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翻译因子活性对六种不同mRNA起始位点选择的影响。

Influence of translation factor activities on start site selection in six different mRNAs.

作者信息

Barth-Baus Daine, Bhasker C Ramana, Zoll Wendy, Merrick William C

机构信息

Department of Biochemistry; School of Medicine; Case Western Reserve University; Cleveland, OH USA.

Carlsbad, CA USA.

出版信息

Translation (Austin). 2013 Apr 1;1(1):e24419. doi: 10.4161/trla.24419. eCollection 2013.

DOI:10.4161/trla.24419
PMID:26824019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4718060/
Abstract

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.

摘要

目前使用生化分析、结构分析和基因操作的文献报道,与起始甲硫氨酰 - tRNA与起始密码子AUG准确匹配相关的关键因素是eIF1、eIF1A和eIF5。然而,这些发现每种情况下都基于单个mRNA的利用,可能存在一些变化。为了评估这一普遍发现,我们测试了六种不同的mRNA。我们的结果证实这三种蛋白质对于起始位点选择很重要。然而,还有两个额外的发现是无法预测的。第一个是eIF1在排除靠近mRNA 5'端(即小于21个核苷酸)的起始密码子方面起主要作用。其次,添加eIF5B的影响几乎与添加eIF5相同。考虑到eIF5和eIF5B在80S起始途径中被认为发挥的不同作用,这是出乎意料的。最后,尽管许多mRNA在定性上似乎以类似方式做出反应,但所观察到的定量差异表明我们的发现仍然存在一些mRNA特异性特征。这种特征可能是5'非翻译区的长度、内部核糖体进入位点(IRES)元件的参与、起始密码子5'或3'端的二级结构,或者与RNA结合蛋白或核糖体相互作用的特定序列/结构元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/f8838e8e7369/ktrs-01-01-10924419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/ac7662054050/ktrs-01-01-10924419-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/6d16beecd854/ktrs-01-01-10924419-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/5777f8808f0a/ktrs-01-01-10924419-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/df26cde1ab51/ktrs-01-01-10924419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/d918cd8b4771/ktrs-01-01-10924419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/1f1fb5bf4076/ktrs-01-01-10924419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/5b70beabb6a2/ktrs-01-01-10924419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/f8838e8e7369/ktrs-01-01-10924419-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/ac7662054050/ktrs-01-01-10924419-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/6d16beecd854/ktrs-01-01-10924419-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/5777f8808f0a/ktrs-01-01-10924419-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/df26cde1ab51/ktrs-01-01-10924419-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/d918cd8b4771/ktrs-01-01-10924419-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/1f1fb5bf4076/ktrs-01-01-10924419-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/5b70beabb6a2/ktrs-01-01-10924419-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/07e5/4718060/f8838e8e7369/ktrs-01-01-10924419-g008.jpg

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