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首页> 外文期刊>Nucleic Acids Research >eIF4G has intrinsic G-quadruplex binding activity that is required for tiRNA function
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eIF4G has intrinsic G-quadruplex binding activity that is required for tiRNA function

机译:EIF4G具有TiRNA功能所需的内在G-Quadruplex结合活动

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摘要

As cells encounter adverse environmental conditions, such as hypoxia, oxidative stress or nutrient deprivation, they trigger stress response pathways to protect themselves until transient stresses have passed. Inhibition of translation is a key component of such cellular stress responses and mounting evidence has revealed the importance of a class of tRNA-derived small RNAs called tiRNAs in this process. The most potent of these small RNAs are those with the capability of assembling into tetrameric G-quadruplex (G4) structures. However, the mechanism by which these small RNAs inhibit translation has yet to be elucidated. Here we show that eIF4G, the major scaffolding protein in the translation initiation complex, directly binds G4s and this activity is required for tiRNA-mediated translation repression. Targeting of eIF4G results in an impairment of 40S ribosome scanning on mRNAs leading to the formation of eIF2 alpha-independent stress granules. Our data reveals the mechanism by which tiRNAs inhibit translation and demonstrates novel activity for eIF4G in the regulation of translation.
机译:随着细胞遭遇不良环境条件,例如缺氧,氧化应激或营养剥夺,它们触发应力响应途径以保护自己直到瞬态应力通过。翻译的抑制是这种细胞应激响应的关键组分,并且安装证据表明,在该过程中,一类称为TiRNA的一类TRNA衍生的小RNA的重要性。这些小RNA中最有效的是具有组装成四聚型G-Quadreplex(G4)结构的能力的那些。然而,这些小RNA抑制翻译尚未阐明的机制。在这里,我们显示EIF4G,在翻译起始复合物中的主要支架蛋白,直接结合G4s,并且该活性对于TiRNA介导的翻译抑制需要。 EIF4G的靶向导致40S核糖体扫描在MRNA上的损伤,导致EIF2无关应力颗粒的形成。我们的数据揭示了Tirnas抑制翻译的机制,并在翻译规范中表明EIF4G的新活动。

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  • 来源
    《Nucleic Acids Research》 |2020年第11期|共11页
  • 作者单位

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

    Boston Univ Sch Med Dept Biochem Boston MA 02118 USA;

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

    IM Sechenov First Moscow State Med Univ Computat Oncol Grp Moscow Russia;

    Case Western Reserve Univ Dept Biochem Cleveland OH 44106 USA;

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

    Brigham &

    Womens Hosp Div Rheumatol Inflammat &

    Immun 75 Francis St Boston MA 02115 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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