A duodenum-specific enhancer regulates expression along three axes in the small intestine

被引:18
作者
Dusing, MR
Brickner, AG
Lowe, SY
Cohen, MB
Wiginton, DA [1 ]
机构
[1] Childrens Hosp Res Fdn, Dept Pediat, Div Dev Biol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Dept Pediat, Div Dev Biol, Cincinnati, OH 45229 USA
[3] Univ Cincinnati, Coll Med, Dept Pediat, Div Pediat Gastroenterol, Cincinnati, OH 45229 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2000年 / 279卷 / 05期
关键词
transgenic mice; PDX-1; temporal regulation; crypt-villus axis; cephalocaudal axis; DNase I footprinting;
D O I
10.1152/ajpgi.2000.279.5.G1080
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Adenosine deaminase (ADA) is expressed at high levels in the epithelium of proximal small intestine. Transgenic mice were used to characterize the regulatory region governing this activation. A duodenum-specific enhancer is located in intron 2 of the human ADA gene at the central site among a cluster of seven DNase I-hypersensitive sites present in duodenal DNA. Flanking DNA, including the remaining hypersensitive sites, is required for consistent high-level enhancer function. The enhancer activates expression in a pattern identical to endogenous ADA along both the anterior-posterior axis of the small intestine and the crypt-villus differentiation axis of the intestinal epithelium. Timing of activation by the central enhancer mimics endogenous mouse ADA activation, occurring at 2-3 wk of age. However, two upstream DNA segments, one proximal and one distal, collaborate to change enhancer activation to a perinatal time point. Studies with duodenal nuclear extracts identified five distinct DNase I footprints within the enhancer. Protected regions encompass six putative binding sites for the transcription factor PDX-1, as well as proposed CDX, hepatocyte nuclear factor-4, and GATA-type sites.
引用
收藏
页码:G1080 / G1093
页数:14
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