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脊髓灰质炎病毒5'非翻译区中一个保守的AUG三联体在体外和体内均可作为起始密码子发挥作用。

A conserved AUG triplet in the 5' nontranslated region of poliovirus can function as an initiation codon in vitro and in vivo.

作者信息

Pestova T V, Hellen C U, Wimmer E

机构信息

A. N. Belozersky Laboratory of Molecular Biology, Moscow State University, Russia.

出版信息

Virology. 1994 Nov 1;204(2):729-37. doi: 10.1006/viro.1994.1588.

DOI:10.1006/viro.1994.1588
PMID:7941341
Abstract

Poliovirus translation is initiated at AUG743, 154 nt downstream of a conserved heptanucleotide CUUAUGG at the 3' border of the internal ribosome entry site. AUG586 is part of this motif and is normally not an initiation codon, but was activated following alteration of its context from CUUAUGG to ACCAUGG. Initiation at AUG586 was efficient and yielded a 7.2-kDa polypeptide translated in an open reading frame that overlapped AUG743 by 38 nt, but the presence of this activated codon reduced initiation at AUG743 by only 50%. Growth of a mutant poliovirus W1-5NC-1 containing the CUU-->ACC substitutions was impaired and was not alleviated by a termination codon placed four triplets downstream of AUG586 in the virus W1-5NC-2. The virus W1-5NC-6 contained the substitution U584A and had a similar sp phenotype; the phenotype of W1-5NC-1 is thus probably due to substitution within the conserved CUUAUGG motif per se rather than to activation of AUG586. A sp mutant virus W1-5NC-3 was derived from W1-5NC-1 by deletion of nt 588-745, indicating that AUG586 could initiate translation in vivo. These observations indicate that although AUG586 can be activated by upstream substitutions, it is nevertheless readily bypassed by ribosomes in mRNAs containing wt downstream elements, resulting in initiation at AUG743.

摘要

脊髓灰质炎病毒的翻译起始于AUG743,位于内部核糖体进入位点3'边界处保守的七核苷酸CUUAUGG下游154个核苷酸处。AUG586是该基序的一部分,通常不是起始密码子,但在其上下文从CUUAUGG改变为ACCAUGG后被激活。在AUG586处起始是有效的,并产生了一个7.2 kDa的多肽,该多肽在一个与AUG743重叠38个核苷酸的开放阅读框中翻译,但这个被激活的密码子的存在仅使AUG743处的起始减少了50%。含有CUU→ACC替换的突变脊髓灰质炎病毒W1-5NC-1的生长受到损害,并且在病毒W1-5NC-2中位于AUG586下游四个三联体处的终止密码子并不能缓解这种损害。病毒W1-5NC-6含有U584A替换,具有类似的sp表型;因此,W1-5NC-1的表型可能是由于保守的CUUAUGG基序本身的替换,而不是由于AUG586的激活。一个sp突变病毒W1-5NC-3是通过缺失核苷酸588 - 745从W1-5NC-1衍生而来的,这表明AUG586可以在体内起始翻译。这些观察结果表明,尽管AUG586可以被上游替换激活,但在含有野生型下游元件的mRNA中,核糖体很容易绕过它,从而在AUG743处起始翻译。

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