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首页> 外文期刊>Developmental dynamics: an official publication of the American Association of Anatomists >Transcriptomic analysis of differential gene expression during chick periocular neural crest differentiation into corneal cells
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Transcriptomic analysis of differential gene expression during chick periocular neural crest differentiation into corneal cells

机译:Chick围眼神经嵴分化术治疗差异基因表达的转录组分分析

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Abstract Background Multipotent neural crest cells (NCC) contribute to the corneal endothelium and keratocytes during ocular development, but the molecular mechanisms that underlie this process remain poorly understood. We performed RNA‐Seq analysis on periocular neural crest (pNC), corneal endothelium, and keratocytes and validated expression of candidate genes by in situ hybridization. Results RNA‐Seq profiling revealed enrichment of genes between pNC and neural crest‐derived corneal cells, which correspond to pathways involved in focal adhesion, ECM‐receptor interaction, cell adhesion, melanogenesis, and MAPK signaling. Comparisons of candidate NCC genes to ocular gene expression revealed that majority of the NCC genes are expressed in the pNC, but they are either differentially expressed or maintained during corneal development. Several genes involved in retinoic acid, transforming growth factor‐β, and Wnt signaling pathways and their modulators are also differentially expressed. We identified differentially expressed transcription factors as potential downstream candidates that may instruct expression of genes involved in establishing corneal endothelium and keratocyte identities. Conclusion Combined, our data reveal novel changes in gene expression profiles as pNC differentiate into highly specialized corneal endothelial cells and keratocytes. These data serve as platform for further analyses of the molecular networks involved in NCC differentiation into corneal cells and provide insights into genes involved in corneal dysgenesis and adult diseases.
机译:摘要背景多能神经嵴细胞(NCC)在眼部发育过程中有助于角膜内皮和角膜细胞,但是该过程的分子机制仍然明白很差。我们对围眼神经嵴(PNC),角膜内皮和角膜细胞进行RNA-SEQ分析,并通过原位杂交验证了候选基因的表达。结果RNA-SEQ分析揭示了PNC和神经嵴衍生的角膜细胞之间基因的富集,其对应于参与局灶性粘附,ECM-受体相互作用,细胞粘附,黑素生成和MAPK信号传导的途径。候选NCC基因对眼基因表达的比较显示,在PNC中表达了大多数NCC基因,但它们在角膜发育过程中差异表达或维持。还差异地表达了参与视黄酸,转化生长因子-β和WNT信号传导途径及其调节剂的几个基因。我们鉴定了差异表达的转录因子,作为可能指示参与建立角膜内皮和角膜织卵物形式的基因表达的潜在下游候选。结论结合,我们的数据显示了基因表达谱的新改变,因为PNC分化成高度专业的角膜内皮细胞和角蛋白酶。这些数据用作进一步分析参与NCC分化的分子网络分析到角膜细胞,并向参与角膜膜体和成人疾病的基因提供有识。

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