A motif in the 5′untranslated region of messenger RNAs regulates protein synthesis in a S6 kinase-dependent manner

Q1 Biochemistry, Genetics and Molecular Biology
Hyun-Chul Shin , Yury A. Bochkov , Kangsan Kim , James E. Gern , Nizar N. Jarjour , Stephane Esnault
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引用次数: 0

Abstract

The 5′ untranslated regions (UTRs) in messenger RNAs (mRNAs) play an important role in the regulation of protein synthesis. We had previously identified a group of mRNAs that includes human semaphorin 7A (SEMA7A) whose translation is upregulated by the Erk/p90S6K pathway in human eosinophils, with a potential negative impact in asthma and airway inflammation. In the current study, we aimed to find a common 5′UTR regulatory cis-element, and determine its impact on protein synthesis. We identified a common and conserved 5′UTR motif GGCTG—[(C/G)T(C/G)]n—GCC that was present in this group of mRNAs. Mutations of the first two GG bases in this motif in SEMA7A 5′UTR led to a complete loss of S6K activity dependence for maximal translation. In conclusion, the newly identified 5′UTR motif present in SEMA7A has a critical role in regulating S6K-dependent protein synthesis.

信使核糖核酸5'非翻译区的基序以S6激酶依赖的方式调节蛋白质合成。
信使核糖核酸(mRNAs)中的5'非翻译区(UTRs)在蛋白质合成的调控中起着重要作用。我们之前已经鉴定了一组信使核糖核酸,其中包括人类信号蛋白7A(SEMA7A),其翻译在人类嗜酸性粒细胞中通过Erk/p90S6K途径上调,对哮喘和气道炎症具有潜在的负面影响。在目前的研究中,我们旨在找到一种常见的5’UTR调控顺式元件,并确定其对蛋白质合成的影响。我们鉴定了一种常见且保守的5’UTR基序GGCTG-[(C/G)T(C/G。SEMA7A 5’UTR中该基序的前两个GG碱基的突变导致S6K活性依赖性的完全丧失以实现最大翻译。总之,SEMA7A中新鉴定的5’UTR基序在调节S6K依赖性蛋白质合成中具有关键作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in biological regulation
Advances in biological regulation Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
8.90
自引率
0.00%
发文量
41
审稿时长
17 days
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