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芜菁黄花叶病毒RNA 3'端假结在病毒RNA依赖的RNA聚合酶负链合成中的作用。

The role of the pseudoknot at the 3' end of turnip yellow mosaic virus RNA in minus-strand synthesis by the viral RNA-dependent RNA polymerase.

作者信息

Deiman B A, Kortlever R M, Pleij C W

机构信息

Leiden Institute of Chemistry, Gorlaeus Laboratories, The Netherlands.

出版信息

J Virol. 1997 Aug;71(8):5990-6. doi: 10.1128/JVI.71.8.5990-5996.1997.

Abstract

The tRNA-like structure at the 3' end of turnip yellow mosaic virus (TYMV) RNA was studied in order to determine the role of this structure in the initiation of minus-strand synthesis in vitro. Deletions in the 5'-to-3' direction up to the pseudoknot structure did not result in a decrease of transcription efficiency. However, transcription efficiency was reduced twofold when a fragment of 21 nucleotides, comprising the 3'-terminal hairpin, was used as a template. tRNA(Phe) from yeast, Escherichia coli 5S rRNA, and the 3'-terminal 208 nucleotides of alfalfa mosaic virus RNA 3 could not be transcribed by the RNA-dependent RNA polymerase (RdRp) of TYMV. Various mutations in the sequences of loop regions L1 and L2 or of stem region S1 of the pseudoknot were tested to further investigate the importance of the pseudoknot structure. The results were compared with those obtained in an earlier study on aminoacylation with the same mutants (R. M. W. Mans, M. H. van Steeg, P. W. G. Verlaan, C. W. A. Pleij, and L. Bosch, J. Mol. Biol. 223:221-232; 1992). Mutants which still harbor a stable pseudoknot, as proven by probing its structure, have a transcription efficiency very close to that of the wild-type virus. Disruption of the pseudoknot structure, however, gives rise to a drop in transcription efficiency to about 50%. No indications of base-specific interactions between L1, L2, or S1 of the pseudoknot and the RdRp were found.

摘要

为了确定芜菁黄花叶病毒(TYMV)RNA 3'端类似 tRNA 的结构在体外负链合成起始过程中的作用,对其进行了研究。在 5'至 3'方向上直至假结结构的缺失并未导致转录效率降低。然而,当使用包含 3'末端发夹结构的 21 个核苷酸片段作为模板时,转录效率降低了两倍。酵母的 tRNA(Phe)、大肠杆菌 5S rRNA 以及苜蓿花叶病毒 RNA 3 的 3'末端 208 个核苷酸均不能被 TYMV 的 RNA 依赖性 RNA 聚合酶(RdRp)转录。对假结的环区 L1 和 L2 或茎区 S1 的序列进行了各种突变测试,以进一步研究假结结构的重要性。将结果与早期关于相同突变体的氨酰化研究(R.M.W. Mans、M.H. van Steeg、P.W.G. Verlaan、C.W.A. Pleij 和 L. Bosch,《分子生物学杂志》223:2–21–232;1992)所得结果进行了比较。通过探测其结构证明仍具有稳定假结的突变体,其转录效率与野生型病毒非常接近。然而,假结结构的破坏会导致转录效率下降至约 50%。未发现假结的 L1、L2 或 S1 与 RdRp 之间存在碱基特异性相互作用的迹象。

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