Screening for novel human genes associated with CRE pathway activation with cell microarray

被引:14
|
作者
Tian, Linjie
Wang, Pingzhang
Guo, Jinhai
Wang, Xinyu
Deng, Weiwei
Zhang, Chenying
Fu, Dongxu
Gao, Xia
Shi, Taiping
Ma, Dalong
机构
[1] Chinese Natl Human Genome Ctr, Beijing 100176, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Lab Med Immunol, Sch Basic Med Sci, Beijing 100083, Peoples R China
[3] Peking Univ, Hlth Sci Ctr, Human Dis Genom Ctr, Beijing 100083, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
reverse transfection; cell microarray; high-throughput screening; cAMP response element; dual luciferase reporter system;
D O I
10.1016/j.ygeno.2007.02.004
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In this study, cell microarray technology is used to identify novel human genes associated with CRE pathway activation. By reverse transfection, expression plasmids containing full-length cDNAs were cotransfected with the reporter plasmid pCRE-d2EGFP to monitor the activation of the CRE pathway via enhanced green fluorescence protein (EGFP) expression. Of the 575 predominantly novel genes screened, 22 exhibited relatively higher EGFP fluorescence compared with a negative control. After a functional validation with a dual luciferase reporter system that included both cis- and trans-luciferase assays, 4 of the 22 genes (RNF41, C8orf32, C6orf208, and MEIS3P1) were confirmed as CRE-pathway activators. Western blot analysis revealed that RNF41 can promote CREB phosphorylation. These results demonstrate the successful combination of cell microarray technology with this reporting system and the potential of this tool to characterize functions of novel genes in a highly parallel format. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:28 / 34
页数:7
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