翻译因子活性对六种不同mrna起始位点选择的影响

Daine Barth-Baus, C. Bhasker, W. Zoll, W. Merrick
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引用次数: 15

摘要

目前的文献通过生化分析、结构分析和遗传操作报道了与启动子met-tRNA与起始密码子AUG忠实匹配相关的关键因素是eIF1、eIF1A和eIF5。然而,这些发现在每种情况下都是基于单一mRNA的利用,可能存在差异。为了评估这一普遍发现,我们测试了六种不同的mrna。我们的结果证实了这三种蛋白在起始位点选择中是重要的。然而,另外两个发现是无法预测的。首先,eIF1在选择靠近mRNA 5 '端(即小于21个核苷酸)的起始密码子中起主要作用。其次,添加eIF5B与添加eIF5的影响几乎相同。考虑到eIF5和eIF5B在80S起始通路中发挥的不同作用,这是出乎意料的。最后,尽管许多mRNA似乎以类似的方式在质量上做出反应,但所注意到的数量差异表明,我们的发现仍然存在一些mRNA的特异性。这个特征可能是5 ' UTR的长度,IRES元件的参与,起始密码子5 '或3 '的二级结构或与RNA结合蛋白或核糖体相互作用的特定序列/结构元件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of translation factor activities on start site selection in six different mRNAs
Current literature using biochemical assays, structural analyses and genetic manipulations has reported that the key factors associated with the faithful matching of the initiator met-tRNA to the start codon AUG are eIF1, eIF1A and eIF5. However, these findings were in each case based upon the utilization of a single mRNA, perhaps with variations. In an effort to evaluate this general finding, we tested six different mRNAs. Our results confirm that these three proteins are important for start site selection. However, two additional findings would not have been predicted. The first is that eIF1 plays a major role in selecting against start codons that are in close proximity to the 5′ end of the mRNA (i.e., less than 21 nucleotides). Second, the addition of eIF5B had nearly the same affect as the addition of eIF5. This is unexpected given the different roles that eIF5 and eIF5B have been proposed to play in the 80S initiation pathway. Finally, although many of the mRNAs appear to respond qualitatively in a similar manner, the quantitative differences noted suggest that there is still some mRNA specific character to our findings. This character may be the length of the 5′ UTR, involvement of an IRES element, secondary structure either 5′ or 3′ of the start codon or specific sequence/structure elements that interact with RNA binding proteins or the ribosome.
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