| Literature DB >> 22802641 |
Katharina Brandl1, Wataru Tomisato, Xiaohong Li, Christina Neppl, Elaine Pirie, Werner Falk, Yu Xia, Eva Marie Y Moresco, Roberto Baccala, Argyrios N Theofilopoulos, Bernd Schnabl, Bruce Beutler.
Abstract
Using an environmentally sensitized genetic screen we identified mutations that cause inflammatory colitis in mice. The X-linked Klein-Zschocher (KLZ) mutation created a null allele of Yipf6, 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.Entities:
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Year: 2012 PMID: 22802641 PMCID: PMC3412000 DOI: 10.1073/pnas.1210366109
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205