Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

MicroRNAs01:22

MicroRNAs

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...
MicroRNAs01:22

MicroRNAs

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 ends...
MicroRNAs01:22

MicroRNAs

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 ends...
piRNA - Piwi-interacting RNAs02:57

piRNA - Piwi-interacting RNAs

PIWI-interacting RNAs, or piRNAs, are the most abundant short non-coding RNAs. More than 20,000 genes have been found in humans that code for piRNAs while only 2000 genes have been found for miRNAs. piRNAs can act at the transcriptional and post-transcriptional levels and have a vital role in silencing transposable elements present in germ cells. They are also involved in epigenetic silencing and activation. Previously, they were thought to function only in germ cells but new evidence suggests...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Clinical features and long-term surgical outcomes of ureteral endometriosis with hydroureteronephrosis: a retrospective study.

BMC women's health·2026
Same author

Comparing incidence of heart failure in individuals with enlarged cardiac chambers versus diabetes.

American journal of preventive cardiology·2026
Same author

Leaching kinetics and mechanisms in efficient chlorination leaching of germanium-rich fume dust.

RSC advances·2026
Same author

Chaperone-Mediated Autophagy-Directed Degradation of PI3K in Tumor Cells: Development of Multifunctional Peptide-Drug Conjugates With Enhanced Penetration and Selectivity.

Archiv der Pharmazie·2026
Same author

AI-quantified Myosteatosis at CAC CT for Prediction of Atrial Fibrillation and Heart Failure: The Multi-Ethnic Study of Atherosclerosis.

Radiology. Cardiothoracic imaging·2026
Same author

CD90 mediates gastric cancer immune evasion though regulating IGF2BP2 to stabilize the m6A-CD47/SIRPα axis.

Cancer cell international·2026

Related Experiment Video

Updated: May 15, 2026

mirMachine: A One-Stop Shop for Plant miRNA Annotation
06:16

mirMachine: A One-Stop Shop for Plant miRNA Annotation

Published on: May 1, 2021

MiRmat: mature microRNA sequence prediction.

Chenfeng He1, Ying-Xin Li, Guangxin Zhang

  • 1The State Key Laboratory of Pharmaceutical Biotechnology and Jiangsu Engineering Research Center for MicroRNA Biology and Biotechnology, School of Life Science, Nanjing University, Nanjing, China.

Plos One
|January 10, 2013
PubMed
Summary

A new method, MiRmat, accurately predicts mature microRNA sequences by analyzing RNA structure and using Random Forest. This tool aids in identifying microRNAs and understanding gene regulation across vertebrates.

More Related Videos

A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source Tools
09:29

A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source Tools

Published on: August 21, 2019

A Reporter Assay to Analyze Intronic microRNA Maturation in Mammalian Cells
06:48

A Reporter Assay to Analyze Intronic microRNA Maturation in Mammalian Cells

Published on: June 16, 2022

Related Experiment Videos

Last Updated: May 15, 2026

mirMachine: A One-Stop Shop for Plant miRNA Annotation
06:16

mirMachine: A One-Stop Shop for Plant miRNA Annotation

Published on: May 1, 2021

A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source Tools
09:29

A Complete Pipeline for Isolating and Sequencing MicroRNAs, and Analyzing Them Using Open Source Tools

Published on: August 21, 2019

A Reporter Assay to Analyze Intronic microRNA Maturation in Mammalian Cells
06:48

A Reporter Assay to Analyze Intronic microRNA Maturation in Mammalian Cells

Published on: June 16, 2022

Area of Science:

  • Bioinformatics
  • Computational Biology
  • Molecular Biology

Background:

  • MicroRNAs (miRNAs) are crucial regulators of gene expression, processed from primary transcripts by Drosha and Dicer enzymes.
  • Mature miRNA sequences, particularly the seed region, dictate target mRNA binding and specificity.
  • Accurate prediction of mature miRNA sequences is essential for discovering novel miRNAs, their targets, and mapping genome-wide post-transcriptional regulatory networks.

Purpose of the Study:

  • To develop and validate a computational method for accurately predicting mature microRNA sequences.
  • To improve the identification of Drosha and Dicer processing sites in microRNA biogenesis.
  • To provide a tool for advancing the study of miRNA function and regulation in vertebrates.

Main Methods:

  • Developed MiRmat, a two-part method for predicting Drosha and Dicer processing sites.
  • Utilized the conserved free energy distribution patterns of vertebrate microRNA hairpin structures.
  • Employed the Random Forest algorithm for sequence prediction based on structural features.

Main Results:

  • MiRmat achieved high accuracy in predicting Drosha (77.8%) and Dicer (92.8%) processing sites within 2 nt deviation on a vertebrate test set.
  • Demonstrated robust performance on novel microRNA families, with identification rates of 71.9% for Drosha and 87.2% for Dicer sites.
  • Outperformed existing state-of-the-art methods in predicting mature microRNA sequences.

Conclusions:

  • MiRmat effectively predicts mature microRNA sequences using RNA stem-loop free energy distributions and Random Forest.
  • The method exhibits superior performance compared to current tools and is applicable across vertebrate species.
  • MiRmat is freely accessible online for research use.