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Related Concept Videos

Multi-species Conserved Sequences02:51

Multi-species Conserved Sequences

Next-generation sequencing technologies have created large genomic databases of a variety of animals and plants. Ever since the human genome project was completed, scientists studied the genome of primates, mammals, and other phylogenetically distant living beings. Such large-scaleĀ  studies have provided new insights into the evolutionary relationship between organisms.
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Evolutionary Relationships through Genome Comparisons

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Next-Generation Sequencing Methods
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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

Longevity genomics across species.

Matt Kaeberlein1

  • 1Department of Pathology, University of Washington, Seattle, WA 98195, USA.

Current Genomics
|July 29, 2008
PubMed
Summary
This summary is machine-generated.

Genome-wide studies identified over 100 longevity genes in yeast and worms, revealing conserved aging pathways. Future research aims to link these findings to human aging and develop therapies for age-related diseases.

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Last Updated: Jul 3, 2026

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High-Throughput Behavioral Aging and Lifespan Assays Using the Lifespan Machine

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Area of Science:

  • Genetics and Molecular Biology
  • Aging Research
  • Comparative Genomics

Background:

  • Genome-wide studies in model organisms like yeast (Saccharomyces cerevisiae) and worms (Caenorhabditis elegans) have identified numerous genes influencing lifespan.
  • These studies have begun to elucidate conserved pathways connecting nutrient availability and growth signals to the aging process.

Purpose of the Study:

  • To summarize findings from unbiased genome-wide studies on longevity in S. cerevisiae and C. elegans.
  • To highlight the identification of genes and pathways involved in aging.
  • To discuss the implications for understanding conserved aging mechanisms and future therapeutic development for human age-associated diseases.

Main Methods:

  • Unbiased genome-wide screening approaches in S. cerevisiae and C. elegans.
  • Comparative analysis of identified longevity genes across species.
  • Investigation of conserved pathways linking nutrient/growth factor signaling to lifespan.

Main Results:

  • Identification of over one hundred genes that determine lifespan in one or both model organisms.
  • Uncovering of key conserved pathways that link nutrient and growth factor cues to longevity.
  • Establishment of quantitative measures for assessing the evolutionary conservation of aging.

Conclusions:

  • Longevity genes and pathways are significantly conserved between yeast and worms.
  • A substantial genetic basis for aging has been uncovered in these model systems.
  • A critical future challenge is to translate these findings to human aging and develop targeted therapies for age-related diseases.