Garcia-Tuñon I, Guallar D, Alonso-Martin S, Benito A A, Benítez-Lázaro A, Pérez-Palacios R, Muniesa P, Climent M, Sánchez M, Vidal M, Schoorlemmer J
Regenerative Medicine Programme, IIS Aragón, Instituto Aragonés de Ciencias de la Salud, Zaragoza, Avda. Gómez Laguna, 25, Pl. 11, 50009 Zaragoza, Spain.
Stem Cell Res. 2011 Jul;7(1):1-16. doi: 10.1016/j.scr.2011.02.005. Epub 2011 Mar 2.
Rex-1/Zfp42 displays a remarkably restricted pattern of expression in preimplantation embryos, primary spermatocytes, and undifferentiated mouse embryonic stem (ES) cells and is frequently used as a marker gene for pluripotent stem cells. To understand the role of Rex-1 in selfrenewal and pluripotency, we used Rex-1 association as a measure to identify potential target genes, and carried out chromatin-immunoprecipitation assays in combination with gene specific primers to identify genomic targets Rex-1 associates with. We find association of Rex-1 to several genes described previously as bivalently marked regulators of differentiation and development, whose repression in mouse embryonic stem (ES) cells is Polycomb Group-mediated, and controlled directly by Ring1A/B. To substantiate the hypothesis that Rex-1 contributes to gene regulation by PcG, we demonstrate interactions of Rex-1 and YY2 (a close relative of YY1) with Ring1 proteins and the PcG-associated proteins RYBP and YAF2, in line with interactions reported previously for YY1. We also demonstrate the presence of Rex-1 protein in both trophectoderm and Inner Cell Mass of the mouse blastocyst and in both ES and in trophectoderm stem (TS) cells. In TS cells, we were unable to demonstrate association of Rex-1 to the genes it associates with in ES cells, suggesting that association may be cell-type specific. Rex-1 might fine-tune pluripotency in ES cells by modulating Polycomb-mediated gene regulation.
Rex-1/Zfp42在植入前胚胎、初级精母细胞和未分化的小鼠胚胎干细胞中表现出极为受限的表达模式,并且经常被用作多能干细胞的标记基因。为了了解Rex-1在自我更新和多能性中的作用,我们以Rex-1的结合作为一种手段来鉴定潜在的靶基因,并结合基因特异性引物进行染色质免疫沉淀试验,以鉴定与Rex-1结合的基因组靶点。我们发现Rex-1与几个先前被描述为分化和发育的双价标记调节因子的基因存在结合,这些基因在小鼠胚胎干细胞中的抑制是由多梳蛋白家族介导的,并直接受Ring1A/B控制。为了证实Rex-1通过多梳蛋白家族促进基因调控的假说,我们证明了Rex-1和YY2(YY1的近亲)与Ring1蛋白以及与多梳蛋白家族相关的蛋白RYBP和YAF2之间的相互作用,这与先前报道的YY1的相互作用一致。我们还证明了Rex-1蛋白在小鼠囊胚的滋养外胚层和内细胞团以及胚胎干细胞和滋养外胚层干细胞中均有存在。在滋养外胚层干细胞中,我们无法证明Rex-1与它在胚胎干细胞中结合的基因存在结合,这表明这种结合可能具有细胞类型特异性。Rex-1可能通过调节多梳蛋白介导的基因调控来微调胚胎干细胞中的多能性。