The dual-specificity kinases, TOPK and DYRK1A, are critical for oocyte maturation induced by wild-type-but not by oncogenic- ras-p21 protein

10.2741/2550 ◽  
2007 ◽  
Vol 12 (12) ◽  
pp. 5089 ◽  
Author(s):  
Yongxia Qu
1992 ◽  
Vol 203 (2) ◽  
pp. 329-335 ◽  
Author(s):  
Denise L. Chung ◽  
Alvin Joran ◽  
Fred Friedman ◽  
Richard Robinson ◽  
Paul W. Brandt-Rauf ◽  
...  

2001 ◽  
Vol 48 (1) ◽  
pp. 9-14 ◽  
Author(s):  
Cecilia Kovac ◽  
Lyndon Chie ◽  
Joseph Morin ◽  
Fred Friedman ◽  
Richard Robinson ◽  
...  

2012 ◽  
Vol 3 (1) ◽  
Author(s):  
Hao-Hsuan Jeng ◽  
Laura J Taylor ◽  
Dafna Bar-Sagi
Keyword(s):  

1987 ◽  
Vol 7 (12) ◽  
pp. 4553-4556
Author(s):  
T Satoh ◽  
S Nakamura ◽  
Y Kaziro

Rat pheochromocytoma (PC12) cells differentiate to neuronal cells in response to nerve growth factor. It has been shown that microinjection of oncogenic but not proto-oncogenic p21 protein induces morphological differentiation in PC12 cells (D. Bar-Sagi and J. R. Feramisco, Cell 42:841-848, 1985). In this paper we describe a recombinant human proto-oncogenic Ha-ras protein which can effectively induce neurite extension of PC12 cells when microinjected as a complex with guanosine-5'-O-(3-thiotriphosphate). The protein was found to be less effective when complexed with GTP. On the other hand, an oncogenic ras protein coinjected with guanosine-5'-O-(2-thiodiphosphate) was entirely inactive. These results indicate that the binary p21-GTP complex, but not the p21-GDP complex, is effective in inducing differentiation in PC12 cells, irrespective of the oncogenic or the proto-oncogenic protein.


ras Oncogenes ◽  
1989 ◽  
pp. 303-309
Author(s):  
U. S. Vogel ◽  
R. E. Diehl ◽  
M. S. Marshall ◽  
M. D. Schaber ◽  
R. B. Register ◽  
...  

1987 ◽  
Vol 7 (12) ◽  
pp. 4553-4556 ◽  
Author(s):  
T Satoh ◽  
S Nakamura ◽  
Y Kaziro

Rat pheochromocytoma (PC12) cells differentiate to neuronal cells in response to nerve growth factor. It has been shown that microinjection of oncogenic but not proto-oncogenic p21 protein induces morphological differentiation in PC12 cells (D. Bar-Sagi and J. R. Feramisco, Cell 42:841-848, 1985). In this paper we describe a recombinant human proto-oncogenic Ha-ras protein which can effectively induce neurite extension of PC12 cells when microinjected as a complex with guanosine-5'-O-(3-thiotriphosphate). The protein was found to be less effective when complexed with GTP. On the other hand, an oncogenic ras protein coinjected with guanosine-5'-O-(2-thiodiphosphate) was entirely inactive. These results indicate that the binary p21-GTP complex, but not the p21-GDP complex, is effective in inducing differentiation in PC12 cells, irrespective of the oncogenic or the proto-oncogenic protein.


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