畜牧兽医学报 ›› 2006, Vol. 37 ›› Issue (11): 1093-1098.

• 遗传繁育 •    下一篇

人类α-actin 启动子真核表达载体的构建及应用

杨玉艾;孙永科;华进联;窦忠英   

  1. 西北农林科技大学 陕西省干细胞工程技术中心,杨凌 712100
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2006-11-25 发布日期:2006-11-25

Construction of Eukaryotic Expression Vector Containing Human Cardiac α-actin Promoter and It’s Application

  • Received:1900-01-01 Revised:1900-01-01 Online:2006-11-25 Published:2006-11-25

摘要: 利用PCR技术克隆了人类α-actin基因的启动子(约450bp),尝试用去掉启动子的pEGFPN1作为框架结构,成功构建了真核表达载体pEGFP-N1-α-actin-P。应用Lipofectamine 2000将所构建的pEGFP-N1-α-actin-P转染入小鼠ES细胞。通过比较,发现在本实验室条件下,质粒DNA浓度以3.0~5.0 μg/mL,转染时间约在2~3 h最佳。200 μg/mL 的G418较适宜于靶细胞的转染与筛选。得到表达心肌α-actin和GFP的小鼠ES细胞,基本维持小鼠ES细胞的形态。PCNA染色结果表明,转染后的小鼠ES细胞具有增殖能力。α-actin抗体免疫组化染色结果表明,转染后细胞表达α-actin和GFP,揭示构建的真核表达载体pEGFP-N1-α-actin-P转染小鼠ES细胞,可能促进其向心肌细胞分化并对其筛选。

关键词: 人类α-actin启动子, 真核表达载体, 小鼠ES细胞, 心肌细胞

Abstract: Human cardiac α-actin promoter obtained from the human heart genome by polymerase chain reaction(PCR) was ligated into the same fragment of pEGFPN1(moved CMV promoter by AseI/Bgl II).The constructed expression vector, named α-actin-pEGFP-N1 which contains neor gene and GFP gene as positive selection markers,was transferred into mice ES cells by Lipofectamine 2000 It’s found that DNA concentration should be 3.0-5.0μg/mL, transfer time was 2-3h, 200μg/mL G418 was used as perfect working concentration. Fluorescent observation and immunocytochemistry assay (PCNA and antibody of α-actin) demonstrated the transfected cells show high levels of α-actin and GFP expression, basically maitain its natural characteristic compared with wild mice ES cells. The results suggest that human cardiac αactin promoter may be useful in the study of mice ES cells specific differentiation into cardiomyocytes.

Key words: human cardiac αactin promoter, the expression vector, mice ES cells(embryonic stem, ES), Cardiomyocytes