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作 者:宣爱国[1] 龙大宏[1] 何峻峰[1] 陈艳[2]
机构地区:[1]广州医学院人体解剖教研室,广东广州510182 [2]广州医学院荔湾医院
出 处:《解剖学研究》2007年第4期250-252,263,共4页Anatomy Research
基 金:广东省医学科研基金(NoB2006075)
摘 要:目的构建神经发育转录因子Brn-4基因真核表达重组质粒,研究Brn-4在神经干细胞(NSC)中的表达情况。方法从新生鼠脑组织提取总RNA,利用RT-PCR的方法获得编码鼠Brn-4的基因片段,应用基因重组技术,将鼠Brn-4基因片段克隆到真核表达载体pEGFP-C2中,应用脂质体转染NSC,荧光显微镜观察该Brn-4基因在NSC中的表达。结果限制性内切酶酶切分析和PCR法鉴定表明为正确重组子,Brn-4基因在NSC中获得表达。结论新构建的真核表达重组质粒pEGFP-Brn-4通过鉴定,结构正确;Brn-4基因可在NSC中表达,可作为后续研究老年性痴呆动物模型转基因实验的基因来源。Objective To construct an eukaryotic expression recombinant plasmid named pEGFP-Brn-4, and research its expression in neural stem cells (NSC). Methods Total RNA was extracted from rat brain as the template and the Brn-4 gene was amplified by reverse transcription-polymerase chain reaction (RT-PCR). By using gene recombination technique, rat Brn-4 eDNA was inserted into eukaryotic expression vector pEGFP-C2. And then, the NSC were transferred by means of lipofectamine media methods. After that, we observed the Brn-4 expressed by NSC. Results The recombinant plasmid was identified to be fight by restriction endonuclease analysis and PCR. The Brn-4 gene could be expressed successfully by NSC. Conclusion The recombinant plasmid pEGFP-Brn-4 is constructed successfully. The Brn-4 gene can be expressed successfully by NSC, which offers a help on gene therapy of Alzheimer disease.
关 键 词:Brn-4基因 真核表达载体 神经干细胞 绿色荧光蛋白
分 类 号:R749.16[医药卫生—神经病学与精神病学]
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