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Genes Dev ; 20(17): 2465-78, 2006 Sep 01.
Article in English | MEDLINE | ID: mdl-16951258

ABSTRACT

The pancreatic and intestinal primordia contain epithelial progenitor cells that generate many cell types. During development, specific programs of gene expression restrict the developmental potential of such progenitors and promote their differentiation. The Insm1 (insulinoma-associated 1, IA-1) gene encodes a Zinc-finger factor that was discovered in an insulinoma cDNA library. We show that pancreatic and intestinal endocrine cells express Insm1 and require Insm1 for their development. In the pancreas of Insm1 mutant mice, endocrine precursors are formed, but only few insulin-positive beta cells are generated. Instead, endocrine precursor cells accumulate that express none of the pancreatic hormones. A similar change is observed in the development of intestine, where endocrine precursor cells are formed but do not differentiate correctly. A hallmark of endocrine cell differentiation is the accumulation of proteins that participate in secretion and vesicle transport, and we find many of the corresponding genes to be down-regulated in Insm1 mutant mice. Insm1 thus controls a gene expression program that comprises hormones and proteins of the secretory machinery. Our genetic analysis has revealed a key role of Insm1 in differentiation of pancreatic and intestinal endocrine cells.


Subject(s)
Cell Differentiation/physiology , DNA-Binding Proteins/physiology , Enteroendocrine Cells/metabolism , Insulin-Secreting Cells/metabolism , Intestinal Mucosa/metabolism , Transcription Factors/physiology , Zinc Fingers , Animals , Cell Differentiation/genetics , DNA-Binding Proteins/biosynthesis , DNA-Binding Proteins/deficiency , DNA-Binding Proteins/genetics , Enteroendocrine Cells/cytology , Female , Gene Expression Regulation, Developmental , Humans , Insulin-Secreting Cells/cytology , Intestinal Mucosa/cytology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Repressor Proteins , Transcription Factors/biosynthesis , Transcription Factors/deficiency , Transcription Factors/genetics , Zinc Fingers/genetics
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