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由病毒基因组编码的开放阅读框可调节猿猴病毒40的病毒体蛋白合成的绝对速率和相对速率。

Leader-encoded open reading frames modulate both the absolute and relative rates of synthesis of the virion proteins of simian virus 40.

作者信息

Sedman S A, Good P J, Mertz J E

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin, Madison 53706.

出版信息

J Virol. 1989 Sep;63(9):3884-93. doi: 10.1128/JVI.63.9.3884-3893.1989.

Abstract

Numerous viral and cellular RNAs are polycistronic, including several of the late mRNA species encoded by simian virus 40 (SV40). The functionally bicistronic major late 16S and functionally tricistronic major late 19S mRNA species of SV40 contain the leader-encoded open reading frames (ORFs) LP1, located upstream of the sequence encoding the virion protein VP1, and LP1*, located upstream of the sequence encoding the virion proteins VP2 and VP3. To determine how these leader ORFs affect synthesis of the virion proteins, monkey cells were transfected with viral mutants in which either the leader-encoded translation initiation signal was mutated or the length and overlap of the leader ORF relative to the ORFs encoding the virion proteins were altered. The levels of initiation at and leaky scanning past each initiation signal were determined directly by quantitative analysis of the viral proteins synthesized in cells transfected with these mutants. Novel findings from these experiments included the following. (i) At least one-third of ribosomes bypass the leader-encoded translation initiation signal, GCCAUGG, on the SV40 major late 16S mRNA. (ii) At least 20% of ribosomes bypass even the consensus translation initiation signal, ACCAUGG, when it is situated 10 bases from the 5' end on the major late 16S mRNA. (iii)O The presence of the leader ORF on the bicistronic 16S mRNA species reduces VP1 synthesis threefold relative to synthesis from a similar RNA that lacks it. (iv) At least half and possibly all VP1 synthesized from the bicistronic 16S mRNA species is made by a leaky scanning mechanism. (v) LP1 and VP1 are synthesized from the bicistronic 16S mRNA species at approximately equal molar ratios. (vi) Approximately half of the VP1 synthesized in SV40-infected cells is synthesized from the minor, monocistronic 16S mRNA even though it accounts for only 20% of the 16S mRNA present. (vii) The presence and site of termination of translation of the leader ORF on the late 19S mRNAs affect the relative as well as absolute rates of synthesis of VP2 and VP3.

摘要

许多病毒RNA和细胞RNA都是多顺反子的,包括猿猴病毒40(SV40)编码的几种晚期mRNA。SV40的功能上双顺反子的主要晚期16S mRNA和功能上三顺反子的主要晚期19S mRNA含有前导编码的开放阅读框(ORF)LP1,位于病毒体蛋白VP1编码序列的上游,以及LP1*,位于病毒体蛋白VP2和VP3编码序列的上游。为了确定这些前导ORF如何影响病毒体蛋白的合成,用病毒突变体转染猴细胞,其中前导编码的翻译起始信号被突变,或者前导ORF相对于病毒体蛋白编码ORF的长度和重叠被改变了。通过对用这些突变体转染的细胞中合成的病毒蛋白进行定量分析,直接确定了每个起始信号处的起始水平和越过起始信号的漏扫描水平。这些实验的新发现包括以下几点。(i)至少三分之一的核糖体绕过SV40主要晚期16S mRNA上前导编码的翻译起始信号GCCAUGG。(ii)当共有翻译起始信号ACCAUGG位于主要晚期16S mRNA 5'端10个碱基处时,至少20%的核糖体甚至会绕过它。(iii)双顺反子16S mRNA上存在前导ORF,相对于缺乏它的类似RNA的合成,VP1的合成减少了三倍。(iv)从双顺反子16S mRNA合成的VP1中,至少一半甚至可能全部是通过漏扫描机制产生的。(v)LP1和VP1从双顺反子16S mRNA以大约相等的摩尔比合成。(vi)在SV40感染的细胞中合成的VP1中约一半是从小的单顺反子16S mRNA合成的,尽管它仅占存在的16S mRNA的20%。(vii)晚期19S mRNA上前导ORF的翻译终止的存在和位点影响VP2和VP3的相对合成速率以及绝对合成速率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8275/250984/58595ed9a31b/jvirol00076-0343-a.jpg

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