Literature DB >> 8510145

Recognition nucleotides of Escherichia coli tRNA(Leu) and its elements facilitating discrimination from tRNASer and tRNA(Tyr).

H Asahara1, H Himeno, K Tamura, T Hasegawa, K Watanabe, M Shimizu.   

Abstract

In order to study how Escherichia coli leucyl-tRNA synthetase recognizes tRNA(Leu) and discriminates it from the other two class II tRNAs, tRNA(Ser) and tRNA(Tyr), various mutations were introduced into class II tRNA transcripts. The discriminator base A73, but not the anticodon sequence, was found to serve as a critical recognition element of tRNA(Leu). A base substitution at the invariant nucleotide A14, but not at any of the other nucleotides characteristic of the E. coli tRNA(Leu) isoacceptors among the three class II tRNAs, caused significantly damaged aminoacylation with leucine. A two base-pair deletion in the long variable arm also resulted in no significant decrease of activity. Transplanting the three tertiary elements characteristic of E. coli tRNA(Leu) (i.e. the location of the G18G19 sequence in the D-loop, the A15 U48 base-pair and the stem pairing pattern of the long variable arm) besides the discriminator base change introduced the leucine charging activity in terms of Vmax/Km, up to 0.1 of that for the normal sequence of tRNA(Leu) into both tRNA(Ser) and tRNA(Tyr). These results indicate that A73 and A14 (or its vicinity) are involved in recognition by leucyl-tRNA synthetase, and that several tertiary elements play a significant role in the discrimination of tRNA(Leu) from the other two class II tRNAs.

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Year:  1993        PMID: 8510145     DOI: 10.1006/jmbi.1993.1277

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  37 in total

1.  Tertiary structure base pairs between D- and TpsiC-loops of Escherichia coli tRNA(Leu) play important roles in both aminoacylation and editing.

Authors:  Xing Du; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

2.  Two distinct domains of the beta subunit of Aquifex aeolicus leucyl-tRNA synthetase are involved in tRNA binding as revealed by a three-hybrid selection.

Authors:  Yong-Gang Zheng; Hui Wei; Chen Ling; Franck Martin; Gilbert Eriani; En-Duo Wang
Journal:  Nucleic Acids Res       Date:  2004-06-18       Impact factor: 16.971

3.  Anticodon-dependent conservation of bacterial tRNA gene sequences.

Authors:  Margaret E Saks; John S Conery
Journal:  RNA       Date:  2007-03-22       Impact factor: 4.942

4.  The crystal structure of the ternary complex of T.thermophilus seryl-tRNA synthetase with tRNA(Ser) and a seryl-adenylate analogue reveals a conformational switch in the active site.

Authors:  S Cusack; A Yaremchuk; M Tukalo
Journal:  EMBO J       Date:  1996-06-03       Impact factor: 11.598

5.  Overexpression, purification and crystallization of tyrosyl-tRNA synthetase from the hyperthermophilic archaeon Aeropyrum pernix K1.

Authors:  Jun Iwaki; Ryuichiro Suzuki; Zui Fujimoto; Mitsuru Momma; Atsushi Kuno; Tsunemi Hasegawa
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-10-25

6.  Bases in the anticodon loop of tRNA(Ala)(GGC) prevent misreading.

Authors:  Hiroshi Murakami; Atsushi Ohta; Hiroaki Suga
Journal:  Nat Struct Mol Biol       Date:  2009-03-22       Impact factor: 15.369

Review 7.  Structure, function and evolution of seryl-tRNA synthetases: implications for the evolution of aminoacyl-tRNA synthetases and the genetic code.

Authors:  M Härtlein; S Cusack
Journal:  J Mol Evol       Date:  1995-05       Impact factor: 2.395

8.  Identity elements of human tRNA(Leu): structural requirements for converting human tRNA(Ser) into a leucine acceptor in vitro.

Authors:  K Breitschopf; T Achsel; K Busch; H J Gross
Journal:  Nucleic Acids Res       Date:  1995-09-25       Impact factor: 16.971

9.  A Flexible peptide tether controls accessibility of a unique C-terminal RNA-binding domain in leucyl-tRNA synthetases.

Authors:  Jennifer L Hsu; Susan A Martinis
Journal:  J Mol Biol       Date:  2007-11-28       Impact factor: 5.469

10.  Chimeric tRNAs as tools to induce proteome damage and identify components of stress responses.

Authors:  Renaud Geslain; Laia Cubells; Teresa Bori-Sanz; Roberto Alvarez-Medina; David Rossell; Elisa Martí; Lluís Ribas de Pouplana
Journal:  Nucleic Acids Res       Date:  2009-12-08       Impact factor: 16.971

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