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Endogenous siRNAs promote proteostasis and longevity in germline-less Caenorhabditis elegans

ABSTRACT: How lifespan and the rate of aging are set is a key problem in biology. Small RNAs are conserved molecules that impact diverse biological processes through the control of gene expression. However, in contrast to miRNAs, the role of endo-siRNAs in aging remains unexplored. Here, by combining deep sequencing and genomic and genetic approaches in C.CaenorhabditisC. elegans elegans, we reveal an unprecedented role for endo-siRNA molecules in the maintenance of proteostasis and lifespan extension in germline-less animals. Furthermore, we identify an endo-siRNA-regulated tyrosine phosphatase, which limits the longevity of germline-less animals by restricting the activity of the heat shock transcription factor HSF-1. Altogether, our findings point to endo-siRNAs as a link between germline removal and the HSF-1 proteostasis and longevity-promoting somatic pathway. This establishes a role for endo siRNAs in the aging process and identifies downstream genes and physiological processes that are regulated by the endo siRNAs to affect longevity.

ORGANISM(S): Caenorhabditis elegans

PROVIDER: GSE128935 | GEO | 2020/04/03

REPOSITORIES: GEO

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Endogenous siRNAs Promote Proteostasis and Longevity in Germline-less C. elegans

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Project description:Endogenous siRNAs Promote Proteostasis and Longevity in Germline-less C. elegans

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