State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China.
Cells. 2019 Sep 5;8(9):1038. doi: 10.3390/cells8091038.
We have previously observed the predominant expression of nucleoporin 62-like (Nup62l mRNA in the pharyngeal region of zebrafish, which raises the question whether Nup62l has important implications in governing the morphogenesis of pharyngeal arches (PA) in zebrafish. Herein, we explored the functions of Nup62l in PA development. The disruption of Nup62l with a CRISPR/Cas9-dependent gene knockout approach led to defective PA, which was characterized by a thinned and shortened pharyngeal region and a significant loss of pharyngeal cartilages. During pharyngeal cartilage formation, prechondrogenic condensation and chondrogenic differentiation were disrupted in homozygous -mutants, while the specification and migration of cranial neural crest cells (CNCCs) were unaffected. Mechanistically, the impaired PA region of -mutants underwent extensive apoptosis, which was mainly dependent on activation of p53-dependent apoptotic pathway. Moreover, aberrant activation of a series of apoptotic pathways in -mutants is closely associated with the inactivation of Wnt/β-catenin signaling. Thus, these findings suggest that the regulation of Wnt/β-catenin activity by Nup62l is crucial for PA formation in zebrafish.
我们之前观察到核孔蛋白 62 样(Nup62l)mRNA 在斑马鱼咽区的主要表达,这就提出了一个问题,即 Nup62l 是否对斑马鱼咽弓(PA)的形态发生有重要影响。在此,我们探讨了 Nup62l 在 PA 发育中的功能。利用 CRISPR/Cas9 依赖性基因敲除方法破坏 Nup62l ,导致 PA 缺陷,其特征是咽区变薄和缩短,以及咽软骨的大量丢失。在咽软骨形成过程中,同源突变纯合子中前软骨形成和软骨分化受到破坏,而颅神经嵴细胞(CNCCs)的特化和迁移不受影响。在机制上,-突变体的受损 PA 区域经历广泛的细胞凋亡,这主要依赖于 p53 依赖性凋亡途径的激活。此外,-突变体中一系列凋亡途径的异常激活与 Wnt/β-catenin 信号的失活密切相关。因此,这些发现表明 Nup62l 对 Wnt/β-catenin 活性的调节对斑马鱼 PA 的形成至关重要。