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In-depth analysis of cis-determinants that either promote or inhibit reinitiation on GCN4 mRNA after translation of its four short uORFs

机译:深入分析促进或抑制GCN4 mRNA四个短uORFs翻译后重新启动的顺式决定簇

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摘要

Translational control in eukaryotes is exerted by many means, one of which involves a ribosome translating multiple cistrons per mRNA as in bacteria. It is called reinitiation (REI) and occurs on mRNAs where the main ORF is preceded by a short upstream uORF(s). Some uORFs support efficient REI on downstream cistrons, whereas some others do not. The mRNA of yeast transcriptional activator GCN4 contains four uORFs of both types that together compose an intriguing regulatory mechanism of its expression responding to nutrients’ availability and various stresses. Here we subjected all GCN4 uORFs to a comprehensive analysis to identify all REI-promoting and inhibiting cis-determinants that contribute either autonomously or in synergy to the overall efficiency of REI on GCN4. We found that the 3′ sequences of uORFs 1–3 contain a conserved AU1-2A/UUAU2 motif that promotes REI in position-specific, autonomous fashion such as the REI-promoting elements occurring in 5′ sequences of uORF1 and uORF2. We also identified autonomous and transferable REI-inhibiting elements in the 3′ sequences of uORF2 and uORF3, immediately following their AU-rich motif. Furthermore, we analyzed contributions of coding triplets and terminating stop codon tetranucleotides of GCN4 uORFs showing a negative correlation between the efficiency of reinitiation and efficiency of translation termination. Together we provide a complex overview of all cis-determinants of REI with their effects set in the context of the overall GCN4 translational control.
机译:真核生物的翻译控制可通过多种手段来实现,其中之一涉及核糖体如细菌中那样翻译每个mRNA的多个顺反子。它被称为重新初始化(REI),发生在主ORF前面是短上游uORF的mRNA上。一些uORF支持下游顺反子的有效REI,而另一些则不支持。酵母转录激活因子GCN4的mRNA包含两种类型的四种uORF,它们共同构成了一种有趣的表达机制,可响应营养物质的可利用性和各种压力。在这里,我们对所有GCN4 uORF进行了全面分析,以确定所有REI促进和抑制的顺式决定簇,这些决定簇对REI在GCN4上的整体效率具有自主性或协同作用。我们发现uORF 1-3的3'序列包含一个保守的AU1-2A / UUAU2基序,它以位置特异性,自主方式促进REI,例如uORF1和uORF2的5'序列中出现的REI促进元件。我们还确定了uORF2和uORF3的3'序列中紧随其富含AU的基序的自主和可转移的REI抑制元件。此外,我们分析了编码三联体和GCN4 uORF的终止终止密码子四核苷酸的贡献,显示了重新初始化效率和翻译终止效率之间的负相关。我们在一起提供了REI所有顺式决定簇的复杂概述,以及它们在整体GCN4翻译控制中的作用集。

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