Mutagenesis screen uncovers lifespan extension through integrated stress response inhibition without reduced mRNA translation

Maxime J. Derisbourg, Laura E. Wester, Ruth Baddi and Martin S. Denzel ()
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Maxime J. Derisbourg: Max Planck Institute for Biology of Ageing
Laura E. Wester: Max Planck Institute for Biology of Ageing
Ruth Baddi: Max Planck Institute for Biology of Ageing
Martin S. Denzel: Max Planck Institute for Biology of Ageing

Nature Communications, 2021, vol. 12, issue 1, 1-14

Abstract: Abstract Protein homeostasis is modulated by stress response pathways and its deficiency is a hallmark of aging. The integrated stress response (ISR) is a conserved stress-signaling pathway that tunes mRNA translation via phosphorylation of the translation initiation factor eIF2. ISR activation and translation initiation are finely balanced by eIF2 kinases and by the eIF2 guanine nucleotide exchange factor eIF2B. However, the role of the ISR during aging remains poorly understood. Using a genomic mutagenesis screen for longevity in Caenorhabditis elegans, we define a role of eIF2 modulation in aging. By inhibiting the ISR, dominant mutations in eIF2B enhance protein homeostasis and increase lifespan. Consistently, full ISR inhibition using phosphorylation-defective eIF2α or pharmacological ISR inhibition prolong lifespan. Lifespan extension through impeding the ISR occurs without a reduction in overall protein synthesis. Instead, we observe changes in the translational efficiency of a subset of mRNAs, of which the putative kinase kin-35 is required for lifespan extension. Evidently, lifespan is limited by the ISR and its inhibition may provide an intervention in aging.

Date: 2021
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DOI: 10.1038/s41467-021-21743-x

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