Das Satyabrata, Gupta Vinayak, Bjorge Johannes, Shi Xiaozhong, Gong Wuming, Garry Mary G, Garry Daniel J
Department of Medicine, Cardiovascular Division, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN, United States.
Department of Physiology, Basic Medical College, Nanchang University, Nanchang, JX, China.
Front Cell Dev Biol. 2023 Feb 27;11:1109648. doi: 10.3389/fcell.2023.1109648. eCollection 2023.
Ets variant 2 (Etv2), a member of the Ets factor family, has an essential role in the formation of endothelial and hematopoietic cell lineages during embryonic development. The functional role of ETS transcription factors is, in part, dependent on the interacting proteins. There are relatively few studies exploring the coordinated interplay between ETV2 and its interacting proteins that regulate mesodermal lineage determination. In order to identify novel ETV2 interacting partners, a yeast two-hybrid analysis was performed and the C2H2 zinc finger transcription factor VEZF1 (vascular endothelial zinc finger 1) was identified as a binding factor, which was specifically expressed within the endothelium during vascular development. To confirm this interaction, co-immunoprecipitation and GST pull down assays demonstrated the direct interaction between ETV2 and VEZF1. During embryoid body differentiation, achieved its peak expression at day 3.0 followed by rapid downregulation, on the other hand expression increased through day 6 of EB differentiation. We have previously shown that ETV2 potently activated gene transcription. Using a promoter-luciferase reporter assay, we demonstrated that VEZF1 co-activated the promoter. Electrophoretic mobility shift assay and Chromatin immunoprecipitation established VEZF1 binding to the promoter. knockout embryonic stem cells had downregulation of hematoendothelial marker genes when undergoing embryoid body mediated mesodermal differentiation whereas overexpression of VEZF1 induced the expression of hematoendothelial genes during differentiation. These current studies provide insight into the co-regulation of the hemato-endothelial lineage development a co-operative interaction between ETV2 and VEZF1.
Ets变体2(Etv2)是Ets因子家族的成员之一,在胚胎发育过程中对内皮细胞和造血细胞谱系的形成起着至关重要的作用。ETS转录因子的功能作用部分取决于相互作用的蛋白质。探索ETV2与其相互作用蛋白之间协调相互作用以调节中胚层谱系确定的研究相对较少。为了鉴定新的ETV2相互作用伙伴,进行了酵母双杂交分析,C2H2锌指转录因子VEZF1(血管内皮锌指1)被鉴定为结合因子,其在血管发育过程中在内皮细胞中特异性表达。为了证实这种相互作用,免疫共沉淀和GST下拉实验证明了ETV2和VEZF1之间的直接相互作用。在胚状体分化过程中, 在第3.0天达到表达峰值,随后迅速下调,另一方面, 在胚状体分化的第6天表达增加。我们之前已经表明ETV2能有效激活 基因转录。使用 启动子-荧光素酶报告基因检测,我们证明VEZF1共同激活了 启动子。电泳迁移率变动分析和染色质免疫沉淀确定VEZF1与 启动子结合。 基因敲除的胚胎干细胞在经历胚状体介导的中胚层分化时,造血内皮标记基因下调,而VEZF1的过表达在分化过程中诱导造血内皮基因的表达。这些当前的研究为造血内皮谱系发育的共同调节提供了见解,即ETV2和VEZF1之间的合作相互作用。 (注:原文中部分基因名称未完整给出,翻译时保留了原文格式)