| Literature DB >> 25910959 |
C Rojas-Marquez1, R Valle-Rios2, E Lopez-Bayghen3, V Ortiz-Navarrete4.
Abstract
T cell activation leads to the induction of genes that are required for appropriate immune responses. This includes CRTAM (Class-I MHC-restricted T cell associated molecule), a protein that plays a key role in T cell development, proliferation, and generating cell polarity during activation. We previously characterized the CRTAM promoter and described how AP-1 family members are important for inducing CRTAM expression upon antigenic activation. Here, we show that CRTAM is a molecular target for ZEB1 (zinc finger E-box-binding protein), a homeodomain/Zn finger transcription factor. Overexpression of ZEB1 repressed CRTAM promoter activity, as well as endogenous CRTAM levels in human T cells. ZEB1-mediated transcriptional repression was abolished when E-box-like elements in the CRTAM promoter are mutated. In summary, ZEB1 functions as a transcriptional repressor for the CRTAM gene in both non-stimulated and stimulated T cells, thereby modulating adaptive immune responses.Entities:
Keywords: CRTAM; E-box-like elements; Promoter; Repression; Transcription; ZEB1
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Year: 2015 PMID: 25910959 DOI: 10.1016/j.molimm.2015.03.253
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407