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一个短开放阅读框在花椰菜花叶病毒RNA前导序列的核糖体跳跃中的作用。

Role of a short open reading frame in ribosome shunt on the cauliflower mosaic virus RNA leader.

作者信息

Pooggin M M, Hohn T, Fütterer J

机构信息

Friedrich Miescher Institute, CH-4002 Basel, Switzerland, the Centre for Bioengineering, Russian Academy of Sciences, 117312 Moscow, Russia.

出版信息

J Biol Chem. 2000 Jun 9;275(23):17288-96. doi: 10.1074/jbc.M001143200.

Abstract

The pregenomic 35 S RNA of cauliflower mosaic virus (CaMV) belongs to the growing number of mRNAs known to have a complex leader sequence. The 612-nucleotide leader contains several short open reading frames (sORFs) and forms an extended hairpin structure. Downstream translation of 35 S RNA is nevertheless possible due to the ribosome shunt mechanism, by which ribosomes are directly transferred from a take-off site near the capped 5' end of the leader to a landing site near its 3' end. There they resume scanning and reach the first long open reading frame. We investigated in detail how the multiple sORFs influence ribosome migration either via shunting or linear scanning along the CaMV leader. The sORFs together constituted a major barrier for the linear ribosome migration, whereas the most 5'-proximal sORF, sORF A, in combination with sORFs B and C, played a positive role in translation downstream of the leader by diverting scanning ribosomes to the shunt route. A simplified, shunt-competent leader was constructed with the most part of the hairpin including all the sORFs except sORF A replaced by a scanning-inhibiting structure. In this leader as well as in the wild type leader, proper translation and termination of sORF A was required for efficient shunt and also for the level of shunt enhancement by a CaMV-encoded translation transactivator. sORF A could be replaced by heterologous sORFs, but a one-codon (start/stop) sORF was not functional. The results implicate that in CaMV, shunt-mediated translation requires reinitiation. The efficiency of the shunt process is influenced by translational properties of the sORF.

摘要

花椰菜花叶病毒(CaMV)的前基因组35S RNA属于已知具有复杂前导序列的mRNA数量不断增加的一类。这个612个核苷酸的前导序列包含几个短开放阅读框(sORF),并形成一个延伸的发夹结构。然而,由于核糖体跳跃机制,35S RNA的下游翻译是可能的,通过该机制,核糖体直接从靠近前导序列加帽5'端的起始位点转移到靠近其3'端的着陆位点。在那里,它们恢复扫描并到达第一个长开放阅读框。我们详细研究了多个sORF如何通过跳跃或沿着CaMV前导序列的线性扫描来影响核糖体迁移。这些sORF共同构成了核糖体线性迁移的主要障碍,而最靠近5'端的sORF,即sORF A,与sORF B和C结合,通过将扫描核糖体转移到跳跃途径,在引导序列下游的翻译中发挥了积极作用。构建了一个简化的、具有跳跃能力的前导序列,其中发夹的大部分包括除sORF A之外的所有sORF都被一个抑制扫描的结构所取代。在这个前导序列以及野生型前导序列中,sORF A的正确翻译和终止对于有效的跳跃以及CaMV编码的翻译反式激活因子增强跳跃的水平都是必需的。sORF A可以被异源sORF取代,但一个密码子(起始/终止)的sORF没有功能。结果表明,在CaMV中,跳跃介导的翻译需要重新起始。跳跃过程的效率受sORF翻译特性的影响。

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