Brooke-Bisschop Travis, Savory Joanne G A, Foley Tanya, Ringuette Randy, Lohnes David
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, Canada.
Dev Biol. 2017 Feb 15;422(2):115-124. doi: 10.1016/j.ydbio.2017.01.002. Epub 2017 Jan 6.
The Cdx transcription factors play essential roles in primitive hematopoiesis in the zebrafish where they exert their effects, in part, through regulation of hox genes. Defects in hematopoiesis have also been reported in Cdx mutant murine embryonic stem cell models, however, to date no mouse model reflecting the zebrafish Cdx mutant hematopoietic phenotype has been described. This is likely due, in part, to functional redundancy among Cdx members and the early lethality of Cdx2 null mutants. To circumvent these limitations, we used Cre-mediated conditional deletion to assess the impact of concomitant loss of Cdx1 and Cdx2 on murine primitive hematopoiesis. We found that Cdx1/Cdx2 double mutants exhibited defects in primitive hematopoiesis and yolk sac vasculature concomitant with reduced expression of several genes encoding hematopoietic transcription factors including Scl/Tal1. Chromatin immunoprecipitation analysis revealed that Scl was occupied by Cdx2 in vivo, and Cdx mutant hematopoietic yolk sac differentiation defects could be rescued by expression of exogenous Scl. These findings demonstrate critical roles for Cdx members in murine primitive hematopoiesis upstream of Scl.
Cdx转录因子在斑马鱼的原始造血过程中发挥着重要作用,它们部分通过调控hox基因来发挥作用。在Cdx突变小鼠胚胎干细胞模型中也报道了造血缺陷,然而,迄今为止,尚未描述反映斑马鱼Cdx突变体造血表型的小鼠模型。这可能部分是由于Cdx成员之间的功能冗余以及Cdx2基因敲除突变体的早期致死性。为了克服这些限制,我们使用Cre介导的条件性缺失来评估Cdx1和Cdx2同时缺失对小鼠原始造血的影响。我们发现Cdx1/Cdx2双突变体在原始造血和卵黄囊脉管系统中表现出缺陷,同时几种编码造血转录因子(包括Scl/Tal1)的基因表达降低。染色质免疫沉淀分析表明,Scl在体内被Cdx2占据,并且通过表达外源性Scl可以挽救Cdx突变体造血卵黄囊分化缺陷。这些发现证明了Cdx成员在小鼠原始造血中Scl上游的关键作用。