Aden K

Barann M

Ellinghaus D

Forster M

Forster P

Franke A

Fritscher-Ravens A

Gilissen C

Jentzsch M

Klostermeier UC

Korbel JO

Krawczak M

Lee CC

Lipinski S

Mayr G

Nothnagel M

Petersen B-S

Piecyk A

Rausch T

Rosenstiel P

Schreiber S

Sheth V

Stengel ST

Tran F

Veltman JA

\ua9 2019 Lipinski et al.; Published by Cold Spring Harbor Laboratory Press. Whole-genome and whole-exome sequencing of individual patients allow the study of rare and potentially causative genetic variation. In this study, we sequenced DNA of a trio comprising a boy with very-early-onset inflammatory bowel disease (veoIBD) and his unaffected parents. We identified a rare, X-linked missense variant in the NAPDH oxidase NOX1 gene (c.C721T, p.R241C) in heterozygous state in the mother and in hemizygous state in the patient. We discovered that, in addition, the patient was homozygous for a common missense variant in the CYBA gene (c.T214C, p.Y72H). CYBA encodes the p22phox protein, a cofactor for NOX1. Functional assays revealed reduced cellular ROS generation and antibacterial capacity of NOX1 and p22phox variants in intestinal epithelial cells. Moreover, the identified NADPH oxidase complex variants affected NOD2-mediated immune responses, and p22phox was identified as a novel NOD2 interactor. In conclusion, we detected missense variants in a veoIBD patient that disrupt the host response to bacterial challenges and reduce protective innate immune signaling via NOD2. We assume that the patient\u27s individual genetic makeup favored disturbed intestinal mucosal barrier function

Newcastle University E-Prints

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2

Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2

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