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MicroRNA (miRNA) are short, regulatory RNA transcribed from introns (non-coding regions of a gene) or intergenic regions (stretches of DNA present between genes). Several processing steps are required to form biologically active, mature miRNA. The initial transcript, called primary miRNA (pri-mRNA), base-pairs with itself, forming a stem-loop structure. Within the nucleus, an endonuclease enzyme, called Drosha, shortens the stem-loop structure into hairpin-shaped pre-miRNA. After the pre-miRNA...
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SPCMLMI: A structural perturbation-based matrix completion method to predict lncRNA-miRNA interactions.

Mei-Neng Wang1, Li-Lan Lei1, Wei He1

  • 1School of Mathematics and Computer Science, Yichun University, Yichun, China.

Frontiers in Genetics
|December 2, 2022
PubMed
Summary
This summary is machine-generated.

This study introduces SPCMLMI, a computational method for predicting long non-coding RNA (lncRNA) and microRNA (miRNA) interactions. The approach accurately identifies these crucial gene regulators, aiding in complex disease diagnosis and treatment.

Keywords:
bilayer networklncRNA–miRNA interactionsmatrix completionstructural consistencystructural perturbation

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • Long non-coding RNA (lncRNA) and microRNA (miRNA) interactions are vital for gene regulation and complex disease development.
  • Experimental identification of lncRNA-miRNA interactions is costly and time-consuming.
  • Accurate computational methods are needed to infer these interactions efficiently.

Purpose of the Study:

  • To develop a novel computational approach, SPCMLMI, for predicting lncRNA-miRNA interactions.
  • To improve the accuracy and efficiency of identifying potential lncRNA-miRNA interactions.

Main Methods:

  • Calculated lncRNA and miRNA similarities (expression profiles, sequences).
  • Constructed a bilayer network integrating known interactions and similarity networks.
  • Applied a structural perturbation-based matrix completion method for prediction.

Main Results:

  • SPCMLMI achieved high prediction performance with AUCs of 0.8984 and 0.9891 on two datasets.
  • Outperformed existing methods in prediction accuracy.
  • Case studies on lncRNA XIST and miRNA hsa-mir-195-5-p validated the method's effectiveness.

Conclusions:

  • SPCMLMI is an effective computational tool for predicting lncRNA-miRNA interactions.
  • The method offers a valuable resource for understanding gene regulation in complex diseases.
  • The structural consistency of the bilayer network contributes to prediction accuracy.