Nucleic Acids Research, Vol 26, Issue 7 1636-1643, Copyright © 1998 by Oxford University Press
M Helm, H Brule, F Degoul, C Cepanec, JP Leroux, R Giege and C Florentz
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.
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The presence of modified nucleotides is required for cloverleaf folding of a human mitochondrial tRNA
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