Lou Ye-jiang, Pan Xiao-rong, Jia Pei-min, Zhang Zhang-lin, Xu Gui-ping, Li Dong, Tong Jian-hua
Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025 PR China.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Jun;27(3):255-8. doi: 10.3760/cma.j.issn.1003-9406.2010.0.004.
To study the regulatory role of interferon-stimulated response elements (ISREs) located on the retinoic acid-induced gene G (RIG-G) promoter in RIG-G expression.
By using point mutation technique, the authors constructed the wide type and site mutant reporter gene plasmids according to the ISRE sequence on RIG-G promoter, and detected the functional activities by luciferase reporter assay.
Mutation in ISRE II alone had no obvious effect on the expression of the reporter gene, whereas mutation in ISRE I dramatically inhibited the transactivity of RIG-G promoter. Mutation in both ISRE I and ISRE II resulted in complete loss of its response to the transcription factors for the reporter gene.
Both ISRE I and ISRE II on the RIG-G promoter are the binding sites for the complex of transcription factors. They are required for RIG-G expression, and ISRE I has a preferential role over ISRE II.
研究维甲酸诱导基因G(RIG-G)启动子上的干扰素刺激反应元件(ISREs)对RIG-G表达的调控作用。
采用点突变技术,根据RIG-G启动子上的ISRE序列构建野生型和位点突变型报告基因质粒,通过荧光素酶报告基因检测法检测其功能活性。
单独ISRE II突变对报告基因表达无明显影响,而ISRE I突变显著抑制RIG-G启动子的转录活性。ISRE I和ISRE II同时突变导致报告基因对转录因子的反应完全丧失。
RIG-G启动子上的ISRE I和ISRE II均为转录因子复合物的结合位点。它们是RIG-G表达所必需的,且ISRE I比ISRE II具有更重要的作用。