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

RNA-seq03:21

RNA-seq

10.4K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.4K
Leaky Scanning02:28

Leaky Scanning

5.2K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.2K
RNA Interference01:23

RNA Interference

26.4K
RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
26.4K
Nonsense-mediated mRNA Decay02:27

Nonsense-mediated mRNA Decay

10.8K
The Upf proteins that carry out nonsense-mediated decay (NMD) are found in all eukaryotic organisms, including humans. Each protein has an individual role, but they need to work in collaboration. Upf1 is an ATP-dependent RNA helicase that unwinds the RNA helix. Because Upf1 can unwind any RNA, Upf2 and Upf3 are required to help Upf1 discriminate between nonsense and normal mRNAs.
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
10.8K

You might also read

Related Articles

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

Sort by
Same author

Hepatic Injury Caused by the Environmental Toxicant Vinyl Chloride is Sex-Dependent in Mice.

Toxicological sciences : an official journal of the Society of Toxicology·2019
Same author

Impact of elevated CO<sub>2</sub> on C:N:P ratio among soybean cultivars.

The Science of the total environment·2019
Same author

Assessment of nephrotoxicity of herbal medicine containing aristolochic acid in mice.

The Korean journal of internal medicine·2019
Same author

Profiles of antibiotic resistome with animal manure application in black soils of northeast China.

Journal of hazardous materials·2019
Same author

Discovery of a First-in-Class Mitogen-Activated Protein Kinase Kinase 1/2 Degrader.

Journal of medicinal chemistry·2019
Same author

Investigating Adsorption/Desorption of DNA on ZIF-8 Surface by Fluorescently Labeled Oligonucleotides.

Langmuir : the ACS journal of surfaces and colloids·2019

Related Experiment Video

Updated: Sep 11, 2025

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

12.2K

RSCNN-PseU: random searching-based convolutional neural network model for identifying RNA pseudouridine.

Jian Jin1, Jie Feng1

  • 1School of Science, Minzu University of China, No. 27 Zhongguancun South Street, Haidian District, Beijing 100081, China.

Briefings in Bioinformatics
|August 15, 2025
PubMed
Summary

This study introduces a novel method for identifying RNA pseudouridine using physicochemical properties and discrete Fourier transform. The developed RSCNN-PseU model demonstrates superior performance in RNA pseudouridine identification.

Keywords:
RNA pseudouridineconvolutional neural networkdiscrete Fourier transformrandom searching

More Related Videos

Identification of Circular RNAs using RNA Sequencing
08:25

Identification of Circular RNAs using RNA Sequencing

Published on: November 14, 2019

12.4K
2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

Published on: July 10, 2020

2.0K

Related Experiment Videos

Last Updated: Sep 11, 2025

Rare Event Detection Using Error-corrected DNA and RNA Sequencing
10:36

Rare Event Detection Using Error-corrected DNA and RNA Sequencing

Published on: August 3, 2018

12.2K
Identification of Circular RNAs using RNA Sequencing
08:25

Identification of Circular RNAs using RNA Sequencing

Published on: November 14, 2019

12.4K
2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications
05:41

2D-HELS MS Seq: A General LC-MS-Based Method for Direct and de novo Sequencing of RNA Mixtures with Different Nucleotide Modifications

Published on: July 10, 2020

2.0K

Area of Science:

  • Biochemistry
  • Bioinformatics
  • Computational Biology

Background:

  • RNA pseudouridine is a crucial post-transcriptional modification impacting RNA structure and function.
  • Accurate identification of RNA pseudouridine is essential for understanding various biological processes.
  • Existing methods for pseudouridine identification may lack efficiency or accuracy.

Purpose of the Study:

  • To develop a more effective feature extraction method for identifying RNA pseudouridine.
  • To propose a novel computational model for enhanced RNA pseudouridine detection.
  • To improve the accuracy and adaptability of pseudouridine identification across different datasets.

Main Methods:

  • RNA sequences were converted into numerical sequences using dinucleotide physicochemical properties (free energy, hydrophilicity).
  • Discrete Fourier Transform (DFT) was applied to extract amplitude features, generating 2(N-1) features for a sequence of length N.
  • A convolutional neural network (CNN) with a dynamic fully connected layer was employed for prediction, optimized using a random search algorithm.

Main Results:

  • The proposed RSCNN-PseU model achieved a better identification effect for RNA pseudouridine.
  • The model demonstrated effective feature extraction and accurate prediction capabilities.
  • Adaptive regulation of model complexity was achieved, accommodating diverse species and datasets.

Conclusions:

  • The novel feature extraction method combined with the RSCNN-PseU model offers a powerful approach for RNA pseudouridine identification.
  • This method enhances the accuracy and efficiency of detecting this important RNA modification.
  • The findings contribute to advancing research in RNA biology and related fields.