A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria

Biochem J. 2011 Feb 1;433(3):441-6. doi: 10.1042/BJ20101902.

Abstract

Mutations in the nuclear gene coding for the mitochondrial aspartyl-tRNA synthetase, a key enzyme for mitochondrial translation, are correlated with leukoencephalopathy. A Ser⁴⁵ to Gly⁴⁵ mutation is located in the predicted targeting signal of the protein. We demonstrate in the present study, by in vivo and in vitro approaches, that this pathology-related mutation impairs the import process across mitochondrial membranes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspartate-tRNA Ligase / genetics*
  • Aspartate-tRNA Ligase / metabolism*
  • Cell Line
  • Humans
  • Leukoencephalopathies / etiology
  • Leukoencephalopathies / genetics
  • Mitochondria / metabolism*
  • Mutation, Missense*
  • Protein Transport

Substances

  • Aspartate-tRNA Ligase