Pal Saumen, Cantor Alan B, Johnson Kirby D, Moran Tyler B, Boyer Meghan E, Orkin Stuart H, Bresnick Emery H
Department of Pharmacology, University of Wisconsin Medical School, 1300 University Avenue, 383 Medical Sciences Center, Madison, WI 53706, USA.
Proc Natl Acad Sci U S A. 2004 Jan 27;101(4):980-5. doi: 10.1073/pnas.0307612100. Epub 2004 Jan 8.
Coregulator recruitment by DNA-bound factors results in chromatin modification and protein-protein interactions, which regulate transcription. However, the mechanism by which the Friend of GATA (FOG) coregulator mediates GATA factor-dependent transcription is unknown. We showed previously that GATA-1 replaces GATA-2 at an upstream region of the GATA-2 locus, and that this GATA switch represses GATA-2. Genetic complementation analysis in FOG-1-null hematopoietic precursors revealed that FOG-1 is not required for establishment or maintenance of the active GATA-2 domain, but is critical for the GATA switch. Analysis of GATA factor binding to additional loci also revealed FOG-1-dependent GATA switches. Thus, FOG-1 facilitates chromatin occupancy by GATA-1 at sites bound by GATA-2. We propose that FOG-1 is a prototype of a new class of coregulators termed chromatin occupancy facilitators, which confer coregulation in certain contexts via enhancing trans-acting factor binding to chromatin in vivo.
与DNA结合的因子招募共调节因子会导致染色质修饰和蛋白质-蛋白质相互作用,从而调节转录。然而,GATA结合因子的辅助蛋白(FOG)共调节因子介导GATA因子依赖性转录的机制尚不清楚。我们之前表明,GATA-1在GATA-2基因座的上游区域取代了GATA-2,并且这种GATA转换会抑制GATA-2。对缺乏FOG-1的造血前体细胞进行的遗传互补分析表明,FOG-1对于活性GATA-2结构域的建立或维持不是必需的,但对GATA转换至关重要。对GATA因子与其他基因座结合的分析也揭示了依赖FOG-1的GATA转换。因此,FOG-1促进了GATA-1在GATA-2结合位点处占据染色质。我们提出,FOG-1是一类新的共调节因子的原型,称为染色质占据促进因子,其通过增强体内反式作用因子与染色质的结合在某些情况下赋予共调节作用。