。病毒相关的RNA和2-氨基嘌呤都可能通过改变真核生物起始因子2的功能水平发挥作用。由于在宿主蛋白合成中没有定性或定量改变,因此显示了通过两种方式介导的翻译刺激仅限于质粒衍生的mRNA。该结果与模型引起双链RNA激活激酶的局部激活导致翻译阻滞的模型一致。

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  • 作者

    Kaufman, R J; Murtha, P;

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  • 年度 1987
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  • 原文格式 PDF
  • 正文语种 en
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