荧光素酶
报告基因
转染
基因
干扰素
分子生物学
发起人
响应元素
生物
化学
细胞生物学
遗传学
基因表达
作者
X.-M. He,Xin Du,Jianzhen Zhuo,Xiaoyan Jing,Xiuqin Yang,D. Liu
标识
DOI:10.1080/09064702.2017.1341952
摘要
Interferon (IFN)-stimulated gene (ISG) 56 family (composed of ISG54, ISG56, ISG58, and ISG60) plays important roles in defense against viral infection in mammalian cells. Numerous studies have been conducted on ISG54, ISG56, and ISG60; however, little is known on ISG58. In the present study, the upstream sequence of porcine ISG58 gene was first characterized as functional promoter by luciferase reporter assay, and then two directly adjacent IFN-stimulated response elements (ISREs), one at −206 to −194 (ISRE-I) and a second one, directly upstream of this element at −219 to −207 bp (ISRE-II), were identified using the bioinformatics method. The subsequent site-directed deletion and transient transfection experiments showed the candidate ISREs are functional. ISRE-I works better than ISRE-II and synergistic cooperation exists between two ISREs. Additionally, the effect of porcine ISG58 on activation of NF-κB was analyzed using the dual-luciferase reporter assay. The results will contribute to revealing the role of ISG58 in immune response.
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