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由于AUG起始密码子前的核苷酸-2和-3缺失导致的α地中海贫血在体外和体内均影响翻译效率。

Alpha-thalassemia due to the deletion of nucleotides -2 and -3 preceding the AUG initiation codon affects translation efficiency both in vitro and in vivo.

作者信息

Morle F, Starck J, Godet J

出版信息

Nucleic Acids Res. 1986 Apr 25;14(8):3279-92. doi: 10.1093/nar/14.8.3279.

Abstract

We previously hypothesized that a 2 nucleotide deletion, causing a A-greater than C change at position -3 preceding the ATG initiation codon of alpha globin gene, reduced translation efficiency of alpha globin mRNA and was responsible for a form of alpha + thalassemia displayed by an Algerian patient. We presently show that this deletion leads to a 30-45% reduction in translation efficiency of synthetic alpha globin mRNA in rabbit reticulocyte lysate. In other experiments, we constructed alpha/G gamma hybrid globin genes in which the 3' end of normal or mutated alpha globin genes downstream to the ATG initiation codon was substituted by the 3' part of a G gamma globin gene. COS cells transfected with either of these 2 hybrid genes were shown to synthesize a similar amount of alpha/G gamma hybrid mRNAs but 50% less G gamma globin when transfected with the alpha/G gamma hybrid gene carrying the deletion. These results definitively establish that the 2 nucleotide deletion reduces translation efficiency by 30-50%. This contrasts with the 93% reduction induced by a similar A-greater than C change at position -3 in the different nucleotide context preceding the ATG codon of the rat preproinsulin gene.

摘要

我们之前曾推测,在α珠蛋白基因ATG起始密码子前第-3位发生的一个2核苷酸缺失,导致A变为C的变化,降低了α珠蛋白mRNA的翻译效率,并导致一名阿尔及利亚患者表现出一种α+地中海贫血形式。我们目前表明,这种缺失导致兔网织红细胞裂解物中合成的α珠蛋白mRNA的翻译效率降低30 - 45%。在其他实验中,我们构建了α/Gγ杂交珠蛋白基因,其中正常或突变的α珠蛋白基因在ATG起始密码子下游的3'端被Gγ珠蛋白基因的3'部分取代。用这两种杂交基因中的任何一种转染COS细胞,结果显示合成的α/Gγ杂交mRNA量相似,但当用携带缺失的α/Gγ杂交基因转染时,合成的Gγ珠蛋白减少50%。这些结果明确证实,2核苷酸缺失使翻译效率降低30 - 50%。这与在大鼠前胰岛素原基因ATG密码子前不同核苷酸背景下第-3位类似的A变为C的变化所导致的93%的降低形成对比。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a90/339764/947fbbe44984/nar00277-0138-a.jpg

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