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Bi-allelic variants in COL3A1 encoding the ligand to GPR56 are associated with cobblestone-like cortical malformation, white matter changes and cerebellar cysts
  1. Laura Vandervore1,2,
  2. Katrien Stouffs1,2,
  3. Ibrahim Tanyalçin1,2,
  4. Tim Vanderhasselt3,
  5. Filip Roelens4,
  6. Muriel Holder-Espinasse5,
  7. Agnete Jørgensen6,
  8. Melanie G Pepin7,
  9. Florence Petit8,
  10. Philippe Khau Van Kien9,
  11. Nadia Bahi-Buisson10,
  12. Willy Lissens1,2,
  13. Alexander Gheldof1,2,
  14. Peter H Byers7,11,
  15. Anna C Jansen1,12
  1. 1 Neurogenetics Research Group, Research Cluster Reproduction, Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium
  2. 2 Center for Medical Genetics, UZ Brussel, Brussels, Belgium
  3. 3 Department of Radiology, UZ Brussel, Brussels, Belgium
  4. 4 Department of Pediatric Neurology, AZ Delta, Roeselare, Belgium
  5. 5 Department of Clinical Genetics, Guy’s Hospital, London, UK
  6. 6 Division of Child and Adolescent Health, Department of Medical Genetics, University Hospital of North Norway, Tromsø, Norway
  7. 7 Department of Pathology, University of Washington, Seattle, Washington, USA
  8. 8 Service de Génétique Clinique, Hôpital J. de Flandre, Lille, France
  9. 9 Unité de Génétique Médicale, Nîmes University Hospital,CHU Carémeau, Nîmes, France
  10. 10 Institut Imagine, Université Paris Descartes - Sorbonne Paris Cités, Paris, France
  11. 11 Department of Medicine (Medical Genetics), University of Washington, Seattle, USA
  12. 12 Department of Pediatrics, Pediatric Neurology Unit, UZ Brussel, Brussels, Belgium
  1. Correspondence to Professor Anna C Jansen, Neurogenetics Research Group, Laarbeeklaan 101, 1090 Brussels,Belgium; anna.jansen{at}uzbrussel.be

Abstract

Background Collagens are one of the major constituents of the pial membrane, which plays a crucial role in neuronal migration and cortical lamination during brain development. Type III procollagen, the chains of which are encoded by COL3A1, is the ligand of the G protein-coupled receptor 56 (GPR56), also known as adhesion G protein-coupled receptor G1. Bi-allelic mutations in GPR56 give rise to cobblestone-like malformation, white matter changes and cerebellar dysplasia. This report shows that bi-allelic mutations in COL3A1 are associated with a similar phenotype.

Methods Exome analysis was performed in a family consisting of two affected and two non-affected siblings. Brain imaging studies of this family and of two previously reported individuals with bi-allelic mutations in COL3A1 were reviewed. Functional assays were performed on dermal fibroblasts.

Results Exome analysis revealed a novel homozygous variant c.145C>G (p.Pro49Ala) in exon 2 of COL3A1. Brain MRI in the affected siblings as well as in the two previously reported individuals with bi-allelic COL3A1 mutations showed a brain phenotype similar to that associated with mutations in GPR56.

Conclusion Homozygous or compound heterozygous mutations in COL3A1 are associated with cobblestone-like malformation in all three families reported to date. The variability of the phenotype across patients suggests that genetic alterations in distinct domains of type III procollagen can lead to different outcomes. The presence of cobblestone-like malformation in patients with bi-allelic COL3A1 mutations emphasises the critical role of the type III collagen–GPR56 axis and the pial membrane in the regulation of brain development and cortical lamination.

  • COL3A1
  • GPR56
  • Cobblestone-like malformation
  • vascular Ehlers-Danlos syndrome

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Footnotes

  • Contributors IT and LV performed molecular, bioinformatics and functional analyses, interpreted the data and contributed to the writing of the manuscript. KS, WL and AG assisted with the molecular, bioinformatics and functional analyses, data interpretation, and contributed to the manuscript. TV reviewed all imaging studies and contributed to the manuscript. FR, MHE, AJ, FP, PKVK and NBB performed patient recruitment, sample acquisition and contributed to the manuscript. MP and PB performed the protein electrophoresis assays and contributed to the manuscript. ACJ conceptualised the study, interpreted clinical and imaging data and contributed to the manuscript.

  • Funding The study was funded by the Scientific Fund Willy Gepts. IT and LV were supported by a research fellowship from the Marguerite-Marie Delacroix Foundation and IT by a Methusalem grant of the Vrije Universiteit Brussel. AJ is supported by a Senior Clinical Investigator Fellowship from FWO.

  • Competing interests None declared.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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