A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease.

ABSTRACT: Mutations in genes encoding subunits of the phagocyte NADPH oxidase complex are recognized to cause chronic granulomatous disease (CGD), a severe primary immunodeficiency. Here we describe how deficiency of CYBC1, a previously uncharacterized protein in humans (C17orf62), leads to reduced expression of NADPH oxidase's main subunit (gp91phox) and results in CGD. Analyzing two brothers diagnosed with CGD we identify a homozygous loss-of-function mutation, p.Tyr2Ter, in CYBC1. Imputation of p.Tyr2Ter into 155K chip-genotyped Icelanders reveals six additional homozygotes, all with signs of CGD, manifesting as colitis, rare infections, or a severely impaired PMA-induced neutrophil oxidative burst. Homozygosity for p.Tyr2Ter consequently associates with inflammatory bowel disease (IBD) in Iceland (P?=?8.3?×?10-8; OR?=?67.6), as well as reduced height (P?=?3.3?×?10-4; -8.5?cm). Overall, we find that CYBC1 deficiency results in CGD characterized by colitis and a distinct profile of infections indicative of macrophage dysfunction.

SUBMITTER: Arnadottir GA 

PROVIDER: S-EPMC6202333 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature