scholarly journals The Forkhead Transcription Factor FOXM1 Controls Cell Cycle-Dependent Gene Expression through an Atypical Chromatin Binding Mechanism

2012 ◽  
Vol 33 (2) ◽  
pp. 227-236 ◽  
Author(s):  
X. Chen ◽  
G. A. Muller ◽  
M. Quaas ◽  
M. Fischer ◽  
N. Han ◽  
...  
2010 ◽  
Vol 38 (1) ◽  
pp. 29-40 ◽  
Author(s):  
Zoulfia Darieva ◽  
Anne Clancy ◽  
Richard Bulmer ◽  
Emma Williams ◽  
Aline Pic-Taylor ◽  
...  

2004 ◽  
Vol 24 (22) ◽  
pp. 10036-10046 ◽  
Author(s):  
Aline Pic-Taylor ◽  
Zoulfia Darieva ◽  
Brian A. Morgan ◽  
Andrew D. Sharrocks

ABSTRACT The forkhead transcription factor Fkh2p acts in a DNA-bound complex with Mcm1p and the coactivator Ndd1p to regulate cell cycle-dependent expression of the CLB2 gene cluster in Saccharomyces cerevisiae. Here, we demonstrate that Fkh2p is a target of cyclin-dependent protein kinases and that phosphorylation of Fkh2p promotes interactions between Fkh2p and the coactivator Ndd1p. These phosphorylation-dependent changes in the Fkh2p-Ndd1p complex play an important role in the cell cycle-regulated expression of the CLB2 cluster. Our data therefore identify an important regulatory target for cyclin-dependent kinases in the cell cycle and further our molecular understanding of the key cell cycle regulatory transcription factor Fkh2p.


2004 ◽  
Vol 3 (4) ◽  
pp. 944-954 ◽  
Author(s):  
Richard Bulmer ◽  
Aline Pic-Taylor ◽  
Simon K. Whitehall ◽  
Kate A. Martin ◽  
Jonathan B. A. Millar ◽  
...  

ABSTRACT In eukaryotes the regulation of gene expression plays a key role in controlling cell cycle progression. Here, we demonstrate that a forkhead transcription factor, Fkh2, regulates the periodic expression of cdc15 + and spo12 + in the M and G1 phases of the cell division cycle in the fission yeast Schizosaccharomyces pombe. We also show that Fkh2 is important for several cell cycle processes, including cell morphology and cell separation, nuclear structure and migration, and mitotic spindle function. We find that the expression of fkh2 + is itself regulated in a cell cycle-dependent manner in G1 coincident with the expression of cdc18 +, a Cdc10-regulated gene. However, fkh2 + expression is independent of Cdc10 function. Fkh2 was found to be phosphorylated during the cell division cycle, with a timing that suggests that this posttranslational modification is important for cdc15 + and spo12 + expression. Related forkhead proteins regulate G2 and M phase-specific gene expression in the evolutionarily distant Saccharomyces cerevisiae, suggesting that these proteins play conserved roles in regulating cell cycle processes in eukaryotes.


2010 ◽  
Vol 285 (46) ◽  
pp. 35728-35739 ◽  
Author(s):  
Anett Marais ◽  
Zongling Ji ◽  
Emma S. Child ◽  
Eberhard Krause ◽  
David J. Mann ◽  
...  

2013 ◽  
Vol 13 (8) ◽  
pp. 585-595 ◽  
Author(s):  
Subhashini Sadasivam ◽  
James A. DeCaprio

2006 ◽  
Vol 20 (10) ◽  
pp. 2304-2314 ◽  
Author(s):  
Wei Wu ◽  
Min Zou ◽  
Deanna R. Brickley ◽  
Travis Pew ◽  
Suzanne D. Conzen

Abstract Activation of the glucocorticoid receptor (GR) plays a critical role in the stress response of virtually all cell types. Despite recent advances in large-scale genomic and proteomic data acquisition, identification of physiologically relevant molecular events downstream of nuclear hormone receptor activation remains challenging. By analyzing gene expression changes 30 min after dexamethasone (Dex) treatment, we previously found that immediate induction of serum and glucocorticoid-regulated kinase-1 (SGK-1) expression is required for GR-mediated mammary epithelial cell survival signaling. We now report that activation of the GR mediates Forkhead transcription factor 3a (FOXO3a) phosphorylation and inactivation in mammary epithelial cells. GR-mediated induction of SGK-1 expression is required for FOXO3a inactivation; additional growth factor stimulation is not required. To further explore the gene expression changes that occur downstream of GR-mediated FOXO3a inactivation, we analyzed temporal gene expression data and selected GR-down-regulated genes containing core FOXO3a binding motifs in their proximal promoters. This approach revealed several previously unrecognized transcriptional target genes of FOXO3a, including IGF binding protein-3 (IGFBP-3). Endogenous IGFBP-3 expression was confirmed to be dependent on the GR-SGK-1-FOXO3a signaling pathway. Moreover, GR activation decreased FOXO3a-induced apoptosis in SK-BR-3 breast cancer cells. Collectively, our data suggest that GR-mediated FOXO3a inactivation is an important mechanism contributing to glucocorticoid-mediated mammary epithelial cell survival.


2018 ◽  
Vol 165 (5) ◽  
pp. 433-446 ◽  
Author(s):  
Gohei Nishibuchi ◽  
Shinichi Machida ◽  
Reiko Nakagawa ◽  
Yuriko Yoshimura ◽  
Kyoko Hiragami-Hamada ◽  
...  

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