期刊文献+

基于数据融合算法的精神分裂症易感基因排序及其信号通路研究 被引量:1

Gene ranking and signaling pathway of schizophrenia susceptible genes based on data fusion arithmetic
下载PDF
导出
摘要 目的利用已有的研究结果,采用数据融合分析方法,对与已知的精神分裂症易感基因有密切关系的候选基因进行统计分析,得出基因排序及其信号通路的结果,以此证明数据融合算法能够有效筛选精神分裂症易感基因。方法根据已知的与精神分裂症相关的基因,利用Endeavour工具,通过数据融合算法将候选基因排序,并用DAVID数据库对基因排序结果进行功能注释和富集分析。结果利用数据融合算法获得的排序较高的基因与已有研究进行比较,证实排名第二的NRG3和排名第三的AKT1与精神分裂症有密切联系。其他排名较高的基因可以作为潜在的疾病易感基因,为精神分裂症的研究提供参考。结论数据融合算法能够准确评价候选基因与精神分裂症的联系,使用该方法能有效地对精神分裂症易感基因进行筛选和判定。 Objective Based on previous studies,this paper applies data fusion arithmetic to extract the potential susceptible genes and signaling pathway related to schizophrenia, which proves that data fusion algorithm is an effective method to filter schizophrenia susceptible genes. Methods By making use of Endeavour tool which is based on data fusion method,the candidate genes were ranked according to their similarity with the tralning genes. Then DAVID database was used to implement the functional annotation and enrichment analysis for the extracted genes. Results Compared with previous studies,the second NRG3 and third AKT1 which are obtalned from higher ranking candidate genes,are closely related to schizophrenia. Other higher ranking genes could be used as potential disease-susceptibility genes to provide reference for the research of schizophrenia. Conclusions Data fusion arithmetic can help to detect the potential schizophrenia candidate genes objectively and correctly,and this method is a powerful tool for identifying schizophrenia susceptible genes.
出处 《北京生物医学工程》 2015年第2期151-155,共5页 Beijing Biomedical Engineering
基金 973计划(2014CB744604) 北京市教委自然基金(KM201010025004 KM201410025013) 北京市脑重大疾病研究院基金(BIBDPXM2014_014226_000016)资助
关键词 精神分裂症易感基因 数据融合算法 基因排序 信号通路 schizophrenia susceptible gene data fusion arithmetic gene ranking signaling pathway
  • 相关文献

参考文献28

  • 1曹玉媛,张景亮,徐朝阳,程晓丽.河南汉族精神分裂症患者线粒体DNA 7445和5178位点突变分析[J].郑州大学学报(医学版),2011,46(4):523-525. 被引量:4
  • 2Jong SD, Boks MPM, Fuller TF, et al. A gene co-expression network in whole blood of schizophrenia patients is independent of antipsychotic-use and enriched for brain-expressed genes [ J ]. Plos One, 2012, 7(6) :e39498.
  • 3Jablensky A. The epidemiology of schizophrenia[ J ]. Aust Nz J Psychiat, 2006, 40(5) :503.
  • 4梁燕,史艺宾,田卫东.精神分裂症相关基因的预测——基于大规模数据的整合分析[J].复旦学报(自然科学版),2013,52(2):255-270. 被引量:4
  • 5Kazuo Yamada, Yoshimi Iwayama, Eiji Hattori, et al. Genome- Wide Association Study of Schizophrenia in Japanese Population [J]. PlosOne, 2011, 6(6):e20468.
  • 6Paul Pavlidis, Jason Weston, Jinsong Cai, et al. Learning Gene Functional Classifications from Multiple Data Types [ J ~. Journal of Computational Biology, 2002, 9(2) :401-411.
  • 7Tijl De Bie, Le'on-Charles Tranchevent, Van Oeffelen LMM, et al. Kernel-based data fusion for gene prioritization [ J ]. Bioinformatics, 2007, 23 ( 13 ) :i125-i132.
  • 8Tranchevent LC, Capdevila F B, Nitsch D, et al. A guide to web tools to prioritize candidate genes [ J ]. Brief Bioinform, 2011, 12(1) :22-32.
  • 9The Gene Ontology Consortium. The gene ontology project in 2008 [ J]. Nucleic Acids Res, 2008, 36 : D440-IM44.
  • 10LiW, Chert LN, He WM, et al. Prioritizing Disease Candidate Proteins in Cardiomyopathy-Specific Protein-Protein Interaction Networks Based on " Guilt by Association" Analysis [ J ]. Plos One, 2013, 8(8) :e71191.

二级参考文献82

  • 1Doi N,Hoshi Y, Itokawa M, et al. Persistence criteria for susceptibility genes for schizophrenia:a discussion from an evolutionary viewpoint[J]. PLoS One,2009,4( 11 ) :e7799.
  • 2Lauritzen KH, Moldestad O, Eide L, et al. Mitochondrial DNA toxicity in forebrain neurons causes apoptosis, neurodegeneration, and impaired behavior[ J]. Mol Cell Biol, 2010,30(6) :1357.
  • 3Jou SH, Chiu NY, Liu CS. Mitochondrial dysfunction and psychiatric disorders [ J ]. Chang Gung Med J, 2009,32 (4) : 370.
  • 4Chen J, Yuan H, Lu J, et al. Mutations at position 7445 in the precursor of mitoehondrial tRNA( Ser(UCN) ) gene in three maternal Chinese pedigrees with sensorineural hearing loss [ J]. Mitochondrion,2008,8(4) :285.
  • 5Lal S, Madhavan M, Heng CK. The association of mitochondrial DNA 5178 C > a polymorphism with plasma lipid levels among three ethnic groups[ J]. Ann Hum Genet, 2005,69( Pt 6) :639.
  • 6Washizuka S, Ikeda A, Kato N,et al. Possible relationship between mitochondrial DNA polymorphisms and lithium response in bipolar disorder[ J]. Int J Neuropsychopharmacol,2003,6(4) :421.
  • 7Kato C, Umekage T, Tochigi M, et al. Mitochondrial DNA polymorphisms and extraversion [ J ]. Am J Med Genet B Neuropsychiatr Genet,2004,128B( 1 ) :76.
  • 8Mueser K T, McGurk S R. Schizophrenia[J]. Lancet, 2004,363(9426) : 2063-2072.
  • 9Christopher A, Ross R L M, Sarah A J. Neurobiology of Sehizophrenia[J]. Neuron, 2006,52: 14.
  • 10Shi J, Levinson D F, Duan J, et al. Common variants on chromosome 6p22. 1 are associated with schizophrenia[J]. Nature, 2009,460(7256) .. 753-757.

共引文献6

同被引文献3

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部