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

Replicative Cell Senescence02:15

Replicative Cell Senescence

Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Replicative Cell Senescence02:15

Replicative Cell Senescence

Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Apoptosis01:30

Apoptosis

Apoptosis is a combination of two Greek words, 'apo' and 'ptosis,' meaning separation and falling off, respectively. Hippocrates used this word to describe gangrene, which was caused due to bandaging of fractured bones. Apoptosis was distinguished from necrosis in 1970 when John Kerr reported observations of morphological changes occurring during apoptosis. During one experiment, he observed that the disruption of blood supply to the liver tissue resulted in a size reduction of the tissue.

You might also read

Related Articles

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

Sort by
Same author

Fasting-mimicking diet counteracts gut microbial dysbiosis in experimental lynch syndrome.

Cancer & metabolism·2026
Same author

Methionine-supplemented longevity diet increases growth hormone, GLP-1, and FGF21; reduces frailty; and promotes healthspan.

Cell metabolism·2026
Same author

A Fasting-Mimicking Diet Affects the Inflammatory Response Following Periodontal Treatment: A Multi-centre Feasibility Randomised Controlled Pilot Trial.

Journal of clinical periodontology·2026
Same author

Senescent obesity signature in breast cancer: a paradigm of reverse cardio-oncology.

European heart journal·2026
Same author

Periodic fasting induced reconstitution of metabolic flexibility improves albuminuria in patients with type 2 diabetes.

Molecular metabolism·2025
Same author

Author Correction: Fasting mimicking diet cycles versus a Mediterranean diet and cardiometabolic risk in overweight and obese hypertensive subjects: a randomized clinical trial.

npj metabolic health and disease·2025

Related Experiment Video

Updated: Jul 5, 2026

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model
08:46

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model

Published on: September 29, 2011

Chronological aging-induced apoptosis in yeast.

Paola Fabrizio1, Valter D Longo

  • 1Andrus Gerontology Center, Division of Biogerontology, University of Southern California, Los Angeles, CA 90089-0191, USA. fabrizio@usc.edu

Biochimica Et Biophysica Acta
|May 1, 2008
PubMed
Summary

Yeast aging studies reveal conserved pathways and programmed death. A specific aging/death program promotes regrowth of adapted mutants in aging Saccharomyces cerevisiae populations.

More Related Videos

Quantifying Yeast Chronological Life Span by Outgrowth of Aged Cells
12:24

Quantifying Yeast Chronological Life Span by Outgrowth of Aged Cells

Published on: May 6, 2009

A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
10:39

A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae

Published on: September 17, 2020

Related Experiment Videos

Last Updated: Jul 5, 2026

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model
08:46

Studying Age-dependent Genomic Instability using the S. cerevisiae Chronological Lifespan Model

Published on: September 29, 2011

Quantifying Yeast Chronological Life Span by Outgrowth of Aged Cells
12:24

Quantifying Yeast Chronological Life Span by Outgrowth of Aged Cells

Published on: May 6, 2009

A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
10:39

A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae

Published on: September 17, 2020

Area of Science:

  • Gerontology
  • Molecular Biology
  • Genetics

Background:

  • Saccharomyces cerevisiae serves as a simple eukaryotic model for aging research.
  • Chronological lifespan measures survival in non-dividing yeast populations, identifying key aging genes and pathways.
  • Schizosaccharomyces pombe exhibits chronological aging similar to S. cerevisiae, involving conserved protein homologues.

Purpose of the Study:

  • To review fundamental genetics of chronological aging in yeast.
  • To explore the overlap between yeast aging and apoptotic processes.
  • To highlight an aging/death program facilitating regrowth of adapted mutants in S. cerevisiae.

Main Methods:

  • Analysis of chronological lifespan paradigms in yeast.
  • Review of genetic studies identifying life-regulatory genes and aging pathways.
  • Description of genome-wide screening techniques for studying programmed death.

Main Results:

  • Identification of conserved pro-aging pathways in yeast.
  • Evidence of apoptotic death features during yeast chronological aging.
  • Discovery of an aging/death program promoting dedifferentiation and regrowth of adapted mutants.

Conclusions:

  • Yeast aging shares fundamental genetic and molecular mechanisms with other eukaryotes.
  • Programmed death pathways in aging yeast populations can lead to the emergence of fitter variants.
  • Genome-wide screening is a powerful tool for elucidating mechanisms of programmed death in aging yeast.