Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
26 Oct 2024
Historique:
received: 31 07 2023
accepted: 15 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 25 10 2024
Statut: epublish

Résumé

Anophthalmia, microphthalmia and coloboma (AMC) comprise a spectrum of developmental eye disorders, accounting for approximately 20% of childhood visual impairment. While non-coding regulatory sequences are increasingly recognised as contributing to disease burden, characterising their impact on gene function and phenotype remains challenging. Furthermore, little is known of the nature and extent of their contribution to AMC phenotypes. We report two families with variants in or near MAB21L2, a gene where genetic variants are known to cause AMC in humans and animal models. The first proband, presenting with microphthalmia and coloboma, has a likely pathogenic missense variant (c.338 G > C; p.[Trp113Ser]), segregating within the family. The second individual, presenting with microphthalmia, carries an ~ 113.5 kb homozygous deletion 19.38 kb upstream of MAB21L2. Modelling of the deletion results in transient small lens and coloboma as well as midbrain anomalies in zebrafish, and microphthalmia and coloboma in Xenopus tropicalis. Using conservation analysis, we identify 15 non-coding conserved elements (CEs) within the deleted region, while ChIP-seq data from mouse embryonic stem cells demonstrates that two of these (CE13 and 14) bind Otx2, a protein with an established role in eye development. Targeted disruption of CE14 in Xenopus tropicalis recapitulates an ocular coloboma phenotype, supporting its role in eye development. Together, our data provides insights into regulatory mechanisms underlying eye development and highlights the importance of non-coding sequences as a source of genetic diagnoses in AMC.

Identifiants

pubmed: 39455595
doi: 10.1038/s41467-024-53553-2
pii: 10.1038/s41467-024-53553-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9245

Informations de copyright

© 2024. The Author(s).

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Auteurs

Fabiola Ceroni (F)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.

Munevver B Cicekdal (MB)

Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.

Richard Holt (R)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.

Elena Sorokina (E)

Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, USA.

Nicolas Chassaing (N)

Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France.
Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.

Samuel Clokie (S)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.

Thomas Naert (T)

Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium.
Institute of Anatomy, University of Zurich, Zurich, Switzerland.
Zurich Kidney Center, University of Zurich, Zurich, Switzerland.

Lidiya V Talbot (LV)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.

Sanaa Muheisen (S)

Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, USA.

Dorine A Bax (DA)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.

Yesim Kesim (Y)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK.
Centre for Human Genetics, University of Oxford, Old Road Campus, Oxford, UK.
NIHR Oxford Biomedical Research Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.

Emma C Kivuva (EC)

Royal Devon University Healthcare NHS Foundation Trust, Exeter, UK.

Catherine Vincent-Delorme (C)

Service de Génétique Clinique Guy Fontaine, Hôpital Jeanne de Flandre, Lille, France.

Soeren S Lienkamp (SS)

Institute of Anatomy, University of Zurich, Zurich, Switzerland.
Zurich Kidney Center, University of Zurich, Zurich, Switzerland.

Julie Plaisancié (J)

Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France.
Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.
Centre de Biologie Intégrative (CBI), Centre de Biologie du Développement (CBD), Université de Toulouse, CNRS, UPS, Toulouse, France.

Elfride De Baere (E)

Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.

Patrick Calvas (P)

Centre de Référence des Affections Rares en Génétique Ophtalmologique CARGO, Site Constitutif, CHU Toulouse, Toulouse, France.
Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.

Kris Vleminckx (K)

Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium. kris.vleminckx@irc.ugent.be.

Elena V Semina (EV)

Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, USA. esemina@mcw.edu.

Nicola K Ragge (NK)

Faculty of Health and Life Sciences, Oxford Brookes University, Oxford, UK. nragge@brookes.ac.uk.
West Midlands Regional Clinical Genetics Service, Birmingham Women's and Children's NHS Foundation Trust and Birmingham Health Partners, Birmingham, UK. nragge@brookes.ac.uk.

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