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Molecular mechanism of lysidine synthesis that determines tRNA identity and codon recognition

机译:赖氨酸合成的分子机制决定了tRNA的同一性和密码子识别

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摘要

Lysidine (2-lysyl cytidine) is a lysine-containing cytidine derivative commonly found at the wobble position of bacterial AUA codon-specific tRNAIle. This modification determines both codon and amino acid specificities of tRNA(IIe). We previously identified tRNA(IIe)-lySidine synthetase (HIS) that synthesizes lysidine, for which it utilizes ATP and lysine as substrates. Here, we show that lysidine synthesis consists of two consecutive reactions that involve an adenylated tRNA intermediate. A mutation study revealed that Escherichia coli TilS discriminates tRNA(IIe) from the structurally similar tRNAMet having the same anticodon loop by recognizing the anticodon loop, the anticodon stem, and the acceptor stem. TilS was shown to bind to the anticodon region and 3' side of the acceptor stem, which cover the recognition sites. These findings reveal a dedicated mechanism embedded in tRNAIIe that controls its recognition and discrimination by TilS, and indicate the significance of this enzyme in the proper deciphering of genetic information.
机译:赖氨酸(2-赖氨酰胞苷)是一种含赖氨酸的胞苷衍生物,通常存在于细菌AUA密码子特异性tRNAIle的摆动位置。这种修饰决定了tRNA(IIe)的密码子和氨基酸特异性。我们之前鉴定了tRNA(IIe)-赖氨酸合成酶(HIS),该酶合成赖氨酸,利用ATP和赖氨酸作为底物。在这里,我们表明赖氨酸的合成是由两个连续的反应组成的,这些反应涉及腺苷酸化的tRNA中间体。一项突变研究表明,大肠杆菌TilS通过识别反密码子环,反密码子茎和受体茎,将tRNA(IIe)与具有相同反密码子环的结构相似的tRNAMet区分开。 TilS已显示与覆盖识别位点的反密码子区域和受体茎的3'侧结合。这些发现揭示了嵌入tRNAIIe的专用机制,该机制控制着TilS对它的识别和区分,并表明该酶在正确解密遗传信息中的重要性。

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