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苜蓿花叶病毒和烟草线条病毒RNA中外壳蛋白假定识别位点的核苷酸序列。

Nucleotide sequence of the putative recognition site for coat protein in the RNAs of alfalfa mosaic virus and tobacco streak virus.

作者信息

Koper-Zwarthoff E C, Bol J F

出版信息

Nucleic Acids Res. 1980 Aug 11;8(15):3307-18. doi: 10.1093/nar/8.15.3307.

DOI:10.1093/nar/8.15.3307
PMID:6160470
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC324154/
Abstract

The sequence of the 3'-terminal 180 and 140 nucleotides of RNAs 2 and 3, respectively, of tobacco streak virus (TSV) was deduced by reverse transcription in the presence of a specific primer and chain terminators. Homology between the two RNAs was found to be restricted to a 3-terminal region of about 45 nucleotides. The data were compared with the sequence of the homologous region of 145 nucleotides occurring at the 3'-termini of the alfalfa mosaic virus (A1MV) RNAs, which contains the specific binding site for coat protein (Koper-Zwarthoff et al., Nucleic Acids Res. 7, 1887-1900 (1979); Houwing and Jaspars, Biochemistry 17, 2927-2933 (1978)). This was done because of the evidence that the RNAs of A1MV and TSV contain specific binding sites for their own as well as each others coat protein, and that binding of coat protein to these sites is required to initiate infection (Van Vloten-Doting, Virology 65, 215-225 (1975)). The 3'-terminal homologous regions of A1MV and TSV have two features in common: the presence of several stable hairpins and the multiple occurrence of the tetranucleotide sequence AUGC. The hairpins cause the linear array of tandemly repeated AUGC-boxes. It is postulated that the primary interaction of coat protein molecules with the RNAs of AlMV and TSV is a cooperative process involving several binding sites each being composed of a hairpin flanked at its 3'-side by an AUGC-sequence.

摘要

在特异性引物和链终止剂存在的情况下,通过逆转录推导了烟草条纹病毒(TSV)RNA 2和RNA 3的3'末端180和140个核苷酸的序列。发现这两种RNA之间的同源性仅限于约45个核苷酸的3'末端区域。将这些数据与苜蓿花叶病毒(A1MV)RNA 3'末端出现的145个核苷酸的同源区域序列进行了比较,该区域包含衣壳蛋白的特异性结合位点(科珀 - 兹瓦特霍夫等人,《核酸研究》7,1887 - 1900(1979);豪温与雅斯帕斯,《生物化学》17,2927 - 2933(1978))。之所以这样做,是因为有证据表明A1MV和TSV的RNA含有自身以及彼此衣壳蛋白的特异性结合位点,并且衣壳蛋白与这些位点的结合是启动感染所必需的(范·弗洛滕 - 多廷,《病毒学》65,215 - 225(1975))。A1MV和TSV的3'末端同源区域有两个共同特征:存在几个稳定的发夹结构以及四核苷酸序列AUGC的多次出现。这些发夹结构导致AUGC框串联重复排列。据推测,衣壳蛋白分子与A1MV和TSV的RNA的主要相互作用是一个协同过程,涉及几个结合位点,每个结合位点由一个在其3'侧侧翼有AUGC序列的发夹结构组成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05fe/324154/b37fbad213e4/nar00432-0070-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05fe/324154/b37fbad213e4/nar00432-0070-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05fe/324154/b37fbad213e4/nar00432-0070-a.jpg

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本文引用的文献

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