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SKN-1 Is a Negative Regulator of DAF-16 and Somatic Stress Resistance in Caenorhabditis elegans

Jianhui Deng, Yuxi Dai, Haiqing Tang, Shanshan Pang

G3 Genes Genomes Genetics · 2020 · ▲ 49 citations

Abstract

ortholog of mammalian Nrf protein, is a well-known longevity factor, and its activation is observed in several long-lived models. SKN-1 also plays essential roles in xenobiotic and oxidative stress responses. Here, we report deleterious functions of SKN-1 in somatic stress resistance that may impair lifespan. Constitutive SKN-1 activation impairs animal resistance to several stresses, including heat, ER stress and mitochondrial stress, which result from the suppression of DAF-16, another master regulator of longevity. SKN-1 activation abrogates DAF-16 nuclear import and downregulates DAF-16 target genes under stress conditions, while SKN-1 inhibition promotes the expression of DAF-16 targets, even in long-lived mutants. Further, SKN-1 activation induces the expression of vitellogenin proteins, which are required for SKN-1-mediated suppression of DAF-16 and stress resistance. Together, these findings identify detrimental roles for SKN-1 activation in animal health, and more importantly, inspire the rethinking of the complex roles for SKN-1 in aging regulation.

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Provenance

Source
OpenAlex
DOI
10.1534/g3.120.401203
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2026-09-02 MST

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APA
Deng, J., Dai, Y., Tang, H., &amp; Pang, S. (2020). SKN-1 Is a Negative Regulator of DAF-16 and Somatic Stress Resistance in Caenorhabditis elegans. <em>G3 Genes Genomes Genetics</em>. https://doi.org/10.1534/g3.120.401203
Vancouver
Deng J, Dai Y, Tang H, Pang S. SKN-1 Is a Negative Regulator of DAF-16 and Somatic Stress Resistance in Caenorhabditis elegans. G3 Genes Genomes Genetics. 2020. doi:10.1534/g3.120.401203.
BibTeX
@article{jianhui2020SKNIsa, title = {SKN-1 Is a Negative Regulator of DAF-16 and Somatic Stress Resistance in Caenorhabditis elegans}, author = {Jianhui Deng and Yuxi Dai and Haiqing Tang and Shanshan Pang}, journal = {G3 Genes Genomes Genetics}, year = {2020}, doi = {10.1534/g3.120.401203}, }

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