Abstract
The nucleus contains diacylglycerol kinases (DGKs), i.e., the enzymes that, by converting diacylglycerol (DG) into phosphatidic acid, terminate DG-dependent events. It has been demonstrated that nuclear DGK-ζ interferes with cell cycle progression. We previously reported that nuclear DGK-ζ expression increased during myogenic differentiation, whereas its down-regulation impaired differentiation. Here, we evaluated the possible involvement of nuclear DGK-ζ in cell cycle progression of C2C12 myoblasts. Overexpression of a wild-type DGK-ζ, which mainly localized to the nucleus (but not of a kinase dead mutant or of a mutant that did not enter the nucleus), blocked the cells in the G1 phase of the cell cycle, as demonstrated by in situ analysis of biotinylated-16-dUTP incorporated into newly synthesized DNA and by flow cytometry. In contrast, down-regulation of endogenous DGK-ζ by short interfering RNA (siRNA) increased the number of cells in both the S and G2/M phases of the cell cycle. Cell cycle arrest of cells overexpressing wild-type DGK-ζ was accompanied by decreased levels of retinoblastoma protein phosphorylated on Ser-807/811. Down-regulation of endogenous DGK-ζ, using siRNA, prevented the cell cycle block characterizing C2C12 cell myogenic differentiation. Overall, our results identify nuclear DGK-ζ as a key determinant of cell cycle progression and differentiation of C2C12 cells. - Evangelisti, C., Tazzari, P. L., Riccio, M., Fiume, R., Hozumi, Y., Falà, F., Goto, K., Manzoli, L., Cocco, L., Martelli, A. M. Nuclear diacylglycerol kinase-ζ is a negative regulator of cell cycle progression in C2C12 mouse myoblasts.
Original language | English |
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Pages (from-to) | 3297-3307 |
Number of pages | 11 |
Journal | FASEB Journal |
Volume | 21 |
Issue number | 12 |
DOIs | |
Publication status | Published - Oct 2007 |
Keywords
- Lipid-dependent signaling pathways
- Nucleus
- Phosphorylated pRB
- siRNA
ASJC Scopus subject areas
- Agricultural and Biological Sciences (miscellaneous)
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Cell Biology
- Medicine(all)