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

Authors :
Marie Messmer
Catherine Florentz
Hagen Schwenzer
Gert C. Scheper
Marjo S. van der Knaap
Laurence Maréchal‑Drouard
Marie Sissler
Source :
Biochemical Journal; Jan2011, Vol. 433 Issue 3, p441-446, 6p
Publication Year :
2011

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02646021
Volume :
433
Issue :
3
Database :
Complementary Index
Journal :
Biochemical Journal
Publication Type :
Academic Journal
Accession number :
57544009
Full Text :
https://doi.org/10.1042/BJ20101902