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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...
Replication in Eukaryotes01:29

Replication in Eukaryotes

In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
Regulation of Expression at Multiple Steps01:23

Regulation of Expression at Multiple Steps

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 addition of a...
Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

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.
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Regulation of Expression Occurs at Multiple Steps02:24

Regulation of Expression Occurs at Multiple Steps

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.
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Related Experiment Video

Updated: Jul 7, 2026

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

Pathways change in expression during replicative aging in Saccharomyces cerevisiae.

Gloria Yiu1, Alejandra McCord, Alison Wise

  • 1Biology Department, Pomona College, Claremont, CA 91711, USA.

The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences
|February 5, 2008
PubMed
Summary

Yeast cells exhibit gene expression changes during aging, mirroring mammalian aging processes. Key findings include altered metabolism, reduced ribosome production, and increased DNA repair, offering insights into aging mechanisms.

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Continuous High-resolution Microscopic Observation of Replicative Aging in Budding Yeast

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Related Experiment Videos

Last Updated: Jul 7, 2026

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

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

Continuous High-resolution Microscopic Observation of Replicative Aging in Budding Yeast
10:41

Continuous High-resolution Microscopic Observation of Replicative Aging in Budding Yeast

Published on: August 20, 2013

Area of Science:

  • Cellular Biology
  • Genetics
  • Molecular Biology

Background:

  • Yeast replicative aging shares similarities with mammalian cellular aging.
  • Phenotypic changes in aging yeast include cell enlargement, sterility, and nucleolar alterations.

Purpose of the Study:

  • To investigate gene expression alterations during yeast replicative aging.
  • To correlate observed gene expression changes with known aging mechanisms in yeast and higher organisms.

Main Methods:

  • Microarray analysis to study global gene expression.
  • Quantitative real-time reverse-transcription polymerase chain reaction (qPCR) to validate mRNA changes.

Main Results:

  • Identified significant messenger RNA (mRNA) changes at 12 and 18-20 generations.
  • Observed shifts towards aerobic metabolism, decreased ribosome gene expression, and partial environmental stress response.
  • Noted pseudostationary phase, downregulated methylation metabolism, increased nucleotide excision repair mRNA, and upregulated protein phosphatase I (Glc7) regulatory subunits.

Conclusions:

  • Yeast aging involves significant, reproducible gene expression changes.
  • These changes reflect metabolic shifts, stress responses, and DNA repair mechanisms.
  • Findings support the role of protein phosphorylation in yeast aging and its parallels with aging in higher eukaryotes.