Systematic exploration of autonomous modules in noisy microRNA-target networks for testing the generality of the

Danny Kit-Sang Yip, Iris K Pang, Kevin Y Yip1

  • 1Department of Computer Science and Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong. kevinyip@cse.cuhk.edu.hk.

BMC Genomics
|December 26, 2014
PubMed
Abstract

Insights

We developed microRNA-target biclusters (MTBs) to analyze competing endogenous RNA (ceRNA) networks. MTBs reveal widespread mRNA expression correlations, supporting the ceRNA hypothesis and enabling functional annotation of microRNAs.

Area of Science:

  • Molecular Biology
  • Systems Biology
  • Bioinformatics

Background:

  • The competing endogenous RNA (ceRNA) hypothesis describes transcript interactions via shared microRNA (miRNA) sponging.
  • While ceRNA's role in gene regulation and cancer is evident, its overall impact on gene expression remains unclear.
  • Analyzing complex miRNA-target networks is challenging due to interconnectedness, hindering the isolation of individual miRNA effects.

Purpose of the Study:

  • To develop computational methods for dissecting complex miRNA-target networks into autonomous modules.
  • To provide objective data for testing the generality of the ceRNA hypothesis.
  • To explore the utility of these modules in functional miRNA annotation.

Main Methods:

  • Proposed computational methods to decompose miRNA-target networks into microRNA-target biclusters (MTBs).
  • MTBs are defined as densely connected miRNA-mRNA modules with minimal external connections.
  • The approach does not require pre-assumptions on expression patterns, allowing objective analysis.

Main Results:

  • Demonstrated significant anti-correlation between miRNA and mRNA expression within MTBs, exceeding random and predicted pairs.
  • Observed widespread expression correlation among mRNAs within the same MTBs, even after controlling for co-regulatory effects.
  • These findings suggest potential expression buffering consistent with the ceRNA hypothesis.

Conclusions:

  • MTBs facilitate the identification of autonomous miRNA-target modules for experimental validation of the ceRNA hypothesis.
  • The identified modules can be leveraged to investigate other properties of miRNA-target networks.

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