| Literature DB >> 19927129 |
Annarita Miccio1, Yuhuan Wang, Wei Hong, Gregory D Gregory, Hongxin Wang, Xiang Yu, John K Choi, Suresh Shelat, Wei Tong, Mortimer Poncz, Gerd A Blobel.
Abstract
GATA transcription factors interact with FOG proteins to regulate tissue development by activating and repressing transcription. FOG-1 (ZFPM1), a co-factor for the haematopoietic factor GATA-1, binds to the NuRD co-repressor complex through a conserved N-terminal motif. Surprisingly, we detected NuRD components at both repressed and active GATA-1/FOG-1 target genes in vivo. In addition, while NuRD is required for transcriptional repression in certain contexts, we show a direct requirement of NuRD also for FOG-1-dependent transcriptional activation. Mice in which the FOG-1/NuRD interaction is disrupted display defects similar to germline mutations in the Gata1 and Fog1 genes, including anaemia and macrothrombocytopaenia. Gene expression analysis in primary mutant erythroid cells and megakaryocytes (MKs) revealed an essential function for NuRD during both the repression and activation of select GATA-1/FOG-1 target genes. These results show that NuRD is a critical co-factor for FOG-1 and underscore the versatile use of NuRD by lineage-specific transcription factors to activate and repress gene transcription in the appropriate cellular and genetic context.Entities:
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Year: 2009 PMID: 19927129 PMCID: PMC2824460 DOI: 10.1038/emboj.2009.336
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598