Literature DB >> 7607232

Mitochondrial and cytoplasmic isoleucyl-, glutamyl- and arginyl-tRNA synthetases of yeast are encoded by separate genes.

A Tzagoloff1, A Shtanko.   

Abstract

Three complementation groups of a pet mutant collection have been found to be composed of respiratory-deficient deficient mutants with lesions in mitochondrial protein synthesis. Recombinant plasmids capable of restoring respiration were cloned by transformation of representatives of each complementation group with a yeast genomic library. The plasmids were used to characterize the complementing genes and to institute disruption of the chromosomal copies of each gene in respiratory-proficient yeast. The sequences of the cloned genes indicate that they code for isoleucyl-, arginyl- and glutamyl-tRNA synthetases. The properties of the mutants used to obtain the genes and of strains with the disrupted genes indicate that all three aminoacyl-tRNA synthetases function exclusively in mitochondrial proteins synthesis. The ISM1 gene for mitochondrial isoleucyl-tRNA synthetase has been localized to chromosome XVI next to UME5. The MSR1 gene for the arginyl-tRNA synthetase was previously located on yeast chromosome VIII. The third gene MSE1 for the mitochondrial glutamyl-tRNA synthetase has not been localized. The identification of three new genes coding for mitochondrial-specific aminoacyl-tRNA synthetases indicates that in Saccharomyces cerevisiae at least 11 members of this protein family are encoded by genes distinct from those coding for the homologous cytoplasmic enzymes.

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Year:  1995        PMID: 7607232     DOI: 10.1111/j.1432-1033.1995.tb20599.x

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


  8 in total

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2.  Saccharomyces cerevisiae imports the cytosolic pathway for Gln-tRNA synthesis into the mitochondrion.

Authors:  Jesse Rinehart; Bethany Krett; Mary Anne T Rubio; Juan D Alfonzo; Dieter Söll
Journal:  Genes Dev       Date:  2005-02-10       Impact factor: 11.361

3.  An efficient genetic screen in Drosophila to identify nuclear-encoded genes with mitochondrial function.

Authors:  T S Vivian Liao; Gerald B Call; Preeta Guptan; Albert Cespedes; Jamie Marshall; Kevin Yackle; Edward Owusu-Ansah; Sudip Mandal; Q Angela Fang; Gelsey L Goodstein; William Kim; Utpal Banerjee
Journal:  Genetics       Date:  2006-07-18       Impact factor: 4.562

4.  In vivo selection of lethal mutations reveals two functional domains in arginyl-tRNA synthetase.

Authors:  R Geslain; F Martin; B Delagoutte; J Cavarelli; J Gangloff; G Eriani
Journal:  RNA       Date:  2000-03       Impact factor: 4.942

5.  Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.

Authors:  Sarah B Pierce; Karen M Chisholm; Eric D Lynch; Ming K Lee; Tom Walsh; John M Opitz; Weiqing Li; Rachel E Klevit; Mary-Claire King
Journal:  Proc Natl Acad Sci U S A       Date:  2011-04-04       Impact factor: 11.205

Review 6.  Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies.

Authors:  Paulien Smits; Jan Smeitink; Lambert van den Heuvel
Journal:  J Biomed Biotechnol       Date:  2010-04-13

7.  Yeast mitochondrial Gln-tRNA(Gln) is generated by a GatFAB-mediated transamidation pathway involving Arc1p-controlled subcellular sorting of cytosolic GluRS.

Authors:  Mathieu Frechin; Bruno Senger; Mélanie Brayé; Daniel Kern; Robert Pierre Martin; Hubert Dominique Becker
Journal:  Genes Dev       Date:  2009-05-01       Impact factor: 11.361

8.  Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia.

Authors:  Simon Edvardson; Avraham Shaag; Olga Kolesnikova; John Moshe Gomori; Ivan Tarassov; Tom Einbinder; Ann Saada; Orly Elpeleg
Journal:  Am J Hum Genet       Date:  2007-08-24       Impact factor: 11.025

  8 in total

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