| Literature DB >> 25935112 |
Maria J Macias1, Pau Martin-Malpartida2, Joan Massagué3.
Abstract
Smad transcription factors are central to the signal transduction pathway that mediates the numerous effects of the transforming growth factor β (TGF-β) superfamily of cytokines in metazoan embryo development as well as in adult tissue regeneration and homeostasis. Although Smad proteins are conserved, recent genome-sequencing projects have revealed their sequence variation in metazoan evolution, human polymorphisms, and cancer. Structural studies of Smads bound to partner proteins and target DNA provide a framework for understanding the significance of these evolutionary and pathologic sequence variations. We synthesize the extant mutational and structural data to suggest how genetic variation in Smads may affect the structure, regulation, and function of these proteins. We also present a web application that compares Smad sequences and displays Smad protein structures and their disease-associated variants.Entities:
Keywords: Smad DNA binding; Smad conservation/variation; Smad proteins; Smad structure; Smad-binding proteins; TGF-β signaling; cancer mutations
Mesh:
Substances:
Year: 2015 PMID: 25935112 PMCID: PMC4485443 DOI: 10.1016/j.tibs.2015.03.012
Source DB: PubMed Journal: Trends Biochem Sci ISSN: 0968-0004 Impact factor: 13.807