» Articles » PMID: 9472014

Expression of NPAT, a Novel Substrate of Cyclin E-CDK2, Promotes S-phase Entry

Overview
Journal Genes Dev
Specialty Molecular Biology
Date 1998 Mar 21
PMID 9472014
Citations 81
Authors
Affiliations
Soon will be listed here.
Abstract

To understand the mechanisms by which CDKs regulate cell cycle progression, it is necessary to identify and characterize the physiological substrates of these kinases. We have developed a screening method to identify novel CDK substrates. One of the cDNAs identified in the screen is identical to the recently isolated NPAT gene. Here we show that NPAT associates with cyclin E-CDK2 in vivo and can be phosphorylated by this CDK. The protein level of NPAT peaks at the G1/S boundary. Overexpression of NPAT accelerates S-phase entry, and this effect is enhanced by coexpression of cyclin E-CDK2. These results suggest that NPAT is a substrate of cyclin E-CDK2 and plays a role in S-phase entry.

Citing Articles

Transcriptional inhibition after irradiation occurs preferentially at highly expressed genes in a manner dependent on cell cycle progression.

Chen Z, Wang X, Gao X, Arslanovic N, Chen K, Tyler J Elife. 2024; 13.

PMID: 39392398 PMC: 11469672. DOI: 10.7554/eLife.94001.


Histone locus bodies: a paradigm for how nuclear biomolecular condensates control cell cycle regulated gene expression.

Geisler M, Kemp Jr J, Duronio R Nucleus. 2023; 14(1):2293604.

PMID: 38095604 PMC: 10730174. DOI: 10.1080/19491034.2023.2293604.


Transcriptional inhibition after irradiation occurs preferentially at highly expressed genes in a manner dependent on cell cycle progression.

Chen Z, Wang X, Gao X, Arslanovic N, Chen K, Tyler J bioRxiv. 2023; .

PMID: 38045243 PMC: 10690177. DOI: 10.1101/2023.11.20.567799.


Cyclin E/CDK2 and feedback from soluble histone protein regulate the S phase burst of histone biosynthesis.

Armstrong C, Passanisi V, Ashraf H, Spencer S Cell Rep. 2023; 42(7):112768.

PMID: 37428633 PMC: 10440735. DOI: 10.1016/j.celrep.2023.112768.


Spatiotemporal higher-order chromatin landscape of human histone gene clusters at histone locus bodies during the cell cycle in breast cancer progression.

Ghule P, Boyd J, Kabala F, Fritz A, Bouffard N, Gao C Gene. 2023; 872:147441.

PMID: 37094694 PMC: 10370284. DOI: 10.1016/j.gene.2023.147441.


References
1.
Ohtsubo M, Roberts J . Cyclin-dependent regulation of G1 in mammalian fibroblasts. Science. 1993; 259(5103):1908-12. DOI: 10.1126/science.8384376. View

2.
Sherr C . Cancer cell cycles. Science. 1996; 274(5293):1672-7. DOI: 10.1126/science.274.5293.1672. View

3.
Tsai L, Lees E, Faha B, Harlow E, Riabowol K . The cdk2 kinase is required for the G1-to-S transition in mammalian cells. Oncogene. 1993; 8(6):1593-602. View

4.
Harper J, Adami G, Wei N, Keyomarsi K, Elledge S . The p21 Cdk-interacting protein Cip1 is a potent inhibitor of G1 cyclin-dependent kinases. Cell. 1993; 75(4):805-16. DOI: 10.1016/0092-8674(93)90499-g. View

5.
Li Y, Graham C, Lacy S, Duncan A, Whyte P . The adenovirus E1A-associated 130-kD protein is encoded by a member of the retinoblastoma gene family and physically interacts with cyclins A and E. Genes Dev. 1993; 7(12A):2366-77. DOI: 10.1101/gad.7.12a.2366. View