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

mRNA Stability and Gene Expression02:51

mRNA Stability and Gene Expression

The structure and stability of mRNA molecules regulates gene expression, as mRNAs are a key step in the pathway from gene to protein. In eukaryotes, the half-life of mRNA varies from a few minutes up to several days. mRNA stability is essential in growth and development. The absence of the proteins regulating its stability, such as tristetraprolin in mice, can cause systemic issues, including bone marrow overgrowth, inflammation, and autoimmunity.
Cis-acting Elements involved in mRNA stability
mRNA Stability and Gene Expression02:51

mRNA Stability and Gene Expression

The structure and stability of mRNA molecules regulates gene expression, as mRNAs are a key step in the pathway from gene to protein. In eukaryotes, the half-life of mRNA varies from a few minutes up to several days. mRNA stability is essential in growth and development. The absence of the proteins regulating its stability, such as tristetraprolin in mice, can cause systemic issues, including bone marrow overgrowth, inflammation, and autoimmunity.
Cis-acting Elements involved in mRNA stability
Stringent Response in E. coli01:23

Stringent Response in E. coli

Bacterial growth is closely tied to nutrient availability, with cells proliferating exponentially under favorable conditions and entering a stationary phase when resources become scarce. This transition is mediated by a regulatory mechanism known as the stringent response, which allows bacteria to adapt to nutrient deprivation by modulating gene expression and metabolic activity.During nutrient scarcity, intracellular amino acid levels decline. It results in the accumulation of uncharged tRNAs...
RNA Stability01:53

RNA Stability

Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
RNA Stability01:53

RNA Stability

Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
Nuclear Export of mRNA02:31

Nuclear Export of mRNA

Before mRNAs are exported to the cytoplasm, it is crucial to check each mRNA for structural and functional integrity. Eukaryotic cells use several different mechanisms, collectively known as mRNA surveillance, to look for irregularities in mRNAs. Irregular or aberrant mRNA are rapidly degraded by various enzymes. If a defective mRNA escapes the surveillance, it would be translated into a protein which would either be non-functional or not function properly. One of the primary irregularities in...

You might also read

Related Articles

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

Sort by
Same author

Functional Analysis of the Zinc Finger Modules of the <i>S. cerevisiae</i> Splicing Factor Luc7.

bioRxiv : the preprint server for biology·2024
Same author

Preface.

The Enzymes·2016
Same author

Splicing-Mediated Autoregulation Modulates Rpl22p Expression in Saccharomyces cerevisiae.

PLoS genetics·2016
Same author

The Rtr1p CTD phosphatase autoregulates its mRNA through a degradation pathway involving the REX exonucleases.

RNA (New York, N.Y.)·2016
Same author

Methylation of yeast ribosomal protein Rpl3 promotes translational elongation fidelity.

RNA (New York, N.Y.)·2016
Same author

Two degrading decades for RNA.

RNA (New York, N.Y.)·2015

Related Experiment Video

Updated: Jun 13, 2026

Isolation of Quiescent Stem Cell Populations from Individual Skeletal Muscles
11:35

Isolation of Quiescent Stem Cell Populations from Individual Skeletal Muscles

Published on: December 9, 2022

InvIGOrating mRNAs during Quiescence.

Guillaume Chanfreau1

  • 1Department of Chemistry & Biochemistry and the Molecular Biology Institute, University of California, Los Angeles, Box 951569, Los Angeles, CA 90095-1569, USA. guillom@chem.ucla.edu

Molecular Cell
|May 18, 2010
PubMed
Summary
This summary is machine-generated.

The Igo1/2 proteins safeguard messenger RNAs (mRNAs) from breakdown during cellular quiescence. This discovery is crucial for understanding gene expression regulation in non-dividing cells.

More Related Videos

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity
09:21

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity

Published on: October 22, 2018

Related Experiment Videos

Last Updated: Jun 13, 2026

Isolation of Quiescent Stem Cell Populations from Individual Skeletal Muscles
11:35

Isolation of Quiescent Stem Cell Populations from Individual Skeletal Muscles

Published on: December 9, 2022

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts
07:03

Determining Genome-wide Transcript Decay Rates in Proliferating and Quiescent Human Fibroblasts

Published on: January 2, 2018

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity
09:21

Saccharomyces cerevisiae Metabolic Labeling with 4-thiouracil and the Quantification of Newly Synthesized mRNA As a Proxy for RNA Polymerase II Activity

Published on: October 22, 2018

Area of Science:

  • Molecular Biology
  • Cellular Biology
  • Gene Expression Regulation

Background:

  • Cellular quiescence, a state of reversible cell cycle arrest, presents unique challenges for maintaining cellular function and integrity.
  • During quiescence, cells must adapt their gene expression programs to survive prolonged periods without growth or division.
  • Understanding the mechanisms that regulate mRNA stability during quiescence is critical for comprehending cellular adaptation.

Discussion:

  • The study by Talarek et al. (2010) in Molecular Cell identifies the Igo1/2 proteins as key players in protecting mRNAs from degradation.
  • These proteins appear to act as a shield, preserving essential mRNA transcripts during the metabolically restricted conditions of quiescence.
  • The findings shed light on a novel mechanism for post-transcriptional gene regulation in quiescent cells.

Key Insights:

  • Identification of Igo1/2 proteins as critical factors for mRNA protection during cellular quiescence.
  • Demonstration of a specific mechanism safeguarding mRNA integrity in non-proliferating cells.
  • Elucidation of a new layer of regulation controlling gene expression in quiescent states.

Outlook:

  • Further investigation into the precise molecular interactions of Igo1/2 with mRNA and other cellular components.
  • Exploring the potential role of Igo1/2 in other cellular stress responses or developmental processes.
  • Investigating therapeutic strategies targeting mRNA stability in diseases associated with quiescence or altered gene expression.