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在mRNA的5'-非翻译区内鉴定最小的强翻译增强子。

Identification of a minimal strong translation enhancer within the 5'-untranslated region of mRNA.

作者信息

Aoki-Mutsuro Hiromi, Tamukai Ryoko, Fukui Miho, Wajiki Mai, Imamura Tomohiro, Ryabova Lyubov A, Schepetilnikov Mikhail V, Teramura Hiroshi, Kusano Hiroaki, Shimada Hiroaki

机构信息

Department of Biological Science and Technology, Tokyo University of Science, Katsushika, Tokyo 125-8585, Japan.

Institut de Biologie Moléculaire des Plantes, CNRS UPR2357, 67084 Strasbourg, France.

出版信息

Plant Biotechnol (Tokyo). 2024 Dec 25;41(4):437-446. doi: 10.5511/plantbiotechnology.24.0909a.

DOI:10.5511/plantbiotechnology.24.0909a
PMID:40083565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11897733/
Abstract

The long 5' untranslated region (5'UTR) exhibits enhancer activity in translation of rice mRNA. In this report, we describe elements of 5'UTR that may be responsible for its enhancer activity, including a long uORF and several secondary structure elements. 5'UTR can be dissected into three stem-loop structures SL1, small SL and SL2, where the uORF starts within SL1 and ends within SL2. As expected, uORF inhibits translation of downstream ORF since deletion of the uORF AUG or the SL1 stem-loop increases translation by approximately two-fold. Thus, the 158 nt 3' region of the 5'UTR lacking SL1 together with the AUG uORF, which has significant enhancer activity, was named dMac3. We investigated two critical regions within dMac3 mRNA that influence its translation: SL2, which destabilization potentially decreases translation activity, and another 13 nt located downstream of SL2. We further confirmed that dMac3 promotes mRNA translation initiation in an in vitro translation system and during transient expression in either cultured cells or leaves. Thus, the dMac3 5'UTR is a useful tool for efficient protein production in various in vitro and in vivo translation systems.

摘要

水稻mRNA的长5'非翻译区(5'UTR)在翻译过程中表现出增强子活性。在本报告中,我们描述了5'UTR中可能与其增强子活性相关的元件,包括一个长的上游开放阅读框(uORF)和几个二级结构元件。5'UTR可分为三个茎环结构,即SL1、小SL和SL2,其中uORF起始于SL1内,终止于SL2内。正如预期的那样,uORF抑制下游开放阅读框的翻译,因为缺失uORF的AUG或SL1茎环会使翻译增加约两倍。因此,5'UTR缺少SL1的158 nt 3'区域与具有显著增强子活性的AUG uORF一起被命名为dMac_3。我们研究了dMac_3 mRNA中影响其翻译的两个关键区域:SL2,其不稳定可能会降低翻译活性,以及位于SL2下游的另一个13 nt区域。我们进一步证实,dMac_3在体外翻译系统以及在培养细胞或叶片中的瞬时表达过程中促进mRNA翻译起始。因此,dMac_3 5'UTR是在各种体外和体内翻译系统中高效生产蛋白质的有用工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/f8901b42e55d/plantbiotechnology-41-4-24.0909a-figure06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/1444c295efdc/plantbiotechnology-41-4-24.0909a-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/2d69e90c49c4/plantbiotechnology-41-4-24.0909a-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/9087d9dd6688/plantbiotechnology-41-4-24.0909a-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/54d27d2f6ae6/plantbiotechnology-41-4-24.0909a-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/b92724379924/plantbiotechnology-41-4-24.0909a-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/f8901b42e55d/plantbiotechnology-41-4-24.0909a-figure06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/1444c295efdc/plantbiotechnology-41-4-24.0909a-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/2d69e90c49c4/plantbiotechnology-41-4-24.0909a-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/9087d9dd6688/plantbiotechnology-41-4-24.0909a-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/54d27d2f6ae6/plantbiotechnology-41-4-24.0909a-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/b92724379924/plantbiotechnology-41-4-24.0909a-figure05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9ea/11897733/f8901b42e55d/plantbiotechnology-41-4-24.0909a-figure06.jpg

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本文引用的文献

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Plant Biotechnol (Tokyo). 2023 Sep 25;40(3):219-227. doi: 10.5511/plantbiotechnology.23.0823a.
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Creation of a potato mutant lacking the starch branching enzyme gene that was generated by genome editing using the CRISPR/dMac3-Cas9 system.利用CRISPR/dMac3-Cas9系统通过基因组编辑创建的缺乏淀粉分支酶基因的马铃薯突变体。
Plant Biotechnol (Tokyo). 2021 Sep 25;38(3):345-353. doi: 10.5511/plantbiotechnology.21.0727a.
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Dissection of a rice OsMac1 mRNA 5' UTR to uncover regulatory elements that are responsible for its efficient translation.
解析水稻 OsMac1 mRNA 5'UTR 以揭示负责其高效翻译的调控元件。
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A novel FLOURY ENDOSPERM2 (FLO2)-interacting protein, is involved in maintaining fertility and seed quality in rice.一种新型的与粉质胚乳2(FLO2)相互作用的蛋白质,参与维持水稻的育性和种子质量。
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