Identification of PCTA, a TGIF antagonist that promotes PML function in TGF-beta signalling. Faresse, N., Colland, F., Ferrand, N., Prunier, C., Bourgeade, M. F., & Atfi, A. EMBO J, 27(13):1804–15, July, 2008.
abstract   bibtex   
The TGIF homoeodomain protein functions as an important negative regulator in the TGF-beta signalling pathway. The inhibitory function of TGIF is executed in part through its ability to sequester the tumour suppressor cytoplasmic promyelocytic leukaemia (cPML) in the nucleus, thereby preventing the phosphorylation of Smad2 by the activated TGF-beta type I receptor. Here, we report on the identification of PCTA (PML competitor for TGIF association), a TGIF antagonist that promotes TGF-beta-induced transcriptional and cytostatic responses. We provide evidence that PCTA functions in TGF-beta signalling by relieving the suppression of Smad2 phosphorylation by TGIF. Furthermore, we demonstrate that PCTA selectively competes with cPML for TGIF association, resulting in the accumulation of cPML in the cytoplasm, where it associates with SARA and coordinates the access of Smad2 for phosphorylation by the activated TGF-beta type I receptor. Thus, our findings on the mode of action of PCTA provide new and important insights into the molecular mechanism underlying the antagonistic interplay between TGIF and cPML in the TGF-beta signalling network.
@article{faresse_identification_2008,
	title = {Identification of {PCTA}, a {TGIF} antagonist that promotes {PML} function in {TGF}-beta signalling},
	volume = {27},
	issn = {1460-2075 (ELECTRONIC); 0261-4189 (LINKING)},
	shorttitle = {Identification of {PCTA}, a {TGIF} antagonist that promotes {PML} function in {TGF}-beta signalling},
	abstract = {The TGIF homoeodomain protein functions as an important negative regulator in the TGF-beta signalling pathway. The inhibitory function of TGIF is executed in part through its ability to sequester the tumour suppressor cytoplasmic promyelocytic leukaemia (cPML) in the nucleus, thereby preventing the phosphorylation of Smad2 by the activated TGF-beta type I receptor. Here, we report on the identification of PCTA (PML competitor for TGIF association), a TGIF antagonist that promotes TGF-beta-induced transcriptional and cytostatic responses. We provide evidence that PCTA functions in TGF-beta signalling by relieving the suppression of Smad2 phosphorylation by TGIF. Furthermore, we demonstrate that PCTA selectively competes with cPML for TGIF association, resulting in the accumulation of cPML in the cytoplasm, where it associates with SARA and coordinates the access of Smad2 for phosphorylation by the activated TGF-beta type I receptor. Thus, our findings on the mode of action of PCTA provide new and important insights into the molecular mechanism underlying the antagonistic interplay between TGIF and cPML in the TGF-beta signalling network.},
	number = {13},
	journal = {EMBO J},
	author = {Faresse, N. and Colland, F. and Ferrand, N. and Prunier, C. and Bourgeade, M. F. and Atfi, A.},
	month = jul,
	year = {2008},
	keywords = {Animals Carrier Proteins/ metabolism Cell Line DNA},
	pages = {1804--15}
}
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