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利用细胞微阵列筛选与CRE通路激活相关的新型人类基因。

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

作者信息

Tian Linjie, Wang Pingzhang, Guo Jinhai, Wang Xinyu, Deng Weiwei, Zhang Chenying, Fu Dongxu, Gao Xia, Shi Taiping, Ma Dalong

机构信息

Chinese National Human Genome Center, Beijing, 3-707 North YongChang Road BDA, Beijing 100176, People's Republic of China.

出版信息

Genomics. 2007 Jul;90(1):28-34. doi: 10.1016/j.ygeno.2007.02.004. Epub 2007 May 8.

Abstract

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.

摘要

在本研究中,细胞微阵列技术用于鉴定与CRE通路激活相关的新型人类基因。通过反向转染,将含有全长cDNA的表达质粒与报告质粒pCRE-d2EGFP共转染,以通过增强型绿色荧光蛋白(EGFP)表达监测CRE通路的激活。在筛选的575个主要为新型基因中,与阴性对照相比,有22个显示出相对较高的EGFP荧光。在用包括顺式和反式荧光素酶测定的双荧光素酶报告系统进行功能验证后,22个基因中的4个(RNF41、C8orf32、C6orf208和MEIS3P1)被确认为CRE通路激活剂。蛋白质印迹分析显示RNF41可促进CREB磷酸化。这些结果证明了细胞微阵列技术与该报告系统的成功结合,以及该工具以高度平行的形式表征新型基因功能的潜力。

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