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Permanent URL to this publication: http://dx.doi.org/10.5167/uzh-51133

Ma, L; Jüttner, M; Kullak-Ublick, G A; Eloranta, J J (2012). Regulation of the gene encoding the intestinal bile acid transporter ASBT by the caudal-type homeobox proteins CDX1 and CDX2. American Journal of Physiology. Gastrointestinal and Liver Physiology, 302(1):G123-33.

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Abstract

The apical sodium-dependent bile acid transporter (ASBT) is expressed abundantly in the ileum and mediates bile acid absorption across the apical membranes. Caudal-type homeobox proteins CDX1 and CDX2 are transcription factors that regulate genes involved in intestinal epithelial differentiation and proliferation. Aberrant expression of both ASBT and CDXs in Barrett's esophagus (BE) prompted us to study, whether the expression of the ASBT gene is regulated by CDXs. Short interfering RNA-mediated knockdown of CDXs resulted in reduced ASBT mRNA expression in intestinal cells. CDXs strongly induced the activity of the ASBT promoter in reporter assays in esophageal and intestinal cells. Nine CDX binding sites were predicted in silico within the ASBT promoter, and binding of CDXs to six of them was verified in vitro and within living cells by electrophoretic mobility shift assays and chromatin immunoprecipitation assays, respectively. RNAs were extracted from esophageal biopsies from 20 BE patients, and analyzed by real-time PCR. Correlation with ASBT expression was found for CDX1, CDX2 and HNF-1α in BE biopsies. In conclusion, the human ASBT promoter is activated transcriptionally by CDX1 and CDX2. Our finding provides a possible explanation for the reported observation that ASBT is aberrantly expressed in esophageal metaplasia that also expresses CDX transcription factors.

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Center for Integrative Human Physiology
04 Faculty of Medicine > University Hospital Zurich > Clinic for Clinical Pharmacology and Toxicology
DDC:570 Life sciences; biology
610 Medicine & health
Language:English
Date:2012
Deposited On:17 Nov 2011 12:43
Last Modified:30 Nov 2013 19:28
Publisher:American Physiological Society
ISSN:0193-1857
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:10.1152/ajpgi.00102.2011
PubMed ID:22016432
Citations:Web of Science®. Times Cited: 6
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