Article Summary
杨 柳,王茂春,肖君华,周宇荀,李 凯,曲妍佳.qPCR array检测分析 C57BL/6小鼠胚胎后肢发育基因表达谱[J].现代生物医学进展英文版,2018,(15):2824-2828.
qPCR array检测分析 C57BL/6小鼠胚胎后肢发育基因表达谱
Detecting and Analyzing Hindlimb Developmental Gene Expression Profiles of C57BL/6 Mouse during Embryonic times by qPCR Array
  Revised:December 25, 2017
DOI:10.13241/j.cnki.pmb.2018.15.005
中文关键词: 实时定量PCR芯片  后肢发育  Hox基因
英文关键词: qPCR array  Hindlimb development  Hox genes
基金项目:上海市科学技术委员会重点项目(12140900404;14140900502)
Author NameAffiliationE-mail
杨 柳 东华大学生物研究所 上海201600 421973071@qq.com 
王茂春 东华大学生物研究所 上海201600  
肖君华 东华大学生物研究所 上海201600  
周宇荀 东华大学生物研究所 上海201600  
李 凯 东华大学生物研究所 上海201600  
曲妍佳 东华大学生物研究所 上海201600  
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中文摘要:
      摘要 目的:胚胎生育过程中因肢体发育异常造成的出生缺陷比率不低,其相关基因表达模式尚不明确。本实验通过建立实时定量PCR芯片(Real-time quantitative polymerasechain reaction array,qPCR array)检测方案,研究C57BL/6品系小鼠后肢发育相关基因的表达谱。方法:以同源异形盒基因家族(Hox)、Wnt5a、配对同源结构域基因(Pitx1)、成纤维生长因子(Fgf8)、音猬因子(Shh)等小鼠肢体发育相关的重要基因制作基因检测表达谱,以C57BL/6品系怀孕雌鼠为材料,取胚胎肢芽发育的四个关键时期(E10.5,E11.5,E12.5,E13.5)的胎鼠后肢,利用qPCR array方案检测表达谱中基因的相对表达水平差异。结果:通过已建立的qPCR array检测了C57BL/6品系小鼠胚胎后肢发育时期Hox家族、Wnt5a、Pitx1、Fgf8、Shh等基因的表达差异。以E10.5为对照,检测出在后肢发育时期基因呈三种表达模式,即Hoxb6、Hoxb8、Hoxc8、Hoxc9、Hoxc10、Hoxd9和Shh基因的表达水平呈上调;Hoxa11、Hoxa13、Hoxc12、Hoxc13、Hoxd13等基因表达出现下调;Hoxc9、Hoxc10、Hoxc11、Hoxd9、Hoxd12、Fgf8和Pitx1等基因的相对表达量呈先上调后下调的曲线表达模式,且有少部分基因在小鼠后肢发育时期表达水平无明显变化。结论:Hox家族、Wnt5a、Pitx1、Fgf8、Shh等基因在小鼠后肢发育时期表达,并且表达模式存在明显差异。
英文摘要:
      ABSTRACT Objective: The rates of birth defects caused by abnormal limb development are not low in the process of embryo devel- opment, however, the expression patterns of the related genes are not clear. In this study, we established a real-time quantitative poly- merasechain reaction array method to study the expression of genes related to hind limb development in C57BL/6 mouse strains. Methods: Hox, Wnt5a, Pitx1, Fgf8 and Shh were used to make the expression profiles of the genes related to hind limb development in mice. The hind limbs of the fetal C57BL/6 mice were taken from the four critical stages (E10.5, E11.5, E12.5, E13.5) of embryonic limb buds de- velopment. We detected relative genetic expression levels by the qPCR array. Results: The expression levels of Hox, Wnt5a, Pitx1, Fgf8 and Shh were detected during the development of the C57BL/6 mouse strains hind limbs by the qPCR array. Using E10.5 as a control, we detected that the genes presented the three expression patterns during the development of the hind limbs. The expression levels of Hoxb6, Hoxb8, Hoxc8, Hoxc9, Hoxc10, Hoxd9 and Shh genes were up-regulated. And the expression levels of Hoxa11, Hoxa13, Hoxc12, Hoxc13 and Hoxd13 genes were down-regulated. The relative expression levels of Hoxc9, Hoxc10, Hoxc11, Hoxd9, Hoxd12, Fgf8 and Pitx1 genes were up-regulated and then down-regulated. And there were no significant changes in the expression levels of a small num- ber of genes. Conclusion: Hox, Wnt5a, Pitx1, Fgf8 and Shh genes were expressed in the development of mice hind limbs, and their ex- pression patterns were significantly different.
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