Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysis.
Dora Janeth FonsecaLuz Adriana CaroDiana Carolina Sierra-DíazCarlos Serrano-ReyesOlga LondoñoYohjana Carolina SuárezHeidi Eliana MateusDavid Bolívar-SalazarAna Francisca RamírezAlejandra de-la-TorrePaul LaissuePublished in: Human genetics (2019)
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare severe cutaneous adverse reactions to drugs. Granulysin (GNLY) plays a key role in keratinocyte apoptosis during SJS/TEN pathophysiology. To determine if GNLY-encoding mutations might be related to the protein's functional disturbances, contributing to SJS/TEN pathogenesis, we performed direct sequencing of GNLY's coding region in a group of 19 Colombian SJS/TEN patients. A GNLY genetic screening was implemented in a group of 249 healthy individuals. We identified the c.11G > A heterozygous sequence variant in a TEN case, which creates a premature termination codon (PTC) (p.Trp4Ter). We show that a mutant protein is synthesised, possibly due to a PTC-readthrough mechanism. Functional assays demonstrated that the mutant protein was abnormally located in the nuclear compartment, potentially leading to a toxic effect. Our results argue in favour of GNLY non-synonymous sequence variants contributing to SJS/TEN pathophysiology, thereby constituting a promising, clinically useful molecular biomarker.
Keyphrases
- amino acid
- end stage renal disease
- protein protein
- newly diagnosed
- early onset
- chronic kidney disease
- ejection fraction
- binding protein
- wild type
- copy number
- case report
- prognostic factors
- oxidative stress
- gene expression
- drug induced
- peritoneal dialysis
- cell proliferation
- dna methylation
- wound healing
- patient reported
- cell cycle arrest