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Updated: Sep 29, 2026

In vitro Organoid Culture of Primary Mouse Colon Tumors
Published on: May 17, 2013
Gut-enriched Kruppel-like factor represses ornithine decarboxylase gene expression and functions as checkpoint
Zhi Y Chen1, Jue-Lon Shie, Chi-Chuan Tseng
1Section of Gastroenterology, Veterans Affairs Boston Healthcare System and Boston University School of Medicine, Boston, Massachusetts, 02118, USA.
Abstract:
Gut-enriched Krüppel-like factor (GKLF, KLF4) is an epithelial-specific transcription factor that expresses in the gastrointestinal tract and mediates growth arrest of colonic epithelium. The molecular mechanisms governing its growth inhibitory effect have not been fully elucidated. In the present study, we showed that induction of GKLF mRNA and protein expression by interferon-gamma treatment was associated with reduction of ornithine decarboxylase (ODC) gene expression and enzyme activity in colon cancer HT-29 cells. Overexpression of GKLF in HT-29 cells significantly reduced ODC mRNA and protein levels as well as enzyme activity and resulted in growth arrest, indicating that ODC might be a downstream target of GKLF. This conclusion was further supported by data showing that GKLF mRNA and protein concentrations were the highest at the G(1)/S boundary of the cell cycle, where ODC mRNA and protein levels were the lowest and that overexpression of GKLF resulted in cell arrested at the G(1) phase. Reporter gene transfection studies and electrophoretic mobility gel shift assays demonstrated that GKLF repressed ODC promoter activity and that these effects appeared to be mediated through interaction with a GC box in the proximal portion of the promoter. Transfection studies using reporter constructs and chromatin immunoprecipitation assays also demonstrated that GKLF inhibited transactivation of the ODC gene by interfering with the binding of Sp1 to the ODC promoter. These results indicate that GKLF may function as a G(1)/S checkpoint regulator and exert its growth arrest effect through down-regulation of ODC gene expression. Furthermore, GKLF is a transcriptional repressor of the ODC gene, and these effects are mediated by interaction with the GC-rich region on the promoter.
Insights
Gut-enriched Krüppel-like factor (GKLF, KLF4) represses ornithine decarboxylase (ODC) gene expression, leading to colon cancer cell growth arrest. This mechanism involves GKLF binding to the ODC promoter, acting as a G1/S checkpoint regulator.
Area of Science:
- Molecular biology
- Cancer research
- Cell cycle regulation
Background:
- Gut-enriched Krüppel-like factor (GKLF, KLF4) is an epithelial-specific transcription factor in the gastrointestinal tract.
- GKLF mediates growth arrest of colonic epithelium, but its molecular mechanisms are not fully understood.
Purpose of the Study:
- To elucidate the molecular mechanisms by which GKLF inhibits colon cancer cell growth.
- To investigate the role of ornithine decarboxylase (ODC) as a downstream target of GKLF.
Main Methods:
- Interferon-gamma treatment to induce GKLF expression in HT-29 colon cancer cells.
- Overexpression studies of GKLF in HT-29 cells.
- Reporter gene assays, electrophoretic mobility gel shift assays (EMSA), and chromatin immunoprecipitation (ChIP) assays.
- Cell cycle analysis.
Main Results:
- GKLF induction/overexpression reduced ODC gene expression, protein levels, and enzyme activity.
- GKLF overexpression led to cell cycle arrest at the G1 phase.
- GKLF repressed ODC promoter activity by interacting with a GC box.
- GKLF inhibited ODC gene transactivation by interfering with Sp1 binding to the ODC promoter.
Conclusions:
- GKLF functions as a transcriptional repressor of the ODC gene.
- GKLF exerts its growth-arresting effect by down-regulating ODC gene expression.
- GKLF acts as a G1/S checkpoint regulator in colon epithelial cells.
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