Potential dual targeting of an Arabidopsis archaebacterial-like histidyl-tRNA synthetase to mitochondria and chloroplasts

被引:68
作者
Akashi, K [1 ]
Grandjean, O [1 ]
Small, I [1 ]
机构
[1] INRA, Genet & Ameliorat Plantes Stn, F-78026 Versailles, France
基金
日本学术振兴会;
关键词
histidyl-tRNA synthetase; mitochondrial protein import; chloroplast transit peptide; GFP; confocal microscopy; Arabidopsis thaliana;
D O I
10.1016/S0014-5793(98)00717-0
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
A cDNA clone encoding a histidyl-tRNA synthetase (HisRS) mas characterized from Arabinopsis thaliana. The deduced amino acid sequence (AtHRS1) is surprisingly more similar to HisRSs from archaebacteria than those from eukaryotes and prokaryotes. AtHRS1 has an N-terminal extension with features characteristic of mitochondrial and chloroplast transit peptides, Transient expression assays in tobacco protoplasts clearly demonstrated efficient targeting of a fusion peptide consisting of the first 71 amino acids of AtHRS1 joined to jellyfish green fluorescent protein (GFP) to both mitochondria and chloroplasts. These observations suggest that the AtHisRS1 cDNA encodes both mitochondrial and chloroplast histidyl-tRNA synthetases. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:39 / 44
页数:6
相关论文
共 36 条
[1]   Crystal structure analysis of the activation of histidine by Thermus thermophilus histidyl-tRNA synthetase [J].
Aberg, A ;
Yaremchuk, A ;
Tukalo, M ;
Rasmussen, B ;
Cusack, S .
BIOCHEMISTRY, 1997, 36 (11) :3084-3094
[2]  
AKASHI K, 1997, PLANT PHYSIOL, V113, P1464
[3]   CRYSTAL-STRUCTURE OF HISTIDYL-TRANSFER-RNA SYNTHETASE FROM ESCHERICHIA-COLI COMPLEXED WITH HISTIDYL-ADENYLATE [J].
ARNEZ, JG ;
HARRIS, DC ;
MITSCHLER, A ;
REES, B ;
FRANCKLYN, CS ;
MORAS, D .
EMBO JOURNAL, 1995, 14 (17) :4143-4155
[4]  
BRINKS S, 1994, J BIOL CHEM, V269, P16478
[5]   TRANSFER RNA-MEDIATED SUPPRESSION OF STOP CODONS IN PROTOPLASTS AND TRANSGENIC PLANTS [J].
CARNEIRO, VTC ;
PELLETIER, G ;
SMALL, I .
PLANT MOLECULAR BIOLOGY, 1993, 22 (04) :681-690
[6]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[7]   A single precursor protein for ferrochelatase-I from Arabidopsis is imported in vitro into both chloroplasts and mitochondria [J].
Chow, KS ;
Singh, DP ;
Roper, JM ;
Smith, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :27565-27571
[8]   Computational method to predict mitochondrially imported proteins and their targeting sequences [J].
Claros, MG ;
Vincens, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 241 (03) :779-786
[9]   SIMULTANEOUS TARGETING OF PEA GLUTATHIONE-REDUCTASE AND OF A BACTERIAL FUSION PROTEIN TO CHLOROPLASTS AND MITOCHONDRIA IN TRANSGENIC TOBACCO [J].
CREISSEN, G ;
REYNOLDS, H ;
XUE, YB ;
MULLINEAUX, P .
PLANT JOURNAL, 1995, 8 (02) :167-175
[10]   A single base change prevents import of cytosolic tRNA(Ala) into mitochondria in transgenic plants [J].
Dietrich, A ;
MarechalDrouard, L ;
Carneiro, V ;
Cosset, A ;
Small, I .
PLANT JOURNAL, 1996, 10 (05) :913-918