P02-014 - Consequences of Arginine 92 mutations in TNFR1 - Inserm - Institut national de la santé et de la recherche médicale Access content directly
Conference Papers Year : 2013

P02-014 - Consequences of Arginine 92 mutations in TNFR1

Abstract

Introduction TNFRSF1A is involved in a Mendelian autosomal dominant autoinflammatory disorder called TNFR-associated periodic syndrome (TRAPS). Most TNFRSF1A mutations are missense changes and, apart from those affecting conserved cysteines, their deleterious effect remains often questionable. This is especially true for the frequent R92Q mutation, which might not be responsible for TRAPS per se but represents a susceptibility factor to multifactorial inflammatory disorders. Objectives This study investigates TRAPS pathophysiology in a family exceptional by its size (13 members). Methods TNFRSF1A screening was performed by PCR-sequencing. Comparison of the 3-dimensional structure and electro- static properties of wild-type and mutated TNFR1 proteins was performed by in silico homology modeling. TNFR1 expression was assessed by western blotting and ELISA in lysates and supernatants of HEK293T cells transfected with plasmids encoding wild-type and mutated TNFR1. Results A TNFRSF1A heterozygous missense mutation, R92W(c.361C>T) perfectly segregated with typical TRAPS mani- festations within the family (p<5.10-4), and was associated with very high disease penetrance (0.9). Prediction of its impact on protein structure revealed local conformational changes and alterations of electrostatic properties. In addition, R92W leads to abrogation of the receptor shedding, whereas TNFR1-R92Q behaves like the wild-type receptor. Conclusion These data demonstrate the pathogenicity of a mutation affecting arginine 92, a residue whose involvement in inflammatory disorders is deeply debated. Combined with previous data on arginine 92 mutations, this study discloses an unusual situation in which different amino acid substitutions at the same position in the protein are associated with a clinical spectrum bridging Mendelian to multifactorial conditions.
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Dates and versions

inserm-00881678 , version 1 (08-11-2013)

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Isabelle Jéru, Serge Charmion, Emmanuelle Cochet, Bruno Copin, Gaëlle Le Borgne, et al.. P02-014 - Consequences of Arginine 92 mutations in TNFR1. Congress of International Society of Systemic Auto-Inflammatory Diseases (ISSAID), May 2013, Lausanne, Switzerland. pp.A121, ⟨10.1186/1546-0096-11-S1-A121⟩. ⟨inserm-00881678⟩
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