Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
EMBO J. 2010 Jan 20;29(2):442-56. doi: 10.1038/emboj.2009.336. Epub 2009 Nov 19.
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.
GATA 转录因子与 FOG 蛋白相互作用,通过激活和抑制转录来调节组织发育。FOG-1(ZFPM1)是造血因子 GATA-1 的辅助因子,通过保守的 N 端基序与 NuRD 共抑制复合物结合。令人惊讶的是,我们在体内检测到了被抑制和活跃的 GATA-1/FOG-1 靶基因都存在 NuRD 成分。此外,虽然在某些情况下 NuRD 是转录抑制所必需的,但我们还表明 NuRD 也直接需要 FOG-1 依赖性转录激活。FOG-1/NuRD 相互作用被破坏的小鼠表现出与 Gata1 和 Fog1 基因种系突变相似的缺陷,包括贫血和巨血小板减少症。在原发性突变红细胞和巨核细胞(MK)中的基因表达分析显示,NuRD 在选择的 GATA-1/FOG-1 靶基因的抑制和激活过程中都具有重要功能。这些结果表明 NuRD 是 FOG-1 的关键共因子,并强调了 NuRD 被谱系特异性转录因子在适当的细胞和遗传背景下激活和抑制基因转录的多功能性。