Genome-wide RNAi analysis in adult Caenorhabditis elegans unveils genes controlling age-related fat accumulation.
Abstract
Fat accumulation with aging occurs in adults across species, yet its underlying mechanisms remain poorly understood, partly due to limited number of studiesspecifically targeting adulthood. Here, we present the first genome-wide analysis of age-associated fat accumulation during adulthood in Caenorhabditis elegans. Unprecedently, our adult-specific RNAi screen identified a limited subset of genes influencing adult fat dynamics, contrasting with the extensive gene sets uncovered in prior developmental RNAi screens. This disparity suggests a unique genetic architecture governing age-related lipid deposition. Central to this network is the evolutionarily conserved transcription factor DAF-16/FoxO, which progressively accumulates in nuclei during aging. Genetic ablation of daf-16 abolished adult fat accumulation, while its adult-specific knockdown reduced adiposity without compromising healthspan or longevity, highlighting its therapeutic potential. Critically, knockdown of the top hits, pals-17 and rege-1, markedly attenuated the nuclear localization of DAF-16 and failed to reduce the adult fat content daf-16-deficient animals, establishing DAF-16 as their essential effector. Overall, our work uncouples developmental and adult lipid regulatory mechanisms and highlights potential targets for understanding and managing adult-onset obesity.
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Research summary
The paper identifies specific genes that control age-related fat accumulation in adult Caenorhabditis elegans, suggesting potential targets for managing adult-onset obesity. This research is relevant as it explores the genetic mechanisms underlying aging-related processes, contributing to the understanding of age-related metabolic changes.
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