Smad2 and Smad3 positively and negatively regulate TGF beta-dependent transcription through the forkhead DNA-binding protein FAST2 - PubMed (original) (raw)
Comparative Study
Smad2 and Smad3 positively and negatively regulate TGF beta-dependent transcription through the forkhead DNA-binding protein FAST2
E Labbé et al. Mol Cell. 1998 Jul.
Free article
Abstract
We identify a mammalian forkhead domain protein, FAST2, that is required for induction of the goosecoid (gsc) promoter by TGF beta or activin signaling. FAST2 binds to a sequence in the gsc promoter, but efficient transcriptional activation and assembly of a DNA-binding complex of FAST2, Smad2, and Smad4 requires an adjacent Smad4 site. Smad3 is closely related to Smad2 but suppresses activation of the gsc promoter. Inhibitory activity is conferred by the MH1 domain, which unlike that of Smad2, binds to the Smad4 site. Through competition for this shared site, Smad3 may prevent transcription by altering the conformation of the DNA-binding complex. Thus, we describe a mechanism whereby Smad2 and Smad3 positively and negatively regulate a TGF beta/activin target gene.
Similar articles
- Homeodomain and winged-helix transcription factors recruit activated Smads to distinct promoter elements via a common Smad interaction motif.
Germain S, Howell M, Esslemont GM, Hill CS. Germain S, et al. Genes Dev. 2000 Feb 15;14(4):435-51. Genes Dev. 2000. PMID: 10691736 Free PMC article. - Characterization of human FAST-1, a TGF beta and activin signal transducer.
Zhou S, Zawel L, Lengauer C, Kinzler KW, Vogelstein B. Zhou S, et al. Mol Cell. 1998 Jul;2(1):121-7. doi: 10.1016/s1097-2765(00)80120-3. Mol Cell. 1998. PMID: 9702198 - Positive and negative regulation of the transforming growth factor beta/activin target gene goosecoid by the TFII-I family of transcription factors.
Ku M, Sokol SY, Wu J, Tussie-Luna MI, Roy AL, Hata A. Ku M, et al. Mol Cell Biol. 2005 Aug;25(16):7144-57. doi: 10.1128/MCB.25.16.7144-7157.2005. Mol Cell Biol. 2005. PMID: 16055724 Free PMC article. - Receptor-regulated Smads in TGF-beta signaling.
Liu F. Liu F. Front Biosci. 2003 Sep 1;8:s1280-303. doi: 10.2741/1149. Front Biosci. 2003. PMID: 12957874 Review. - [The cellular signal transduction of TGF-beta family].
Huang JF, Fang DC, Lu R. Huang JF, et al. Sheng Li Ke Xue Jin Zhan. 1999 Jul;30(3):255-8. Sheng Li Ke Xue Jin Zhan. 1999. PMID: 12532793 Review. Chinese. No abstract available.
Cited by
- TGF-β family signaling in stem cells.
Sakaki-Yumoto M, Katsuno Y, Derynck R. Sakaki-Yumoto M, et al. Biochim Biophys Acta. 2013 Feb;1830(2):2280-96. doi: 10.1016/j.bbagen.2012.08.008. Epub 2012 Aug 16. Biochim Biophys Acta. 2013. PMID: 22959078 Free PMC article. Review. - Nodal signaling activates differentiation genes during zebrafish gastrulation.
Bennett JT, Joubin K, Cheng S, Aanstad P, Herwig R, Clark M, Lehrach H, Schier AF. Bennett JT, et al. Dev Biol. 2007 Apr 15;304(2):525-40. doi: 10.1016/j.ydbio.2007.01.012. Epub 2007 Jan 12. Dev Biol. 2007. PMID: 17306247 Free PMC article. - Foxh1 recruits Gsc to negatively regulate Mixl1 expression during early mouse development.
Izzi L, Silvestri C, von Both I, Labbé E, Zakin L, Wrana JL, Attisano L. Izzi L, et al. EMBO J. 2007 Jul 11;26(13):3132-43. doi: 10.1038/sj.emboj.7601753. Epub 2007 Jun 14. EMBO J. 2007. PMID: 17568773 Free PMC article. - BF-1 interferes with transforming growth factor beta signaling by associating with Smad partners.
Dou C, Lee J, Liu B, Liu F, Massague J, Xuan S, Lai E. Dou C, et al. Mol Cell Biol. 2000 Sep;20(17):6201-11. doi: 10.1128/MCB.20.17.6201-6211.2000. Mol Cell Biol. 2000. PMID: 10938097 Free PMC article. - Erbin inhibits transforming growth factor beta signaling through a novel Smad-interacting domain.
Dai F, Chang C, Lin X, Dai P, Mei L, Feng XH. Dai F, et al. Mol Cell Biol. 2007 Sep;27(17):6183-94. doi: 10.1128/MCB.00132-07. Epub 2007 Jun 25. Mol Cell Biol. 2007. PMID: 17591701 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous