A coherent FOXO3-SNAI2 feed-forward loop in autophagy.

Proc Natl Acad Sci U S A

Institute of Intervention Vessel, Shanghai 10th People's Hospital, Shanghai Key Laboratory of Signaling and Diseases Research, School of Life Science and Technology, Tongji University, 200092 Shanghai, China.

Published: March 2022

SignificanceUnderstanding autophagy regulation is instrumental in developing therapeutic interventions for autophagy-associated disease. Here, we identified SNAI2 as a regulator of autophagy from a genome-wide screen in HeLa cells. Upon energy stress, SNAI2 is transcriptionally activated by FOXO3 and interacts with FOXO3 to form a feed-forward regulatory loop to reinforce the expression of autophagy genes. Of note, SNAI2-increased FOXO3-DNA binding abrogates CRM1-dependent FOXO3 nuclear export, illuminating a pivotal role of DNA in the nuclear retention of nucleocytoplasmic shuttling proteins. Moreover, a dFoxO-Snail feed-forward loop regulates both autophagy and cell size in , suggesting this evolutionarily conserved regulatory loop is engaged in more physiological activities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931368PMC
http://dx.doi.org/10.1073/pnas.2118285119DOI Listing

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