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Publication : Control of endodermal endocrine development by Hes-1.

First Author  Jensen J Year  2000
Journal  Nat Genet Volume  24
Issue  1 Pages  36-44
PubMed ID  10615124 Mgi Jnum  J:59312
Mgi Id  MGI:1351379 Doi  10.1038/71657
Citation  Jensen J, et al. (2000) Control of endodermal endocrine development by Hes-1. Nat Genet 24(1):36-44
abstractText  Development of endocrine cells in the endoderm involves Atonal and Achaete/Scute-related basic helix-loop-helix (bHLH) proteins. These proteins also serve as neuronal determination and differentiation factors, and are antagonized by the Notch pathway partly acting through Hairy and Enhancer-of-split (HES)-type proteins. Here we show that mice deficient in Hes1 (encoding Hes-1) display severe pancreatic hypoplasia caused by depletion of pancreatic epithelial precursors due to accelerated differentiation of post-mitotic endocrine cells expressing glucagon. Moreover, upregulation of several bHLH components is associated with precocious and excessive differentiation of multiple endocrine cell types in the developing stomach and gut, showing that Hes-1 operates as a general negative regulator of endodermal endocrine differentiation.
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