A large-scale analysis of autophagy-related gene expression identifies new regulators of autophagy

被引:61
|
作者
Bernard, Amelie
Jin, Meiyan
Xu, Ziheng
Klionsky, Daniel J. [1 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
关键词
autophagy; gene expression; stress; transcription factor; yeast; TRANSCRIPTION FACTOR; INDUCTION; YEAST; VACUOLE; PROTEIN;
D O I
10.1080/15548627.2015.1099796
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is a pathway mediating vacuolar degradation and recycling of proteins and organelles, which plays crucial roles in cellular physiology. To ensure its proper cytoprotective function, the induction and amplitude of autophagy are tightly regulated, and defects in its regulation are associated with various diseases. Transcriptional control of autophagy is a critical aspect of autophagy regulation, which remains largely unexplored. In particular, very few transcription factors involved in the activation or repression of autophagy-related gene expression have been characterized. To identify such regulators, we analyzed the expression of representative ATG genes in a large collection of DNA-binding mutant deletion strains in growing conditions as well as after nitrogen or glucose starvation. This analysis identified several proteins involved in the transcriptional control of ATG genes. Further analyses showed a correlation between variations in expression and autophagy magnitude, thus identifying new positive and negative regulators of the autophagy pathway. By providing a detailed analysis of the regulatory network of the ATG genes our study paves the way for future research on autophagy regulation and signaling.
引用
收藏
页码:2114 / 2122
页数:9
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