Dual mode recognition of two isoacceptor tRNAs by mammalian mitochondrial seryl-tRNA synthetase

被引:50
作者
Shimada, N
Suzuki, T
Watanabe, K
机构
[1] Univ Tokyo, Dept Chem & Biotechnol, Grad Sch Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Univ Tokyo, Dept Integrated Biosci, Grad Sch Frontier Sci, Kashiwa, Chiba 2778583, Japan
关键词
D O I
10.1074/jbc.M105150200
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
Animal mitochondrial translation systems contain two serine tRNAs, corresponding to the codons AGY (Y = U and C) and UCN (N = U, C, A, and G), each possessing an unusual secondary structure; tRNA(GCU)(Ser) (for AGY) lacks the entire D arm, whereas tRNA(UGA)(Ser) (for UCN) has an unusual cloverleaf configuration. We previously demonstrated that a single bovine mitochondrial seryl-tRNA synthetase (mt SerRS) recognizes these topologically distinct isoacceptors having no common sequence or structure. Recombinant mt SerRS clearly footprinted at the T PsiC loop of each isoacceptor, and kinetic studies revealed that mt SerRS specifically recognized the T PsiC loop sequence in each isoacceptor. However, in the case of tRNA(UGA)(Ser), T PsiC loop-D loop interaction was further required for recognition, suggesting that mt SerRS recognizes the two substrates by distinct mechanisms. mt SerRS could slightly but significantly misacylate mitochondrial tRNA(Gln), which has the same T PsiC loop sequence as tRNA(UGA)(Ser), implying that the fidelity of mitochondrial translation is maintained by kinetic discrimination of tRNAs in the network of aminoacyl-tRNA synthetases.
引用
收藏
页码:46770 / 46778
页数:9
相关论文
共 48 条
[12]   AMINOACYLATION OF RNA MINIHELICES WITH ALANINE [J].
FRANCKLYN, C ;
SCHIMMEL, P .
NATURE, 1989, 337 (6206) :478-481
[13]   Expression of bovine mitochondrial tRNA(GCU)(Ser) derivatives in Escherichia coli [J].
Hayashi, I ;
Kawai, G ;
Watanabe, K .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3503-3507
[14]   Higher-order structure and thermal instability of bovine mitochondrial tRNASerUGA investigated by proton NMR spectroscopy [J].
Hayashi, I ;
Kawai, G ;
Watanabe, K .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 284 (01) :57-69
[15]   CONVERSION OF AMINOACYLATION SPECIFICITY FROM TRANSFER RNA(TYR) TO TRANSFER RNA(SER) INVITRO [J].
HIMENO, H ;
HASEGAWA, T ;
UEDA, T ;
WATANABE, K ;
SHIMIZU, M .
NUCLEIC ACIDS RESEARCH, 1990, 18 (23) :6815-6819
[16]   Only one nucleotide insertion to the long variable arm confers an efficient serine acceptor activity upon Saccharomyces cerevisiae tRNA(Leu) in vitro [J].
Himeno, H ;
Yoshida, S ;
Soma, A ;
Nishikawa, K .
JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (04) :704-711
[17]   In vitro selected RNA molecules that bind to elongation factor Tu [J].
Hornung, V ;
Hofmann, HP ;
Sprinzl, M .
BIOCHEMISTRY, 1998, 37 (20) :7260-7267
[18]   THE CODON CUG IS READ AS SERINE IN AN ASPOROGENIC YEAST CANDIDA-CYLINDRACEA [J].
KAWAGUCHI, Y ;
HONDA, H ;
TANIGUCHIMORIMURA, J ;
IWASAKI, S .
NATURE, 1989, 341 (6238) :164-166
[19]   UNILATERAL AMINOACYLATION SPECIFICITY BETWEEN BOVINE MITOCHONDRIA AND EUBACTERIA [J].
KUMAZAWA, Y ;
HIMENO, H ;
MIURA, KI ;
WATANABE, K .
JOURNAL OF BIOCHEMISTRY, 1991, 109 (03) :421-427
[20]   tRNA recognition and evolution of determinants in seryl-tRNA synthesis [J].
Lenhard, B ;
Orellana, O ;
Ibba, M ;
Weygand-Durasevic, I .
NUCLEIC ACIDS RESEARCH, 1999, 27 (03) :721-729