修饰GLP2分泌性表达载体的构建及促增殖活性测定的实验研究

谭虎; 杨天德; 粟永萍; 艾国平; 黄岚; 陶军; 刘晓宏; 楼淑芬

您当前的位置：

首页 >

文章列表页 >

修饰GLP2分泌性表达载体的构建及促增殖活性测定的实验研究

论著 | 更新时间：2026-01-09

- 修饰GLP2分泌性表达载体的构建及促增殖活性测定的实验研究
- Construction of secretary expression vector of mutation chimeric GLP2 and detection of its proliferation-promoting activity
- 陆军军医大学学报 2007年29卷第17期页码：1650-1653
- 作者机构：
- 作者简介：
- 基金信息：
- DOI：
  中图分类号： R329.25;R394-33;R394.2
- 纸质出版：2007
- 稿件说明：
移动端阅览
谭虎,杨天德,粟永萍,艾国平,黄岚,陶军,刘晓宏,楼淑芬.修饰GLP2分泌性表达载体的构建及促增殖活性测定的实验研究[J].陆军军医大学学报(原第三军医大学学报),2007,29(17):1650-1653.

　TAN Hu,YANG Tian-de,SU Yong-ping,AI Guo-ping,HUANG Lan,TAO Jun,LIU Xiao-hong,LOU Shu-fen.Construction of secretary expression vector of mutation chimeric GLP2 and detection of its proliferation-promoting activity[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(17):1650-1653.
谭虎,杨天德,粟永萍,艾国平,黄岚,陶军,刘晓宏,楼淑芬.修饰GLP2分泌性表达载体的构建及促增殖活性测定的实验研究[J].陆军军医大学学报(原第三军医大学学报),2007,29(17):1650-1653. DOI：

　TAN Hu,YANG Tian-de,SU Yong-ping,AI Guo-ping,HUANG Lan,TAO Jun,LIU Xiao-hong,LOU Shu-fen.Construction of secretary expression vector of mutation chimeric GLP2 and detection of its proliferation-promoting activity[J].J Amry Med Univ (J Third Mil Med Univ),2007,29(17):1650-1653. DOI：

摘要

目的对胰高血糖素样肽-2（glucagon-like peptid-2， GLP-2）进行基因修饰，观察其促细胞增殖活性。方法通过RT-PCR方法获得含GLP2编码序列的高血糖素原cDNA片段；通过PCR重叠延伸技术得到GLP2信号肽及成熟肽的嵌合分子，并将编码GLP2成熟肽N-末端第二位丙氨酸的序列(GCT)突变为编码甘氨酸的序列(GGT)；将其插入真核表达质粒pVITRO3，转染至肠上皮细胞（Caco-2），观察其对细胞增殖活性的影响。结果克隆的修饰GLP2基因与国外报道的核苷酸序列及其编码的氨基酸序列完全一致，并成功拼接GLP2的信号肽及成熟肽；且加入pVITRO3-GLP2-Caco-2培养上清的细胞生长明显快于对照组。结论 PCR重叠延伸技术适用于分泌性载体构建。构建的修饰GLP2表达系统所表达的蛋白具有促进肠上皮细胞增殖的作用。

Abstract

Objective To construct the secretary expression vector of mutation chimeric GLP2 by clone technology and detect its effect on cell proliferation. Methods The proglucagon cDNA was generated by the reverse transcription. The PCR product of signal and mature peptides of GLP2 was linked by SOE (splicing by overlap extension) and the gene

which coded the second amino acid in the N-terminal of GLP2

was mutated from GCT to GGT by PCR. Then the chimeric GLP2 cDNA was cloned into pVITRO3 vector and the recombinant plasmid was transfected to Caco-2. The cell proliferation was detected by MTT. Results The sequences of signal peptide

and mature peptide of GLP2 were connected successfully and the mature peptide sequence was mutated. MTT and

H-TdR showed that rGLP2 could accelerate the proliferation of Caco-2 cell significantly. Conclusion SOE is appropriate in establishing secretion type of expression vector and the secretary expression vector of mutation chimeric GLP2 has accelerating effect on cell proliferation.

关键词

Keywords

references

浏览量

下载量

CSCD

文章被引用时，请邮件提醒。

提交

工具集

关联资源

超低浓度二甲基亚砜促进皮肤成纤维细胞增殖作用及机制研究

谷胱甘肽过氧化物酶7通过PI3K-AKT通路调控肝癌细胞增殖和衰老

静息期精原前体细胞Rb1基因敲除致精原干细胞特化异常机制初探

生物钟基因PER1调控口腔鳞癌细胞中BAX、BCL2和PCNA表达的昼夜节律