Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW), University Medical Centre Utrecht, CancerGenomiCs.nl, Uppsalalaan 8, 3584 CT Utrecht, the Netherlands.
Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Centre Utrecht, 3508 AB Utrecht, the Netherlands.
Cell Stem Cell. 2015 Feb 5;16(2):158-70. doi: 10.1016/j.stem.2014.12.006. Epub 2015 Jan 22.
The Wnt signaling pathway controls stem cell identity in the intestinal epithelium and in many other adult organs. The transcription factor Ascl2 (a Wnt target gene) is a master regulator of intestinal stem cell identity. It is unclear how the continuous Wnt gradient along the crypt axis is translated into discrete expression of Ascl2 and discrete specification of stem cells at crypt bottoms. We show that (1) Ascl2 is regulated in a direct autoactivatory loop, leading to a distinct on/off expression pattern, and (2) Wnt/R-spondin can activate this regulatory loop. This mechanism interprets the Wnt levels in the intestinal crypt and translates the continuous Wnt signal into a discrete Ascl2 "on" or "off" decision. In turn, Ascl2, together with β-catenin/Tcf, activates the genes fundamental to the stem cell state. In this manner, Ascl2 forms a transcriptional switch that is both Wnt responsive and Wnt dependent to define stem cell identity.
Wnt 信号通路控制着肠道上皮和许多其他成年器官中的干细胞特性。转录因子 Ascl2(Wnt 的靶基因)是肠道干细胞特性的主要调节因子。目前尚不清楚沿隐窝轴的连续 Wnt 梯度如何转化为 Ascl2 的离散表达以及隐窝底部干细胞的离散特化。我们发现:(1)Ascl2 在直接的自动激活回路中受到调控,导致明显的开/关表达模式;(2)Wnt/R-spondin 可以激活这个调节回路。该机制解释了肠道隐窝中的 Wnt 水平,并将连续的 Wnt 信号转化为离散的 Ascl2“开”或“关”决定。反过来,Ascl2 与 β-catenin/Tcf 一起激活了干细胞状态所必需的基因。通过这种方式,Ascl2 形成了一个转录开关,它对 Wnt 有反应并且依赖于 Wnt 来定义干细胞特性。