DOI: 10.1101/gad.12.22.3499. Glycogen synthase kinase-3β regulates cyclin D1 proteolysis and subcellular localization

Glycogen synthase kinase-3β regulates cyclin D1 proteolysis and subcellular localization

10.1101/gad.12.22.3499

Crossref journal-article

Cold Spring Harbor Laboratory

Genes & Development (246)

Abstract

The activities of cyclin D-dependent kinases serve to integrate extracellular signaling during G1 phase with the cell-cycle engine that regulates DNA replication and mitosis. Induction of D-type cyclins and their assembly into holoenzyme complexes depend on mitogen stimulation. Conversely, the fact that D-type cyclins are labile proteins guarantees that the subunit pool shrinks rapidly when cells are deprived of mitogens. Phosphorylation of cyclin D1 on a single threonine residue near the carboxyl terminus (Thr-286) positively regulates proteasomal degradation of D1. Now, we demonstrate that glycogen synthase kinase-3β (GSK-3β) phosphorylates cyclin D1 specifically on Thr-286, thereby triggering rapid cyclin D1 turnover. Because the activity of GSK-3β can be inhibited by signaling through a pathway that sequentially involves Ras, phosphatidylinositol-3-OH kinase (PI3K), and protein kinase B (Akt), the turnover of cyclin D1, like its assembly, is also Ras dependent and, hence, mitogen regulated. In contrast, Ras mutants defective in PI3K signaling, or constitutively active mitogen-activated protein kinase-kinase (MEK1) mutants that act downstream of Ras to activate extracellular signal-regulated protein kinases (ERKs), cannot stabilize cyclin D1. In direct contrast to cyclin D1, which accumulates in the nucleus during G1 phase and exits into the cytoplasm during S phase, GSK-3β is predominantly cytoplasmic during G1 phase, but a significant fraction enters the nucleus during S phase. A highly stable D1 mutant in which an alanine is substituted for the threonine at position 286 and that is refractory to phosphorylation by GSK-3β remained in the nucleus throughout the cell cycle. Overexpression of an active, but not a kinase-defective, form of GSK-3β in mouse fibroblasts caused a redistribution of cyclin D1 from the cell nucleus to the cytoplasm. Therefore, phosphorylation and proteolytic turnover of cyclin D1 and its subcellular localization during the cell division cycle are linked through the action of GSK-3β.

Bibliography

Diehl, J. A., Cheng, M., Roussel, M. F., & Sherr, C. J. (1998). Glycogen synthase kinase-3Î² regulates cyclin D1 proteolysis and subcellular localization. Genes & Development, 12(22), 3499â3511.

Authors 4

J. Alan Diehl (first)
Mangeng Cheng (additional)
Martine F. Roussel (additional)
Charles J. Sherr (additional)

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Dates

Type	When
Created	17 years, 6 months ago (Feb. 20, 2008, 5:52 p.m.)
Deposited	3 years, 9 months ago (Nov. 14, 2021, 10:24 p.m.)
Indexed	5 days, 11 hours ago (Aug. 26, 2025, 2:45 a.m.)
Issued	26 years, 9 months ago (Nov. 15, 1998)
Published	26 years, 9 months ago (Nov. 15, 1998)
Published Online	26 years, 9 months ago (Nov. 15, 1998)
Published Print	26 years, 9 months ago (Nov. 15, 1998)

Funders 0

None

BibTeX

@article{Diehl_1998, title={Glycogen synthase kinase-3β regulates cyclin D1 proteolysis and subcellular localization}, volume={12}, ISSN={1549-5477}, url={http://dx.doi.org/10.1101/gad.12.22.3499}, DOI={10.1101/gad.12.22.3499}, number={22}, journal={Genes & Development}, publisher={Cold Spring Harbor Laboratory}, author={Diehl, J. Alan and Cheng, Mangeng and Roussel, Martine F. and Sherr, Charles J.}, year={1998}, month=nov, pages={3499–3511} }

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