Huggins G S, Bacani C J, Boltax J, Aikawa R, Leiden J M
Cardiovascular Biology Laboratory, Harvard School of Public Health, Cardiac Unit, Massachusetts General Hospital, USA.
J Biol Chem. 2001 Jul 27;276(30):28029-36. doi: 10.1074/jbc.M103577200. Epub 2001 May 29.
Friend of GATA (FOG)-2 is a multi-zinc finger transcriptional corepressor protein that binds specifically to GATA4. Gene targeting studies have demonstrated that FOG-2 is required for normal cardiac morphogenesis, including the development of the coronary vasculature, left ventricular compact zone, and heart valves. To better understand the molecular mechanisms by which FOG-2 regulates these cardiac developmental programs, we screened a mouse day 11 embryo library using a yeast two-hybrid interaction trap with the fifth and sixth zinc fingers of FOG-2 as bait. Using this approach, we isolated clones encoding the orphan nuclear receptors chicken ovalbumin upstream promoter-transcription factor (COUP-TF) 2 and COUP-TF3. COUP-TF2-null embryos die during embryonic development with defective angiogenesis and cardiac defects, a pattern that partly resembles the FOG-2-null phenotype. The interaction between COUP-TF2 and FOG-2 in mammalian cells was confirmed by co-immunoprecipitation of these proteins from transfected COS-7 cells. The sites of binding interaction between COUP-TF2 and FOG-2 were mapped to zinc fingers 5 and 6 and fingers 7 and 8 of FOG-2 and to the carboxyl terminus of the COUP-TF proteins. Binding to COUP-TF2 was specific because FOG-2 did not interact with the ligand-binding domains of retinoid X receptor alpha, glucocorticoid receptor, and peroxisome proliferating antigen receptor gamma, which are related to the COUP-TF proteins. Full-length FOG-2 markedly enhanced transcriptional repression by GAL4-COUP-TF2(117-414), but not by a COUP-TF2 repression domain mutant. Moreover, FOG-2 repressed COUP-TF2dependent synergistic activation of the atrial natriuretic factor promoter by both GATA4 and the FOG-2-independent mutant GATA4-E215K. Taken together, these findings suggest that FOG-2 functions as a corepressor for both GATA and COUP-TF proteins.
GATA结合因子(FOG)-2是一种多锌指转录共抑制蛋白,它能特异性地与GATA4结合。基因靶向研究表明,FOG-2是正常心脏形态发生所必需的,包括冠状血管系统、左心室致密区和心脏瓣膜的发育。为了更好地理解FOG-2调节这些心脏发育程序的分子机制,我们以FOG-2的第五和第六个锌指为诱饵,利用酵母双杂交相互作用陷阱筛选了小鼠第11天胚胎文库。通过这种方法,我们分离出了编码孤儿核受体鸡卵清蛋白上游启动子转录因子(COUP-TF)2和COUP-TF3的克隆。COUP-TF2基因敲除胚胎在胚胎发育过程中因血管生成缺陷和心脏缺陷而死亡,这种模式部分类似于FOG-2基因敲除表型。通过从转染的COS-7细胞中共免疫沉淀这些蛋白,证实了COUP-TF2与FOG-2在哺乳动物细胞中的相互作用。COUP-TF2与FOG-2的结合相互作用位点定位于FOG-2的锌指5和6以及锌指7和8,以及COUP-TF蛋白的羧基末端。与COUP-TF2的结合是特异性的,因为FOG-2不与视黄酸X受体α、糖皮质激素受体和过氧化物酶体增殖抗原受体γ的配体结合域相互作用,这些受体与COUP-TF蛋白相关。全长FOG-2显著增强了GAL4-COUP-TF2(117-414)的转录抑制作用,但对COUP-TF2抑制域突变体则没有增强作用。此外,FOG-2抑制了GATA4和不依赖FOG-2的突变体GATA4-E215K对心房钠尿肽启动子的COUP-TF2依赖性协同激活。综上所述,这些发现表明FOG-2作为GATA和COUP-TF蛋白的共抑制因子发挥作用。