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FMR1信使核糖核酸的翻译不受AGG中断的影响。

Translation of the FMR1 mRNA is not influenced by AGG interruptions.

作者信息

Ludwig Anna L, Raske Christopher, Tassone Flora, Garcia-Arocena Dolores, Hershey John W, Hagerman Paul J

机构信息

Department of Biochemistry and Molecular Medicine, School of Medicine, University of California Davis, 4303 Tupper Hall, Davis, CA 95616, USA.

出版信息

Nucleic Acids Res. 2009 Nov;37(20):6896-904. doi: 10.1093/nar/gkp713. Epub 2009 Sep 14.

DOI:10.1093/nar/gkp713
PMID:19752155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2777427/
Abstract

The fragile X mental retardation 1 (FMR1) gene contains a CGG-repeat element within its 5' untranslated region (5'UTR) which, for alleles with more than approximately 40 repeats, increasingly affects both transcription (up-regulation) and translation (inhibition) of the repeat-containing RNA with increasing CGG-repeat length. Translational inhibition is thought to be due to impaired ribosomal scanning through the CGG-repeat region, which is postulated to form highly stable secondary/tertiary structure. One striking difference between alleles in the premutation range (55-200 CGG repeats) and those in the normal range (< approximately 40 repeats) is the reduced number/absence of 'expansion stabilizing' AGG interruptions in the larger alleles. Such interruptions, which generally occur every 9-11 repeats in normal alleles, are thought to disrupt the extended CGG-repeat hairpin structure, thus facilitating translational initiation. To test this hypothesis, we have measured the translational efficiency of CGG-repeat mRNAs with 0-2 AGG interruptions, both in vitro (rabbit reticulocyte lysates) and in cell culture (HEK-293 cells). We demonstrate that the AGG interruptions have no detectable influence on translational efficiency in either a cell-free system or cell culture, indicating that any AGG-repeat-induced alterations in secondary/tertiary structure, if present, do not involve the rate-limiting step(s) in translational initiation.

摘要

脆性X智力低下1(FMR1)基因在其5'非翻译区(5'UTR)包含一个CGG重复元件,对于具有超过约40个重复的等位基因,随着CGG重复长度的增加,越来越多地影响含重复序列RNA的转录(上调)和翻译(抑制)。翻译抑制被认为是由于核糖体扫描通过CGG重复区域受损,该区域被假定形成高度稳定的二级/三级结构。前突变范围内的等位基因(55 - 200个CGG重复)与正常范围内的等位基因(<约40个重复)之间的一个显著差异是较大等位基因中“扩展稳定”AGG中断的数量减少/缺失。这种中断通常在正常等位基因中每9 - 11个重复出现一次,被认为会破坏扩展的CGG重复发夹结构,从而促进翻译起始。为了验证这一假设,我们在体外(兔网织红细胞裂解物)和细胞培养(HEK - 293细胞)中测量了具有0 - 2个AGG中断的CGG重复mRNA的翻译效率。我们证明,AGG中断在无细胞系统或细胞培养中对翻译效率均无可检测到的影响,这表明如果存在任何由AGG重复诱导的二级/三级结构改变,并不涉及翻译起始中的限速步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/c78702bd74c8/gkp713f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/17ee5eea1660/gkp713f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/6a440cf7642b/gkp713f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/0bee858022f4/gkp713f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/c78702bd74c8/gkp713f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/17ee5eea1660/gkp713f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/6a440cf7642b/gkp713f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/0bee858022f4/gkp713f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f792/2777427/c78702bd74c8/gkp713f4.jpg

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