Emechebe Uchenna, Kumar P Pavan, Rozenberg Julian M, Moore Bryn, Firment Ashley, Mirshahi Tooraj, Moon Anne M
Department of Neurobiology and Anatomy, University of Utah, Salt Lake City, United States.
Weis Center for Research, Geisinger Clinic, Danville, United States.
Elife. 2016 Apr 5;5:e07897. doi: 10.7554/eLife.07897.
Crucial roles for T-box3 in development are evident by severe limb malformations and other birth defects caused by T-box3 mutations in humans. Mechanisms whereby T-box3 regulates limb development are poorly understood. We discovered requirements for T-box at multiple stages of mouse limb development and distinct molecular functions in different tissue compartments. Early loss of T-box3 disrupts limb initiation, causing limb defects that phenocopy Sonic Hedgehog (Shh) mutants. Later ablation of T-box3 in posterior limb mesenchyme causes digit loss. In contrast, loss of anterior T-box3 results in preaxial polydactyly, as seen with dysfunction of primary cilia or Gli3-repressor. Remarkably, T-box3 is present in primary cilia where it colocalizes with Gli3. T-box3 interacts with Kif7 and is required for normal stoichiometry and function of a Kif7/Sufu complex that regulates Gli3 stability and processing. Thus, T-box3 controls digit number upstream of Shh-dependent (posterior mesenchyme) and Shh-independent, cilium-based (anterior mesenchyme) Hedgehog pathway function.
T-box3在发育过程中的关键作用通过人类中由T-box3突变引起的严重肢体畸形和其他出生缺陷得以体现。T-box3调节肢体发育的机制目前还知之甚少。我们发现了T-box在小鼠肢体发育多个阶段的需求以及在不同组织区域的独特分子功能。T-box3的早期缺失会破坏肢体起始,导致出现类似于音猬因子(Shh)突变体的肢体缺陷。后期在后肢间充质中敲除T-box3会导致指(趾)缺失。相反,前侧T-box3的缺失会导致多指(趾)畸形,这与初级纤毛功能障碍或Gli3阻遏物功能异常时的情况相同。值得注意的是,T-box3存在于初级纤毛中,并与Gli3共定位。T-box3与Kif7相互作用,是调节Gli3稳定性和加工的Kif7/Sufu复合物正常化学计量和功能所必需的。因此,T-box3在依赖Shh的(后肢间充质)和不依赖Shh的、基于纤毛的(前肢间充质)刺猬信号通路功能的上游控制指(趾)数量。