Sinha Tanvi, Lammerts van Bueren Kelly, Dickel Diane E, Zlatanova Ivana, Thomas Reuben, Lizama Carlos O, Xu Shan-Mei, Zovein Ann C, Ikegami Kohta, Moskowitz Ivan P, Pollard Katherine S, Pennacchio Len A, Black Brian L
Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA 94143, USA.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; U.S. Department of Energy Joint Genome Institute, 1 Cyclotron Road, Berkeley, CA 94720, USA; Comparative Biochemistry Program, University of California, Berkeley, Berkeley, CA 94720, USA.
Cell Rep. 2022 May 31;39(9):110881. doi: 10.1016/j.celrep.2022.110881.
Endothelial and erythropoietic lineages arise from a common developmental progenitor. Etv2 is a master transcriptional regulator required for the development of both lineages. However, the mechanisms through which Etv2 initiates the gene-regulatory networks (GRNs) for endothelial and erythropoietic specification and how the two GRNs diverge downstream of Etv2 remain incompletely understood. Here, by analyzing a hypomorphic Etv2 mutant, we demonstrate different threshold requirements for initiation of the downstream GRNs for endothelial and erythropoietic development. We show that Etv2 functions directly in a coherent feedforward transcriptional network for vascular endothelial development, and a low level of Etv2 expression is sufficient to induce and sustain the endothelial GRN. In contrast, Etv2 induces the erythropoietic GRN indirectly via activation of Tal1, which requires a significantly higher threshold of Etv2 to initiate and sustain erythropoietic development. These results provide important mechanistic insight into the divergence of the endothelial and erythropoietic lineages.
内皮细胞谱系和红细胞生成谱系起源于一个共同的发育祖细胞。Etv2是这两个谱系发育所需的主要转录调节因子。然而,Etv2启动内皮细胞和红细胞生成特异性的基因调控网络(GRN)的机制,以及这两个GRN在Etv2下游如何分化,仍未完全了解。在这里,通过分析一个低表达的Etv2突变体,我们证明了内皮细胞和红细胞生成发育的下游GRN启动存在不同的阈值要求。我们表明,Etv2直接作用于血管内皮发育的一个连贯前馈转录网络,低水平的Etv2表达足以诱导和维持内皮细胞GRN。相比之下,Etv2通过激活Tal1间接诱导红细胞生成GRN,这需要显著更高的Etv2阈值来启动和维持红细胞生成发育。这些结果为内皮细胞和红细胞生成谱系的分化提供了重要的机制见解。