Abstract:[Background] Autophagy plays a pivotal role in regulating the cell lifespan and aging. Our previous study showed that deletion of the autophagy-related gene ATG8 significantly decreased the replicative lifespan of yeast cells, while the specific mechanism remains to be explored. [Objective] To study the effect and potential mechanism of ATG8 in regulating the cellular lifespan of Saccharomyces cerevisiae. [Methods] The yeast strain overexpressing ATG8 (ATG8 OE) was constructed by homologous recombination. The chronological lifespans (CLS) of ATG8-deleted (atg8Δ) and ATG8 OE strains were measured. The proliferative rates of yeast cells were analyzed by a Bioscreen C MB instrument based on growth curves. The production of reactive oxygen species (ROS) was measured by flow cytometry. The expression levels of oxidative stress-related genes were determined by quantitative RT-PCR (RT-qPCR). The activity of the key apoptotic enzyme, Caspase-3, was measured by the colorimetric method. [Results] The deletion of ATG8 shortened the chronological lifespan and weakened the proliferation of yeast cells. Meanwhile, it increased the production of intracellular ROS, down-regulated the expression levels of oxidative stress-related genes, and enhanced the activity of caspase-3. The overexpression of ATG8 decreased the production of intracellular ROS and up-regulated the expression levels of oxidative stress-related genes in yeast cells. The ATG8 OE strain showed no significant change in the chronological lifespan, proliferation, or caspase-3 activity. [Conclusion] The autophagy-related gene ATG8 plays a role in regulating the chronological lifespan and oxidative stress response of yeast cells.