4.8 Article

Combinatorial network of primary and secondary microRNA-driven regulatory mechanisms

Journal

NUCLEIC ACIDS RESEARCH
Volume 37, Issue 18, Pages 5969-5980

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nar/gkp638

Keywords

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Funding

  1. National High-Tech RD Program [2006AA02Z334, 2007AA02Z304, 2006AA02Z330, 2009AA02Z304]
  2. International collaboration program [2007DFA31040]
  3. Key Research Program of CAS [KSCX2-YW-R-112]
  4. China National Key Projects for Infectious Disease [2008ZX10002-021]
  5. Shanghai Natural Science Foundation [08ZR1415800]
  6. Science and Technology Commission of Shanghai Municipality [2008PJ14084]
  7. National Natural Science Foundation of China [30770497]

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Recent miRNA transfection experiments show strong evidence that miRNAs influence not only their target but also non-target genes; the precise mechanism of the extended regulatory effects of miRNAs remains to be elucidated. A hypothetical two-layer regulatory network in which transcription factors (TFs) function as important mediators of miRNA-initiated regulatory effects was envisioned, and a comprehensive strategy was developed to map such miRNA-centered regulatory cascades. Given gene expression profiles after miRNA-perturbation, along with putative miRNA-gene and TF-gene regulatory relationships, highly likely degraded targets were fetched by a non-parametric statistical test; miRNA-regulated TFs and their downstream targets were mined out through linear regression modeling. When applied to 53 expression datasets, this strategy discovered combinatorial regulatory networks centered around 19 miRNAs. A tumor-related regulatory network was diagrammed as an example, with the important tumor-related regulators TP53 and MYC playing hub connector roles. A web server is provided for query and analysis of all reported data in this article. Our results reinforce the growing awareness that non-coding RNAs may play key roles in the transcription regulatory network. Our strategy could be applied to reveal conditional regulatory pathways in many more cellular contexts.

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