Literature DB >> 11680848

tRNA recognition by tRNA-guanine transglycosylase from Escherichia coli: the role of U33 in U-G-U sequence recognition.

S T Nonekowski1, G A Garcia.   

Abstract

In eubacteria, the biosynthesis of queuine, a modified base found in the wobble position (#34) of tRNAs coding for Tyr, His, Asp, and Asn, occurs via a multistep pathway. One of the key enzymes in this pathway, tRNA-guanine transglycosylase (TGT), exchanges the genetically encoded guanine at position 34 with a queuine precursor, preQ1. Previous studies have identified a minimal positive RNA recognition motif for Escherichia coli TGT consisting of a stable minihelix that contains a U-G-U sequence starting at the second position of its seven base anticodon loop. Recently, we reported that TGT was capable of recognizing the U-G-U sequence outside of this limited structural context. To further characterize the ability of TGT to recognize the U-G-U sequence in alternate contexts, we constructed mutants of the previously characterized E. coli tRNA(Tyr) minihelix. The U-G-U sequence was shifted to various positions within the anticodon loop of these mutants. Characterization of these analogs demonstrates that in addition to the normal U33G34U35 position, TGT can also recognize the U34G35U36 analog (UGU(+1)). The other analogs were not active. This indicates that the recognition of the U-G-U sequence is not strictly dependent upon its position relative to the stem. In E. coli, the full-length tRNA with a U34G35U36 anticodon sequence is one of the isoacceptors that codes for threonine. We found that TGT is able to recognize tRNA(Thr(UGU)) but only in the absence of a uridine at position 33. U33, an invariant base present in all tRNAs, has been shown to strongly influence the conformation of the anticodon loop of certain tRNAs. We find that mutation of this base confers on TGT the ability to recognize U34G35U36, and suggests that loop conformation affects recognition. The fact that the other analogs were not active indicates that although TGT is capable of recognizing the U-G-U sequence in additional contexts, this recognition is not indiscriminate.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11680848      PMCID: PMC1370187     

Source DB:  PubMed          Journal:  RNA        ISSN: 1355-8382            Impact factor:   4.942


  52 in total

Review 1.  Structural motifs in RNA.

Authors:  P B Moore
Journal:  Annu Rev Biochem       Date:  1999       Impact factor: 23.643

2.  Isolation and characterization of a guanine insertion enzyme, a specific tRNA transglycosylase, from Escherichia coli.

Authors:  N Okada; S Nishimura
Journal:  J Biol Chem       Date:  1979-04-25       Impact factor: 5.157

3.  Structure of a hexanucleotide RNA hairpin loop conserved in ribosomal RNAs.

Authors:  S Huang; Y X Wang; D E Draper
Journal:  J Mol Biol       Date:  1996-05-03       Impact factor: 5.469

4.  tRNA-guanine transglycosylase from Escherichia coli: recognition of noncognate-cognate chimeric tRNA and discovery of a novel recognition site within the TpsiC arm of tRNA(Phe).

Authors:  F L Kung; S Nonekowski; G A Garcia
Journal:  RNA       Date:  2000-02       Impact factor: 4.942

5.  Nucleotide sequence of threonine tRNA from Bacillus subtilis.

Authors:  T Hasegawa; H Ishikura
Journal:  Nucleic Acids Res       Date:  1978-02       Impact factor: 16.971

6.  Specific function of a G.U wobble pair from an adjacent helical site in tRNA(Ala) during recognition by alanyl-tRNA synthetase.

Authors:  W H McClain; K Gabriel; J Schneider
Journal:  RNA       Date:  1996-02       Impact factor: 4.942

7.  Structural domains of transfer RNA molecules.

Authors:  G J Quigley; A Rich
Journal:  Science       Date:  1976-11-19       Impact factor: 47.728

8.  Specific replacement of Q base in the anticodon of tRNA by guanine catalyzed by a cell-free extract of rabbit reticulocytes.

Authors:  N Okada; F Harada; S Nishimura
Journal:  Nucleic Acids Res       Date:  1976-10       Impact factor: 16.971

9.  Synthesis of aspartyl-tRNA(Asp) in Escherichia coli--a snapshot of the second step.

Authors:  S Eiler; A Dock-Bregeon; L Moulinier; J C Thierry; D Moras
Journal:  EMBO J       Date:  1999-11-15       Impact factor: 11.598

10.  Novel mechanism of post-transcriptional modification of tRNA. Insertion of bases of Q precursors into tRNA by a specific tRNA transglycosylase reaction.

Authors:  N Okada; S Noguchi; H Kasai; N Shindo-Okada; T Ohgi; T Goto; S Nishimura
Journal:  J Biol Chem       Date:  1979-04-25       Impact factor: 5.157

View more
  4 in total

Review 1.  Probing the intermediacy of covalent RNA enzyme complexes in RNA modification enzymes.

Authors:  Stephanie M Chervin; Jeffrey D Kittendorf; George A Garcia
Journal:  Methods Enzymol       Date:  2007       Impact factor: 1.600

2.  Identification of the rate-determining step of tRNA-guanine transglycosylase from Escherichia coli.

Authors:  George A Garcia; Stephanie M Chervin; Jeffrey D Kittendorf
Journal:  Biochemistry       Date:  2009-12-01       Impact factor: 3.162

Review 3.  Transglycosylation: a mechanism for RNA modification (and editing?).

Authors:  George A Garcia; Jeffrey D Kittendorf
Journal:  Bioorg Chem       Date:  2005-02-23       Impact factor: 5.275

4.  Site-specific modification of Shigella flexneri virF mRNA by tRNA-guanine transglycosylase in vitro.

Authors:  Julie K Hurt; Sureyya Olgen; George A Garcia
Journal:  Nucleic Acids Res       Date:  2007-07-10       Impact factor: 16.971

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.