Ontology highlight
ABSTRACT: Objectives
TNFAIP3 encodes A20 that negatively regulates nuclear factor kappa light chain enhancer of activated B cells (NF-κB), the major transcription factor coordinating inflammatory gene expression. TNFAIP3 polymorphisms have been linked with a spectrum of inflammatory and autoimmune diseases and, recently, loss-of-function mutations in A20 were found to cause a novel inflammatory disease 'haploinsufficiency of A20' (HA20). Here we describe a family with HA20 caused by a novel TNFAIP3 loss-of-function mutation and elucidate the upstream molecular mechanisms linking HA20 to dysregulation of NF-κB and the related inflammasome pathway.Methods
NF-κB activation was studied in a mutation-expressing cell line using luciferase reporter assay. Physical and c
SUBMITTER: Rajamaki K
PROVIDER: S-EPMC6203104 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature