TY - JOUR T1 - Biallelic <em>GINS2</em> variant p.(Arg114Leu) causes Meier-Gorlin syndrome with craniosynostosis JF - Journal of Medical Genetics JO - J Med Genet SP - 776 LP - 780 DO - 10.1136/jmedgenet-2020-107572 VL - 59 IS - 8 AU - Maria J Nabais Sá AU - Kerry A Miller AU - Mary McQuaid AU - Nils Koelling AU - Andrew O M Wilkie AU - Hugo Wurtele AU - Arjan P M de Brouwer AU - Jorge Oliveira Y1 - 2022/08/01 UR - http://jmg.bmj.com/content/59/8/776.abstract N2 - Introduction Replication of the nuclear genome is an essential step for cell division. Pathogenic variants in genes coding for highly conserved components of the DNA replication machinery cause Meier-Gorlin syndrome (MGORS).Objective Identification of novel genes associated with MGORS.Methods Exome sequencing was performed to investigate the genotype of an individual presenting with prenatal and postnatal growth restriction, a craniofacial gestalt of MGORS and coronal craniosynostosis. The analysis of the candidate variants employed bioinformatic tools, in silico structural protein analysis and modelling in budding yeast.Results A novel homozygous missense variant NM_016095.2:c.341G&gt;T, p.(Arg114Leu), in GINS2 was identified. Both non-consanguineous healthy parents carried this variant. Bioinformatic analysis supports its classification as pathogenic. Functional analyses using yeast showed that this variant increases sensitivity to nicotinamide, a compound that interferes with DNA replication processes. The phylogenetically highly conserved residue p.Arg114 localises at the docking site of CDC45 and MCM5 at GINS2. Moreover, the missense change possibly disrupts the effective interaction between the GINS complex and CDC45, which is necessary for the CMG helicase complex (Cdc45/MCM2–7/GINS) to accurately operate. Interestingly, our patient’s phenotype is strikingly similar to the phenotype of patients with CDC45-related MGORS, particularly those with craniosynostosis, mild short stature and patellar hypoplasia.Conclusion GINS2 is a new disease-associated gene, expanding the genetic aetiology of MGORS. ER -