Coexpression Network Analysis of miRNA-142 Overexpression in Neuronal Cells.

MicroRNAs are small noncoding RNA molecules, which are differentially expressed in diverse biological processes and are also involved in the regulation of multiple genes. A number of sites in the 3′ untranslated regions (UTRs) of different mRNAs allow complimentary binding for a microRNA, leading to...

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Publicado en:BioMed Research International Vol. 2015; pp. 1 - 10
Autores principales: Thapa, Ishwor, Fox, Howard S., Bastola, Dhundy
Formato: Journal Article
Publicado: Wiley-Blackwell 10/11/2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 10/11/2015
      vid: 2015
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        110561951
        10.1155/2015/921517
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        atl: Coexpression Network Analysis of miRNA-142 Overexpression in Neuronal Cells.
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          Thapa, Ishwor
          Fox, Howard S.
          Bastola, Dhundy
        affil: College of Information Science and Technology, University of Nebraska Omaha, Omaha, NE 68182, USA
      sug:
      ab: MicroRNAs are small noncoding RNA molecules, which are differentially expressed in diverse biological processes and are also involved in the regulation of multiple genes. A number of sites in the 3′ untranslated regions (UTRs) of different mRNAs allow complimentary binding for a microRNA, leading to their posttranscriptional regulation. The miRNA-142 is one of the microRNAs overexpressed in neurons that is found to regulate SIRT1 and MAOA genes. Differential analysis of gene expression data, which is focused on identifying up- or downregulated genes, ignores many relationships between genes affected by miRNA-142 overexpression in a cell. Thus, we applied a correlation network model to identify the coexpressed genes and to study the impact of miRNA-142 overexpression on this network. Combining multiple sources of knowledge is useful to infer meaningful relationships in systems biology. We applied coexpression model on the data obtained from wild type and miR-142 overexpression neuronal cells and integrated miRNA seed sequence mapping information to identify genes greatly affected by this overexpression. Larger differences in the enriched networks revealed that the nervous system development related genes such as TEAD2, PLEKHA6, and POGLUT1 were greatly impacted due to miRNA-142 overexpression.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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