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

نویسندگان

  • Marie Messmer
  • Catherine Florentz
  • Hagen Schwenzer
  • Gert C Scheper
  • Marjo S van der Knaap
  • Laurence Maréchal-Drouard
  • Marie Sissler
چکیده

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.

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عنوان ژورنال:
  • The Biochemical journal

دوره 433 3  شماره 

صفحات  -

تاریخ انتشار 2011