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首页> 外文期刊>Journal of Molecular Biology >MAJOR IDENTITY DETERMINANTS FOR ENZYMATIC FORMATION OF RIBOTHYMIDINE AND PSEUDOURIDINE IN THE T-PSI-LOOP OF YEAST TRNAS
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MAJOR IDENTITY DETERMINANTS FOR ENZYMATIC FORMATION OF RIBOTHYMIDINE AND PSEUDOURIDINE IN THE T-PSI-LOOP OF YEAST TRNAS

机译:酵母T-PSI-环中核糖嘧啶和假丝胺碱酶形成的主要同一性决定因素

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Almost all transfer RNA molecules sequenced so far contain two universal modified nucleosides at positions 54 and 55, respectively: ribothymidine (T-54) and pseudouridine (psi(55)). To identify the tRNA elements recognized by tRNA:m(5)uridine-54 methyltransferase and tRNA:pseudouridine-55 synthase from the yeast Saccharomyces cerevisiae, a set of 43 yeast tRNA(Asp) mutants were used. Some variants contained point mutations, while the others included progressive reductions in size down to a tRNA minisubstrate consisting of the T psi-loop with only one G . C base-pair as stem (9-mer). All substrates !full-sized tRNA(Asp) and various minihelices) were produced ill vitro by T7 transcription and tested using yeast extract (S100) as a source of enzymatic activities and S-adenosyl-L-methionine as a methyl donor. The results indicate that the minimal substrate for enzymatic formation of psi(55) is a stem/loop structure with only four G . C base-pairs in the stem, while a longer stem is required for efficient T-54 formation. None of the conserved nucleotides (G(53), C-56, A(58) and C-61) and U-54 for psi(55) or U-55 for T-54 formation can be replaced by any of the other three canonical nucleotides. Yeast tRNA:m(5)uridine-54 methyltransferase additionally requires the presence of a pyrimidine-60 in the loop. interestingly, in a tRNA(Asp) variant in which the T psi-loop was permuted Mi with the anticodon-loop, I;he new U-32 and U-33 residues derived from the T psi-loop were quantitatively converted to T-32 and psi(33), respectively. Structural mapping of this variant with ethylnitrosourea confirmed that the intrinsic characteristic structure of the T psi-loop was conserved upon permutation and that the displaced anticodon-loop did not acquire a T psi-loop structure. These results demonstrate that a local conformation rather than the exact location of the U-U sequence within the tRNA architecture is the important identity determinant for recognition by yeast tRNA:m(5)uridine-54 methyltransferase and tRNA:pseudouridine-55 synthase. (C) 1997 Academic Press Limited. [References: 53]
机译:到目前为止,几乎所有已测序的转移RNA分子在位置54和55处都包含两个通用的修饰核苷:核糖胸苷(T-54)和假尿苷(psi(55))。为了从酿酒酵母中鉴定出被tRNA:m(5)uridine-54甲基转移酶和tRNA:pseudouridine-55合酶识别的tRNA元件,使用了一组43个酵母tRNA(Asp)突变体。一些变体包含点突变,而其他变体包括大小逐渐减小到仅包含一个G的t psi环组成的tRNA微型底物。 C碱基对作为茎(9聚体)。通过T7转录在体外产生所有底物(全长tRNA(Asp)和各种小螺旋),并使用酵母提取物(S100)作为酶活性来源,并使用S-腺苷-L-蛋氨酸作为甲基供体进行测试。结果表明,酶促形成psi(55)的最小底物是只有四个G的茎/环结构。茎中有C个碱基对,而有效的T-54形成则需要更长的茎。 psi(55)的U-54或T-54形成的U-55的任何保守核苷酸(G(53),C-56,A(58)和C-61)和U-54均不能被其他任何一个取代三个规范核苷酸。酵母tRNA:m(5)尿苷54甲基转移酶还需要在环中存在嘧啶60。有趣的是,在一个tRNA(Asp)变体中,其中T psi环与反密码子环置换成Mi,I;从T psi环衍生的新U-32和U-33残基被定量转化为T- 32和psi(33)。该变异体与乙基亚硝基脲的结构图证实,排列后T psi环的固有特征结构得以保留,置换的反密码子环未获得T psi环结构。这些结果表明,在tRNA结构内局部构象而不是U-U序列的确切位置是酵母tRNA:m(5)尿苷-54甲基转移酶和tRNA:伪尿苷-55合酶识别的重要同一性决定因素。 (C)1997 Academic Press Limited。 [参考:53]

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