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NGX6对Wnt/β-连环蛋白信号通路中β-连环蛋白/TCF/LEF转录激活的影响

[Effects of NGX6 on the transcriptional activation of beta-catenin/TCF/LEF in Wnt/beta-catenin signal pathway].

作者信息

Liu Fen, Shen Shou-rong, Li Hong-tao, Wang Xiao-yan, Peng Ya, Liao Man-tian, Guo Qin

机构信息

Department of Gastroenterology, Third Xiangya Hospital, Central South University, Changsha 410013, China.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2007 Dec;32(6):985-91.

Abstract

OBJECTIVE

To explore the effects of NGX6 on the transcriptional activation of beta-catenin/TCF/LEF in Wnt/beta-catenin signal pathway, and to identify the role of NGX6 in Wnt signal pathway.

METHODS

The eukaryotic expression vector pcDNA3.1(+)-beta-catenin (WT) was constructed. pcDNA3.1(+)-beta-catenin (WT) and pCMV-myc-NGX6 were cotransfected to COS-7 and the transcriptional activity of TCF/LEF was detected by TCF-4 luciferase report system. Without extro-genous beta-catenin, pCMV-myc-NGX6 was transfected alone to COS-7 and colon cancer cell line SW620, and the transcriptional activity of TCF/LEF was detected by TCF-4 luciferase report system, and then the expression of nucleus beta-catenin and TCF-4 was detected by Western blot.

RESULTS

The eukaryotic expression vector pcDNA3.1(+)-beta-catenin (WT) was successfully constructed. The activation of TCF-4 luciferase report gene in the cotransfection group in COS-7 was less than that in NGX6 alone transfection group (P<0.05). The activation of TCF-4 luciferase report gene in NGX6 alone transfection group without extro-genous beta-catenin was less than that in pCMV-myc transfection group in COS-7 and SW620. The expression of beta-catenin and TCF-4 was decreased after the NGX6 transfection in COS-7 and SW620 cells.

CONCLUSION

NGX6 can inhibit the transcriptional activation of beta-catenin/TCF/LEF in Wnt signal pathway by its negative regulation in the nuclear translocation of beta-catenin.

摘要

目的

探讨NGX6对Wnt/β-连环蛋白信号通路中β-连环蛋白/TCF/LEF转录激活的影响,明确NGX6在Wnt信号通路中的作用。

方法

构建真核表达载体pcDNA3.1(+)-β-连环蛋白(野生型)。将pcDNA3.1(+)-β-连环蛋白(野生型)与pCMV-myc-NGX6共转染至COS-7细胞,采用TCF-4荧光素酶报告系统检测TCF/LEF的转录活性。在无外源性β-连环蛋白的情况下,将pCMV-myc-NGX6单独转染至COS-7细胞和结肠癌细胞系SW620,采用TCF-4荧光素酶报告系统检测TCF/LEF的转录活性,然后通过蛋白质免疫印迹法检测细胞核内β-连环蛋白和TCF-4的表达。

结果

成功构建真核表达载体pcDNA3.1(+)-β-连环蛋白(野生型)。COS-7细胞中共转染组的TCF-4荧光素酶报告基因激活程度低于NGX6单独转染组(P<0.05)。在无外源性β-连环蛋白时,NGX6单独转染组的TCF-4荧光素酶报告基因激活程度低于COS-7细胞和SW620细胞中的pCMV-myc转染组。NGX6转染COS-7细胞和SW620细胞后,β-连环蛋白和TCF-4的表达降低。

结论

NGX6可通过对β-连环蛋白核转位的负性调节作用,抑制Wnt信号通路中β-连环蛋白/TCF/LEF的转录激活。

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