Yip1 domain family, member 6 (Yipf6) mutation induces spontaneous intestinal inflammation in mice
Author(s) -
Katharina Brandl,
Wataru Tomisato,
Xiaohong Li,
Christieppl,
Elaine Pirie,
Werner Falk,
Yu Xia,
Eva Marie Y. Moresco,
Roberto Baccalà,
Argyrios N. Theofilopoulos,
Bernd Schnabl,
Bruce Beutler
Publication year - 2012
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1210366109
Subject(s) - paneth cell , biology , null allele , colitis , mutant , microbiology and biotechnology , ileitis , secretion , inflammation , genetics , gene , allele , golgi apparatus , mutation , immunology , small intestine , pathology , disease , biochemistry , crohn's disease , medicine , endoplasmic reticulum
Using an environmentally sensitized genetic screen we identified mutations that cause inflammatory colitis in mice. The X-linkedKlein-Zschocher (KLZ ) mutation created a null allele ofYipf6 , a member of a gene family believed to regulate vesicular transport in yeast, but without known functions in mammals. Yipf6 is a five transmembrane-spanning protein associated with Golgi compartments.Klein-Zschocher mutants were extremely sensitive to colitis induced by dextran sodium sulfate (DSS) and developed spontaneous ileitis and colitis after 16 mo of age in specific pathogen-free housing conditions. Electron microscopy, gene expression, and immunocytochemistry analyses provided evidence that impaired intestinal homeostasis stemmed from defective formation and secretion of large secretory granules from Paneth and goblet cells. These studies support a tissue- and organ-specific function for Yipf6 in the maintenance of intestinal homeostasis and implicate the orthologous human gene as a disease susceptibility locus.
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