Literature DB >> 2180700

The contacts of yeast tRNA(Ser) with seryl-tRNA synthetase studied by footprinting experiments.

A C Dock-Bregeon1, A Garcia, R Giegé, D Moras.   

Abstract

Yeast tRNA(Ser) is a member of the class II tRNAs, whose characteristic is the presence of an extended variable loop. This additional structural feature raises questions about the recognition of these class II tRNAs by their cognate synthetase and the possibility of the involvement of the extra arm in the recognition process. A footprinting study of yeast tRNA(Ser) complexed with its cognate synthetase, yeast seryl-tRNA synthetase (an alpha 2 dimer), was undertaken. Chemical (ethylnitrosourea) and enzymatic (nucleases S1 and V1) probes were used in the experiments. A map of the contact points between the tRNA and the synthetase was established and results were analyzed with respect to a three-dimensional model of yeast tRNA(Ser). Regions in close vicinity with the synthetase are clustered on one face of tRNA. The extra arm, which is strongly protected from chemical modifications, appears as an essential part of the contact area. The anticodon triplet and a large part of the anticodon arm are, in contrast, still accessible to the probes when the complex is formed. These results are discussed in the context of the recognition of tRNAs in the aminoacylation reaction.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2180700     DOI: 10.1111/j.1432-1033.1990.tb15401.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  14 in total

1.  Interaction of Escherichia coli tRNA(Ser) with its cognate aminoacyl-tRNA synthetase as determined by footprinting with phosphorothioate-containing tRNA transcripts.

Authors:  D Schatz; R Leberman; F Eckstein
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

2.  Eight base changes are sufficient to convert a leucine-inserting tRNA into a serine-inserting tRNA.

Authors:  J Normanly; T Ollick; J Abelson
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

3.  Conversion of aminoacylation specificity from tRNA(Tyr) to tRNA(Ser) in vitro.

Authors:  H Himeno; T Hasegawa; T Ueda; K Watanabe; M Shimizu
Journal:  Nucleic Acids Res       Date:  1990-12-11       Impact factor: 16.971

4.  Crystallization and preliminary X-ray diffraction analysis of human cytosolic seryl-tRNA synthetase.

Authors:  Jean Baptiste Artero; Susana C M Teixeira; Edward P Mitchell; Michael A Kron; V Trevor Forsyth; Michael Haertlein
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2010-10-29

5.  Aminoacyl-tRNA synthetase-induced cleavage of tRNA.

Authors:  S Beresten; M Jahn; D Söll
Journal:  Nucleic Acids Res       Date:  1992-04-11       Impact factor: 16.971

Review 6.  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

Review 7.  An operational RNA code for amino acids and possible relationship to genetic code.

Authors:  P Schimmel; R Giegé; D Moras; S Yokoyama
Journal:  Proc Natl Acad Sci U S A       Date:  1993-10-01       Impact factor: 11.205

8.  Idiosyncratic helix-turn-helix motif in Methanosarcina barkeri seryl-tRNA synthetase has a critical architectural role.

Authors:  Silvija Bilokapic; Nives Ivic; Vlatka Godinic-Mikulcic; Ivo Piantanida; Nenad Ban; Ivana Weygand-Durasevic
Journal:  J Biol Chem       Date:  2009-02-19       Impact factor: 5.157

9.  Coexpression of eukaryotic tRNASer and yeast seryl-tRNA synthetase leads to functional amber suppression in Escherichia coli.

Authors:  I Weygand-Durasević; M Nalaskowska; D Söll
Journal:  J Bacteriol       Date:  1994-01       Impact factor: 3.490

10.  Recognition of the bacterial second messenger cyclic diguanylate by its cognate riboswitch.

Authors:  Nadia Kulshina; Nathan J Baird; Adrian R Ferré-D'Amaré
Journal:  Nat Struct Mol Biol       Date:  2009-11-08       Impact factor: 15.369

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.