Literature DB >> 25913036

Biallelic Mutations of Methionyl-tRNA Synthetase Cause a Specific Type of Pulmonary Alveolar Proteinosis Prevalent on Réunion Island.

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.
Copyright © 2015 The American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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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


  22 in total

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Journal:  J Mol Biol       Date:  1999-12-17       Impact factor: 5.469

Review 2.  Pulmonary alveolar proteinosis.

Authors:  Bruce C Trapnell; Jeffrey A Whitsett; Koh Nakata
Journal:  N Engl J Med       Date:  2003-12-25       Impact factor: 91.245

3.  Site-directed mutagenesis by overlap extension using the polymerase chain reaction.

Authors:  S N Ho; H D Hunt; R M Horton; J K Pullen; L R Pease
Journal:  Gene       Date:  1989-04-15       Impact factor: 3.688

4.  Role for a conserved structural motif in assembly of a class I aminoacyl-tRNA synthetase active site.

Authors:  Veronica C Casina; Andrew A Lobashevsky; William E McKinney; Cassidy L Brown; Rebecca W Alexander
Journal:  Biochemistry       Date:  2011-01-11       Impact factor: 3.162

5.  Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders.

Authors:  Gaia Novarino; Ali G Fenstermaker; Maha S Zaki; Matan Hofree; Jennifer L Silhavy; Andrew D Heiberg; Mostafa Abdellateef; Basak Rosti; Eric Scott; Lobna Mansour; Amira Masri; Hulya Kayserili; Jumana Y Al-Aama; Ghada M H Abdel-Salam; Ariana Karminejad; Majdi Kara; Bulent Kara; Bita Bozorgmehri; Tawfeg Ben-Omran; Faezeh Mojahedi; Iman Gamal El Din Mahmoud; Naima Bouslam; Ahmed Bouhouche; Ali Benomar; Sylvain Hanein; Laure Raymond; Sylvie Forlani; Massimo Mascaro; Laila Selim; Nabil Shehata; Nasir Al-Allawi; P S Bindu; Matloob Azam; Murat Gunel; Ahmet Caglayan; Kaya Bilguvar; Aslihan Tolun; Mahmoud Y Issa; Jana Schroth; Emily G Spencer; Rasim O Rosti; Naiara Akizu; Keith K Vaux; Anide Johansen; Alice A Koh; Hisham Megahed; Alexandra Durr; Alexis Brice; Giovanni Stevanin; Stacy B Gabriel; Trey Ideker; Joseph G Gleeson
Journal:  Science       Date:  2014-01-31       Impact factor: 47.728

6.  Exome sequencing identifies a significant variant in methionyl-tRNA synthetase (MARS) in a family with late-onset CMT2.

Authors:  Michael Gonzalez; Heather McLaughlin; Henry Houlden; Min Guo; Liu Yo-Tsen; Marios Hadjivassilious; Fiorella Speziani; Xiang-Lei Yang; Anthony Antonellis; Mary M Reilly; Stephan Züchner
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-06-01       Impact factor: 10.154

7.  In vivo analysis of mtDNA replication defects in yeast.

Authors:  Enrico Baruffini; Iliana Ferrero; Françoise Foury
Journal:  Methods       Date:  2010-03-02       Impact factor: 3.608

8.  Pulmonary alveolar proteinosis in children on La Réunion Island: a new inherited disorder?

Authors:  Laurent Enaud; Alice Hadchouel; Aurore Coulomb; Laureline Berteloot; Florence Lacaille; Liliane Boccon-Gibod; Vincent Boulay; Françoise Darcel; Matthias Griese; Mélinée Linard; Malek Louha; Michel Renouil; Jean-Pierre Rivière; Bruno Toupance; Virginie Verkarre; Christophe Delacourt; Jacques de Blic
Journal:  Orphanet J Rare Dis       Date:  2014-06-14       Impact factor: 4.123

9.  Rare recessive loss-of-function methionyl-tRNA synthetase mutations presenting as a multi-organ phenotype.

Authors:  Eline van Meel; Daniel J Wegner; Paul Cliften; Marcia C Willing; Frances V White; Stuart Kornfeld; F Sessions Cole
Journal:  BMC Med Genet       Date:  2013-10-08       Impact factor: 2.103

10.  VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies.

Authors:  Daria Diodato; Laura Melchionda; Tobias B Haack; Cristina Dallabona; Enrico Baruffini; Claudia Donnini; Tiziana Granata; Francesca Ragona; Paolo Balestri; Maria Margollicci; Eleonora Lamantea; Alessia Nasca; Christopher A Powell; Michal Minczuk; Tim M Strom; Thomas Meitinger; Holger Prokisch; Costanza Lamperti; Massimo Zeviani; Daniele Ghezzi
Journal:  Hum Mutat       Date:  2014-06-24       Impact factor: 4.878

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  29 in total

Review 1.  Emerging mechanisms of aminoacyl-tRNA synthetase mutations in recessive and dominant human disease.

Authors:  Rebecca Meyer-Schuman; Anthony Antonellis
Journal:  Hum Mol Genet       Date:  2017-10-01       Impact factor: 6.150

2.  Mutations in methionyl-tRNA synthetase gene in a Chinese family with interstitial lung and liver disease, postnatal growth failure and anemia.

