Bernard Amélie, Jin Meiyan, Xu Ziheng, Klionsky Daniel J
a Life Sciences Institute , and the Department of Molecular ; Cellular and Developmental Biology; University of Michigan ; Ann Arbor , MI USA.
Autophagy. 2015 Nov 2;11(11):2114-2122. doi: 10.1080/15548627.2015.1099796.
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.
自噬是一种介导蛋白质和细胞器的液泡降解及循环利用的途径,在细胞生理学中发挥着关键作用。为确保其正常的细胞保护功能,自噬的诱导及强度受到严格调控,其调控缺陷与多种疾病相关。自噬的转录调控是自噬调控的一个关键方面,在很大程度上仍未被探索。特别是,很少有参与自噬相关基因表达激活或抑制的转录因子得到表征。为了鉴定此类调节因子,我们分析了大量DNA结合突变缺失菌株在生长条件下以及氮或葡萄糖饥饿后代表性自噬相关基因(ATG基因)的表达。该分析鉴定出了几种参与ATG基因转录调控的蛋白质。进一步分析表明表达变化与自噬强度之间存在相关性,从而鉴定出自噬途径新的正调控因子和负调控因子。通过对ATG基因调控网络进行详细分析,我们的研究为未来自噬调控和信号传导的研究铺平了道路。