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Published on: April 25, 2022
Identification of miRNA-mRNA regulatory modules by exploring collective group relationships
S M Masud Karim1, Lin Liu2, Thuc Duy Le3
1School of Information Technology and Mathematical Sciences, University of South Australia, Mawson Lakes, Adelaide, 5095, SA, Australia. masud.karim@mymail.unisa.edu.au.
Background:
microRNAs (miRNAs) play an essential role in the post-transcriptional gene regulation in plants and animals. They regulate a wide range of biological processes by targeting messenger RNAs (mRNAs). Evidence suggests that miRNAs and mRNAs interact collectively in gene regulatory networks. The collective relationships between groups of miRNAs and groups of mRNAs may be more readily interpreted than those between individual miRNAs and mRNAs, and thus are useful for gaining insight into gene regulation and cell functions. Several computational approaches have been developed to discover miRNA-mRNA regulatory modules (MMRMs) with a common aim to elucidate miRNA-mRNA regulatory relationships. However, most existing methods do not consider the collective relationships between a group of miRNAs and the group of targeted mRNAs in the process of discovering MMRMs. Our aim is to develop a framework to discover MMRMs and reveal miRNA-mRNA regulatory relationships from the heterogeneous expression data based on the collective relationships.
Results:
We propose DIscovering COllective group RElationships (DICORE), an effective computational framework for revealing miRNA-mRNA regulatory relationships. We utilize the notation of collective group relationships to build the computational framework. The method computes the collaboration scores of the miRNAs and mRNAs on the basis of their interactions with mRNAs and miRNAs, respectively. Then it determines the groups of miRNAs and groups of mRNAs separately based on their respective collaboration scores. Next, it calculates the strength of the collective relationship between each pair of miRNA group and mRNA group using canonical correlation analysis, and the group pairs with significant canonical correlations are considered as the MMRMs. We applied this method to three gene expression datasets, and validated the computational discoveries.
Conclusions:
Analysis of the results demonstrates that a large portion of the regulatory relationships discovered by DICORE is consistent with the experimentally confirmed databases. Furthermore, it is observed that the top mRNAs that are regulated by the miRNAs in the identified MMRMs are highly relevant to the biological conditions of the given datasets. It is also shown that the MMRMs identified by DICORE are more biologically significant and functionally enriched.
Insights
We developed DICORE, a computational framework to find miRNA-mRNA regulatory modules by analyzing collective relationships. This method identifies biologically significant gene regulatory networks and enhances understanding of gene regulation.
Area of Science:
- Computational Biology
- Genomics
- Bioinformatics
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression, targeting messenger RNAs (mRNAs) post-transcriptionally.
- Understanding collective miRNA-mRNA interactions within gene regulatory networks is crucial for biological insights.
- Existing computational methods often overlook the collective relationships between miRNA and mRNA groups.
Purpose of the Study:
- To develop a novel computational framework, DICORE, for discovering miRNA-mRNA regulatory modules (MMRMs).
- To reveal miRNA-mRNA regulatory relationships by focusing on collective interactions within groups.
- To analyze heterogeneous expression data for identifying biologically significant MMRMs.
Main Methods:
- DICORE utilizes collective group relationships to model miRNA-mRNA interactions.
- It computes collaboration scores for miRNAs and mRNAs to form distinct groups.
- Canonical correlation analysis identifies significant collective relationships between miRNA and mRNA groups, defining MMRMs.
Main Results:
- DICORE successfully identified miRNA-mRNA regulatory relationships from gene expression datasets.
- The discovered regulatory relationships show high consistency with experimentally validated databases.
- Identified MMRMs revealed top mRNAs highly relevant to specific biological conditions.
Conclusions:
- DICORE effectively discovers biologically significant and functionally enriched miRNA-mRNA regulatory modules.
- The framework provides a novel approach to understanding gene regulation through collective interactions.
- The findings contribute to a deeper insight into miRNA-mRNA networks and cellular functions.
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