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The transcription factor Cdx2 regulates the intestine-specific expression of human peptide transporter 1 through
Jin Shimakura1, Tomohiro Terada, Yutaka Shimada
1Department of Pharmacy, Kyoto University Hospital, Faculty of Medicine, Kyoto University, Sakyo-ku, Kyoto 606-8507, Japan.
Insights
Cdx2 significantly enhances the intestine-specific expression of H(+)/peptide cotransporter 1 (PEPT1) by interacting with transcription factor Sp1. This interaction is crucial for PEPT1 gene regulation in intestinal cells.
Area of Science:
- Molecular biology
- Gastroenterology
- Gene regulation
Background:
- H(+)/peptide cotransporter 1 (PEPT1, SLC15A1) is vital for intestinal absorption of peptides and drugs.
- Transcription factor Sp1 regulates basal PEPT1 expression.
- The factor driving intestine-specific PEPT1 expression was previously unknown.
Purpose of the Study:
- To identify intestinal transcription factors regulating PEPT1 gene expression.
- To elucidate the mechanism of intestine-specific PEPT1 transcription.
Main Methods:
- Investigated effects of intestinal transcription factors on the PEPT1 promoter.
- Utilized in vitro experiments with Caco-2 cells, including promoter analysis and co-immunoprecipitation.
- Analyzed Cdx2 and PEPT1 mRNA levels in human gastric and intestinal metaplasia tissues.
Main Results:
- Cdx2 markedly trans-activated the PEPT1 promoter, despite the absence of a typical Cdx2-binding sequence.
- Mutation of Sp1-binding sites reduced Cdx2's effect.
- Co-expression of Cdx2 and Sp1 synergistically activated the PEPT1 promoter, and Cdx2 and Sp1 proteins interacted.
- A strong correlation was observed between Cdx2 and PEPT1 mRNA levels in human tissues.
Conclusions:
- Cdx2 plays a critical role in the intestine-specific transcriptional regulation of PEPT1.
- Cdx2 likely modulates PEPT1 expression through interaction with Sp1.
- Findings provide insight into the molecular mechanisms of intestinal transporter gene regulation.
Abstract:
H(+)/peptide cotransporter 1 (PEPT1, SLC15A1) localized at the brush-border membranes of intestinal epithelial cells plays important roles in the intestinal absorption of small peptides and a variety of peptidemimetic drugs. We previously demonstrated that transcription factor Sp1 functions as a basal transcriptional regulator of human PEPT1. However, the factor responsible for the intestine-specific expression of PEPT1 remains unknown. In the present study, we investigated the effect of the intestinal transcription factors on the transcription of the PEPT1 gene and found that only Cdx2 markedly trans-activated the PEPT1 promoter. However, the promoter region responsible for this effect lacked a typical Cdx2-binding sequence, but instead, possessed some Sp1-binding sites. In vitro experiments using Caco-2 cells showed that (1) mutation of the Sp1-binding site diminished the effect of Cdx2, (2) co-expression of Cdx2 and Sp1 synergistically trans-activated the PEPT1 promoter and (3) Sp1 protein was immunoprecipitated with Cdx2 protein. These results raise the possibility that Cdx2 modulates the PEPT1 promoter by interaction with Sp1. The significance of Cdx2 in vivo for PEPT1 regulation was shown by the determination of mRNA levels of Cdx2 and PEPT1 in human tissue. In gastric samples, some with intestinal metaplasia, the levels of PEPT1 and Cdx2 mRNA were highly correlated. Taken together, the present study suggests that Cdx2 plays a key role in the transcriptional regulation of the intestine-specific expression of PEPT1, possibly through interaction with Sp1.
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