Literature DB >> 27426735

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

Robert Kopajtich1, Kei Murayama2, Andreas R Janecke3, Tobias B Haack1, Maximilian Breuer4, A S Knisely5, Inga Harting6, Toya Ohashi7, Yasushi Okazaki8, Daisaku Watanabe9, Yoshimi Tokuzawa10, Urania Kotzaeridou4, Stefan Kölker4, Sven Sauer4, Matthias Carl11, Simon Straub12, Andreas Entenmann12, Elke Gizewski13, René G Feichtinger14, Johannes A Mayr14, Karoline Lackner15, Tim M Strom1, Thomas Meitinger1, Thomas Müller12, Akira Ohtake16, Georg F Hoffmann4, Holger Prokisch1, Christian Staufner17.   

Abstract

tRNA synthetase deficiencies are a growing group of genetic diseases associated with tissue-specific, mostly neurological, phenotypes. In cattle, cytosolic isoleucyl-tRNA synthetase (IARS) missense mutations cause hereditary weak calf syndrome. Exome sequencing in three unrelated individuals with severe prenatal-onset growth retardation, intellectual disability, and muscular hypotonia revealed biallelic mutations in IARS. Studies in yeast confirmed the pathogenicity of identified mutations. Two of the individuals had infantile hepatopathy with fibrosis and steatosis, leading in one to liver failure in the course of infections. Zinc deficiency was present in all affected individuals and supplementation with zinc showed a beneficial effect on growth in one.
Copyright © 2016 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27426735      PMCID: PMC4974065          DOI: 10.1016/j.ajhg.2016.05.027

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  36 in total

1.  Heterozygous bile salt export pump deficiency: a possible genetic predisposition to transient neonatal cholestasis.

Authors:  Bogdan Hermeziu; Damien Sanlaville; Muriel Girard; Claude Léonard; Stanislas Lyonnet; Emmanuel Jacquemin
Journal:  J Pediatr Gastroenterol Nutr       Date:  2006-01       Impact factor: 2.839

2.  High-resolution in situ hybridization to whole-mount zebrafish embryos.

Authors:  Christine Thisse; Bernard Thisse
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

3.  Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizures.

Authors:  Xiaochang Zhang; Jiqiang Ling; Giulia Barcia; Lili Jing; Jiang Wu; Brenda J Barry; Ganeshwaran H Mochida; R Sean Hill; Jill M Weimer; Quinn Stein; Annapurna Poduri; Jennifer N Partlow; Dorothée Ville; Olivier Dulac; Tim W Yu; Anh-Thu N Lam; Sarah Servattalab; Jacqueline Rodriguez; Nathalie Boddaert; Arnold Munnich; Laurence Colleaux; Leonard I Zon; Dieter Söll; Christopher A Walsh; Rima Nabbout
Journal:  Am J Hum Genet       Date:  2014-03-20       Impact factor: 11.025

Review 4.  The role of aminoacyl-tRNA synthetases in genetic diseases.

Authors:  Anthony Antonellis; Eric D Green
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

Review 5.  Mitochondrial aminoacyl-tRNA synthetases in human disease.

Authors:  Svetlana Konovalova; Henna Tyynismaa
Journal:  Mol Genet Metab       Date:  2013-01-26       Impact factor: 4.797

Review 6.  Aminoacyl-tRNA synthetase-interacting multifunctional proteins (AIMPs): a triad for cellular homeostasis.

Authors:  Sang Gyu Park; Eung-Chil Choi; Sunghoon Kim
Journal:  IUBMB Life       Date:  2010-04       Impact factor: 3.885

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

Authors:  Alice Hadchouel; Thomas Wieland; Matthias Griese; Enrico Baruffini; Bettina Lorenz-Depiereux; Laurent Enaud; Elisabeth Graf; Jean Christophe Dubus; Sonia Halioui-Louhaichi; Aurore Coulomb; Christophe Delacourt; Gertrud Eckstein; Ralf Zarbock; Thomas Schwarzmayr; François Cartault; Thomas Meitinger; Tiziana Lodi; Jacques de Blic; Tim M Strom
Journal:  Am J Hum Genet       Date:  2015-04-23       Impact factor: 11.025

