| Literature DB >> 15317935 |
Joshua R Friedman1, Brian Larris, Phillip P Le, T Harshani Peiris, Athanasios Arsenlis, Jonathan Schug, John W Tobias, Klaus H Kaestner, Linda E Greenbaum.
Abstract
CCAAT enhancer-binding protein beta (C/EBPbeta), a basic-leucine zipper transcription factor, is an important effector of signals in physiologic growth and cancer. The identification of direct C/EBPbeta targets in vivo has been limited by functional compensation by other C/EBP family proteins and the low stringency of the consensus sequence. Here we use the combined power of expression profiling and high-throughput chromatin immunoprecipitation to identify direct and biologically relevant targets of C/EBPbeta. We identified 25 potential C/EBPbeta targets, of which 88% of those tested were confirmed as in vivo C/EBPbeta-binding sites. Six of these genes also displayed differential expression in C/EBPbeta-/- livers. Computational analysis revealed that bona fide C/EBPbeta target genes can be distinguished by the presence of binding motifs for specific additional transcription factors in the vicinity of the C/EBPbeta site. This approach is generally applicable to the discovery of direct, biologically relevant targets of mammalian transcription factors. Copyright 2004 The National Academy of Sciencs of the USAEntities:
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Year: 2004 PMID: 15317935 PMCID: PMC516505 DOI: 10.1073/pnas.0402875101
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205