自噬
FOXO3公司
细胞生物学
循环(图论)
生物
物理
计算机科学
数学
遗传学
磷酸化
组合数学
细胞凋亡
蛋白激酶B
作者
Xiaowei Guo,Zhuojie Li,Xiaojie Zhu,Meixiao Zhan,Chenxi Wu,Xiang Ding,Kai Peng,Wenzhe Li,Xianjue Ma,Zhongwei Lv,Ligong Lu,Lei Xue
标识
DOI:10.1073/pnas.2118285119
摘要
Significance Understanding 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 Drosophila , suggesting this evolutionarily conserved regulatory loop is engaged in more physiological activities.
科研通智能强力驱动
Strongly Powered by AbleSci AI