Identification of the disease-associated genes in periodontitis using the co-expression network

被引:0
作者
G. P. Sun
T. Jiang
P. F. Xie
J. Lan
机构
[1] the Third Hospital of Ji’nan,Department of Stomatology
[2] Ji’nan Stomatological Hospital,General Department
[3] Ji’nan Stomatological Hospital,Department of Oral and Maxillofacial Surgery
[4] Shandong University,Department of Prosthodontics, College of Stomatology
来源
Molecular Biology | 2016年 / 50卷
关键词
periodontitis; differentially expressed genes; co-expression;
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学科分类号
摘要
The aim of this study was to investigate the disease-associated genes in periodontitis. In the present experiments, the topological analysis of the differential co-expression network was proposed. Using the GSE16134 dataset downloaded from the European Molecular Biology Laboratory-European Bioinformatics Institute, a co-expression network was constructed after the differentially expressed genes (DEGs) were identified between the diseased (242 samples) and healthy (69 samples) gingival tissues from periodontitis patients. The topological properties of the modules obtained from the network as well as an analysis of transcription factors (TFs) were used to determine the disease-associated genes. The gene ontology and pathway enrichment analysis was performed to investigate the underlying mechanisms of these disease related genes. A total of 524 DEGs, including 19 TFs were identified and a co-expression network with 2569 edges was obtained. Among the 7 modules gained in the network, the TFs (ZNF215, ZEN273, NFAT5, TRPS1, MEF2C and FLI1) were considered to be important in periodontitis. The functional and pathway enrichment analysis revealed that the DEGs were highly involved in the immune system. The co-expression network analysis and TFs identified in periodontitis may provide opportunities for biomarker development and novel insights into the therapeutics of periodontitis.
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页码:124 / 131
页数:7
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  • [1] Duran-Pinedo A.E.(2011)Correlation network analysis applied to complex biofilm communities PloS ONE. 6 28438-1130
  • [2] Paster B.(2010)Evidences of the cooperative role of the chemokines CCL3, CCL4 and CCL5 and its receptors CCR1+ and CCR5+ in RANKL+ cell migration throughout experimental periodontitis in mice Bone. 46 1122-540
  • [3] Teles R.(2010)Effects of adenoviral-mediated coexpression of bone morphogenetic protein-7 and insulinlike growth factor-1 on human periodontal ligament cells J. Periodont. Res. 45 532-571
  • [4] Frias-Lopez J.(2010)Diseases as network perturbations Curr. Opin. Biotechnol. 21 566-542
  • [5] Repeke C.E.(2013)Network topology reveals key cardiovascular disease genes PLoS ONE. 8 71537-532
  • [6] Ferreira S.B.(2012)Exploring the human diseasome: the human disease network Brief. Funct. Genomics. 11 533-1420
  • [7] Claudino M.(2012)Biological function through network topology: a survey of the human diseasome Brief. Funct. Genomics. 11 522-276
  • [8] Silveira E.M.(2014)A systems biology analysis of brain microvascular endothelial cell lipotoxicity BMC Syst. Biol. 8 80-315
  • [9] de Assis G.F.(2008)A systems level analysis of transcriptional changes in Alzheimer’s disease and normal aging J. Neurosci. 28 1410-821
  • [10] Avila-Campos M.J.(2010)Analysis of Alzheimer’s disease severity across brain regions by topological analysis of gene co-expression networks BMC Syst. Biol. 4 136-9551