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RESEARCH PAPER / 2024-11-23

DEAD-box RNA helicase DDX-23 mediates dietary restriction induced health span in Caenorhabditis elegans.

Yi Xiao, Hongjiao Zhang, Xiaocong Li, Chao Han, Fang Liu

Guizhou Provincial College-Based Key Lab for Tumor Prevention and Treatment With Distinctive Medicines, Zunyi Medical University, Zunyi Guizhou, 563000, China. [email protected]. · pubmed

Abstract

Dietary restriction (DR) extends lifespan in diverse species, from yeast to mammals. However, its underlying mechanisms are not well understood. In this study, through using the tractable model Caenorhabditis elegans, we show a role for the DEAD-box RNA helicase, DDX-23 (homologous to mammal DDX23) as a regulator of healthspan in response to dietary restriction. Meanwhile, DDX-23 is also required for heat and oxidative stress response in C. elegans. Intriguingly, DDX-23 functions in the germline during adult to regulate dietary restriction-induced longevity. We then find that PHA-4/FOXA acts downstream of DDX-23 to mediate the transcriptional response of SOD-related genes and consequently the lifespan of the animals. Furthermore, we find that the DEAD-box RNA helicase, DDX-23 negatively regulates the healthy lifespan extension by up-regulating the expression of miR-231, and resulting in suppressing the activation of FOXO transcription factor DAF-16. Our work shows a newly discovered for DEAD-box RNA helicase DDX-23 in the regulation of dietary restriction-mediated longevity in C. elegans and reveals the downstream transcriptional regulation mechanisms.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper investigates the role of DDX-23 in mediating healthspan in response to dietary restriction in C. elegans, which is directly related to mechanisms of aging and longevity. While the findings contribute to understanding the molecular pathways involved in dietary restriction and longevity, the study appears to provide solid but incremental advances rather than groundbreaking insights. The focus on a specific RNA helicase and its downstream effects is valuable, but the overall impact on the broader field of longevity research seems limited.

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