Disease-causing mutations in the promoter and enhancer of the ornithine transcarbamylase gene.
Yoon J JangAbigail L LaBellaTimothy P FeeneyNancy BravermanMendel TuchmanHiroki MorizonoNicholas Ah MewLjubica CaldovicPublished in: Human mutation (2018)
The ornithine transcarbamylase (OTC) gene is on the X chromosome and its product catalyzes the formation of citrulline from ornithine and carbamylphosphate in the urea cycle. About 10%-15% of patients, clinically diagnosed with OTC deficiency (OTCD), lack identifiable mutations in the coding region or splice junctions of the OTC gene on routine molecular testing. We collected DNA from such patients via retrospective review and by prospective enrollment. In nine of 38 subjects (24%), we identified a sequence variant in the OTC regulatory regions. Eight subjects had unique sequence variants in the OTC promoter and one subject had a novel sequence variant in the OTC enhancer. All sequence variants affect positions that are highly conserved in mammalian OTC genes. Functional studies revealed reduced reporter gene expression with all sequence variants. Two sequence variants caused decreased binding of the HNF4 transcription factor to its mutated binding site. Bioinformatic analyses combined with functional assays can be used to identify and authenticate pathogenic sequence variants in regulatory regions of the OTC gene, in other urea cycle disorders or other inborn errors of metabolism.
Keyphrases
- copy number
- transcription factor
- genome wide identification
- genome wide
- gene expression
- dna methylation
- end stage renal disease
- ejection fraction
- newly diagnosed
- dna binding
- binding protein
- single molecule
- prognostic factors
- emergency department
- high throughput
- patient reported outcomes
- inflammatory response
- crispr cas
- patient reported
- health insurance
- toll like receptor
- adverse drug
- nuclear factor
- affordable care act
- cell free
- case control