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Pseudouridine and ribothymidine formation in the tRNA-like domain of turnip yellow mosaic virus RNA.

机译:萝卜黄色花叶病毒RNA的tRNA样结构域中的假尿苷和核苷胸苷的形成。

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摘要

The last 82 nucleotides of the 6.3 kb genomic RNA of plant turnip yellow mosaic virus (TYMV), the so-called 'tRNA-like' domain, presents functional, structural and primary sequence homologies with canonical tRNAs. In particular, one of the stem-loops resembles the TPsi(pseudouridine)-branch of tRNA, except for the presence of a guanosine at position 37 (numbering is from the 3'-end) instead of the classical uridine-55 in tRNA (numbering is from the 5'-end). Both the wild-type TYMV-RNA fragment and a variant, TYMV-mut G37U in which G-37 has been replaced by U-37, have been tested as potential substrates for the yeast tRNA modification enzymes. Results indicate that two modified nucleotides were formed upon incubation of the wild-type TYMV-fragment in a yeast extract: one Psi which formed quantitatively at position 65, and one ribothymidine (T) which formed at low level at position U-38. In the TYMV-mutant G37U, besides the quantitative formation of both Psi-65 and T-38, an additional Psi was detected at position 37. Modified nucleotides Psi-65, T-38 and Psi-37 in TYMV RNA are equivalent to Psi-27, T-54 and Psi-55 in tRNA, respectively. Purified yeast recombinant tRNA:Psisynthases (Pus1 and Pus4), which catalyze respectively the formation of Psi-27 and Psi-55 in yeast tRNAs, are shown to catalyze the quantitative formation of Psi-65 and Psi-37, respectively, in the tRNA-like 3'-domain of mutant TYMV RNA in vitro . These results are discussed in relation to structural elements that are needed by the corresponding enzymes in order to catalyze these post-transcriptional modification reactions.
机译:植物芜菁黄花叶病毒(TYMV)6.3 kb基因组RNA的最后82个核苷酸,即所谓的“ tRNA样”结构域,与标准tRNA呈现功能性,结构性和一级序列同源性。特别是,一个茎环类似于tRNA的TPsi(伪尿苷)分支,除了在第37位上存在鸟苷(编号从3'端开始)而不是在tRNA中存在经典的尿苷55外(编号是从5'端开始)。野生型TYMV-RNA片段和TYMV-mut G37U变体(其中G-37已被U-37取代)均已作为酵母tRNA修饰酶的潜在底物进行了测试。结果表明,在酵母提取物中温育野生型TYMV片段时,形成了两个修饰的核苷酸:一个在定量位置65定量形成的Psi,一个在U-38定量水平形成的核苷(T)。在TYMV突变体G37U中,除了定量形成Psi-65和T-38外,还在位置37检测到另外的Psi。TYMV RNA中修饰的核苷酸Psi-65,T-38和Psi-37与Psi等效。 tRNA中分别为-27,T-54和Psi-55。纯化的酵母重组tRNA:Pynynase(Pus1和Pus4)分别催化酵母tRNA中Psi-27和Psi-55的形成,分别催化tRNA中Psi-65和Psi-37的定量形成。 TYMV RNA体外的类3'-结构域。这些结果是与相应的酶催化这些转录后修饰反应所需的结构元件有关的。

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