Jove
Visualize
Contact Us

Related Concept Videos

RNA-seq03:21

RNA-seq

11.6K
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...
11.6K
Ribosome Profiling02:24

Ribosome Profiling

4.0K
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...
4.0K
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

1.3K
The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
1.3K
Real Time RT-PCR02:57

Real Time RT-PCR

64.3K
Real-time reverse transcription-polymerase chain reaction, or Real-time RT-PCR, is an analytical tool used to determine the expression level of target genes. The method involves converting mRNA to complementary DNA with the help of an enzyme known as reverse transcriptase, followed by the PCR amplification of the cDNA. These two processes can be performed simultaneously in a single tube or separately as a two-step reaction.
The real-time quantification of the number of amplified products is...
64.3K
Transcriptional Regulation: Riboswitches01:23

Transcriptional Regulation: Riboswitches

493
Riboswitches are RNA elements that regulate gene expression by altering their secondary structures in response to specific effector molecules. These elements, located in the leader regions of certain mRNAs, act as transcriptional regulators by toggling between alternative conformations to control downstream gene expression. Riboswitch-mediated regulation is a precise mechanism for modulating biosynthetic pathways, as exemplified by the riboflavin biosynthesis pathway in Bacillus...
493
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

25.6K
Gene expression can be regulated at almost every step from gene to protein. Transcription is the step that is most commonly regulated. This involves the binding of proteins to short regulatory sequences on the DNA. This association can either promote or inhibit the transcription of a gene associated with the respective sequence.
Transcription results in the generation of precursor (pre-mRNA) that consists of both exons and introns, which needs further processing before being translated to a...
25.6K

You might also read

Related Articles

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

Sort by
Same author

Transcription initiation profiling defines the regulatory logic of astrocyte gene regulation.

bioRxiv : the preprint server for biology·2026
Same author

<i>Mysm1</i> mutations in <i>meander tail</i> mice cause anterior-selective cerebellum malformation.

bioRxiv : the preprint server for biology·2026
Same author

SETD5 dysfunction in human astrocytes drives IL-6-mediated neuronal impairments via the JAK/STAT signaling pathway.

bioRxiv : the preprint server for biology·2026
Same author

Profiling active RNA polymerase II transcription start sites from total RNA by capped small RNA sequencing (csRNA-seq).

Nature protocols·2026
Same author

Multiplexed measurements of protein-protein interactions and protein abundance across cellular conditions using Prod&PQ-seq.

bioRxiv : the preprint server for biology·2026
Same author

Improved spike-in normalization clarifies the relationship between active histone modifications and transcription.

bioRxiv : the preprint server for biology·2025
Same journal

High-accuracy SNV calling for bacterial isolates using deep learning with AccuSNV.

Genome research·2026
Same journal

Complete sequencing of medaka genomes reveals the architecture of centromeric satellites, giant mobile elements, and sex chromosomes.

Genome research·2026
Same journal

Convergence and conflict among telomere specialized transposons across 60 million years of Drosophilid evolution.

Genome research·2026
Same journal

A unified analysis of cell type- and trajectory-associated pathways in single-cell data using Phoenix.

Genome research·2026
Same journal

Resf1 is required for proper placental development and configuration of trophoblast cell-specific heterochromatin.

Genome research·2026
Same journal

Telomere-driven replicative crisis is driven by large-scale changes in genomic architecture.

Genome research·2026
See all related articles
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 Experiment Video

Updated: Jan 5, 2026

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
12:54

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

14.0K

Identification and dynamic quantification of regulatory elements using total RNA.

Sascha H Duttke1, Max W Chang1, Sven Heinz1

  • 1Department of Medicine, University of California, San Diego, La Jolla, California 92093, USA.

Genome Research
|October 26, 2019
PubMed
Summary
This summary is machine-generated.

We developed capped-small RNA-seq (csRNA-seq) to detect transcription start sites for stable and unstable RNAs. This method reveals more regulated transcripts and ancient regulatory elements across eukaryotes.

More Related Videos

Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
05:12

Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms

Published on: February 2, 2024

1.3K
An Assay for Quantifying Protein-RNA Binding in Bacteria
07:02

An Assay for Quantifying Protein-RNA Binding in Bacteria

Published on: June 12, 2019

6.9K

Related Experiment Videos

Last Updated: Jan 5, 2026

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
12:54

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation

Published on: March 7, 2018

14.0K
Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
05:12

Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms

Published on: February 2, 2024

1.3K
An Assay for Quantifying Protein-RNA Binding in Bacteria
07:02

An Assay for Quantifying Protein-RNA Binding in Bacteria

Published on: June 12, 2019

6.9K

Area of Science:

  • Molecular Biology
  • Genomics
  • Epigenetics

Background:

  • Gene expression regulation relies on precise control of transcription initiation.
  • Detecting both stable and unstable RNA transcripts is crucial for understanding gene regulation dynamics.
  • Current methods like RNA-seq have limitations in sensitivity and scope for detecting all transcript types.

Purpose of the Study:

  • To introduce a novel method, capped-small RNA-seq (csRNA-seq), for high-resolution detection of transcription start sites (TSSs).
  • To characterize stable and unstable RNA transcripts across diverse eukaryotic species.
  • To investigate the evolutionary conservation of transcriptional regulatory elements and associated histone modifications.

Main Methods:

  • Developed capped-small RNA-seq (csRNA-seq) using total RNA for sensitive detection of TSSs.
  • Applied csRNA-seq to tissues from multiple eukaryotic kingdoms (animals, plants, fungi).
  • Integrated csRNA-seq data with epigenomic data, including histone modifications like H3K4me3 and H3K27ac.

Main Results:

  • csRNA-seq identified an order of magnitude more regulated transcripts compared to standard RNA-seq.
  • Detected evolutionarily conserved unstable transcripts (e.g., enhancer RNAs, pri-miRNAs) across eukaryotes.
  • Found H3K4me3 enriched at stable TSSs and H3K27ac downstream of all active TSSs, indicating ancient roles for these marks.

Conclusions:

  • Total RNA is sufficient for comprehensive analysis of stable and unstable transcripts and their regulatory elements.
  • csRNA-seq provides single-nucleotide resolution for capturing transcription dynamics.
  • Histone modifications have ancient roles in marking active transcription start sites and downstream regulatory regions.