John T. Milliken Department of Medicine, Division of Nephrology, Washington University School of Medicine, St. Louis, Mo 63110 USA.
Division of Pediatric Hematology/Oncology, Departement of Pediatrics and Department of Biochemistry & Molecular Biology, Pennsylvania State University, Hershey, PA 17033 USA.
Dev Biol. 2020 Aug 15;464(2):176-187. doi: 10.1016/j.ydbio.2020.05.008. Epub 2020 Jun 3.
Chromatin-remodeling complexes play critical roles in establishing gene expression patterns in response to developmental signals. How these epigenetic regulators determine the fate of progenitor cells during development of specific organs is not well understood. We found that genetic deletion of Brg1 (Smarca4), the core enzymatic protein in SWI/SNF, in nephron progenitor cells leads to severe renal hypoplasia. Nephron progenitor cells were depleted in Six2-Cre, Brg1 mice due to reduced cell proliferation. This defect in self-renewal, together with impaired differentiation resulted in a profound nephron deficit in Brg1 mutant kidneys. Sall1, a transcription factor that is required for expansion and maintenance of nephron progenitors, associates with SWI/SNF. Brg1 and Sall1 bind promoters of many progenitor cell genes and regulate expression of key targets that promote their proliferation.
染色质重塑复合物在响应发育信号建立基因表达模式方面发挥着关键作用。这些表观遗传调节剂如何在特定器官的发育过程中决定祖细胞的命运还不是很清楚。我们发现,SWI/SNF 的核心酶蛋白 Brg1(Smarca4)在肾祖细胞中的遗传缺失导致严重的肾发育不全。由于细胞增殖减少,Six2-Cre、Brg1 小鼠中的肾祖细胞被耗尽。这种自我更新的缺陷,加上分化受损,导致 Brg1 突变肾脏中的肾单位严重不足。Sall1 是一种转录因子,对于肾祖细胞的扩增和维持是必需的,它与 SWI/SNF 相关。Brg1 和 Sall1 结合许多祖细胞基因的启动子,并调节促进其增殖的关键靶基因的表达。