Literature DB >> 22119658

Few Smad proteins and many Smad-interacting proteins yield multiple functions and action modes in TGFβ/BMP signaling in vivo.

Andrea Conidi1, Silvia Cazzola, Karen Beets, Kathleen Coddens, Clara Collart, Frederique Cornelis, Luk Cox, Debruyn Joke, Mariya P Dobreva, Ruben Dries, Camila Esguerra, Annick Francis, Abdelilah Ibrahimi, Roel Kroes, Flore Lesage, Elke Maas, Ivan Moya, Paulo N G Pereira, Elke Stappers, Agata Stryjewska, Veronique van den Berghe, Liesbeth Vermeire, Griet Verstappen, Eve Seuntjens, Lieve Umans, An Zwijsen, Danny Huylebroeck.   

Abstract

Signaling by the many ligands of the TGFβ family strongly converges towards only five receptor-activated, intracellular Smad proteins, which fall into two classes i.e. Smad2/3 and Smad1/5/8, respectively. These Smads bind to a surprisingly high number of Smad-interacting proteins (SIPs), many of which are transcription factors (TFs) that co-operate in Smad-controlled target gene transcription in a cell type and context specific manner. A combination of functional analyses in vivo as well as in cell cultures and biochemical studies has revealed the enormous versatility of the Smad proteins. Smads and their SIPs regulate diverse molecular and cellular processes and are also directly relevant to development and disease. In this survey, we selected appropriate examples on the BMP-Smads, with emphasis on Smad1 and Smad5, and on a number of SIPs, i.e. the CPSF subunit Smicl, Ttrap (Tdp2) and Sip1 (Zeb2, Zfhx1b) from our own research carried out in three different vertebrate models.
Copyright © 2011. Published by Elsevier Ltd.

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Year:  2011        PMID: 22119658     DOI: 10.1016/j.cytogfr.2011.11.006

Source DB:  PubMed          Journal:  Cytokine Growth Factor Rev        ISSN: 1359-6101            Impact factor:   7.638


  49 in total

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