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Nucleoporin 62-Like Protein Is Required for the Development of Pharyngeal Arches through Regulation of Wnt/β-Catenin Signaling and Apoptotic Homeostasis in Zebrafish

机译:通过调节Wnt /β-Catenin信号传导和斑马鱼的细胞凋亡稳态需要咽核蛋白62类蛋白来促进咽弓的发展。

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摘要

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 nup62l-mutants, while the specification and migration of cranial neural crest cells (CNCCs) were unaffected. Mechanistically, the impaired PA region of nup62l-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 nup62l-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.
机译:我们之前已经观察到斑马鱼的咽区域中核孔蛋白62样(Nup62l)mRNA的主要表达,这引起了一个问题,即Nup62l是否在控制斑马鱼的咽弓(PA)的形态发生中具有重要意义。在本文中,我们探讨了Nup62l在PA开发中的功能。用CRISPR / Cas9依赖性基因敲除方法破坏Nup62l会导致PA缺陷,其特征是咽部区域变薄和变短,咽软骨明显丧失。在咽软骨形成过程中,纯合nup62l突变体的软骨前凝结和软骨分化受到破坏,而颅神经rest细胞(CNCC)的规格和迁移不受影响。从机理上讲,受损的nup62l突变体的PA区域经历了广泛的凋亡,这主要取决于p53依赖性凋亡途径的激活。此外,nup62l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活性的调节对于斑马鱼PA的形成至关重要。

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