Regulation of kidney-specific Ksp-cadherin gene promoter by hepatocyte nuclear factor-1β

被引:42
作者
Bai, Y
Pontoglio, M
Hiesberger, T
Sinclair, AM
Igarashi, P
机构
[1] Univ Texas, SW Med Ctr Dallas, Dept Internal Med, Div Nephrol, Dallas, TX 75390 USA
[2] Inst Pasteur, Dept Dev Biol, Unite Express Genet & Malad, CNRS,URA 1644, F-75724 Paris 15, France
关键词
transcription factor; kidney-specific gene regulation; mouse inner medullary collecting duct-3 cells; deoxyribonuclease hypersensitive sites; maturity-onset diabetes of the young;
D O I
10.1152/ajprenal.00128.2002
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Kidney-specific cadherin (Ksp-cadherin) is a tissue-specific member of the cadherin family that is expressed exclusively in the kidney and developing genitourinary tract. Recent studies have shown that the proximal 250 bp of the Ksp-cadherin gene promoter are sufficient to direct tissue-specific gene expression in vivo and in vitro. The proximal 120 bp of the promoter are evolutionarily conserved between mouse and human and contain a DNase I hypersensitive site that is kidney cell specific. At position -55, the promoter contains a consensus recognition site for hepatocyte nuclear factor-1 (HNF-1). Mutations of the consensus HNF-1 site and downstream GC-boxes inhibit promoter activity in transfected cells. HNF-1alpha and HNF-1beta bind specifically to the -55 site, and both proteins transactivate the promoter directly. Expression of Ksp-cadherin is not altered in the kidneys of HNF-1alpha-deficient mice. However, expression of a gain-of-function HNF-1beta mutant stimulates Ksp-cadherin promoter activity in transfected cells, whereas expression of a dominant-negative mutant inhibits activity. These studies identify Ksp-cadherin as the first kidney-specific promoter that has been shown to be regulated by HNF-1beta. Mutations of HNF-1beta, as occur in humans with inherited renal cysts and diabetes, may cause dysregulated Ksp-cadherin promoter activity.
引用
收藏
页码:F839 / F851
页数:13
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