实用医学杂志 ›› 2024, Vol. 40 ›› Issue (13): 1778-1784.doi: 10.3969/j.issn.1006-5725.2024.13.003

• 基础研究 • 上一篇    下一篇

核糖体S6蛋白激酶4基因在多种肿瘤中的表达及其生物信息学分析

杨江林1,2,许远红3,廖德仲4()   

  1. 1.贵州医科大学医学检验学院(贵阳 550004);贵州医科大学附属医院
    2.贵州医科大学附属医院 临床检验中心
    3. 贵州中医药大学基础医学院,贵阳 550025
    4.贵州医科大学附属医院 病理科 贵阳, 550004
  • 收稿日期:2023-11-17 出版日期:2024-07-10 发布日期:2024-07-09
  • 通讯作者: 廖德仲 E-mail:djliao@gmc.edu.cn
  • 基金资助:
    国家自然科学基金资助项目(82060489)

Expression of RSK4 gene in a variety of tumors and an analysis on the bioinformatics of this gene

Jianglin YANG1,2,Yuanhong XU3,Dezhong. LIAO4()   

  1. 1.School of Clinical Laboratory Science,Guizhou Medical University,Guiyang 550004,China
    2.Center for Clinical Laboratory,the Affiliated Hospital of Guizhou Medical University,Guiyang 550004,China
  • Received:2023-11-17 Online:2024-07-10 Published:2024-07-09
  • Contact: Dezhong. LIAO E-mail:djliao@gmc.edu.cn

摘要:

目的 探讨在不同肿瘤细胞中核糖体S6蛋白激酶4(ribosomal protein S6 kinase 4, RSK4)的表达谱是否存在差异,以及预测可能存在的蛋白亚型及其生物学特性。 方法 提取神经胶质瘤细胞GL261、卵巢癌细胞ID8、乳腺癌细胞4T1和168FARN、结肠癌细胞mc38和CT26、胃癌细胞MFC和肺癌细胞LLC1的RNA,采用RT?PCR技术检测RSK4的表达及其剪接异构体,生物信息学分析RSK4的生物学特征及其功能。 结果 RT?PCR结果显示在GL261、4T1、mc38、CT26、MFC和LLC1中均表达RSK4,且不同的肿瘤细胞中表达了多个剪接异构体,开放阅读框分析RSK4可能至少编码11个蛋白亚型;二级结构分析显示,这些剪接异构体编码的蛋白亚型均由α?螺旋、延伸链、β?转角和无规则卷曲组成,且保守结构域均相同;蛋白互作网络富集分析显示,RSK4主要通过mTOR信号通路和突触持续增强等信号通路在核质和胞浆中发挥激酶的活性。 结论 RSK4在不同的肿瘤细胞中存在不同的表达谱,可能产生多种氮端不同的蛋白异构体,能够通过多种信号通路参与不同的生物学途径。

关键词: 核糖体S6蛋白激酶4, 转录本, 可变剪接, 生物信息学, 基因表达谱

Abstract:

Objective The aim of this study was to investigate whether there are differences in the expression spectrums of RSK4 in different tumor cells and to predict the possible protein subtypes and their biological characteristics. Methods RNA was extracted from glioma cells GL261, ovarian cancer cells ID8, breast cancer cells 4T1 and 168FARN, colon cancer cells mc38 and CT26, gastric cancer cells MFC and lung cancer cells LLC1. The expressions and splicing isomers of RSK4 were detected by RT?PCR. The biological characteristics and functions of RSK4 were analyzed by bioinformatics. Results RT?PCR results showed that RSK4 was expressed in GL261, 4T1, mc38, CT26, MFC and LLC1; and multiple splicing isomers were expressed in different tumor cells. Open reading frame analysis revealed RSK4 may encode at least 11 protein subtypes. Secondary structure analysis showed that these protein subtypes encoded by the splicing isomers were composed of α?helix, extended strand, β?turn and random coil, and had the same conserved domain. The results of protein interaction network enrichment analysis showed that RSK4 exerted kinase activity in the nucleus and cytoplasm mainly through the mTOR signaling pathway and long?term potentiation. Conclusions RSK4 has different expression spectrums in different tumor cells, and may produces a variety of protein isoforms with different nitrogen terminals, which can be involved in different biological processes through multiple signaling pathways.

Key words: ribosomal protein S6 kinase 4, transcripts, alternative splicing, bioinformatics, gene expression spectrum

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