Department of Biomedical Sciences, University of North Dakota, Grand Forks, ND 58202, USA.
Hubei Cancer Hospital, Wuhan, Hubei 430079, China.
Hum Mol Genet. 2020 Jun 3;29(9):1405-1416. doi: 10.1093/hmg/ddz185.
Dominant TBX5 mutation causes Holt-Oram syndrome (HOS), which is characterized by limb defects in humans, but the underlying mechanistic basis is unclear. We used a mouse model with Tbx5 conditional knockdown in Hh-receiving cells (marked by Gli1+) during E8 to E10.5, a previously established model to study atrial septum defects, which displayed polydactyly or hypodactyly. The results suggested that Tbx5 is required for digit identity in a subset of limb mesenchymal cells. Specifically, Tbx5 deletion in this cell population decreased cell apoptosis and increased the proliferation of handplate mesenchymal cells. Furthermore, Tbx5 was found to negatively regulate the Hh-signaling activity through transcriptional regulation of Ptch1, a known Hh-signaling repressor. Repression of Hh-signaling through Smo co-mutation in Tbx5 heterozygotes rescued the limb defects, thus placing Tbx5 upstream of Hh-signaling in limb defects. This work reveals an important missing component necessary for understanding not only limb development but also the molecular and genetic mechanisms underlying HOS.
TBX5 显性突变导致 Holt-Oram 综合征(HOS),其特征是人类肢体缺陷,但潜在的机制基础尚不清楚。我们使用了一种在 E8 至 E10.5 期间在 HH 受体细胞(由 Gli1+标记)中进行 Tbx5 条件性敲低的小鼠模型,这是一种用于研究房间隔缺损的先前建立的模型,该模型显示多指或少指。结果表明,Tbx5 在手板间充质细胞亚群的数字身份中是必需的。具体而言,该细胞群中 Tbx5 的缺失减少了细胞凋亡并增加了手板间充质细胞的增殖。此外,发现 Tbx5 通过对已知的 HH 信号抑制剂 Ptch1 的转录调控来负调控 HH 信号活性。在 Tbx5 杂合子中通过 Smo 共突变抑制 HH 信号可挽救肢体缺陷,因此将 Tbx5 置于 HH 信号在肢体缺陷中的上游。这项工作揭示了一个重要的缺失组成部分,不仅对于理解肢体发育,而且对于 Holt-Oram 综合征的分子和遗传机制都是必要的。