等位基因
补体系统
生物
发起人
转录因子
单核苷酸多态性
分子生物学
基因敲除
基因
U937电池
报告基因
细胞培养
基因表达
免疫学
遗传学
基因型
抗体
作者
А. Н. Уварова,E. A. Tkachenko,E. M. Stasevich,Е. А. Богомолова,Elina A. Zheremyan,Dmitry V. Kuprash,Kirill V. Korneev
标识
DOI:10.31857/s0026898424020089
摘要
The complement inhibitor CD55/DAF is expressed on many cell types. Dysregulation of CD55 expression is associated with increased disease severity in influenza A infection and vascular complications in pathologies that involve excessive activation of the complement system. A luciferase reporter system was used to functionally analyze the single nucleotide polymorphism rs2564978 in the U937 human promonocytic cell line. The polymorphism is in the promoter of the CD55 gene, and its minor allele T is associated with a severe course of influenza A(H1N1)pdm09. A decreased activity of the CD55 promoter carrying the minor rs2564978(T) allele was observed in activated U937 cells, which provide a cell model of human macrophages. Using bioinformatics resources, PU.1 was identified as a potential transcription factor that may bind to the CD55 promoter at the rs2564978 site in an allele-specific manner. The involvement of PU.1 in modulating CD55 promoter activity was verified by a PU.1 genetic knockdown with small interfering RNAs under specific monocyte activation conditions.
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