Variants in NR6A1 cause a novel oculo-vertebral-renal (OVR) syndrome
Uma M NeelathiiD, Ehsan UllahiD, Aman GeorgeiD, Mara I MafteiiD, Elangovan BoobalaniD, Daniel Sanchez-MendozaiD, Chloe AdamsiD, David M. McGaugheyiD, Yuri V. SergeeviD, Ranya Al Rawi, Amelia NaikiD, Chelsea Bender, Irene Hussels MaumeneeiD, Michel MichaelidesiD, Tun Giap TaniD, Siying LiniD, Rafael VillasmiliD, Delphine BlainiD, Robert B. HufnageliD, Gavin ArnoiD, Rodrigo YoungiD, Bin GuaniD, Brian P. BrooksiD
Abstract
Colobomatous microphthalmia is a potentially blinding congenital ocular malformation that can present either in isolation or together with other syndromic features. Despite a strong genetic component to disease, many cases lack a molecular diagnosis. We describe a novel autosomal dominant oculo-vertebral-renal (OVR) syndrome in six independent families characterized by colobomatous microphthalmia, missing vertebrae and congenital kidney abnormalities. Genome sequencing identified six rare variants in the orphan nuclear receptor gene NR6A1 in these families. We performed in silico, cellular and zebrafish experiments to demonstrate the NR6A1 variants were pathogenic or likely pathogenic for OVR syndrome. Knockdown of either or both zebrafish paralogs of NR6A1 results in abnormal eye and somite development, which was rescued by wild-type but not variant NR6A1 mRNA. Illustrating the power of genomic ascertainment in medicine, our study establishes NR6A1 as a critical factor in eye and vertebral development and a pleiotropic gene responsible for OVR syndrome.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 10
- FWCI
- 5.88
- Field percentile
- top 3%
- Organism
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Variants in NR6A1 as a cause for congenital renal, vertebral and uterine anomalies
Adeline Jacquinet, Lydie C. Flasse, … Bernard Peers·medRxiv·Jan 8, 2025
- Identification of novel coloboma candidate genes through conserved gene expression analyses across four vertebrate species
Violeta Trejo-Reveles, Nicholas Owen, … Joe Rainger·BiomoleculesPeer-reviewed·Feb 4, 2023
- Whole genome sequencing of a family with autosomal dominant features within the oculoauriculovertebral spectrum
Aline Lourenço Petrin, Ligiane Alves Machado‐Paula, … Lina M. Moreno Uribe·medRxiv·Feb 7, 2024
- Domain-specific mechanisms of YAP1 variants in ocular coloboma revealed by in-vitro and organoid studies
Srishti Silvano, Van Annika Zean Rick-Lenze, … Cerys S Manning·Biochimica et Biophysica Acta (BBA) - Molecular Basis of DiseasePeer-reviewed·Apr 6, 2026
- Mutations in SIX1 associated with Branchio-oto-renal Syndrome (BOR) differentially affect otic expression of putative target genes
Tanya Mehdizadeh, Himani Datta Majumdar, … Sally A. Moody·Journal of Developmental BiologyPeer-reviewed·Jun 30, 2021
- Nf2 fine-tunes proliferation and tissue alignment during closure of the optic fissure in the embryonic mouse eye
Wesley Sun, Sara Ramirez, … Sabine Fuhrmann·Human Molecular GeneticsPeer-reviewed·Oct 13, 2020