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Structural Elements in the 5′-Untranslated Region of Giardiavirus Transcript Essential for Internal Ribosome Entry Site-Mediated Translation Initiation

机译:内部核糖体进入位点介导的翻译起始必不可少的贾第鞭毛病毒转录本的5'-非翻译区的结构元素。

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Translation of uncapped giardiavirus (GLV) mRNA in Giardia lamblia requires the presence of a 5′-untranslated region (5′-UTR) and a viral capsid coding region. We used dicistronic viral constructs to show that the downstream 253 nucleotides (nt) of the 5′-UTR plus the initial 264-nt capsid coding region constitute an internal ribosome entry site (IRES). Predicted secondary structures in the 253-nt 5′-UTR include stem-loops U3, U4a, U4b, U4c, and U5. Chemical and enzymatic probing analysis confirmed the presence of all predicted stem-loops except U4a. Disruption of stem-loop structures U3 and U5 by site-directed mutagenesis resulted in a drastic reduction in translation of a monocistronic viral transcript, which could be restored by compensatory sequence changes. Mutations disrupting stem-loops U4b and U4c do not exert an appreciable effect on translation, but certain sequences in the U4a region and in U4b do appear to play important roles in the IRES. Structural analysis also suggests that an 8-nt U3 loop sequence (nt 147 to 154) pairs with an 8-nt downstream sequence (nt 168 to 175) to form a pseudoknot. Disruption of this pseudoknot by mutagenesis resulted in a drastic reduction in translation, which could be restored by compensatory sequence changes. This study has defined the secondary structure in the 5′-UTR of the IRES. Together with the previous results, we have now completed analysis of the entire structure of GLV IRES and fully defined the functionally essential structural elements in it.
机译:兰氏贾第鞭毛虫中未封盖的贾第鞭毛虫病毒(GLV)mRNA的翻译需要存在5'非翻译区(5'-UTR)和病毒衣壳编码区。我们使用双顺反子病毒构建体显示5'-UTR的下游253个核苷酸(nt)加上起始的264-nt衣壳编码区构成了内部核糖体进入位点(IRES)。 253-nt 5'-UTR中预测的二级结构包括茎环U3,U4a,U4b,U4c和U5。化学和酶促探测分析证实,除了U4a外,所有预测的茎环均存在。通过定点诱变破坏茎环结构U3和U5导致单顺反子病毒转录物翻译的急剧减少,可以通过补偿性序列改变来恢复。破坏茎环U4b和U4c的突变不会对翻译产生明显影响,但U4a区和U4b中的某些序列确实在IRES中起重要作用。结构分析还表明,一个8-nt U3环序列(nt 147至154)与一个8-nt下游序列(nt 168至175)配对以形成假结。通过诱变破坏该假结导致翻译急剧减少,可以通过补偿序列改变来恢复。这项研究定义了IRES 5'-UTR中的二级结构。连同以前的结果,我们现在已经完成了对GLV IRES整个结构的分析,并在其中完全定义了功能上必不可少的结构元素。

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