Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
29
pubmed:dateCreated
1999-8-19
pubmed:databankReference
pubmed:abstractText
Activation of transforming growth factor beta receptors causes the phosphorylation and nuclear translocation of Smad proteins, which then participate in the regulation of expression of target genes. We describe a novel Smad-interacting protein, SIP1, which was identified using the yeast two-hybrid system. Although SIP1 interacts with the MH2 domain of receptor-regulated Smads in yeast and in vitro, its interaction with full-length Smads in mammalian cells requires receptor-mediated Smad activation. SIP1 is a new member of the deltaEF1/Zfh-1 family of two-handed zinc finger/homeodomain proteins. Like deltaEF1, SIP1 binds to 5'-CACCT sequences in different promoters, including the Xenopus brachyury promoter. Overexpression of either full-length SIP1 or its C-terminal zinc finger cluster, which bind to the Xbra2 promoter in vitro, prevented expression of the endogenous Xbra gene in early Xenopus embryos. Therefore, SIP1, like deltaEF1, is likely to be a transcriptional repressor, which may be involved in the regulation of at least one immediate response gene for activin-dependent signal transduction pathways. The identification of this Smad-interacting protein opens new routes to investigate the mechanisms by which transforming growth factor beta members exert their effects on expression of target genes in responsive cells and in the vertebrate embryo.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
16
pubmed:volume
274
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
20489-98
pubmed:dateRevised
2008-11-21
pubmed:meshHeading
pubmed-meshheading:10400677-Amino Acid Sequence, pubmed-meshheading:10400677-Animals, pubmed-meshheading:10400677-Base Sequence, pubmed-meshheading:10400677-Binding Sites, pubmed-meshheading:10400677-COS Cells, pubmed-meshheading:10400677-Cloning, Molecular, pubmed-meshheading:10400677-DNA, Complementary, pubmed-meshheading:10400677-DNA-Binding Proteins, pubmed-meshheading:10400677-Down-Regulation, pubmed-meshheading:10400677-Homeodomain Proteins, pubmed-meshheading:10400677-Molecular Sequence Data, pubmed-meshheading:10400677-Promoter Regions, Genetic, pubmed-meshheading:10400677-Protein Binding, pubmed-meshheading:10400677-Repressor Proteins, pubmed-meshheading:10400677-Sequence Homology, Amino Acid, pubmed-meshheading:10400677-Trans-Activators, pubmed-meshheading:10400677-Xenopus, pubmed-meshheading:10400677-Xenopus Proteins, pubmed-meshheading:10400677-Zinc Fingers
pubmed:year
1999
pubmed:articleTitle
SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5'-CACCT sequences in candidate target genes.
pubmed:affiliation
Department of Cell Growth, Differentiation and Development (VIB-07), Flanders Interuniversity Institute for Biotechnology (VIB), Herestraat49, B-3000 Leuven, Belgium.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't