copGFP和PuroR双标记基因慢病毒融合表达载体的构建及应用*

doi:10.12047/j.cjap.6215.2022.028

中国应用生理学杂志 ›› 2022, Vol. 38 ›› Issue (2): 108-112.doi: 10.12047/j.cjap.6215.2022.028

copGFP和Puro^R双标记基因慢病毒融合表达载体的构建及应用^*

张浩¹⁺, 朱文琦¹⁺, 赵思捷¹⁺, 李永利¹, 侯俊², 卞成蓉¹, 鲍春梅¹, 卫桢¹, 孙杰¹, 李波^1△, 李伯安^1△

1.解放军总医院第五医学中心检验科, 2.解放军总医院第五医学中心感染病研究所, 北京 100039

收稿日期:2021-05-13 修回日期:2022-03-24 出版日期:2022-03-28 发布日期:2022-08-29
通讯作者: ^△Tel: 010-66933393; E-mail: lba@263.com,pipi780816@aliyun.com
作者简介:⁺共同第一作者
基金资助:
^*军队重大科研项目(AWS14C003)

Construction and application of lentivirus overexpression vector with two labeling genes fused with CopGFP and Puro^R

ZHANG Hao¹⁺, ZHU Wen-qi¹⁺, ZHAO Si-jie¹⁺, LI Yong-li¹, HOU Jun², BIAN Cheng-rong¹, BAO Chun-mei¹, WEI Zhen¹, SUN Jie¹, LI Bo^1△, LI Bo-an^1△

1. Center for Clinical Laboratory, 2. Infectious Medicine Institute, the Fifth Medical Center, General Hospital of Chinese PLA, Beijing 100039, China

Received:2021-05-13 Revised:2022-03-24 Online:2022-03-28 Published:2022-08-29

摘要/Abstract

摘要： 目的: 构建具有绿色荧光蛋白(copGFP)和嘌呤霉素抗性基因(PuroR)融合表达双筛选标记的慢病毒过表达载体,检测其嘌呤霉素抗性和绿色荧光蛋白表达的特性。方法: 从pCDH-CMV-MCS-copGFP载体中扩增copGFP编码区DNA序列,从pLKO.1载体中扩增Puro^R编码区DNA序列,运用重组PCR方法,扩增copGFP与Puro^R基因融合编码序列并克隆至经BamH Ⅰ+Sal Ⅰ双酶切的pCDH-CMV-MCS-copGFP载体片段中,构建含copGFP和Puro^R融合表达双筛选标记的慢病毒过表达载体;载体的融合标签序列进行测序确证;将该载体用辅助包装质粒PLP1、PLP2、VSVG在293T细胞中包装成慢病毒后感染肝癌细胞MHCC97H,检测感染细胞对嘌呤霉素的抵抗作用以及绿色荧光蛋白的表达情况;为验证该载体表达外源目的基因的有效性,将Sp1编码区DNA序列插入该载体中包装成慢病毒,用对照及表达Sp1的慢病毒感染肝癌细胞MHCC97H,感染细胞经1 mg/ml嘌呤霉素筛选7 d后获得稳定感染细胞株,提取稳定感染细胞的总RNA及总蛋白,分别运用RT-qPCR和Western blot方法检测Sp1在对照及表达Sp1的慢病毒感染的肝癌MHCC97H细胞中的mRNA和蛋白表达水平的差异。结果: 成功构建含copGFP和Puro^R融合表达双筛选标记的慢病毒过表达载体;该载体与辅助质粒包装出的慢病毒感染肝癌细胞后,感染细胞同时具有嘌呤霉素抗性和表达绿色荧光蛋白特性;将Sp1编码序列插入该载体,包装慢病毒并肝癌细胞,Sp1 的mRNA水平对照细胞相比分别升高3.3倍,蛋白水平升高2.2倍(P＜0.01)。 结论: 成功构建含copGFP和Puro^R融合表达双筛选标记的慢病毒过表达载体,该载体编码的融合双标记基因具有嘌呤霉素抗性和绿色荧光蛋白表达的特性,可高水平表达长片段的目的基因。

关键词: 桡足类绿色荧光蛋白, 嘌呤霉素抗性基因, 融合表达, 慢病毒载体, 特异性蛋白1

Abstract: Objective: To construct the lentivirus overexpression vector with two label genes fused with CopGFP and Puro^R and to detect the emission of green fluorescence as well as resistance to puromycin in liver cancer cells infected with lentivirus packaged with the above vector. Methods: Firstly, two fragments containing copGFP and Puro^R coding sequences were amplified from pCDH-CMV-MCS-copGFP and pLKO.1 respectively; secondly, the two amplified regions were fused with each other by recombinant PCR; thirdly, the fusion DNA fragment was cut and inserted into pCDH-CMV-MCS-copGFP vector, which was linearized with the same restriction endonuclease as used to digest fusion DNA fragment: BamH Ⅰ and Sal Ⅰ. The fusion region in the constructed vector was confirmed by DNA sequencing. The checked vector was co-transfected with package assistant plasmids, namely PLP1, PLP2 and VSVG into in 293T cells and the culture supernatant was subjected to centrifuge and infect liver cancer MHCC97H cells, which were then used to detect their resistance to puromycin (infected cells were treated with 1 mg/ml puromycin for 7 days after infection) and to observe green fluorescence emission in microscope. To determine its efficiency in expressing foreign target protein, the Sp1 coding region was inserted into the MCS sites of the vector, and Sp1 mRNA and protein expression levels were compared with the vehicle vector by RT-qPCR and Western blot. Results: The lentivirus overexpression vector with two label genes fused with CopGFP and Puro^R was successfully constructed, and the liver cancer cells infected with lentivirus packaged with the vector expressing two labeling genes fused with CopGFP and Puro^Rshowed both emission of green fluorescence and resistance to puromycin simultaneously, while cells containing with the vector inserted with Sp1 coding region improved Sp1 mRNA level with 3.3 fold and protein level with 2.2 fold higher in comparison with cells containing the vehicle vector (P＜0.01). Conclusion: The fused label genes consisting of copGFP and Puro^R are correctly cloned into the lentivirus vector and confer cells with the ability to emission of green fluorescence and resistance to puromycin, besides, the vector may promote the expression of the target gene with long coding sequence.

Key words: copGFP, Puro^R, fusion expression, lentivirus vector, Sp1

中图分类号:

张浩, 朱文琦, 赵思捷, 李永利, 侯俊, 卞成蓉, 鲍春梅, 卫桢, 孙杰, 李波, 李伯安. copGFP和Puro^R双标记基因慢病毒融合表达载体的构建及应用^*[J]. 中国应用生理学杂志, 2022, 38(2): 108-112.

ZHANG Hao, ZHU Wen-qi, ZHAO Si-jie, LI Yong-li, HOU Jun, BIAN Cheng-rong, BAO Chun-mei, WEI Zhen, SUN Jie, LI Bo, LI Bo-an. Construction and application of lentivirus overexpression vector with two labeling genes fused with CopGFP and Puro^R[J]. CJAP, 2022, 38(2): 108-112.

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copGFP和Puro^R双标记基因慢病毒融合表达载体的构建及应用^*

Construction and application of lentivirus overexpression vector with two labeling genes fused with CopGFP and Puro^R

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copGFP和PuroR双标记基因慢病毒融合表达载体的构建及应用*

Construction and application of lentivirus overexpression vector with two labeling genes fused with CopGFP and PuroR

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copGFP和Puro^R双标记基因慢病毒融合表达载体的构建及应用^*

Construction and application of lentivirus overexpression vector with two labeling genes fused with CopGFP and Puro^R