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.

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.

Related Concept Videos

Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

Role Of Notch Signalling In Intestinal Stem Cell Renewal

Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...
Role of Ephrin-Eph Signalling in Intestinal Stem Cell Renewal01:22

Role of Ephrin-Eph Signalling in Intestinal Stem Cell Renewal

Erythropoietin-producing hepatocellular carcinoma receptor (Eph) and its ligand, Eph receptor-interacting protein (Ephrin) were first discovered in the human carcinoma cell line, hence the name. Ephrin-Eph interaction guides cells to reach their appropriate location in adult tissues. They also play an essential role in the immune system by helping in immune cell migration, adhesion, and activation. Based on their structure and function, Eph is divided into two classes — EphA and EphB.
Abnormal Proliferation02:23

Abnormal Proliferation

Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
Renewal of Intestinal Stem Cells01:23

Renewal of Intestinal Stem Cells

The intestinal epithelial lining rapidly renews every 4 to 5 days. The renewal is facilitated by intestinal stem cells (ISCs) located at the base of the crypt– a gland located at the bottom of each villus. ISCs divide asymmetrically to form new stem cells and progenitor daughter cells. The daughter cells are called transit-amplifying (TA) cells which move upwards along the crypt and either differentiate into absorptive cells– the enterocytes or secretory cells– including the goblet,...
Epigenetic Regulation01:37

Epigenetic Regulation

Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...