Guo Bin, Huang Xinxin, Zhang Peipei, Qi Linxiang, Liang Qianqian, Zhang Xuebo, Huang Jie, Fang Bin, Hou Wenru, Han Jinghua, Zhang Hong
College of Life Sciences China Agricultural University, Beijing, China State Key Laboratory of Biomacromolecules, Institute of Biophysics Chinese Academy of Sciences, Beijing, China National Institute of Biological Sciences, Beijing, China.
National Institute of Biological Sciences, Beijing, China.
EMBO Rep. 2014 Jun;15(6):705-13. doi: 10.1002/embr.201338310. Epub 2014 Apr 24.
The mechanisms that coordinate the regulation of autophagy with developmental signaling during multicellular organism development remain largely unknown. Here, we show that impaired function of ribosomal protein RPL-43 causes an accumulation of SQST-1 aggregates in the larval intestine, which are removed upon autophagy induction. Using this model to screen for autophagy regulators, we identify 139 genes that promote autophagy activity upon inactivation. Various signaling pathways, including Sma/Mab TGF-β signaling, lin-35/Rb signaling, the XBP-1-mediated ER stress response, and the ATFS-1-mediated mitochondrial stress response, regulate the expression of autophagy genes independently of the TFEB homolog HLH-30. Our study thus provides a framework for understanding the role of signaling pathways in regulating autophagy under physiological conditions.
在多细胞生物体发育过程中,协调自噬调节与发育信号传导的机制在很大程度上仍然未知。在此,我们表明核糖体蛋白RPL-43的功能受损会导致幼虫肠道中SQST-1聚集体的积累,自噬诱导后这些聚集体会被清除。利用该模型筛选自噬调节因子,我们鉴定出139个基因,这些基因失活后会促进自噬活性。包括Sma/Mab TGF-β信号传导、lin-35/Rb信号传导、XBP-1介导的内质网应激反应和ATFS-1介导的线粒体应激反应在内的各种信号通路,独立于TFEB同源物HLH-30调节自噬基因的表达。因此,我们的研究为理解信号通路在生理条件下调节自噬中的作用提供了一个框架。