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首页|期刊导航|激光生物学报|斑马鱼egr1基因敲除品系的构建及其颅面软骨发育异常分析

斑马鱼egr1基因敲除品系的构建及其颅面软骨发育异常分析

阳剑波 苏娜 赵琳慧 黄淑兰 颜峰 胡翔 刘爱龙 李翔

激光生物学报2025,Vol.34Issue(2):148-156,9.
激光生物学报2025,Vol.34Issue(2):148-156,9.DOI:10.3969/j.issn.1007-7146.2025.02.007

斑马鱼egr1基因敲除品系的构建及其颅面软骨发育异常分析

Construction of Zebrafish egr1 Gene Knockout Strains and Analysis of Craniofacial Cartilage Developmental Anomalies

阳剑波 1苏娜 2赵琳慧 2黄淑兰 2颜峰 3胡翔 2刘爱龙 3李翔4

作者信息

  • 1. 湖南师范大学附属长沙市妇幼保健院,长沙 410007||湖南师范大学生命科学学院,长沙 410081
  • 2. 湖南师范大学生命科学学院,长沙 410081
  • 3. 湖南南华生物技术有限公司干细胞外泌体工程技术研究中心,长沙 410027
  • 4. 湖南师范大学附属长沙市妇幼保健院,长沙 410007
  • 折叠

摘要

Abstract

The EGR1 protein encoded by early growth response factor 1(egr1)belongs to the Cys2-His2 type zinc finger protein family.Previous studies have demonstrated its critical roles in animal growth,development,reproduction,and immune processes;however,its function in craniofacial development remains unreported.In this study,we utilized in situ hybridization to identify the specific expression of the egr1 gene in the head region of zebrafish during early cartilage development.To elucidate the function of EGR1 in this context,we employed CRISPR/Cas9 gene editing to generate egr1 knockout zebrafish and analyzed their phenotypes.Alcian blue staining revealed abnormalities in craniofacial cartilage development in egr1-/-mutant embryos,including deformities in Meckel's cartilage and ceratohyal,as well as disarray in the opercular and branchial regions.Our findings demonstrated the critical impact of egr1 gene deficiency on early craniofacial cartilage development in zebrafish,offering valuable insights into the pathogenesis of cartilage-related diseases and potential therapeutic strategies.

关键词

斑马鱼/egr1/原位杂交/CRISPR/Cas9/软骨发育

Key words

zebrafish/egr1/in situ hybridization/CRISPR/Cas9/cartilage development

分类

生物学

引用本文复制引用

阳剑波,苏娜,赵琳慧,黄淑兰,颜峰,胡翔,刘爱龙,李翔..斑马鱼egr1基因敲除品系的构建及其颅面软骨发育异常分析[J].激光生物学报,2025,34(2):148-156,9.

基金项目

长沙市自然科学基金项目(kq2208477) (kq2208477)

国家自然科学基金面上项目(81972642) (81972642)

湖南师范大学大学生创新训练计划项目(2024054). (2024054)

激光生物学报

1007-7146

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