Inactivation of DRG1, encoding a translation factor GTPase, causes a Recessive Neurodevelopmental Disorder.

Christian A E Westrip, Franziska Paul, Fathiya Al-Murshedi, Hashim Qaitoon, Breana Cham, Sally C Fletcher, Eline Hendrix, Uncaar Boora, Alvin Yu Jin Ng, Carine Bonnard, Maryam Najafi, Salem Alawbathani, Imelda Lambert, Gabriel Fox, Byrappa Venkatesh, Aida Bertoli-Avella, Ee Shien Tan, Almundher Al-Maawali, Bruno Reversade, Mathew L Coleman

Research output: Contribution to journalArticlepeer-review

Abstract

Purpose: Developmentally-regulated GTP-binding protein 1 (DRG1) is a highly conserved member of a class of GTPases implicated in translation. Although the expression of mammalian DRG1 is elevated in the central nervous system (CNS) during development, and its function has been implicated in fundamental cellular processes, no pathogenic germline variants have yet been identified. Here, we characterize the clinical and biochemical consequences of DRG1 variants. Methods: We collate clinical information of four individuals with germline DRG1 variants and employ in silico, in vitro, and cell-based studies to study the pathogenicity of these alleles. Results: We identified private germline DRG1 variants including three stop-gained p.Gly54*, p.Arg140*, p.Lys263* and a p.Asn248Phe missense variant. These alleles are recessively inherited in four affected individuals from three distinct families and cause a neurodevelopmental disorder with global developmental delay, primary microcephaly, short stature and craniofacial anomalies. We show that these loss-of-function variants: 1) severely disrupt DRG1 mRNA/protein stability in patient-derived fibroblasts, 2) impair its GTPase activity and 3) compromise its binding to partner protein ZC3H15. Consistent with the importance of DRG1 in humans, targeted inactivation of mouse Drg1 resulted in pre-weaning lethality. Conclusion: Our work defines a new Mendelian disorder of DRG1 deficiency. This study highlights DRG1’s importance for normal mammalian development and underscores the significance of translation factor GTPases in human physiology and homeostasis.
Original languageEnglish (US)
Pages (from-to)100893
JournalGenetics in medicine : official journal of the American College of Medical Genetics
DOIs
StatePublished - May 11 2023

ASJC Scopus subject areas

  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Inactivation of DRG1, encoding a translation factor GTPase, causes a Recessive Neurodevelopmental Disorder.'. Together they form a unique fingerprint.

Cite this