Roles of HNF-1β in kidney development and congenital cystic diseases

Peter Igarashi, Xinli Shao, Brian T. McNally, Thomas Hiesberger

Research output: Contribution to journalArticlepeer-review

85 Scopus citations

Abstract

Hepatocyte nuclear factor-1β (HNF-1β) is a Pit-1/Oct-1/Unc-86 (POU)/homeodomain-containing transcription factor that regulates tissue-specific gene expression in the kidney, liver, pancreas, and other epithelial organs. Mutations of HNF-1β produce maturity-onset diabetes of the young type 5 (MODY5) and are associated with congenital cystic abnormalities of the kidney. Transgenic mice expressing mutant HNF-1β under the control of a kidney-specific promoter develop kidney cysts and renal failure, which is similar to the phenotype of humans with MODY5. Similarly, kidney-specific deletion of HNF-1β using Cre/loxP recombination results in renal cyst formation. HNF-1β directly regulates the Pkhd1 promoter. HNF-1β mutant mice show decreased expression of Pkhd1, the gene that is mutated in humans with autosomal-recessive polycystic kidney disease (ARPKD). These studies demonstrate that HNF-1β is required for the development of the mammalian kidney. They establish a previously unrecognized link between two renal cystic diseases, MODY5 and ARPKD, and suggest that the mechanism of cyst formation in humans with mutations of HNF-1β involves down-regulation of PKHD1 gene transcription.

Original languageEnglish (US)
Pages (from-to)1944-1947
Number of pages4
JournalKidney international
Volume68
Issue number5
DOIs
StatePublished - Nov 2005

Bibliographical note

Funding Information:
Work from the authors' laboratory is supported by grants from the National Institute of Diabetes and Digestive and Kidney Diseases, Texas Advanced Technology Program, and PKD Foundation.

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