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

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

10.1K
In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
10.1K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.8K
3.8K
Alternative RNA Splicing02:18

Alternative RNA Splicing

26.1K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
26.1K
Alternative RNA Splicing02:18

Alternative RNA Splicing

5.5K
5.5K
Diversity in Cell Signaling Responses01:22

Diversity in Cell Signaling Responses

8.4K
The physiological function of a cell and cellular communication are outcomes of a range of extrinsic signals, intracellular signaling pathways, and cellular responses. No two cell types express the same repertoire of signaling components. Receptors are highly selective for their cognate ligands, but once activated, they can alter multiple cellular processes such as DNA transcription, protein synthesis, and metabolic activity. 
Graded and Abrupt Responses
Some signaling systems generate...
8.4K
RNA Splicing01:32

RNA Splicing

61.2K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
61.2K

You might also read

Related Articles

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

Sort by
Same author

Neuregulin-1β Mitigates Doxorubicin-Induced Cardiotoxicity via <i>Serping1</i> in Cardiac Fibroblasts.

International journal of molecular sciences·2026
Same author

Hypoxia-driven microRNA-27b underlies pathologic cardiac endoreplication in heart disease.

Signal transduction and targeted therapy·2026
Same author

Decoding Fibroblast Diversity Associated with the Postnatal Loss of Cardiac Regenerative Capacity.

International journal of molecular sciences·2026
Same author

<i>CLIPPER</i> Regulates LPIN1-Mediated Mitochondrial Biogenesis and Heart Regeneration.

Circulation research·2026
Same author

Circular Tale of Micropeptides in Cardiac Hypertrophy.

Circulation research·2025
Same author

Powering up piRNAs for heart regeneration.

Nature cardiovascular research·2025
Same journal

Patient-derived organoids reveal ductal dysfunction and CFTR-modulator responses in chronic pancreatitis.

Cell stem cell·2026
Same journal

Lineage plasticity driven by GATA6 loss fuels colorectal cancer metastasis.

Cell stem cell·2026
Same journal

Quantitative molecular cartography of emergency myelopoiesis reveals conserved modules of hematopoietic activation.

Cell stem cell·2026
Same journal

Paired pre- and post-transplant human immunoprofiling identifies an IFN-γ-JAK1 axis limiting stem-cell-derived RPE engraftment.

Cell stem cell·2026
Same journal

ENPP1 blockade with a humanized monoclonal antibody enhances renal repair after acute kidney injury.

Cell stem cell·2026
Same journal

ZNF512B safeguards genome integrity at regulatory regions to repress the SASP and inflammation.

Cell stem cell·2026
See all related articles

Related Experiment Video

Updated: Mar 21, 2026

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
12:44

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis

Published on: November 11, 2014

12.8K

Divergent Paths Lnc Cell Fates.

Samir Ounzain1, Thierry Pedrazzini1

  • 1Experimental Cardiology Unit, Department of Medicine, University of Lausanne Medical School, 1011 Lausanne, Switzerland.

Cell Stem Cell
|May 7, 2016
PubMed
Summary
This summary is machine-generated.

Specific long noncoding RNAs (lncRNAs) activate key developmental genes. These regulatory molecules control embryonic stem cell fate and properties, offering new insights into stem cell biology.

More Related Videos

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
09:36

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA

Published on: April 10, 2018

26.5K
Isolate Cell-Type-Specific RNAs from Snap-Frozen Heterogeneous Tissue Samples without Cell Sorting
08:30

Isolate Cell-Type-Specific RNAs from Snap-Frozen Heterogeneous Tissue Samples without Cell Sorting

Published on: December 8, 2021

2.6K

Related Experiment Videos

Last Updated: Mar 21, 2026

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis
12:44

Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis

Published on: November 11, 2014

12.8K
RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
09:36

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA

Published on: April 10, 2018

26.5K
Isolate Cell-Type-Specific RNAs from Snap-Frozen Heterogeneous Tissue Samples without Cell Sorting
08:30

Isolate Cell-Type-Specific RNAs from Snap-Frozen Heterogeneous Tissue Samples without Cell Sorting

Published on: December 8, 2021

2.6K

Area of Science:

  • Molecular Biology
  • Genetics
  • Stem Cell Biology

Background:

  • Long noncoding RNAs (lncRNAs) are recognized as crucial regulators of gene expression.
  • Their role in controlling stem cell properties is an area of active investigation.
  • Understanding lncRNA function is key to deciphering stem cell differentiation and development.

Purpose of the Study:

  • To investigate the function of a specific class of lncRNAs in embryonic stem cell regulation.
  • To determine how divergently transcribed lncRNAs influence stem cell fate.
  • To identify the mechanisms by which lncRNAs activate developmental genes.

Main Methods:

  • Analysis of lncRNA transcription patterns in embryonic stem cells.
  • Functional studies to assess the impact of specific lncRNAs on gene expression.
  • Investigation of lncRNA interactions with key developmental genes.

Main Results:

  • A distinct group of lncRNAs, transcribed divergently from protein-coding genes, was identified.
  • These lncRNAs were shown to activate critical developmental genes essential for stem cell fate.
  • The study provides evidence for a novel regulatory mechanism involving lncRNAs in stem cell differentiation.

Conclusions:

  • Divergent lncRNAs play a significant role in controlling embryonic stem cell fate.
  • These lncRNAs act by activating key developmental genes, thereby regulating stem cell properties.
  • The findings expand our understanding of the regulatory landscape governing stem cell pluripotency and differentiation.