首页|期刊导航|山东医药|肥胖小鼠血清外泌体差异表达LncRNAs筛选、功能及调控蛋白互作网络分析

肥胖小鼠血清外泌体差异表达LncRNAs筛选、功能及调控蛋白互作网络分析OACSTPCD

Screening,function and regulatory protein interaction network analysis of differentially expressed LncRNAs in serum exosomes of obese mice

中文摘要英文摘要

目的 筛选肥胖小鼠与对照组小鼠血清外泌体差异表达的LncRNAs,分析差异表达LncRNAs相关靶基因的基因本体功能及相关信号通路,并对差异表达LncRNAs调控的蛋白进行互作网络分析,以探讨差异表达的LncRNAs与肥胖发生的关系.方法 用高脂饲料(肥胖组)和普通饲料(对照组)分别饲养C57BL/6小鼠各12只,喂养8周后通过对小鼠体质量的检测确定肥胖小鼠模型构建成功.提取两组小鼠血清外泌体,进行高通量测序以筛选差异表达的LncRNAs,应用TopGO软件和KEGG数据库对差异表达基因进行GO、KEGG分析.采用STRING蛋白质相互作用网络数据库构建差异表达基因蛋白互作网络,筛选差异表达的LncRNAs调控的蛋白.结果 两组血清外泌体中,共筛选出201个差异表达LncRNAs,其中32个表达上调,169个表达下调,主要存在于细胞内部分(intracellular part,其中富集712个候选基因)、细胞内(intracellular,其中富集730个候选基因)、细胞器部分(organelle part,其中富集483个候选基因),主要涉及脂肪酸降解、MAPK信号通路等相关通路.初步筛选出了8个肥胖相关LncRNAs调控的蛋白(Ehmt1、Epha3、MAPK13、Mark4、Irak2、Fgfr4、Prkce、MAPK1).结论 肥胖小鼠与对照组小鼠血清外泌体中共筛选出201个差异表达LncRNAs,其中32个表达上调,169个表达下调.差异表达LncRNAs主要涉及脂肪酸降解、MAPK信号通路等.初步筛选出8个LncRNAs调控的肥胖相关蛋白(Ehmt1、Epha3、MAPK13、Mark4、Irak2、Fgfr4、Prkce、MAPK1);差异表达LncRNAs与肥胖发生可能有关.

Objective To screen the differentially expressed LncRNAs in serum exosomes of obese mice and control mice,to analyse the gene ontology function and related signaling pathways of the target genes associated with the differen-tially expressed LncRNAs,and to conduct interaction network analysis of proteins regulated by differentially expressed ln-cRNAs,in order to explore the relationship between the differentially expressed LncRNAs and the occurrence of obesity.Methods Twelve C57BL/6 mice were fed with high-fat diet(obese group)and 12 were fed with normal diet(control group),and the body mass of the mice was examined after 8 weeks of feeding to determine the success of the construction of the obese mouse models.The serum exosomes of mice in the two groups were extracted and were subjected to high-throughput sequencing to screen for differentially expressed LncRNAs,and GO and KEGG analyses of the differentially ex-pressed genes were performed by applying TopGO software and KEGG database.The STRING protein interaction network database was used to construct the protein interaction network of differentially expressed genes and we screened the obesity closely related proteins regulated by differentially expressed lncRNAs.Results In serum exosomes of the two groups,a total of 201 differentially expressed lncRNAs were screened out,of which 32 were up-regulated and 169 were down-regulat-ed,and were mainly found in the intracellular part(of which 712 candidate genes were enriched),intracellular(of which 730 candidate genes were enriched),and organelle part(of which 483 candidate genes were enriched),mainly involving fatty acid degradation,MAPK signaling pathway and other related pathways.Eight obesity closely related proteins(Ehmt1,Epha3,MAPK13,Mark4,Irak2,Fgfr4,Prkce,and MAPK1)were initially screened out.Conclusion A to-tal of 201 differentially expressed lncRNAs were screened out in serum exosomes of obese and control mice,of which 32 were up-regulated and 169 were down-regulated.The differentially expressed lncRNAs were mainly involved in fatty acid degradation and MAPK signalling pathway.Eight obesity-related proteins(Ehmt1,Epha3,MAPK13,Mark4,Irak2,Fg-fr4,Prkce,and MAPK1)were preliminarily screened out;the differentially expressed lncRNAs might be related to the oc-currence of obesity.

王昶赞;仪雯瑛;李祥辉;努尔比耶·努尔麦麦提

新疆医科大学临床医学部,乌鲁木齐 830054新疆医科大学基础医学院生物化学与分子生物学教研室新疆地方病分子生物学重点实验室

临床医学

长链非编码RNA外泌体肥胖

long non-coding RNAexosomesobesity

《山东医药》 2024 (027)

35-39 / 5

10.3969/j.issn.1002-266X.2024.27.008

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