Crystal structure of the catalytic subunit of Cdc25B required for G 2 /M phase transition of the cell cycle 1 1Edited by I. A. Wilson

1999 ◽  
Vol 293 (3) ◽  
pp. 559-568 ◽  
Author(s):  
Ross A Reynolds ◽  
Anthony W Yem ◽  
Cindy L Wolfe ◽  
Martin R Deibel ◽  
Constance G Chidester ◽  
...  
1998 ◽  
Vol 111 (12) ◽  
pp. 1751-1757 ◽  
Author(s):  
A. Abrieu ◽  
T. Brassac ◽  
S. Galas ◽  
D. Fisher ◽  
J.C. Labbe ◽  
...  

We have investigated whether Plx1, a kinase recently shown to phosphorylate cdc25c in vitro, is required for activation of cdc25c at the G2/M-phase transition of the cell cycle in Xenopus. Using immunodepletion or the mere addition of an antibody against the C terminus of Plx1, which suppressed its activation (not its activity) at G2/M, we show that Plx1 activity is required for activation of cyclin B-cdc2 kinase in both interphase egg extracts receiving recombinant cyclin B, and cycling extracts that spontaneously oscillate between interphase and mitosis. Furthermore, a positive feedback loop allows cyclin B-cdc2 kinase to activate Plx1 at the G2/M-phase transition. In contrast, activation of cyclin A-cdc2 kinase does not require Plx1 activity, and cyclin A-cdc2 kinase fails to activate Plx1 and its consequence, cdc25c activation in cycling extracts.


1990 ◽  
Vol 10 (7) ◽  
pp. 3847-3851
Author(s):  
C H McGowan ◽  
P Russell ◽  
S I Reed

The product of the CDC2Hs gene is the protein kinase subunit of the M-phase promoting factor, which is required for entry into mitosis. The activity of this kinase is regulated in a cell cycle-dependent manner by reversible phosphorylation and through association with other proteins. We report here that in HeLa cells, the abundance of the CDC2Hs mRNA and the rate of synthesis of the encoded protein, p34, vary in a cell cycle-dependent manner.


2014 ◽  
Vol 68 (4) ◽  
pp. 255-259 ◽  
Author(s):  
Justyna Polit

In eukaryotes, the 34kDa kinase (p34) encoded by the <em>cdc2</em> gene is a key regulator of both the onset of DNA synthesis (G<sub>1</sub> to S phase transition) and the onset of mitosis (G<sub>1</sub> to M phase transition). Using mouse anti-human PSTAIRE and FITClabelled goat antibodies, indirect semiquantitative determination of p34<sup><em>cdc2</em></sup> levels was performed in meristematic cells from the control (intact) and excised, carbohydrate-starved main roots of Vicia faba var. minor. No evident differences in the intensity of fluorescence was found either between the G<sub>1</sub> and G<sub>2</sub> cells or between the control cells and the cells arrested at both Principal Control Points by carbohydrate starvation. It seems thus, that the cell cycle block induced in meristematic cells of <em>V. faba</em> var. <em>minor</em> is not correlated with the absolute level of the key cell cycle enzyme responsible for phosphory-lution of cellular proteins, but primarily with the altered activity of p34<sup><em>cdc2</em></sup>.


1998 ◽  
Vol 18 (1) ◽  
pp. 546-557 ◽  
Author(s):  
Vjekoslav Dulić ◽  
Gretchen H. Stein ◽  
Dariush Farahi Far ◽  
Steven I. Reed

ABSTRACT Cell cycle arrest in G1 in response to ionizing radiation or senescence is believed to be provoked by inactivation of G1 cyclin-cyclin-dependent kinases (Cdks) by the Cdk inhibitor p21Cip1/Waf1/Sdi1. We provide evidence that in addition to exerting negative control of the G1/S phase transition, p21 may play a role at the onset of mitosis. In nontransformed fibroblasts, p21 transiently reaccumulates in the nucleus near the G2/M-phase boundary, concomitant with cyclin B1 nuclear translocation, and associates with a fraction of cyclin A-Cdk and cyclin B1-Cdk complexes. Premitotic nuclear accumulation of cyclin B1 is not detectable in cells with low p21 levels, such as fibroblasts expressing the viral human papillomavirus type 16 E6 oncoprotein, which functionally inactivates p53, or in tumor-derived cells. Moreover, synchronized E6-expressing fibroblasts show accelerated entry into mitosis compared to wild-type cells and exhibit higher cyclin A- and cyclin B1-associated kinase activities. Finally, primary embryonic fibroblasts derived from p21−/− mice have significantly reduced numbers of premitotic cells with nuclear cyclin B1. These data suggest that p21 promotes a transient pause late in G2 that may contribute to the implementation of late cell cycle checkpoint controls.


1990 ◽  
Vol 10 (7) ◽  
pp. 3847-3851 ◽  
Author(s):  
C H McGowan ◽  
P Russell ◽  
S I Reed

The product of the CDC2Hs gene is the protein kinase subunit of the M-phase promoting factor, which is required for entry into mitosis. The activity of this kinase is regulated in a cell cycle-dependent manner by reversible phosphorylation and through association with other proteins. We report here that in HeLa cells, the abundance of the CDC2Hs mRNA and the rate of synthesis of the encoded protein, p34, vary in a cell cycle-dependent manner.


2002 ◽  
Vol 178 (2) ◽  
pp. 117-125 ◽  
Author(s):  
Ma Aileen C. Mendoza ◽  
Rafael A. Ponce ◽  
Ying C. Ou ◽  
Elaine M. Faustman

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