A pathogenic point mutation reduces stability of mitochondrial mutant tRNA(Ile)

Takehiro Yasukawa, Narumi Hino, Tsutomu Suzuki, Kimitsuna Watanabe, Takuya Ueda, Shigeo Ohta*

*この研究の対応する著者

研究成果: Article査読

48 被引用数 (Scopus)

抄録

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(Ile) 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(Ile) 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(Ile) both in vitro and in vivo, as well as by monitoring its melting profile. Our finding indicates that the mutant tRNA(Ile) itself is intrinsically unstable.

本文言語English
ページ(範囲)3779-3784
ページ数6
ジャーナルNucleic acids research
28
19
DOI
出版ステータスPublished - 2000 10 1
外部発表はい

ASJC Scopus subject areas

  • 遺伝学

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