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人FOXP3基因的生物信息学分析

Bioinformatic Analysis of the Human FOXP3 Gene

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在正常生理和应激生物环境中,叉头转录因子3(FOXP3)是调节性T细胞发育和抑制功能的重要转录因子.试验利用生物信息学在线工具及软件对FOXP3 蛋白的理化性质、蛋白晶体结构、翻译后修饰以及其相互作用蛋白等进行了研究.研究发现FOXP3 蛋白复合物主要包含NFAT1 DNA结合域和与脱氧核糖核酸结合的FOXP3 FKH结构域,并且通过多种翻译后修饰影响FOXP3 蛋白构象和与其互作蛋白的相互作用,最终改变FOXP3 蛋白活性以调节Treg抑制特征.研究结果可为今后深入研究FOXP3 如何调节Treg抑制的新方法和增强自身免疫性疾病免疫耐受的新疗法提供参考.
Forkhead transcription factor 3(FOXP3)played an important role in regulating regulatory T cell development and inhibiting function in normal physiological and stressed biological environments.The physical and chemical properties of FOXP3 protein,its crystal structure,post-translational modification and its interacting proteins were investigated using bioinformatics online tools and software.It was found that FOXP3 protein complex mainly contained the NFAT1 DNA-binding domain and the FOXP3 FKH domain bound to DNA,and affected the conformation of FOXP3 protein and its interaction with proteins through various post-translational modifications,and finally changed FOXP3 protein activity to regulate the inhibition of Treg.The results might provide a reference for further research on how FOXP 3 regulates the inhibition of Treg and new therapies to enhance immune tolerance in autoimmune diseases.

Treg cellsFOXP3 geneimmunologic tolerancebioinformatics analysis

陈倩、戴凌燕、李宇琦、李爽、申雪、佟春玉、宋博翠

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黑龙江八一农垦大学生命科学技术学院,大庆 163319

Treg细胞 FOXP3基因 免疫耐受 生物信息学分析

黑龙江省博士后启动基金项目

LBH-Q21158

2023

黑龙江八一农垦大学学报
黑龙江八一农垦大学

黑龙江八一农垦大学学报

影响因子:0.888
ISSN:1002-2090
年,卷(期):2023.35(6)
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