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The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNA.

机译:人线粒体tRNA的四叶形折叠需要修饰的核苷酸的存在。

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摘要

Direct sequencing of human mitochondrial tRNALysshows the absence of editing and the occurrence of six modified nucleotides (m1A9, m2G10, Psi27, Psi28 and hypermodified nucleotides at positions U34 and A37). This tRNA folds into the expected cloverleaf, as confirmed by structural probing with nucleases. The solution structure of the corresponding in vitro transcript unexpectedly does not fold into a cloverleaf but into an extended bulged hairpin. This non-canonical fold, established according to the reactivity to a large set of chemical and enzymatic probes, includes a 10 bp aminoacyl acceptor stem (the canonical 7 bp and 3 new pairs between residues 8-10 and 65-63), a 13 nt large loop and an anticodon-like domain. It is concluded that modified nucleotides have a predominant role in canonical folding of human mitochondrial tRNALys. Phylogenetic comparisons as well as structural probing of selected in vitro transcribed variants argue in favor of a major contribution of m1A9 in this process.
机译:人线粒体tRNALys的直接测序显示没有编辑,并且存在六个修饰的核苷酸(m1A9,m2G10,Psi27,Psi28和超修饰的核苷酸,位于U34和A37位)。该tRNA折叠成预期的苜蓿叶形,如通过核酸酶的结构探测所证实的。相应的体外转录本的溶液结构出乎意料地不会折叠成苜蓿叶形而是折叠成一个伸出的凸起的发夹。根据与大量化学和酶探针的反应性而建立的这种非经典折叠,包括一个10 bp的氨酰基受体茎(在残基8-10和65-63之间为经典的7 bp和3对新对),一个13 nt大环和反密码子样结构域。结论是,修饰的核苷酸在人线粒体tRNALys的标准折叠中起主要作用。系统发育比较以及所选体外转录变异的结构探测表明,m1A9在这一过程中起了重要作用。

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