Citron Kinase Is a Cell Cycle-dependent, Nuclear Protein Required for G2/M Transition of Hepatocytes
Citron Kinase Is a Cell Cycle-dependent, Nuclear Protein Required for G2/M Transition of Hepatocytes
Citron Kinase (Citron-K) is a cell cycle-dependent protein regulating the G(2)/M transition in hepatocytes. Synchronization studies demonstrated that expression of the Citron-K protein starts at the late S and/or the early G(2) phase after that of cyclin B1. Expression of Citron-K is developmentally regulated. Levels of Citron-K mRNA and protein are highest in embryonic liver and gradually decrease after birth. Citron-K exists in interphase nuclei and begins to disperse into the cytoplasm at prophase. It concentrates at the cleavage furrow and midbody during anaphase, telophase, and cytokinesis, implicating a role in the control of cytokinesis. However, studies with knockouts show that Citron-K is not essential for cytokinesis in hepatocytes. Instead, loss of Citron-K causes a significant increase of G(2) tetraploid nuclei in one-week-old rat and mouse liver. In addition, Citron-K deficiency triggers apoptosis in a small subset of embryonic liver cells. In summary, our data demonstrate that Citron-K has a distinct cell cycle-dependent expression pattern and cellular localization as a downstream target of Rho-GTPase and functions in the control of G(2)/M transition in the hepatocyte cell cycle.
- University of North Carolina at Chapel Hill United States
- University of Turin Italy
Cell Nucleus, Male, Microscopy, Confocal, Blotting, Western, Cell Cycle, Intracellular Signaling Peptides and Proteins, Apoptosis, Immunohistochemistry, Precipitin Tests, Perfusion, Mice, Liver, Microscopy, Fluorescence, Hepatocytes, Animals, Humans, Female, Cells, Cultured, In Situ Hybridization, Metaphase
Cell Nucleus, Male, Microscopy, Confocal, Blotting, Western, Cell Cycle, Intracellular Signaling Peptides and Proteins, Apoptosis, Immunohistochemistry, Precipitin Tests, Perfusion, Mice, Liver, Microscopy, Fluorescence, Hepatocytes, Animals, Humans, Female, Cells, Cultured, In Situ Hybridization, Metaphase
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