| Literature DB >> 31642954 |
Dora Janeth Fonseca1, Luz Adriana Caro2, Diana Carolina Sierra-Díaz1, Carlos Serrano-Reyes3, Olga Londoño1, Yohjana Carolina Suárez1, Heidi Eliana Mateus1, David Bolívar-Salazar1, Ana Francisca Ramírez4, Alejandra de-la-Torre5, Paul Laissue6.
Abstract
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.Entities:
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Year: 2019 PMID: 31642954 DOI: 10.1007/s00439-019-02066-w
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132