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Naturally occurring aminoacyl-tRNA synthetases editing-domain mutations that cause mistranslation in Mycoplasma parasites.
Li, Li; Boniecki, Michal T; Jaffe, Jacob D; Imai, Brian S; Yau, Peter M; Luthey-Schulten, Zaida A; Martinis, Susan A.
Affiliation
  • Li L; Center for Biophysics and Computational Biology, Department of Biochemistry, University of Illinois, Urbana, IL 61801, USA.
Proc Natl Acad Sci U S A ; 108(23): 9378-83, 2011 Jun 07.
Article in En | MEDLINE | ID: mdl-21606343
Mycoplasma parasites escape host immune responses via mechanisms that depend on remarkable phenotypic plasticity. Identification of these mechanisms is of great current interest. The aminoacyl-tRNA synthetases (AARSs) attach amino acids to their cognate tRNAs, but occasionally make errors that substitute closely similar amino acids. AARS editing pathways clear errors to avoid mistranslation during protein synthesis. We show here that AARSs in Mycoplasma parasites have point mutations and deletions in their respective editing domains. The deleterious effect on editing was confirmed with a specific example studied in vitro. In vivo mistranslation was determined by mass spectrometric analysis of proteins produced in the parasite. These mistranslations are uniform cases where the predicted closely similar amino acid replaced the correct one. Thus, natural AARS editing-domain mutations in Mycoplasma parasites cause mistranslation. We raise the possibility that these mutations evolved as a mechanism for antigen diversity to escape host defense systems.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Biosynthesis / Amino Acyl-tRNA Synthetases / Mutation / Mycoplasma Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2011 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein Biosynthesis / Amino Acyl-tRNA Synthetases / Mutation / Mycoplasma Limits: Animals / Humans Language: En Journal: Proc Natl Acad Sci U S A Year: 2011 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos