Deiman B A, Koenen A K, Verlaan P W, Pleij C W
Gorlaeus Laboratories, Leiden Institute of Chemistry, The Netherlands.
J Virol. 1998 May;72(5):3965-72. doi: 10.1128/JVI.72.5.3965-3972.1998.
From mutational analysis of the 3'-terminal hairpin of turnip yellow mosaic virus (TYMV) RNA and use of nonstructured C-rich RNA templates, we conclude that the main determinant in the tRNA-like structure of TYMV RNA for initiation of minus-strand synthesis by the viral RNA-dependent RNA polymerase (RdRp) is the non-base-paired 3' ACC(A) end. Base pairing of this 3' end reduces the transcription efficiency drastically, and deletion of only the 3'-terminal A residue results in a fivefold drop in efficiency. The two C residues of the 3' ACCA end are required for efficient transcription, as shown by substitution mutations. However, the 5' A residue is not specifically involved in initiation of transcription, as shown by substitution mutations. Furthermore, the hairpin stem and loop upstream of the 3' ACCA end also do not interact with the RdRp in a base-specific way. However, for efficient transcription, the hairpin stem should be at least five bp in length, while the calculated deltaG value should be less than -10.5 kcal/mol. Unexpectedly, the use of nonstructured C-rich RNA templates showed that the RdRp can start internally on an NCCN or NUCN sequence. Therefore, a possible function of the tRNA-like structure of TYMV RNA may be to prevent internal initiation of minus-strand synthesis.
通过对芜菁黄花叶病毒(TYMV)RNA 3'末端发夹结构的突变分析以及使用非结构化富含 C 的 RNA 模板,我们得出结论,TYMV RNA 类似 tRNA 结构中,病毒 RNA 依赖的 RNA 聚合酶(RdRp)起始负链合成的主要决定因素是未碱基配对的 3' ACC(A)末端。该 3'末端的碱基配对会大幅降低转录效率,仅缺失 3'末端的 A 残基会导致效率下降五倍。如取代突变所示,3' ACCA 末端的两个 C 残基是高效转录所必需的。然而,如取代突变所示,5' A 残基并非特异性参与转录起始。此外,3' ACCA 末端上游的发夹茎环也不以碱基特异性方式与 RdRp 相互作用。然而,为实现高效转录,发夹茎的长度应至少为 5 个碱基对,同时计算得出的ΔG 值应小于-10.5 kcal/mol。出乎意料的是,使用非结构化富含 C 的 RNA 模板表明,RdRp 可在 NCCN 或 NUCN 序列上从内部起始。因此,TYMV RNA 类似 tRNA 结构的一个可能功能可能是防止负链合成的内部起始。