8.  Mutations in DARS cause hypomyelination with brain stem and spinal cord involvement and leg spasticity.

Authors:  Ryan J Taft; Adeline Vanderver; Richard J Leventer; Stephen A Damiani; Cas Simons; Sean M Grimmond; David Miller; Johanna Schmidt; Paul J Lockhart; Kate Pope; Kelin Ru; Joanna Crawford; Tena Rosser; Irenaeus F M de Coo; Monica Juneja; Ishwar C Verma; Prab Prabhakar; Susan Blaser; Julian Raiman; Petra J W Pouwels; Marianna R Bevova; Truus E M Abbink; Marjo S van der Knaap; Nicole I Wolf
Journal:  Am J Hum Genet       Date:  2013-05-02       Impact factor: 11.025

9.  Contribution of variant alleles of ABCB11 to susceptibility to intrahepatic cholestasis of pregnancy.

Authors:  P H Dixon; S W C van Mil; J Chambers; S Strautnieks; R J Thompson; F Lammert; R Kubitz; V Keitel; A Glantz; L-A Mattsson; H-U Marschall; M Molokhia; G E Moore; K J Linton; C Williamson
Journal:  Gut       Date:  2008-11-05       Impact factor: 23.059

10.  Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease.

Authors:  Cornelia Kornblum; Thomas J Nicholls; Tobias B Haack; Susanne Schöler; Viktoriya Peeva; Katharina Danhauser; Kerstin Hallmann; Gábor Zsurka; Joanna Rorbach; Arcangela Iuso; Thomas Wieland; Monica Sciacco; Dario Ronchi; Giacomo P Comi; Maurizio Moggio; Catarina M Quinzii; Salvatore DiMauro; Sarah E Calvo; Vamsi K Mootha; Thomas Klopstock; Tim M Strom; Thomas Meitinger; Michal Minczuk; Wolfram S Kunz; Holger Prokisch
Journal:  Nat Genet       Date:  2013-01-13       Impact factor: 38.330

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  25 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.  Bi-allelic IARS mutations in a child with intra-uterine growth retardation, neonatal cholestasis, and mild developmental delay.

Authors:  N Orenstein; K Weiss; S N Oprescu; R Shapira; D Kidron; L Vanagaite-Basel; A Antonellis; M Muenke
Journal:  Clin Genet       Date:  2017-02-22       Impact factor: 4.438

Review 3.  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

4.  Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.

Authors:  Rick Kamps; Radek Szklarczyk; Tom E Theunissen; Debby M E I Hellebrekers; Suzanne C E H Sallevelt; Iris B Boesten; Bart de Koning; Bianca J van den Bosch; Gajja S Salomons; Marisa Simas-Mendes; Rob Verdijk; Kees Schoonderwoerd; Irenaeus F M de Coo; Jo M Vanoevelen; Hubert J M Smeets
Journal:  Eur J Hum Genet       Date:  2018-02-13       Impact factor: 4.246

5.  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

Review 6.  tRNA Metabolism and Neurodevelopmental Disorders.

Authors:  Ashleigh E Schaffer; Otis Pinkard; Jeffery M Coller
Journal:  Annu Rev Genomics Hum Genet       Date:  2019-05-13       Impact factor: 8.929

Review 7.  Genetic Approaches to Understanding Psychiatric Disease.

Authors:  Jacob J Michaelson
Journal:  Neurotherapeutics       Date:  2017-07       Impact factor: 7.620

Review 8.  Recent topics: the diagnosis, molecular genesis, and treatment of mitochondrial diseases.

Authors:  Kei Murayama; Masaru Shimura; Zhimei Liu; Yasushi Okazaki; Akira Ohtake
Journal:  J Hum Genet       Date:  2018-11-21       Impact factor: 3.172

9.  Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy.

Authors:  Joshi Stephen; Sheela Nampoothiri; Aditi Banerjee; Nathanial J Tolman; Josef Martin Penninger; Ullrich Elling; Chukwuma A Agu; John D Burke; Kalpana Devadathan; Rajesh Kannan; Yan Huang; Peter J Steinbach; Susan A Martinis; William A Gahl; May Christine V Malicdan
Journal:  Hum Genet       Date:  2018-04-24       Impact factor: 4.132

10.  Identification of Mutator-Derived Alternative Splicing Signatures of Genomic Instability for Improving the Clinical Outcome of Cholangiocarcinoma.

Authors:  Zijing Lin; Jianping Gong; Guochao Zhong; Jiejun Hu; Dong Cai; Lei Zhao; Zhibo Zhao
Journal:  Front Oncol       Date:  2021-05-14       Impact factor: 6.244

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