Authors:  Yu Sun; Guorui Hu; Jihang Luo; Di Fang; Yongguo Yu; Xiang Wang; Jing Chen; Wenjuan Qiu
Journal:  J Hum Genet       Date:  2017-02-02       Impact factor: 3.172

3.  MARS variant associated with both recessive interstitial lung and liver disease and dominant Charcot-Marie-Tooth disease.

Authors:  Jonathan Rips; Rebecca Meyer-Schuman; Oded Breuer; Reuven Tsabari; Avraham Shaag; Shoshana Revel-Vilk; Shimon Reif; Orly Elpeleg; Anthony Antonellis; Tamar Harel
Journal:  Eur J Med Genet       Date:  2018-04-12       Impact factor: 2.708

Review 4.  Predicting the pathogenicity of aminoacyl-tRNA synthetase mutations.

Authors:  Stephanie N Oprescu; Laurie B Griffin; Asim A Beg; Anthony Antonellis
Journal:  Methods       Date:  2016-11-20       Impact factor: 3.608

5.  Compound heterozygosity for loss-of-function FARSB variants in a patient with classic features of recessive aminoacyl-tRNA synthetase-related disease.

Authors:  Anthony Antonellis; Stephanie N Oprescu; Laurie B Griffin; Amer Heider; Andrea Amalfitano; Jeffrey W Innis
Journal:  Hum Mutat       Date:  2018-04-10       Impact factor: 4.878

6.  Cysteinyl-tRNA Synthetase Mutations Cause a Multi-System, Recessive Disease That Includes Microcephaly, Developmental Delay, and Brittle Hair and Nails.

Authors:  Molly E Kuo; Arjan F Theil; Anneke Kievit; May Christine Malicdan; Wendy J Introne; Thomas Christian; Frans W Verheijen; Desiree E C Smith; Marisa I Mendes; Lidia Hussaarts-Odijk; Eric van der Meijden; Marjon van Slegtenhorst; Martina Wilke; Wim Vermeulen; Anja Raams; Catherine Groden; Shino Shimada; Rebecca Meyer-Schuman; Ya Ming Hou; William A Gahl; Anthony Antonellis; Gajja S Salomons; Grazia M S Mancini
Journal:  Am J Hum Genet       Date:  2019-02-26       Impact factor: 11.025

7.  Biallelic IARS Mutations Cause Growth Retardation with Prenatal Onset, Intellectual Disability, Muscular Hypotonia, and Infantile Hepatopathy.

Authors:  Robert Kopajtich; Kei Murayama; Andreas R Janecke; Tobias B Haack; Maximilian Breuer; A S Knisely; Inga Harting; Toya Ohashi; Yasushi Okazaki; Daisaku Watanabe; Yoshimi Tokuzawa; Urania Kotzaeridou; Stefan Kölker; Sven Sauer; Matthias Carl; Simon Straub; Andreas Entenmann; Elke Gizewski; René G Feichtinger; Johannes A Mayr; Karoline Lackner; Tim M Strom; Thomas Meitinger; Thomas Müller; Akira Ohtake; Georg F Hoffmann; Holger Prokisch; Christian Staufner
Journal:  Am J Hum Genet       Date:  2016-07-14       Impact factor: 11.025

Review 8.  The future is here: Integrating genetics into the pediatric pulmonary clinic.

Authors:  Megan H Hawley; Peter P Moschovis; Mengdi Lu; T Bernard Kinane; Lael M Yonker
Journal:  Pediatr Pulmonol       Date:  2020-07

Review 9.  Pulmonary Alveolar Proteinosis Syndrome.

Authors:  Takuji Suzuki; Bruce C Trapnell
Journal:  Clin Chest Med       Date:  2016-06-17       Impact factor: 2.878

10.  Emergent high fatality lung disease in systemic juvenile arthritis.

Authors:  Gail H Deutsch; R Paul Guillerman; Johannes Birgmeier; Karthik Jagadeesh; Scott Canna; Grant Schulert; Vivian E Saper; Guangbo Chen; Robin Deterding; Jianpeng Xu; Ann N Leung; Layla Bouzoubaa; Khalid Abulaban; Kevin Baszis; Edward M Behrens; James Birmingham; Alicia Casey; Michal Cidon; Randy Q Cron; Aliva De; Fabrizio De Benedetti; Ian Ferguson; Martha P Fishman; Steven I Goodman; T Brent Graham; Alexei A Grom; Kathleen Haines; Melissa Hazen; Lauren A Henderson; Assunta Ho; Maria Ibarra; Christi J Inman; Rita Jerath; Khulood Khawaja; Daniel J Kingsbury; Marisa Klein-Gitelman; Khanh Lai; Sivia Lapidus; Clara Lin; Jenny Lin; Deborah R Liptzin; Diana Milojevic; Joy Mombourquette; Karen Onel; Seza Ozen; Maria Perez; Kathryn Phillippi; Sampath Prahalad; Suhas Radhakrishna; Adam Reinhardt; Mona Riskalla; Natalie Rosenwasser; Johannes Roth; Rayfel Schneider; Dieneke Schonenberg-Meinema; Susan Shenoi; Judith A Smith; Hafize Emine Sönmez; Matthew L Stoll; Christopher Towe; Sara O Vargas; Richard K Vehe; Lisa R Young; Jacqueline Yang; Tushar Desai; Raymond Balise; Ying Lu; Lu Tian; Gill Bejerano; Mark M Davis; Purvesh Khatri; Elizabeth D Mellins
Journal:  Ann Rheum Dis       Date:  2019-09-27       Impact factor: 19.103

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