Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY, 40536, USA.
Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY, 40292, USA; KY INBRE Bioinformatics Core, University of Louisville, Louisville, KY, 40292, USA.
Dev Biol. 2022 Dec;492:156-171. doi: 10.1016/j.ydbio.2022.10.010. Epub 2022 Oct 18.
The extracellular signal-regulated kinase (ERK1/2) pathway is essential in embryonic development. The scaffold protein Shoc2 is a critical modulator of ERK1/2 signals, and mutations in the shoc2 gene lead to the human developmental disease known as Noonan-like syndrome with loose anagen hair (NSLH). The loss of Shoc2 and the shoc2 NSLH-causing mutations affect the tissues of neural crest (NC) origin. In this study, we utilized the zebrafish model to dissect the role of Shoc2-ERK1/2 signals in the development of NC. These studies established that the loss of Shoc2 significantly altered the expression of transcription factors regulating the specification and differentiation of NC cells. Using comparative transcriptome analysis of NC-derived cells from shoc2 CRISPR/Cas9 mutant larvae, we found that Shoc2-mediated signals regulate gene programs at several levels, including expression of genes coding for the proteins of extracellular matrix (ECM) and ECM regulators. Together, our results demonstrate that Shoc2 is an essential regulator of NC development. This study also indicates that disbalance in the turnover of the ECM may lead to the abnormalities found in NSLH patients.
细胞外信号调节激酶(ERK1/2)通路在胚胎发育中至关重要。支架蛋白 Shoc2 是 ERK1/2 信号的关键调节因子,shoc2 基因的突变导致人类发育性疾病,称为具有疏松生长期毛发的类诺南综合征(NSLH)。Shoc2 的缺失和 shoc2 NSLH 致病突变影响神经嵴(NC)起源的组织。在这项研究中,我们利用斑马鱼模型来剖析 Shoc2-ERK1/2 信号在 NC 发育中的作用。这些研究表明,Shoc2 的缺失显著改变了调节 NC 细胞特化和分化的转录因子的表达。通过对 shoc2 CRISPR/Cas9 突变幼虫衍生的 NC 细胞的比较转录组分析,我们发现 Shoc2 介导的信号在几个水平上调节基因程序,包括编码细胞外基质(ECM)和 ECM 调节剂的蛋白质的基因表达。总之,我们的结果表明 Shoc2 是 NC 发育的必需调节因子。这项研究还表明,ECM 周转率的失衡可能导致 NSLH 患者的异常。