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Thoc1真核表达载体构建及其与ClC-3蛋白在人宫颈癌细胞HeLa中的共定位观察

刘学强 郑兆广 王汝上 钟杰 何桂芳 徐彬

山东医药2018,Vol.58Issue(16):26-29,4.
山东医药2018,Vol.58Issue(16):26-29,4.DOI:10.3969/j.issn.1002-266X.2018.16.007

Thoc1真核表达载体构建及其与ClC-3蛋白在人宫颈癌细胞HeLa中的共定位观察

Construction of Thoc1 eukaryotic expression vector,and its co-localization with ClC-3 in human cervical cancer HeLa cells

刘学强 1郑兆广 2王汝上 2钟杰 1何桂芳 1徐彬1

作者信息

  • 1. 广东药科大学生命科学与生物制药学院,广州510006
  • 2. 广州康臣药业有限公司肾病药物研究中心
  • 折叠

摘要

Abstract

Objective To clone human Thoc1 gene and construct the eukaryotic expression vector pThoc 1-DsRed2-N1,to observe the co-localization of Thoc1 with voltage-gated chloride channel 3(ClC-3)in human cervical cancer HeLa cells,and to analyze whether ClC-3 is involved in the cell transcription.Methods Thoc1 coding sequence was amplified by RT-PCR and cloned into the pDsRed2-N1 vector to construct the eukaryotic expression vector pThoc 1-DsRed2-N1, which was then identified by PCR,enzyme digestion(SacⅠand BamHⅠ),and gene sequencing.HeLa cells in the loga-rithmic phase were divided into 3 groups:the transfection group,empty transfection group,and control group,which were transfected with pThoc1-DsRed2-N1 plasmid,pDsRed2-N1 plasmid,and lipidosome by Lipofectamine 2000,respectively. At 48 h,the gene expression was observed under inverted fluorescence microscope.The co-localization of Thoc1 with ClC-3 was detected by immunofluorescence in the the transfection group.Results PCR results showed that there was a 2.1 kb target band,and meanwhile,4.7 kb and 2.1 kb bands were obtained by enzyme digestion.Sequencing proved that the se-quence and splicing order of Thoc1 gene was matched with Genebank,suggesting that the fluorescent eukaryotic expression vector pThoc1-DsRed2-N1 was constructed successfully.Overt red fluorescence was observed in the empty transfection group.The red fluorescence intensity of the transfection group was between those of the empty transfection group and the blank control group,suggesting that Thoc1 was expressed in HeLa cells.ClC-3 was localized both in the nucleus and cyto-plasm,mainly in nucleus.At the same time,Thoc1was localized in the nucleus only,and yellow fluorescence was observed after we merged ClC-3 with Thoc1,indicating that ClC-3 and Thoc1 were co-located in the nucleus.Conclusion The eu-karyotic expression vector pThoc1-DsRed2-N1 is successfully constructed, Thoc1 co-localizes with ClC-3 in the nucleus, suggesting that ClC-3 may be involved in the cell transcription process.

关键词

Thoc1基因/真核表达载体/氯离子通道3/共定位/人宫颈癌细胞HeLa

Key words

Thoc1 gene/eukaryotic expression vector/chloride channel-3/co-localization/human cervical cancer HeLa

分类

医药卫生

引用本文复制引用

刘学强,郑兆广,王汝上,钟杰,何桂芳,徐彬..Thoc1真核表达载体构建及其与ClC-3蛋白在人宫颈癌细胞HeLa中的共定位观察[J].山东医药,2018,58(16):26-29,4.

基金项目

国家自然科学基金资助项目(81101666). (81101666)

山东医药

OACSTPCD

1002-266X

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