Gene-diet interactions and aging in C. elegans
Open accessAbstract
Diet is the most variable aspect of life history, as most individuals have a large diversity of food choices, varying in the type and amount that they ingest. In the short-term, diet can affect metabolism and energy levels. However, in the long run, the net deficiency or excess of calories from diet can influence the progression and severity of age-related diseases. An old and yet still debated question is: how do specific dietary choices impact health- and lifespan? It is clear that genetics can play a critical role - perhaps just as important as diet choices. For example, poor diet in combination with genetic susceptibility can lead to metabolic disorders, such as obesity and type 2 diabetes. Recent work in Caenorhabditis elegans has identified the existence of diet-gene pairs, where the consequence of mutating a specific gene is only realized on specific diets. Many core metabolic pathways are conserved from worm to human. Although only a handful of these diet-gene pairs has been characterized, there are potentially hundreds, if not thousands, of such interactions, which may explain the variability in the rates of aging in humans and the incidence and severity of age-related diseases.
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Differences in experimental approaches and the techniques used to measure metabolic flexibility may influence outcomes.
“Differences in experimental approaches and the techniques used to measure metabolic flexibility may influence outcomes (305).”
From Metabolic Flexibility as an Adaptation to Energy Resources and Requirements in Health and Disease (2018) · cites this paper as [305]
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References 143 · Cited by 38
Research works printed but not linked: 1
- Hansen M New genes tied to endocrine, metabolic, and dietary regulation of lifespan from a Caenorhabditis elegans genomic RNAi screen PLoS Genet 2005b 1 1 e17 PMC1183531 16103914
- Authors
- Yen, C. A., & Curran, S. P.
- Affiliations
- University of Southern California (US)
- Corresponding author
- Curran, Sean P.
- ORCID
- Curran, Sean P.
- Venue
- Experimental Gerontology
- Publisher
- Elsevier BV
- Published
- 2016-12
- Volume
- 86
- Pages
- 106-112
- ISSN
- 0531-5565 (ISSN-L)
- PMC
- PMC5001925
- OpenAlex
- W2277288473
- Cited by
- 38
- References
- 143
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 7 · 2020: 5 · 2019: 3 · 2018: 2 · 2017: 2 · 2015: 1
- FWCI
- 1.26
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Experimental Gerontology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (R00AG032308)
- National Institute of General Medical Sciences (R01GM109028)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- gene-diet interaction, aging, Caenorhabditis elegans, lifespan, age-related diseases, food choice, metabolic pathways, obesity, type 2 diabetes, genetic susceptibility
- MeSH terms
- Aging, Animals, Diet, Eating, Forecasting, Genes, Insulin, Signal Transduction, Caenorhabditis elegans, Caloric Restriction
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