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呼肠孤病毒信使核糖核酸5'末端的核苷酸序列。

Nucleotide sequences at the 5' termini of reovirus mRNA's.

作者信息

Hastings K E, Millward S

出版信息

J Virol. 1978 Nov;28(2):490-8. doi: 10.1128/JVI.28.2.490-498.1978.

DOI:10.1128/JVI.28.2.490-498.1978
PMID:722859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC354298/
Abstract

During in vitro synthesis of reovirus mRNA by viral cores, methyl groups from S-adenosylmethionine are incorporated only into 5'-terminal cap structures, i.e., m7GpppGmCp.... Thus, mRNA synthesized in the presence of S-adenosyl-[methyl-3H]methionine is 3H labeled specifically at the 5' terminus. This circumstance was exploited in the determination of 5'-terminal nucleotide sequences. Seven 5'-terminal fragments derived by complete RNase T1, digestion of methyl-3Hlabeled mRNA were partially degraded with RNase T2, and the products were separated by electrophoresis-homochromatography. From the patterns formed by the methyl-3H-labeled RNase T2 products, the sequences of the seven RNase T1-generated fragments were deduced. All seven fragments started with the sequence m7GpppGmCUA, after which the sequences diverged, with a tendency to be either U-rich or A-rich. Their chain lengths ranged from 7 to 10 nucleotides (excluding the m7G residue), and none of them contained an initiator AUG triplet. The sequences obtained support the hypothesis that virion-associated oligonucleotides arise through abortive transcription of the viral genome. There is no apparent 5'-terminal sequence feature distinctive of early versus late mRNA species within the small-mRNA size class.

摘要

在病毒核心进行呼肠孤病毒mRNA的体外合成过程中,来自S-腺苷甲硫氨酸的甲基仅掺入5'-末端帽结构,即m7GpppGmCp.... 因此,在S-腺苷-[甲基-3H]甲硫氨酸存在下合成的mRNA在5'末端被特异性地3H标记。这种情况被用于确定5'-末端核苷酸序列。通过用RNase T1完全消化甲基-3H标记的mRNA得到的七个5'-末端片段用RNase T2进行部分降解,产物通过电泳-同系层析法分离。根据甲基-3H标记的RNase T2产物形成的图谱,推导了七个RNase T1产生的片段的序列。所有七个片段均以m7GpppGmCUA序列起始,此后序列 diverged,倾向于富含U或富含A。它们的链长范围为7至10个核苷酸(不包括m7G残基),并且它们均不包含起始AUG三联体。获得的序列支持这样的假设,即病毒体相关的寡核苷酸通过病毒基因组的流产转录产生。在小mRNA大小类别中,早期与晚期mRNA种类之间没有明显的5'-末端序列特征。

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Nucleotide sequences at the 5' termini of reovirus mRNA's.呼肠孤病毒信使核糖核酸5'末端的核苷酸序列。
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引用本文的文献

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Assignment of reovirus mRNA ribosome binding sites to virion genome segments by nucleotide sequence analyses.通过核苷酸序列分析将呼肠孤病毒mRNA核糖体结合位点定位到病毒粒子基因组片段上。
Nucleic Acids Res. 1980 Jan 25;8(2):337-50. doi: 10.1093/nar/8.2.337.
2
Reovirus progeny subviral particles synthesize uncapped mRNA.呼肠孤病毒子代亚病毒颗粒合成无帽mRNA。
J Virol. 1980 May;34(2):497-505. doi: 10.1128/JVI.34.2.497-505.1980.
3
Sequences of ribosome binding sites from the large size class of reovirus mRNA.呼肠孤病毒大尺寸类mRNA的核糖体结合位点序列。

本文引用的文献

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CHROMATOGRAPHY OF RIBONUCLEASE T1 DIGESTS OF RNA ON THE DEAE-CELLULOSE OF 7 M UREA.核糖核酸酶T1对RNA的消化产物在7M尿素的二乙氨基乙基纤维素上的色谱分析
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Homologous terminal sequences of the genome double-stranded RNAs of bluetongue virus.蓝舌病病毒基因组双链RNA的同源末端序列
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Resolution of multiple ribonucleic acid species by polyacrylamide gel electrophoresis.通过聚丙烯酰胺凝胶电泳分离多种核糖核酸种类
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A simple method for the preparation of 32-P-labelled adenosine triphosphate of high specific activity.一种制备高比活度32-P标记三磷酸腺苷的简单方法。
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Regulation of transcription of the Reovirus genome.呼肠孤病毒基因组转录的调控
J Mol Biol. 1968 Aug 28;36(1):107-23. doi: 10.1016/0022-2836(68)90223-4.
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Reovirus: RNA polymerase activity in purified virions.呼肠孤病毒:纯化病毒颗粒中的RNA聚合酶活性
Biochem Biophys Res Commun. 1968 Dec 30;33(6):895-901. doi: 10.1016/0006-291x(68)90396-3.
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Separation of ten reovirus genome segments by polyacrylamide gel electrophoresis.通过聚丙烯酰胺凝胶电泳分离十种呼肠孤病毒基因组片段。
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