Cytokine-induced phosphoinositide 3-kinase activity promotes Cdk2 activation in factor-dependent hematopoietic cells

2004 ◽  
Vol 299 (1) ◽  
pp. 257-266 ◽  
Author(s):  
Matthew K Henry ◽  
Dipali Nimbalkar ◽  
Raymond J Hohl ◽  
Frederick W Quelle
Cell ◽  
1994 ◽  
Vol 77 (1) ◽  
pp. 83-93 ◽  
Author(s):  
L. Stephens ◽  
A. Smrcka ◽  
F.T. Cooke ◽  
T.R. Jackson ◽  
P.C. Sternweis ◽  
...  

2002 ◽  
Vol 13 (2) ◽  
pp. 480-492 ◽  
Author(s):  
Tom D. Wolkow ◽  
Tamar Enoch

Fission yeast Rad3 is a member of a family of phosphoinositide 3-kinase -related kinases required for the maintenance of genomic stability in all eukaryotic cells. In fission yeast, Rad3 regulates the cell cycle arrest and recovery activities associated with the G2/M checkpoint. We have developed an assay that directly measures Rad3 kinase activity in cells expressing physiological levels of the protein. Using the assay, we demonstrate directly that Rad3 kinase activity is stimulated by checkpoint signals. Of the five other G2/M checkpoint proteins (Hus1, Rad1, Rad9, Rad17, and Rad26), only Rad26 was required for Rad3 kinase activity. Because Rad26 has previously been shown to interact constitutively with Rad3, our results demonstrate that Rad26 is a regulatory subunit, and Rad3 is the catalytic subunit, of the Rad3/Rad26 kinase complex. Analysis of Rad26/Rad3 kinase activation in rad26.T12, a mutant that is proficient for cell cycle arrest, but defective in recovery, suggests that these two responses to checkpoint signals require quantitatively different levels of kinase activity from the Rad3/Rad26 complex.


Cell Cycle ◽  
2012 ◽  
Vol 11 (19) ◽  
pp. 3523-3524
Author(s):  
Ana González-García ◽  
Ana C. Carrera

1985 ◽  
Vol 5 (10) ◽  
pp. 2543-2551 ◽  
Author(s):  
I MacDonald ◽  
J Levy ◽  
T Pawson

The avian c-fps and mammalian c-fes proto-oncogenes are cognate cellular sequences. Antiserum raised against the P140gag-fps transforming protein of Fujinami avian sarcoma virus specifically recognized a 92,000-Mr protein in human and mouse hematopoietic cells which was closely related in structure to Snyder-Theilen feline sarcoma virus P87gag-fes. This polypeptide was apparently the product of the human c-fes gene and was therefore designated p92c-fes. Human p92c-fes was associated with a tyrosine-specific protein kinase activity in vitro and was capable of both autophosphorylation and phosphorylation of enolase as an exogenous protein substrate. The synthesis of human and mouse p92c-fes was largely, though not entirely, confined to myeloid cells. p92c-fes was expressed to relatively high levels in a multipotential murine myeloid cell line, in more mature human and mouse granulocyte-macrophage progenitors, and in differentiated macrophage like cells as well as in the mononuclear fraction of normal and leukemic human peripheral blood. p92c-fes was not found in erythroid cells, with the exception of a human erythroleukemia line which retains the capacity to differentiate into macrophage like cells. These results suggest a normal role for the p92c-fes tyrosine kinase in hematopoiesis, particularly in granulocyte-macrophage differentiation. In addition, a distinct 94,000-Mr polypeptide, antigenically related to p92c-fes, was identified in a number of hematopoietic and nonhematopoietic human and mouse cells and was also found to be associated with a tyrosine-specific protein kinase activity.


2012 ◽  
Vol 26 (S1) ◽  
Author(s):  
Marciano Sablad ◽  
Glenda Castro ◽  
Natasha Rozenkrants ◽  
Karen Ngo ◽  
Tadimeti Rao ◽  
...  

2010 ◽  
Vol 185 (7) ◽  
pp. 4042-4052 ◽  
Author(s):  
Julia Rolf ◽  
Sarah E. Bell ◽  
Dorottya Kovesdi ◽  
Michelle L. Janas ◽  
Dalya R. Soond ◽  
...  

2006 ◽  
Vol 9 (7) ◽  
pp. 565-570 ◽  
Author(s):  
Xiaoke Yang ◽  
Puyao Li ◽  
Larry Feldberg ◽  
Steven Kim ◽  
Michael Bowman ◽  
...  

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