| 马娜 陈天姬 李珑 陈婧 杜娟△.Dppa2 基因启动子区Oct4 结合位点突变对其活性的影响[J].,2015,15(21):4001-4004 |
| Dppa2 基因启动子区Oct4 结合位点突变对其活性的影响 |
| The Mutation of Oct4 Binding Site in Promoter Region of Dppa2 Gene andits Impacts on the Dppa2 Gene Expression |
| |
| DOI： |
| 中文关键词: Dppa2 启动子 Oct4 结合位点 荧光素酶 |
| 英文关键词: Dppa2 promoter Oct4 binding site Luciferase |
| 基金项目:湖南省科技厅科技计划项目（2009FJ3058）；中南大学中央高校基本科研业务费专项资金项目（2013zzts273）；
中南大学教师研究基金（905010042） |
|
| 摘要点击次数: 677 |
| 全文下载次数: 0 |
| 中文摘要: |
| 目的：探讨Dppa2 基因5' 端启动子区Oct4 结合位点突变对Dppa2基因启动子活性的影响。方法：PCR 扩增包括Oct4 结合
位点的Dppa2 基因5' 端转录起始点上游-2439～+293 bp 的启动子序列，片段长度为2732 bp。将该片段连接到pGL3-Basic 载体，
构建野生型pGL3-2439表达载体。采用定点突变法，将-1959～-1957 位碱基的GCA突变成TAG，构建Oct4 结合位点突变型
pGL3-mo2439 表达载体。用上述两种表达载体、PGL3-basic 载体和Oct4 表达载体分别瞬时转染HEK 293 细胞。细胞培养48 h
后，利用双荧光素酶报告系统测定各组细胞表达的荧光素酶的相对活性。结果：经琼脂糖凝胶电泳及测序鉴定，证实野生型
(pGL3-2439)和突变型(pGL3-mo2439)载体构建成功。荧光素酶活性测定结果显示，转染Dapp2 基因启动子野生型pGL3-2439 表
达载体的细胞组荧光素酶的相对活性为16.307，突变型pGL3-mo2439 表达载体的细胞组荧光素酶的相对活性为10.634。Oct4 结
合位点突变后，Dppa2 基因启动子区转录活性较野生型降低了35 %。结论：Dppa2基因5'端启动子区-1959～-1957 位的Oct4 结
合位点突变可能导致Dppa2 基因启动子活性下降 |
| 英文摘要: |
| Objective:To investigate the mutation of Oct4 binding site in promoter region of Dppa2 gene and its impacts on the
Dppa2 gene expression.Methods:The promoter sequence, -2439~+293 bp region upstream of Dppa2 which contain the recognition site
of Oct4, was amplified through PCR method. The mutation of GCA→TAG (-2439～+293 bp) in the conserved recognition site of Oct4
was obtained using site directed mutagenesis method. The wild type and mutant were subcloned into pGL3 luciferase reporter vectors to
construct recombinant eukaryotic expression vector, named as pGL3-2439 and pGL3-mo2439 respectively. These two recombinant plasmids,
pGL3-basic plasmids or control vector and Oct4 plasmids were transient transfected into HEK 293 cells using lipofectamin 2000.
After cultured 48 hours, the activity of promoters was determined by examine the relative activity of luciferase by dual Luciferase Reporter
Assay System.Results:Wild-type and mutant promoter sequence of Dppa2 was successfully cloned into recombinant vectors,
which was vertified by Gel electrophoresis and DNA sequencing methods. The expression activity of human wild-type and mutant was
also confirmed in the transfected HEK 293 cell. The relative activity of luciferase was 16.307 in the cells transfected with wild-type promoter,
and 10.643 in the cells transfected with mutant promoter. When compared with wild type, the promoter activity of Dppa2 gene decreased
35 %in the promoter with mutation of Oct4 binding site.Conclusion:The mutation of Oct4 binding site in the promoter region
may down-regulates the transciption activity of Dppa2 gene. |
|
查看全文
查看/发表评论 下载PDF阅读器 |
| 关闭 |
