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小鼠膜联蛋白A1真核表达载体的构建及其细胞内定位
  • ISSN号:0577-7402
  • 期刊名称:《解放军医学杂志》
  • 时间:0
  • 分类:Q291[生物学—细胞生物学]
  • 作者机构:[1]南方医科大学病理生理学教研室、广东省蛋白质组学重点实验室,广州510515
  • 相关基金:国家自然科学基金(30670828;30572151); 国家自然科学基金委员会-广东省人民政府自然科学联合基金重点项目(U0632004); 长江学者和创新团队发展计划项目(IRT0731)
中文摘要:

目的构建小鼠膜联蛋白A1(annexin-A1,ANXA1)真核表达载体,并检测其在NIH3T3细胞中的表达和定位。方法采用PCR法从小鼠肝cDNA文库扩增ANXA1基因编码序列,并将其克隆至带有血凝素(HA)标记的真核表达载体pcDNA3-HA上,经PCR、酶切和测序鉴定后,将重组质粒pcDNA3-HA-ANXA1瞬时转染NIH3T3细胞,采用细胞免疫荧光法检测目的基因表达情况。结果菌液PCR、双酶切和DNA测序结果均表明重组质粒pcDNA3-HA-ANXA1构建正确,并可在NIH3T3细胞的胞质、胞核和胞膜中广泛表达。结论成功构建了pcDNA3-HA-ANXA1真核表达载体,该载体中的HA-ANXA1融合基因能在哺乳动物中有效表达并正确定位,为下一步深入研究ANXA1相关的信号通路奠定了基础。

英文摘要:

Objective To construct the eukaryotic expression vector of mouse Annexin-A1 (ANXA1),and detect its expression and localization in NIH3T3 fibroblast cell lines. Methods The corresponding coding sequences of mouse ANXA1 (GenBank accession No. AK140838) were amplified by polymerase chain reaction (PCR) from mouse liver cDNA library and then cloned into hemagglutinin (HA)-tagged vector pcDNA3-HA following the routine procedures to construct a new recombinant plasmid named pcDNA3-HA-ANXA1. After identification by double digestion with restriction endonucleases,PCR and DNA sequencing,the recombinant plasmid pcDNA3-HA-ANXA1 was transiently transfected into NIH3T3 cells with the Polyfect transfectant reagent. The transfected cells were then cultured for a certain time,and labeled with antibody against HA and fluorescence conjugated second antibody to detect the expression and localization of HA-ANXA1 with immunocytochemical method. Results The results of identification by PCR,digestion with restriction endonucleases and DNA sequencing proved that the construction of the eukaryotic expression vector for ANXA1 was successful. After transfection into NIH 3T3 cells with the expression vector for ANXA1,it was found that the ANXA1 fusion protein was highly expressed in NIH 3T3 cells and diffusely distributed throughout the plasma membrane,the cytoplasm and the nucleus as shown by fluorescence microscopy. Conclusions The eukaryotic expression vector of HA-tagged ANXA1 was successfully constructed,which could effectively expressed in mammalian cells with a correct localization,and it could serve as an important tool in the further study of the signal pathway of ANXA1in mammalian cells.

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期刊信息
  • 《解放军医学杂志》
  • 中国科技核心期刊
  • 主管单位:中国人民解放军总后勤部卫生部
  • 主办单位:人民军医出版社
  • 主编:
  • 地址:北京市100036信箱188分箱
  • 邮编:100036
  • 邮箱:mjcpla@pmmp.com.cn
  • 电话:010-51927306
  • 国际标准刊号:ISSN:0577-7402
  • 国内统一刊号:ISSN:11-1056/R
  • 邮发代号:2-74
  • 获奖情况:
  • 全军医学期刊质量评比优秀期刊奖,北京市全优期刊奖,中国科学引文数据库来源期刊
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  • 俄罗斯文摘杂志,美国化学文摘(网络版),波兰哥白尼索引,荷兰文摘与引文数据库,荷兰医学文摘,日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版),瑞典开放获取期刊指南,中国北大核心期刊(2000版)
  • 被引量:30614