A pathogenic point mutation reduces stability of mitochondrial mutant tRNAlle

被引:47
作者
Yasukawa, T
Hino, N
Suzuki, T
Watanabe, K
Ueda, T
Ohta, S [1 ]
机构
[1] Nippon Med Sch, Inst Gerontol, Dept Biochem & Cell Biol, Nakahara Ku, Kawasaki, Kanagawa 2118533, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
[3] Univ Tokyo, Grad Sch Frontier Sci, Dept Integrated Biosci, Bunkyo Ku, Tokyo 1138656, Japan
关键词
D O I
10.1093/nar/28.19.3779
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Point mutations in mitochondrial tRNA genes are responsible for individual subgroups of mitochondrial encephalomyopathies, We have recently reported that point mutations in the tRNA(Leu)(UUR) and tRNA(Lys) genes cause a defect in the normal modification at the first nucleotide of the anticodon, As part of a systematic analysis of pathogenic mutant mitochondrial tRNAs, we purified tRNA(lle) with a point mutation at nucleotide 4269 to determine its nucleotide sequence, including modified nucleotides, We found that, instead of causing a defect in the post-transcriptional modification, a pathogenic point mutation in the mitochondrial tRNA(lle) reduced the stability of the mutant tRNA molecule, resulting in a low steady-state level of aminoacyl-tRNA. The reduced stability was confirmed by examining the life-span of the mutant tRNA(lle) both in vitro and in vivo, as well as by monitoring its melting profile. Our finding indicates that the mutant tRNA(lle) itself is intrinsically unstable.
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页码:3779 / 3784
页数:6
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