Hypomorphic mutations of TRIP11 cause odontochondrodysplasia.

Bone Biology Bone development Genetics Molecular pathology Protein traffic

Journal

JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073

Informations de publication

Date de publication:
07 Feb 2019
Historique:
received: 07 09 2018
accepted: 20 12 2018
pubmed: 8 2 2019
medline: 8 2 2019
entrez: 8 2 2019
Statut: epublish

Résumé

Odontochondrodysplasia (ODCD) is an unresolved genetic disorder of skeletal and dental development. Here, we show that ODCD is caused by hypomorphic TRIP11 mutations, and we identify ODCD as the nonlethal counterpart to achondrogenesis 1A (ACG1A), the known null phenotype in humans. TRIP11 encodes Golgi-associated microtubule-binding protein 210 (GMAP-210), an essential tether protein of the Golgi apparatus that physically interacts with intraflagellar transport 20 (IFT20), a component of the ciliary intraflagellar transport complex B. This association and extraskeletal disease manifestations in ODCD point to a cilium-dependent pathogenesis. However, our functional studies in patient-derived primary cells clearly support a Golgi-based disease mechanism. In spite of reduced abundance, residual GMAP variants maintain partial Golgi integrity, normal global protein secretion, and subcellular distribution of IFT20 in ODCD. These functions are lost when GMAP-210 is completely abrogated in ACG1A. However, a similar defect in chondrocyte maturation is observed in both disorders, which produces a cellular achondrogenesis phenotype of different severity, ensuing from aberrant glycan processing and impaired extracellular matrix proteoglycan secretion by the Golgi apparatus.

Identifiants

pubmed: 30728324
pii: 124701
doi: 10.1172/jci.insight.124701
pmc: PMC6413787
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical Research Council
ID : MR/N000366/1
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : R01 DK103632
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM060992
Pays : United States

Auteurs

Anika Wehrle (A)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Tomasz M Witkos (TM)

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.

Sheila Unger (S)

Division of Genetic Medicine, University of Lausanne, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Judith Schneider (J)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

John A Follit (JA)

Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Johannes Hermann (J)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Tim Welting (T)

Laboratory for Experimental Orthopedics, Department of Orthopaedic Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.

Virginia Fano (V)

Hospital de Pediatria JP Garrahan, Buenos Aires, Argentina.

Marja Hietala (M)

Medical Biochemistry and Genetics, University of Turku, Turku, Finland.

Nithiwat Vatanavicharn (N)

Department of Paediatrics, Mahidol University, Bangkok, Thailand.

Katharina Schoner (K)

Institute of Pathology, Philipps-University Marburg, Marburg, Germany.

Jürgen Spranger (J)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Miriam Schmidts (M)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Bernhard Zabel (B)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Gregory J Pazour (GJ)

Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA.

Agnes Bloch-Zupan (A)

Centre de Référence des Manifestations Odontologiques des Maladies Rares, Pôle de Médecine et Chirurgie Bucco-dentaires, Hôpitaux Universitaires de Strasbourg (HUS), Faculté de Chirurgie Dentaire, Université de Strasbourg, Strasbourg, France.
Université de Strasbourg, Faculté de Chirurgie Dentaire, Institute of Advanced Studies, USIAS, Strasbourg, France.
HUS, Pôle de Médecine et Chirurgie Bucco-dentaires Hôpital Civil, Centre de référence des maladies rares orales et dentaires, O-Rares, Filière Santé Maladies rares TETE COU, European Reference Network ERN CRANIO, Strasbourg, France.
Université de Strasbourg, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), CERBM, INSERM U1258, CNRS- UMR7104, Illkirch, France.

Gen Nishimura (G)

Department of Radiology and Medical Imaging, Tokyo Metropolitan Kiyose Children's Hospital, Kiyose, Japan.

Andrea Superti-Furga (A)

Division of Genetic Medicine, University of Lausanne, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland.

Martin Lowe (M)

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, United Kingdom.

Ekkehart Lausch (E)

Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Classifications MeSH