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Measurement of Lifespan in Drosophila melanogaster
Published on: January 7, 2013
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Transposable Element Landscape in Drosophila Populations Selected for Longevity
Daniel K Fabian1,2, Handan Melike Dönertaş1, Matías Fuentealba1,2
1European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, United Kingdom.
Genome Biology and Evolution
|February 17, 2021
Summary
Long-lived flies showed increased transposable element (TE) abundance, contrary to expectations. Reduced TE expression, particularly telomeric TEs, may contribute to longevity, suggesting TEs can be passed on with minimal impact on lifespan.
Area of Science:
- Genetics
- Aging Research
- Genomics
Background:
- Transposable elements (TEs) can negatively impact health and fitness by integrating into the genome.
- TE activity increases with age, contributing to genomic instability and age-related diseases.
- It is hypothesized that long-lived individuals possess enhanced TE silencing mechanisms.
Purpose of the Study:
- To investigate the relationship between TE insertions, expression, and longevity in Drosophila melanogaster.
- To determine if populations selected for longevity exhibit different TE profiles compared to controls.
Main Methods:
- Genome-wide analysis of TE insertions and expression in Drosophila melanogaster populations selected for longevity.
- RNA sequencing (RNA-seq) to quantify TE expression levels.
- Simulations to assess TE abundance under neutrality.
Main Results:
- Long-lived populations showed higher overall TE family abundance than controls, contrary to initial hypotheses.
- A trend towards reduced TE expression was observed in selected populations.
- Telomeric TEs were more abundant both genomically and transcriptionally in long-lived flies.
Conclusions:
- Increased TE abundance in long-lived flies suggests reproduction at old age facilitates TE transmission.
- Reduced TE expression, especially of telomeric TEs, may be a key mechanism for promoting longevity.
- Improved telomere maintenance linked to TEs presents a novel pathway for lifespan extension.
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