Major identity determinants in the ''augmented D helix'' of tRNA(Glu) from Escherichia coli

被引:60
作者
Sekine, S
Nureki, O
Sakamoto, K
Niimi, T
Tateno, M
Go, M
Kohno, T
Brisson, A
Lapointe, J
Yokoyama, S
机构
[1] UNIV TOKYO, SCH SCI, DEPT BIOPHYS & BIOCHEM, BUNKYO KU, TOKYO 113, JAPAN
[2] NAGOYA UNIV, FAC SCI, DEPT BIOL, CHIKUSA KU, NAGOYA, AICHI 46401, JAPAN
[3] UNIV LAVAL, FAC SCI & GENIE, DEPT BIOCHIM, Ste Foy, PQ G1K 7P4, CANADA
关键词
aminoacyl-tRNA synthetase; footprinting; steady-state kinetics; tRNA identity; tRNA variant;
D O I
10.1006/jmbi.1996.0118
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
By a kinetic analysis of 59 variant transcripts of Escherichia coli tRNA(Glu) with glutamyl-tRNA synthetase (GluRS), the U11 . A24 base-pair, the U13 . G22 .. A46 base-triple, and the lack of residue 47 (Delta 47) were found to serve as major determinants for tRNA(Glu) identity. This is the first system for which major identity determinants are reported to be clustered in the ''augmented D helix'', consisting of the D stem with some neighboring residues and the variable loop. Other identity determinants are U34, U35, C36 and A37 in the anticodon loop, and G1 . C72 and U2 . A71 in the acceptor stem. Phosphate-group protection by GluRS from ethylnitrosourea was observed most strongly for the minor groove side of D-stem helix, indicating that GluRS tightly binds to the D stem for recognition, on the minor groove side, of the potent identity-determinant groups of the U11 . A24 and U13 . G22 base-pairs. A46 is not involved in direct recognition by GluRS; the U13 . G22 .. A46 base-triple is required probably for formation of the structural features that are recognized by GluRS. In this context, the essential role of Characteristic Delta 47 in tRNA(Glu) identity may be to maintain the U13 . G22 .. A46 base-triple. (C) 1996 Academic Press Limited
引用
收藏
页码:685 / 700
页数:16
相关论文
共 79 条
[1]   BIOLOGICAL FUNCTION OF 2-THIOURIDINE IN ESCHERICHIA-COLI GLUTAMIC-ACID TRANSFER RIBONUCLEIC-ACID [J].
AGRIS, PF ;
SOLL, D ;
SENO, T .
BIOCHEMISTRY, 1973, 12 (22) :4331-4337
[2]   ESCHERICHIA-COLI SERYL-TRANSFER-RNA SYNTHETASE RECOGNIZES TRNA(SER) BY ITS CHARACTERISTIC TERTIARY STRUCTURE [J].
ASAHARA, H ;
HIMENO, H ;
TAMURA, K ;
NAMEKI, N ;
HASEGAWA, T ;
SHIMIZU, M .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 236 (03) :738-748
[3]   THE 2.9 ANGSTROM CRYSTAL-STRUCTURE OF THERMUS-THERMOPHILUS SERYL-TRANSFER-RNA SYNTHETASE COMPLEXED WITH TRNA(SER) [J].
BIOU, V ;
YAREMCHUK, A ;
TUKALO, M ;
CUSACK, S .
SCIENCE, 1994, 263 (5152) :1404-1410
[4]  
BRETON R, 1990, J BIOL CHEM, V265, P18248
[5]  
BRETON R, 1986, J BIOL CHEM, V261, P610
[6]  
BRISSON A, 1992, THESIS U LAVAL QUEBE
[7]   YEAST TRANSFER RNA(ASP) RECOGNITION BY ITS COGNATE CLASS-II AMINOACYL-TRANSFER RNA-SYNTHETASE [J].
CAVARELLI, J ;
REES, B ;
RUFF, M ;
THIERRY, JC ;
MORAS, D .
NATURE, 1993, 362 (6416) :181-184
[8]   PARTITION OF TRANSFER-RNA SYNTHETASES INTO 2 CLASSES BASED ON MUTUALLY EXCLUSIVE SETS OF SEQUENCE MOTIFS [J].
ERIANI, G ;
DELARUE, M ;
POCH, O ;
GANGLOFF, J ;
MORAS, D .
NATURE, 1990, 347 (6289) :203-206
[9]   THE MIDAS DISPLAY SYSTEM [J].
FERRIN, TE ;
HUANG, CC ;
JARVIS, LE ;
LANGRIDGE, R .
JOURNAL OF MOLECULAR GRAPHICS, 1988, 6 (01) :13-&
[10]   AMINOACYLATION OF RNA MINIHELICES WITH ALANINE [J].
FRANCKLYN, C ;
SCHIMMEL, P .
NATURE, 1989, 337 (6206) :478-481