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拟南芥多胺氧化酶-2上游开放阅读框是下游翻译调控所必需的。

Arabidopsis Polyamine oxidase-2 uORF is required for downstream translational regulation.

作者信息

Guerrero-González María de la Luz, Ortega-Amaro María Azucena, Juárez-Montiel Margarita, Jiménez-Bremont Juan Francisco

机构信息

Facultad de Agronomía y Veterinaria, Universidad Autónoma de San Luis Potosí, San Luis Potosí, Mexico.

Instituto Potosino de Investigación Científica y Tecnológica AC, División de Biología Molecular, San Luis Potosí, Mexico.

出版信息

Plant Physiol Biochem. 2016 Nov;108:381-390. doi: 10.1016/j.plaphy.2016.08.006. Epub 2016 Aug 5.

Abstract

In eukaryotic mRNAs, small upstream open reading frames (uORFs) located in the 5'-untranslated region control the translation of the downstream main ORF. Polyamine oxidase (PAO) enzymes catalyze the oxidation of higher polyamines such as spermidine and spermine, and therefore contribute to the maintenance of intracellular polyamine content and to the regulation of physiological processes through their catabolic products. Recently, we reported that the Arabidopsis thaliana Polyamine Oxidase 2 (AtPAO2) is post-transcriptionally regulated by its 5'-UTR region through an uORF. In the present study, we analyzed whether the translation of the uORF is needed for the translational repression of the main ORF, and whether the inactivation of the uORF had an effect on the translational control mediated by polyamines. To this aim, we generated diverse single mutations in the uORF sequence; these mutant 5'-UTRs were fused to the GUS reporter gene, and tested in onion monolayer cells and A. thaliana transgenic seedlings. Removal of the start codon or introduction of a premature stop codon in the AtPAO2 uORF sequence abolished the negative regulation of the GUS expression exerted by the wild-type AtPAO2 uORF. An artificial uORF (32 amino acids in length) generated by the addition of a single nucleotide in AtPAO2 uORF proved to be less repressive than the wild-type uORF. Thus, our findings suggest that translation of the AtPAO2 uORF is necessary for the translational repression of the main ORF.

摘要

在真核生物的信使核糖核酸(mRNA)中,位于5'-非翻译区的小上游开放阅读框(uORF)控制着下游主要开放阅读框的翻译。多胺氧化酶(PAO)催化亚精胺和精胺等高阶多胺的氧化反应,因此通过其分解代谢产物有助于维持细胞内多胺含量并调节生理过程。最近,我们报道了拟南芥多胺氧化酶2(AtPAO2)在转录后通过其5'-非翻译区的一个uORF受到调控。在本研究中,我们分析了主开放阅读框的翻译抑制是否需要uORF的翻译,以及uORF的失活是否会对多胺介导的翻译控制产生影响。为此,我们在uORF序列中产生了多种单突变;这些突变的5'-非翻译区与GUS报告基因融合,并在洋葱单层细胞和拟南芥转基因幼苗中进行测试。在AtPAO2 uORF序列中去除起始密码子或引入提前终止密码子消除了野生型AtPAO2 uORF对GUS表达的负调控。通过在AtPAO2 uORF中添加单个核苷酸产生的人工uORF(长度为32个氨基酸)被证明比野生型uORF的抑制作用更小。因此,我们的研究结果表明AtPAO2 uORF的翻译对于主开放阅读框的翻译抑制是必要的。

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