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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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Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
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Updated: Jul 31, 2025

Characterization of Functionally Associated miRNAs in Glioblastoma and their Engineering into Artificial Clusters for Gene Therapy
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GKLOMLI: a link prediction model for inferring miRNA-lncRNA interactions by using Gaussian kernel-based method on

Leon Wong1,2, Lei Wang3,4, Zhu-Hong You5

  • 1Guangxi Key Lab of Human-machine Interaction and Intelligent Decision, Guangxi Academy of Sciences, Nanning, 530007, China.

BMC Bioinformatics
|May 9, 2023
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Summary

This study introduces GKLOMLI, a computational tool for predicting microRNA-lncRNA interactions. This method offers a cost-effective and reliable approach to understanding gene regulation in human diseases.

Keywords:
Competing endogenous RNA (ceRNA)Computational biologyGaussian kernelLink predictionmiRNA–lncRNA interaction

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Limited understanding of microRNA-lncRNA interactions hinders the elucidation of regulatory mechanisms in human diseases.
  • Experimental validation of these interactions, such as CLIP-seq, is costly and time-consuming.
  • Computational tools are increasingly vital for predicting potential miRNA-lncRNA interactions for further experimental validation.

Purpose of the Study:

  • To develop a novel computational model for predicting miRNA-lncRNA interactions.
  • To provide a reliable and efficient tool for identifying potential miRNA-lncRNA interactions.
  • To facilitate the study of gene expression modulation in human diseases.

Main Methods:

  • Proposed a novel link prediction model named GKLOMLI (Gaussian kernel-based method and linear optimization algorithm for inferring miRNA-lncRNA interactions).
  • Utilized a Gaussian kernel-based method to generate miRNA and lncRNA similarity matrices from an observed interaction network.
  • Employed a linear optimization algorithm trained on an integrated matrix for predicting interactions.

Main Results:

  • The GKLOMLI model demonstrated high performance in predicting miRNA-lncRNA interactions.
  • Cross-validation experiments, including k-fold CV and leave-one-out CV, yielded high Area Under the Curves (AUCs).
  • Achieved AUCs of 0.8623 ± 0.0027 (2-fold CV), 0.9053 ± 0.0017 (5-fold CV), 0.9151 ± 0.0013 (10-fold CV), and 0.9236 (LOO-CV).

Conclusions:

  • The proposed GKLOMLI method is a high-performance tool for predicting miRNA-lncRNA interactions.
  • GKLOMLI is expected to aid in uncovering underlying interactions and deciphering mechanisms of complex diseases.
  • This computational approach offers a valuable resource for future biological experiments and disease research.