Shih Hung Ping, Seymour Philip A, Patel Nisha A, Xie Ruiyu, Wang Allen, Liu Patrick P, Yeo Gene W, Magnuson Mark A, Sander Maike
Departments of Pediatrics and Cellular & Molecular Medicine, Pediatric Diabetes Research Center, University of California San Diego, La Jolla, CA 92093, USA.
Departments of Pediatrics and Cellular & Molecular Medicine, Pediatric Diabetes Research Center, University of California San Diego, La Jolla, CA 92093, USA; DanStem, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen N, Denmark.
Cell Rep. 2015 Oct 13;13(2):326-36. doi: 10.1016/j.celrep.2015.08.082. Epub 2015 Oct 1.
The generation of pancreas, liver, and intestine from a common pool of progenitors in the foregut endoderm requires the establishment of organ boundaries. How dorsal foregut progenitors activate pancreatic genes and evade the intestinal lineage choice remains unclear. Here, we identify Pdx1 and Sox9 as cooperative inducers of a gene regulatory network that distinguishes the pancreatic from the intestinal lineage. Genetic studies demonstrate dual and cooperative functions for Pdx1 and Sox9 in pancreatic lineage induction and repression of the intestinal lineage choice. Pdx1 and Sox9 bind to regulatory sequences near pancreatic and intestinal differentiation genes and jointly regulate their expression, revealing direct cooperative roles for Pdx1 and Sox9 in gene activation and repression. Our study identifies Pdx1 and Sox9 as important regulators of a transcription factor network that initiates pancreatic fate and sheds light on the gene regulatory circuitry that governs the development of distinct organs from multi-lineage-competent foregut progenitors.
前肠内胚层中共同的祖细胞群生成胰腺、肝脏和肠道需要建立器官边界。前肠背侧祖细胞如何激活胰腺基因并避免选择肠道谱系尚不清楚。在这里,我们确定Pdx1和Sox9是一个基因调控网络的协同诱导因子,该网络区分胰腺谱系和肠道谱系。遗传学研究表明,Pdx1和Sox9在胰腺谱系诱导和肠道谱系选择抑制中具有双重和协同作用。Pdx1和Sox9与胰腺和肠道分化基因附近的调控序列结合,并共同调节它们的表达,揭示了Pdx1和Sox9在基因激活和抑制中的直接协同作用。我们的研究确定Pdx1和Sox9是启动胰腺命运的转录因子网络的重要调节因子,并阐明了控制具有多谱系能力的前肠祖细胞发育出不同器官的基因调控回路。