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 Structure01:23

RNA Structure

79.8K
Overview
The basic structure of RNA consists of a five-carbon sugar and one of four nitrogenous bases. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
There are three main types of ribonucleic acid (RNA): messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). All three RNA types consist of a...
79.8K
RNA Structure01:19

RNA Structure

8.0K
The basic structure of RNA consists of a string of ribonucleotides attached by phosphodiester bonds. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
There are three main types of ribonucleic acid (RNA) involved in protein synthesis: messenger RNA (mRNA), transfer RNA (tRNA), and ribosomal RNA (rRNA). All three...
8.0K
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

7.5K
Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific...
7.5K
Structure of a Gene01:30

Structure of a Gene

16.5K
A gene is the fundamental unit of heredity. Every individual has two copies of each gene, one inherited from each parent. Although most people contain the same genes, there is a small fraction that is slightly different amongst people. A gene with a small difference in its sequence of DNA bases forms different alleles, contributing to different phenotypes.
However, only 1% of the DNA is composed of genes that encode proteins; the rest, 99% is non-coding DNA. This non-coding DNA performs...
16.5K
Genomic DNA in Eukaryotes00:58

Genomic DNA in Eukaryotes

53.6K
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
53.6K
Ribosome Profiling02:24

Ribosome Profiling

4.2K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
4.2K

You might also read

Related Articles

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

Sort by
Same author

Prognostic markers, quality of life (QoL) and value of health (V-He) in advanced biliary cancers (ABC) treated with second-line active symptom control (ASC) alone or ASC with oxaliplatin-5-FU chemotherapy (ASC + FOLFOX) in the randomised phase III, multicentre, open-label ABC-06 clinical trial.

ESMO open·2026
Same author

Effect of recombinant equine chorionic gonadotropin on fertility of lactating dairy cows.

Theriogenology·2026
Same author

Comparison of short-read and long-read metagenome assemblies in a natural soil community highlights systematic bias in recovery of high-diversity populations.

NAR genomics and bioinformatics·2025
Same author

A genome-wide investigation of insidious uveitis in Appaloosa horses.

BMC genomics·2025
Same author

The Great Genotyper: a graph-based method for population genotyping of small and structural variants.

GigaScience·2025
Same author

Anna: an open-source platform for real-time integration of machine learning classifiers with veterinary electronic health records.

BMC veterinary research·2025
Same journal

Chromosomal scale genome assembly of medicinal plant Sophora tonkinensis.

BMC genomics·2026
Same journal

Variant-specific RNA testing resolves variants of uncertain significance in exome testing.

BMC genomics·2026
Same journal

Kaiso overexpression promotes an interferon immune response in murine intestines.

BMC genomics·2026
Same journal

Genomic evidence of ecological flexibility and cross-niche CRISPR spacerome targeting phage-plasmid hybrids in Latilactobacillus curvatus.

BMC genomics·2026
Same journal

Fgf evolution in vertebrates: insights from cyclostomes.

BMC genomics·2026
Same journal

Metabolic reprogramming, oxidative stress, and mitophagy in JSRV Env-transformed BEAS-2B cells: insights from integrated transcriptomics and metabolomics.

BMC genomics·2026
See all related articles

Related Experiment Video

Updated: Mar 8, 2026

Large-scale Zebrafish Embryonic Heart Dissection for Transcriptional Analysis
10:00

Large-scale Zebrafish Embryonic Heart Dissection for Transcriptional Analysis

Published on: January 12, 2015

15.3K

Tissue resolved, gene structure refined equine transcriptome.

T A Mansour1,2, E Y Scott3, C J Finno1

  • 1Department of Population Health and Reproduction, University of California, Davis, Davis, USA.

BMC Genomics
|January 22, 2017
PubMed
Summary
This summary is machine-generated.

This study presents a new equine transcriptome, improving gene expression analysis and genetic variant assessment. The refined transcriptome offers enhanced tissue-specific resolution for various downstream applications.

Keywords:
Equine transcriptomeRNA-seqTissue-specificity

More Related Videos

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
10:44

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp

Published on: June 20, 2018

10.4K
Single-Animal, Single-Tube RNA Extraction for Comparison of Relative Transcript Levels via qRT-PCR in the Tardigrade Hypsibius exemplaris
08:11

Single-Animal, Single-Tube RNA Extraction for Comparison of Relative Transcript Levels via qRT-PCR in the Tardigrade Hypsibius exemplaris

Published on: January 3, 2025

951

Related Experiment Videos

Last Updated: Mar 8, 2026

Large-scale Zebrafish Embryonic Heart Dissection for Transcriptional Analysis
10:00

Large-scale Zebrafish Embryonic Heart Dissection for Transcriptional Analysis

Published on: January 12, 2015

15.3K
Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp
10:44

Single Cell Multiplex Reverse Transcription Polymerase Chain Reaction After Patch-clamp

Published on: June 20, 2018

10.4K
Single-Animal, Single-Tube RNA Extraction for Comparison of Relative Transcript Levels via qRT-PCR in the Tardigrade Hypsibius exemplaris
08:11

Single-Animal, Single-Tube RNA Extraction for Comparison of Relative Transcript Levels via qRT-PCR in the Tardigrade Hypsibius exemplaris

Published on: January 3, 2025

951

Area of Science:

  • Genomics
  • Transcriptomics
  • Bioinformatics

Background:

  • Accurate gene expression quantification and genetic variant analysis depend on high-quality reference transcriptomes.
  • Current horse genome annotations are insufficient for precise gene expression assessment, particularly at the isoform level, and lack detailed untranslated region (UTR) usage information.

Purpose of the Study:

  • To develop an improved annotation pipeline for the horse genome.
  • To create a refined equine transcriptome by integrating extensive RNA-seq data.
  • To enhance the accuracy and resolution of gene expression analysis and functional genomics in horses.

Main Methods:

  • An annotation pipeline was developed for horse transcriptomes.
  • 1.9 billion RNA-seq reads from multiple datasets were integrated.
  • Four levels of transcript filtration were applied to generate multiple transcriptome versions.

Main Results:

  • A new equine transcriptome was generated, integrating data from eight tissues across 59 individuals.
  • The refined transcriptome features improved gene structure and isoform resolution, offering significant tissue-specific insights.
  • The most comprehensive version includes 36,876 genes, 76,125 isoforms, and 6,474 novel transcriptional loci.

Conclusions:

  • The developed pipeline and resulting equine transcriptomes provide superior tissue-specific resolution compared to existing resources.
  • The transcriptomes are flexible and suitable for diverse downstream analyses, including gene expression and variant studies.
  • Further integration of equine transcriptomes with the pipeline is encouraged to continuously improve equine genomic annotation.