Negi Soumya, Bolt Christopher Chase, Zhang Huimin, Stubbs Lisa
Department of Cell and Developmental Biology, University of Illinois, Urbana-Champaign, United States.
École Polytechnique Fédérale de Lausanne, SV ISREC UPDUB, 1015 Lausanne, Switzerland.
Dev Biol. 2019 Feb 15;446(2):180-192. doi: 10.1016/j.ydbio.2018.11.023. Epub 2018 Dec 27.
The evolutionarily conserved transcription factor, Tbx18, is expressed in a dynamic pattern throughout embryonic and early postnatal life and plays crucial roles in the development of multiple organ systems. Previous studies have indicated that this dynamic function is controlled by an expansive regulatory structure, extending far upstream and downstream of the gene. With the goal of identifying elements that interact with the Tbx18 promoter in developing prostate, we coupled chromatin conformation capture (4C) and ATAC-seq from embryonic day 18.5 (E18.5) mouse urogenital sinus (UGS), where Tbx18 is highly expressed. The data revealed dozens of active chromatin elements distributed throughout a 1.5 million base pair topologically associating domain (TAD). To identify cell types contributing to this chromatin signal, we used lineage tracing methods with a Tbx18 Cre "knock-in" allele; these data show clearly that Tbx18-expressing precursors differentiate into wide array of cell types in multiple tissue compartments, most of which have not been previously reported. We also used a 209 kb Cre-expressing Tbx18 transgene, to partition enhancers for specific precursor types into two rough spatial domains. Within this central 209 kb compartment, we identified ECR1, previously described to regulate Tbx18 expression in ureter, as an active regulator of UGS expression. Together these data define the diverse fates of Tbx18+ precursors in prostate-associated tissues for the first time, and identify a highly active TAD controlling the gene's essential function in this tissue.
进化上保守的转录因子Tbx18在胚胎期和出生后早期以动态模式表达,并在多个器官系统的发育中发挥关键作用。先前的研究表明,这种动态功能受一个广泛的调控结构控制,该结构延伸至基因的上下游很远的位置。为了确定在发育中的前列腺中与Tbx18启动子相互作用的元件,我们将染色质构象捕获技术(4C)与来自胚胎第18.5天(E18.5)小鼠泌尿生殖窦(UGS)的ATAC-seq相结合,Tbx18在该部位高度表达。数据显示,数十个活跃的染色质元件分布在一个150万个碱基对的拓扑相关结构域(TAD)中。为了确定对这种染色质信号有贡献的细胞类型,我们使用谱系追踪方法和Tbx18 Cre“敲入”等位基因;这些数据清楚地表明,表达Tbx18的前体可分化为多个组织隔室中的多种细胞类型,其中大多数此前尚未见报道。我们还使用了一个表达Cre的209 kb Tbx18转基因,将特定前体类型的增强子分为两个大致的空间结构域。在这个中央209 kb的结构域内,我们确定了先前描述为在输尿管中调节Tbx18表达的ECR1,它是UGS表达的一个活跃调节因子。这些数据首次定义了前列腺相关组织中Tbx18+前体的多种命运,并确定了一个高度活跃的TAD控制该基因在该组织中的基本功能。