染色质免疫沉淀
基因敲除
转录因子
电泳迁移率测定
发起人
基因
基因表达
分子生物学
抄写(语言学)
信使核糖核酸
生物
遗传学
语言学
哲学
作者
Weiyi Zhu,Xiangjun Dong,Shuang Luo,Shipeng Guo,Weihui Zhou,Weihong Song
标识
DOI:10.1016/j.bbrc.2023.01.087
摘要
CSTB has been reported to be associated with the pathogenesis of many malignant tumors, especially hepatocellular carcinoma (HCC). However, how the expression of this gene is regulated is largely unknown. We initially cloned and analyzed the promoter region of the CSTB gene by luciferase assay and the Sp3 binding site (CCCCGCCCCGCG) was found in it. The results of electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP) experiments verified that the transcription factor, Sp3 could bind to the " CCCCGCCCCGCG ″ site of the CSTB gene promoter. We showed that the overexpression of Sp3 significantly increased the endogenous mRNA and protein expression levels of CSTB, whereas knockdown of Sp3 decreased the mRNA and protein expression levels according to quantitative real-time PCR (qRT‒PCR) and western blotting. In conclusion, CSTB gene expression is closely regulated by transcription factor Sp3, which may be a potential mechanism for the dysregulation of CSTB expression in HCC.
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