作者: Rixun Fang , Nilda A. Santiago , Lynne C. Olds , Eric Sibley
DOI: 10.1016/S0016-5085(00)70420-3
关键词: Electrophoretic mobility shift assay 、 Expression vector 、 Cellular differentiation 、 Molecular biology 、 Enterocyte 、 Lactase 、 Nuclear protein 、 Biology 、 Promoter 、 Enterocyte differentiation
摘要: Abstract Background & Aims: Lactase is the intestinal disaccharidase responsible for digestion of lactose, predominant carbohydrate in milk. Transcription lactase gene activated during enterocyte differentiation. We have characterized interaction between promoter and Cdx2, a homeodomain protein involved regulating development Methods: Nuclear bound to cis element, CE-LPH1, was analyzed by electrophoretic mobility shift assays supershifts with Cdx2 antibody. activities were assayed cells transfected luciferase reporter constructs expression construct. Results: Electrophoretic assay CE-LPH1 yields specific DNA/protein complex that requires caudal-related binding site, TTTAC. The recognized antibody more abundant differentiated enterocytes. A construct able activate transcription driven wild-type, but not mutated, results increased endogenous messenger RNA. Conclusions: interacts capable activating gene. In contrast previous report, correlates These conclusions are consistent role cell GASTROENTEROLOGY 2000;118:115-127