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The h subunit of eIF3 promotes reinitiation competence during translation of mRNAs harboring upstream open reading frames

机译:eIF3的h亚基在具有上游开放阅读框的mRNA的翻译过程中促进重新启动能力

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摘要

Upstream open reading frames (uORFs) are protein coding elements in the 5′ leader of messenger RNAs. uORFs generally inhibit translation of the main ORF because ribosomes that perform translation elongation suffer either permanent or conditional loss of reinitiation competence. After conditional loss, reinitiation competence may be regained by, at the minimum, reacquisition of a fresh methionyl-tRNA. The conserved h subunit of Arabidopsis eukaryotic initiation factor 3 (eIF3) mitigates the inhibitory effects of certain uORFs. Here, we define more precisely how this occurs, by combining gene expression data from mutated 5′ leaders of Arabidopsis AtbZip11 (At4g34590) and yeast GCN4 with a computational model of translation initiation in wild-type and eif3h mutant plants. Of the four phylogenetically conserved uORFs in AtbZip11, three are inhibitory to translation, while one is anti-inhibitory. The mutation in eIF3h has no major effect on uORF start codon recognition. Instead, eIF3h supports efficient reinitiation after uORF translation. Modeling suggested that the permanent loss of reinitiation competence during uORF translation occurs at a faster rate in the mutant than in the wild type. Thus, eIF3h ensures that a fraction of uORF-translating ribosomes retain their competence to resume scanning. Experiments using the yeast GCN4 leader provided no evidence that eIF3h fosters tRNA reaquisition. Together, these results attribute a specific molecular function in translation initiation to an individual eIF3 subunit in a multicellular eukaryote.
机译:上游开放阅读框(uORF)是信使RNA 5'前导序列中的蛋白质编码元件。 uORF通常会抑制主要ORF的翻译,因为执行翻译延伸的核糖体会永久或有条件地丧失重新启动能力。有条件的损失后,至少可以通过重新获得新鲜的甲硫氨酰-tRNA来恢复重新启动的能力。拟南芥真核生物起始因子3(eIF3)的保守的h亚基可减轻某些uORF的抑制作用。在这里,我们将拟南芥AtbZip11(At4g34590)和酵母GCN4的突变5'前导序列的基因表达数据与野生型和eif3h突变植物中翻译起始的计算模型结合起来,从而更精确地定义了这种情况的发生方式。在AtbZip11中的四个系统发育上保守的uORF中,有三个抑制翻译,而一个则具有抗抑制作用。 eIF3h中的突变对uORF起始密码子识别没有重大影响。相反,eIF3h支持uORF转换后的有效重新初始化。模型表明,在突变体中,uORF翻译过程中永久性的重新启动能力丧失比野生型更快。因此,eIF3h确保了一部分翻译uORF的核糖体保留其恢复扫描的能力。使用酵母GCN4前导序列进行的实验没有提供eIF3h促进tRNA吸收的证据。总之,这些结果将翻译起始中的特定分子功能归因于多细胞真核生物中的单个eIF3亚基。

著录项

  • 来源
    《RNA》 |2010年第4期|748-761|共14页
  • 作者单位

    Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

    Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

    Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

    Graduate Program in Genome Science and Technology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

    Department of Ecology and Evolutionary Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

    Department of Biochemistry and Cellular and Molecular Biology, The University of Tennessee, Knoxville, Tennessee 37996, USA|Graduate Program in Genome Science and Technology, The University of Tennessee, Knoxville, Tennessee 37996, USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    translation regulation; uORF; reinitiation; eIF3; modeling;

    机译:翻译规则;uORF;重新初始化;eIF3;建模;

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