Literature DB >> 1420150

Functional compensation of a recognition-defective transfer RNA by a distal base pair substitution.

Y M Hou1, P Schimmel.   

Abstract

A single G3:U70 base pair in the acceptor helix is the major determinant of alanine acceptance in alanine transfer RNAs. Transfer of this base pair into other transfer RNAs confers alanine acceptance. A G3:C70 substitution eliminates alanine acceptance in vivo and in vitro. In this work, a population of mutagenized G3:C70 alanine tRNA amber suppressors was subjected to a selection for mutations that compensate for the inactivating G3:C70 substitution. No compensatory mutations located in the acceptor helix were obtained. Instead, a U27:U43 substitution that replaced the wild-type C27:G43 in the anticodon stem created a U27:U43/G3:C70 mutant alanine tRNA that inserts alanine at amber codons in vivo. The U27:U43 substitution is at a location where previous footprinting work established an RNA-protein contact. Thus, this mutation may act by functionally coupling a distal part of the tRNA structure to the active site.

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Year:  1992        PMID: 1420150     DOI: 10.1021/bi00157a019

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  10 in total

1.  Specific atomic groups and RNA helix geometry in acceptor stem recognition by a tRNA synthetase.

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2.  Arginine aminoacylation identity is context-dependent and ensured by alternate recognition sets in the anticodon loop of accepting tRNA transcripts.

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3.  Genetic selection for active E.coli amber tRNA(Asn) exclusively led to glutamine inserting suppressors.

Authors:  F Martin; G Eriani; J Reinbolt; G Dirheimer; J Gangloff
Journal:  Nucleic Acids Res       Date:  1995-03-11       Impact factor: 16.971

4.  Search for characteristic structural features of mammalian mitochondrial tRNAs.

Authors:  M Helm; H Brulé; D Friede; R Giegé; D Pütz; C Florentz
Journal:  RNA       Date:  2000-10       Impact factor: 4.942

5.  The RNA sequence context defines the mechanistic routes by which yeast arginyl-tRNA synthetase charges tRNA.

Authors:  M Sissler; R Giegé; C Florentz
Journal:  RNA       Date:  1998-06       Impact factor: 4.942

Review 6.  Functions of the gene products of Escherichia coli.

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7.  Wide cross-species aminoacyl-tRNA synthetase replacement in vivo: yeast cytoplasmic alanine enzyme replaced by human polymyositis serum antigen.

Authors:  T L Ripmaster; K Shiba; P Schimmel
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8.  Compensatory mutations cause excess of antagonistic epistasis in RNA secondary structure folding.

Authors:  Claus O Wilke; Richard E Lenski; Christoph Adami
Journal:  BMC Evol Biol       Date:  2003-02-05       Impact factor: 3.260

9.  Extensive sequence turnover of the signal peptides of members of the GDF/BMP family: exploring their evolutionary landscape.

Authors:  Reiner A Veitia; Sandrine Caburet
Journal:  Biol Direct       Date:  2009-07-16       Impact factor: 4.540

10.  Relaxed sequence constraints favor mutational freedom in idiosyncratic metazoan mitochondrial tRNAs.

Authors:  Bernhard Kuhle; Joseph Chihade; Paul Schimmel
Journal:  Nat Commun       Date:  2020-02-20       Impact factor: 14.919

  10 in total

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