Search for characteristic structural features of mammalian mitochondrial tRNAs

被引:248
作者
Helm, M
Brulé, H
Friede, D
Giegé, R
Pütz, D
Florentz, C
机构
[1] CNRS, Inst Biol Mol & Cellulaire, UPR 9002, Dept Mecanismes & Macromol Synth Prot & Cristallo, F-67084 Strasbourg, France
[2] Inst Theoret Chem, A-1090 Vienna, Austria
关键词
aminoacylation identity; bizarre tRNAs; compilation; G-U pairs; neurodegenerative disorders; T-loop;
D O I
10.1017/S1355838200001047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A number of mitochondrial (mt) tRNAs have strong structural deviations from the classical tRNA cloverleaf secondary structure and from the conventional L-shaped tertiary structure, As a consequence, there is a general trend to consider all mitochondrial tRNAs as "bizarre" tRNAs, Here, a large sequence comparison of the 22 tRNA genes within 31 fully sequenced mammalian mt genomes has been performed to define the structural characteristics of this specific group of tRNAs, Vertical alignments define the degree of conservation/variability of primary sequences and secondary structures and search for potential tertiary interactions within each of the 22 families, Further horizontal alignments ascertain that, with the exception of serine-specific tRNAs, mammalian mt tRNAs do fold into cloverleaf structures with mostly classical features. However, deviations exist and concern large variations in size of the D- and T-loops. The predominant absence of the conserved nucleotides G18G19 and T54T55C56, respectively in these loops, suggests that classical tertiary interactions between both domains do not take place, Classification of the tRNA sequences according to their genomic origin (G-rich or G-poor DNA strand) highlight specific features such as richness/poorness in mismatches or G-T pairs in stems and extremely low G-content or C-content in the D- and T-loops. The resulting 22 "typical" mammalian mitochondrial sequences built up a phylogenetic basis for experimental structural and functional investigations. Moreover, they are expected to help in the evaluation of the possible impacts of those point mutations detected in human mitochondrial tRNA genes and correlated with pathologies.
引用
收藏
页码:1356 / 1379
页数:24
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