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甲基营养型酵母多形汉逊酵母中mRNA翻译的内部起始

Internal Initiation of Translation of mRNA in the Methylotrophic Yeast Hansenula polymorpha.

作者信息

Mardanova E S, Beletsky A V, Ravin N V

机构信息

Institute of Bioengineering, Research Center of Biotechnology, Russian Academy of Sciences, Moscow, 119071, Russia.

出版信息

Biochemistry (Mosc). 2016 May;81(5):521-9. doi: 10.1134/S0006297916050096.

Abstract

Besides regular cap-dependent translation of mRNA, eukaryotes exploit internal initiation of translation driven by internal ribosome entry sites (IRESs). It is supposed that internal initiation provides translation of cellular mRNAs under stress conditions where the cap-dependent initiation is reduced. A number of IRESs have been characterized in mammalian mRNAs, but only a few examples are known in lower eukaryotes, particularly in yeasts. Here we identified two IRESs in the thermotolerant methylotrophic yeast Hansenula polymorpha DL-1. These sites are located in 5'-untranslated regions of genes HPODL_02249 and HPODL_04025 encoding a hypothetical membrane protein and actin-binding protein, respectively. In Saccharomyces cerevisiae cells, both IRESs drive expression of a second gene of a bicistronic mRNA, as well as translation of hairpin-containing monocistronic mRNA. The possibility of spurious splicing or presence of a cryptic promoter in the IRES sequences was ruled out, indicating that expression of a second gene of a bicistronic mRNA was IRES-dependent. We evaluated IRES activity of both elements and found that under normal physiological conditions its contribution to the overall translation of the respective mRNAs in yeast cells is about 0.3-0.4%. Therefore, these results suggest that the IRES-dependent translation initiation mechanism exists in Hansenula polymorpha.

摘要

除了常规的依赖帽结构的mRNA翻译外,真核生物还利用由内部核糖体进入位点(IRESs)驱动的内部翻译起始。据推测,内部起始在帽依赖性起始减少的应激条件下提供细胞mRNA的翻译。在哺乳动物mRNA中已经鉴定出许多IRES,但在低等真核生物中,特别是在酵母中,只有少数例子。在这里,我们在耐热甲基营养酵母多形汉逊酵母DL-1中鉴定出两个IRES。这些位点分别位于基因HPODL_02249和HPODL_04025的5'非翻译区,它们分别编码一种假定的膜蛋白和肌动蛋白结合蛋白。在酿酒酵母细胞中,两个IRES都驱动双顺反子mRNA第二个基因的表达,以及含发夹的单顺反子mRNA的翻译。排除了IRES序列中假剪接或隐蔽启动子存在的可能性,表明双顺反子mRNA第二个基因的表达是IRES依赖性的。我们评估了这两个元件的IRES活性,发现在正常生理条件下,其对酵母细胞中相应mRNA整体翻译的贡献约为0.3-0.4%。因此,这些结果表明多形汉逊酵母中存在IRES依赖性翻译起始机制。

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