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Biotin-based Pulldown Assay to Validate mRNA Targets of Cellular miRNAs
Published on: June 12, 2018
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.
Background:
In the competing endogenous RNA (ceRNA) hypothesis, different transcripts communicate through a competition for their common targeting microRNAs (miRNAs). Individual examples have clearly shown the functional importance of ceRNA in gene regulation and cancer biology. It remains unclear to what extent gene expression levels are regulated by ceRNA in general. One major hurdle to studying this problem is the intertwined connections in miRNA-target networks, which makes it difficult to isolate the effects of individual miRNAs.
Results:
Here we propose computational methods for decomposing a complex miRNA-target network into largely autonomous modules called microRNA-target biclusters (MTBs). Each MTB contains a relatively small number of densely connected miRNAs and mRNAs with few connections to other miRNAs and mRNAs. Each MTB can thus be individually analyzed with minimal crosstalk with other MTBs. Our approach differs from previous methods for finding modules in miRNA-target networks by not making any pre-assumptions about expression patterns, thereby providing objective information for testing the ceRNA hypothesis. We show that the expression levels of miRNAs and mRNAs in an MTB are significantly more anti-correlated than random miRNA-mRNA pairs and other validated and predicted miRNA-target pairs, demonstrating the biological relevance of MTBs. We further show that there is widespread correlation of expression between mRNAs in same MTBs under a wide variety of parameter settings, and the correlation remains even when co-regulatory effects are controlled for, which suggests potential widespread expression buffering between these mRNAs, which is consistent with the ceRNA hypothesis. Lastly, we also propose a potential use of MTBs in functional annotation of miRNAs.
Conclusions:
MTBs can be used to help identify autonomous miRNA-target modules for testing the generality of the ceRNA hypothesis experimentally. The identified modules can also be used to test other properties of miRNA-target networks in general.
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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