Literature DB >> 22733991

GATA6 is required for proliferation, migration, secretory cell maturation, and gene expression in the mature mouse colon.

Eva Beuling1, Boaz E Aronson, Luc M D Tran, Kelly A Stapleton, Ellis N ter Horst, Laurens A T M Vissers, Michael P Verzi, Stephen D Krasinski.   

Abstract

Controlled renewal of the epithelium with precise cell distribution and gene expression patterns is essential for colonic function. GATA6 is expressed in the colonic epithelium, but its function in the colon is currently unknown. To define GATA6 function in the colon, we conditionally deleted Gata6 throughout the epithelium of small and large intestines of adult mice. In the colon, Gata6 deletion resulted in shorter, wider crypts, a decrease in proliferation, and a delayed crypt-to-surface epithelial migration rate. Staining techniques and electron microscopy indicated deficient maturation of goblet cells, and coimmunofluorescence demonstrated alterations in specific hormones produced by the endocrine L cells and serotonin-producing cells. Specific colonocyte genes were significantly downregulated. In LS174T, the colonic adenocarcinoma cell line, Gata6 knockdown resulted in a significant downregulation of a similar subset of goblet cell and colonocyte genes, and GATA6 was found to occupy active loci in enhancers and promoters of some of these genes, suggesting that they are direct targets of GATA6. These data demonstrate that GATA6 is necessary for proliferation, migration, lineage maturation, and gene expression in the mature colonic epithelium.

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Year:  2012        PMID: 22733991      PMCID: PMC3422006          DOI: 10.1128/MCB.00070-12

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  38 in total

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  23 in total

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Review 4.  Role of GATA factors in development, differentiation, and homeostasis of the small intestinal epithelium.

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Review 5.  GATA factors in endocrine neoplasia.

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10.  Simultaneous gene deletion of gata4 and gata6 leads to early disruption of follicular development and germ cell loss in the murine ovary.

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