Computational Prediction of Functional MicroRNA-mRNA Interactions

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Date

2019

Journal Title

Journal ISSN

Volume Title

Publisher

Humana Press Inc

Open Access Color

Green Open Access

No

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Top 10%
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Average
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Top 10%

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Abstract

Proteins have a strong influence on the phenotype and their aberrant expression leads to diseases. MicroRNAs (miRNAs) are short RNA sequences which posttranscriptionally regulate protein expression. This regulation is driven by miRNAs acting as recognition sequences for their target mRNAs within a larger regulatory machinery. A miRNA can have many target mRNAs and an mRNA can be targeted by many miRNAs which makes it difficult to experimentally discover all miRNA-mRNA interactions. Therefore, computational methods have been developed for miRNA detection and miRNA target prediction. An abundance of available computational tools makes selection difficult. Additionally, interactions are not currently the focus of investigation although they more accurately define the regulation than pre-miRNA detection or target prediction could perform alone. We define an interaction including the miRNA source and the mRNA target. We present computational methods allowing the investigation of these interactions as well as how they can be used to extend regulatory pathways. Finally, we present a list of points that should be taken into account when investigating miRNA-mRNA interactions. In the future, this may lead to better understanding of functional interactions which may pave the way for disease marker discovery and design of miRNA-based drugs.

Description

Allmer, Jens/0000-0002-2164-7335; Sacar Demirci, Muserref Duygu/0000-0003-2012-0598;

Keywords

MicroRNA, Target, Regulation, Posttranscriptional Regulation, Pathway Extension, miRNA-mRNA Interaction, Target, Sequence Analysis, RNA, Gene Expression Profiling, Computational Biology, High-Throughput Nucleotide Sequencing, MicroRNA, Pathway extension, MiRNA–mRNA interaction, Machine Learning, MicroRNAs, Databases, Genetic, Animals, Humans, Gene Regulatory Networks, RNA, Messenger, Posttranscriptional regulation, Software, Regulation

Fields of Science

0301 basic medicine, 0303 health sciences, 03 medical and health sciences

Citation

WoS Q

N/A

Scopus Q

Q4
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OpenCitations Citation Count
23

Source

Methods in Molecular Biology

Volume

1912

Issue

Start Page

175

End Page

196
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19

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6

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