| Literature DB >> 25913036 |
Alice Hadchouel1, Thomas Wieland2, Matthias Griese3, Enrico Baruffini4, Bettina Lorenz-Depiereux2, Laurent Enaud5, Elisabeth Graf2, Jean Christophe Dubus6, Sonia Halioui-Louhaichi7, Aurore Coulomb8, Christophe Delacourt9, Gertrud Eckstein2, Ralf Zarbock3, Thomas Schwarzmayr2, François Cartault10, Thomas Meitinger11, Tiziana Lodi4, Jacques de Blic12, Tim M Strom13.
Abstract
Methionyl-tRNA synthetase (MARS) catalyzes the ligation of methionine to tRNA and is critical for protein biosynthesis. We identified biallelic missense mutations in MARS in a specific form of pediatric pulmonary alveolar proteinosis (PAP), a severe lung disorder that is prevalent on the island of Réunion and the molecular basis of which is unresolved. Mutations were found in 26 individuals from Réunion and nearby islands and in two families from other countries. Functional consequences of the mutated alleles were assessed by growth of wild-type and mutant strains and methionine-incorporation assays in yeast. Enzyme activity was attenuated in a liquid medium without methionine but could be restored by methionine supplementation. In summary, identification of a founder mutation in MARS led to the molecular definition of a specific type of PAP and will enable carrier screening in the affected community and possibly open new treatment opportunities.Entities:
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Year: 2015 PMID: 25913036 PMCID: PMC4570277 DOI: 10.1016/j.ajhg.2015.03.010
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025