TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes

HGG Advances

Dan Doherty¹  Caitlin V. Miller²  Dorien Lugtenberg³  Deborah A. Nickerson⁴  Reza Maroofian⁵  Inge B. Mathijssen⁶  Jennifer C. Dempsey⁷  Majid Mojarrad⁸  Michael J. Bamshad⁸  Eva Pajkrt⁸  Aoife M. Waters⁹  Jessica L. Giordano^1,10  Caroline C.W. Klaver^1,11  Henry Houlden^1,11  Atieh Eslahi^1,12  Mahsa Sadat Asl Mohajeri^1,13  Bert B.A. de Vries^1,13  Elizabeth van Leeuwen^1,13  Julie C. Van De Weghe^1,13  Vimla S. Aggarwal^1,14 

[1] Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA;Genetic Center of Khorasan Razavi, Mashhad, Iran;Genetic Research Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran;Student Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran;University of Washington Center for Mendelian Genomics, Seattle, WA 98195, USA;Department of Clinical Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands;Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands;Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran;Department of Neuromuscular Disorders, University College London Institute of Neurology, Queen Square, London WC1N 3BG, UK;Department of OB/GYN, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA;Department of Obstetrics and Gynecology, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands;Department of Ophthalmology, Radboud University Medical Center, Nijmegen, the Netherlands;Department of Pediatrics, University of Washington, Seattle, WA 98195, USA;Great Ormond Street Hospital NHS Foundation Trust, London WC1N 1LE, UK;

关键词: TMEM218;    Joubert syndrome;    Meckel syndrome;    ciliopathy;    cilia;    primary cilia;   

DOI  :  

来源: DOAJ

【 摘 要 】

Summary: The Joubert-Meckel syndrome spectrum is a continuum of recessive ciliopathy conditions caused by primary cilium dysfunction. The primary cilium is a microtubule-based, antenna-like organelle that projects from the surface of most human cell types, allowing them to respond to extracellular signals. The cilium is partitioned from the cell body by the transition zone, a known hotspot for ciliopathy-related proteins. Despite years of Joubert syndrome (JBTS) gene discovery, the genetic cause cannot be identified in up to 30% of individuals with JBTS, depending on the cohort, sequencing method, and criteria for pathogenic variants. Using exome and targeted sequencing of 655 families with JBTS, we identified three individuals from two families harboring biallelic, rare, predicted-deleterious missense TMEM218 variants. Via MatchMaker Exchange, we identified biallelic TMEM218 variants in four additional families with ciliopathy phenotypes. Of note, four of the six families carry missense variants affecting the same highly conserved amino acid position 115. Clinical features included the molar tooth sign (N = 2), occipital encephalocele (N = 5, all fetuses), retinal dystrophy (N = 4, all living individuals), polycystic kidneys (N = 2), and polydactyly (N = 2), without liver involvement. Combined with existing functional data linking TMEM218 to ciliary transition zone function, our human genetic data make a strong case for TMEM218 dysfunction as a cause of ciliopathy phenotypes including JBTS with retinal dystrophy and Meckel syndrome. Identifying all genetic causes of the Joubert-Meckel spectrum enables diagnostic testing, prognostic and recurrence risk counseling, and medical monitoring, as well as work to delineate the underlying biological mechanisms and identify targets for future therapies.

【 授权许可】

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