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Cited by 178

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Longevity genes in the nematode Caenorhabditis elegans also mediate increased resistance to stress and prevent disease

Johnson, T. E., Henderson, S., Murakami, S., de Castro, E., de Castro, S. H., Cypser, J., Rikke, B., Tedesco, P., Link, C.·2002·Journal of Inherited Metabolic Disease

Abstract

More than 40 single‐gene mutants in Caenorhabditis elegans have been demonstrated to lead to increased lifespan (a rigorous, operational test for being a gerontogene) of 20% or more; these are referred to collectively as ‘Age’ mutants. Age mutants must change key functions that are rate‐limiting determinants of longevity; moreover, important genes can be identified independently of prior hypotheses as to actual mode of gene action in extending longevity and/or ‘slowing’ of ageing. These Age mutants define as many as nine (possibly) distinct pathways and/or modes of action, as defined by primary phenotype. Each of three well‐studied mutants (age‐1, clk‐1, and spe‐26) alters age‐specific mortality rates in a fashion unique to itself. In age‐1 mutants, the decreases in mortality rates are quite dramatic, with an almost tenfold drop in mortality throughout most of life. All Age mutants (so far without exception) increase the ability of the worm to respond to several (but not all) stresses, including heat, UV, and reactive oxidants. We have used directed strategies as well as random mutagenesis to identify novel genes that increase the worm's ability to resist stress. Two genes (daf‐16 and old‐1) are epistatic to the long‐life phenotype of most mutants and also yield over‐expression strains that are stress‐resistant and long‐lived. We have also used a variety of approaches to determine what transcriptional alterations are associated with increased longevity (and with ageing itself), including whole‐genome expression studies using microarrays and GFP reporter constructs. We suggest that the role of the Age genes in both longevity and stress resistance indicates that a major evolutionary determinant of longevity is the ability to respond to stress. In mammals, both dietary restriction and hormesis are phenomena in which the endogenous level of resistance to stress has been upregulated; both of these interventions extend longevity, suggesting possible evolutionary conservation.

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Metadata

Authors
Johnson, T. E., Henderson, S., Murakami, S., de Castro, E., de Castro, S. H., Cypser, J., Rikke, B., Tedesco, P., & Link, C.
Venue
Journal of Inherited Metabolic Disease
Publisher
Wiley
Published
2002-05
Volume
25
Issue
3
Pages
197-206
ISSN
  • 0141-8955 (ISSN-L)
  • 1573-2665
OpenAlex
W60943716
Cited by
178
References
2
FWCI
2.80
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Longevity genes in the nematode Caenorhabditis elegans also mediate increased resistance to stress and prevent disease. https://app.cochat.ai/papers/10.1023/a:1015677828407
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Johnson, T. E., Henderson, S., Murakami, S., de Castro, E., de Castro, S. H., Cypser, J., Rikke, B., Tedesco, P., & Link, C. (2002). Longevity genes in the nematode Caenorhabditis elegans also mediate increased resistance to stress and prevent disease. Journal of Inherited Metabolic Disease. https://doi.org/10.1023/a%3A1015677828407

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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