State Key Laboratory of Biomembrane and Membrane Biotechnology, Tsinghua University-Peking University Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, Beijing, China.
Autophagy. 2012 Oct;8(10):1529-30. doi: 10.4161/auto.21156. Epub 2012 Jun 26.
Mounting evidence suggests that acetylation plays an important role in various biological processes including transcriptional regulation, DNA damage repair, cell cycle progression, aging, and glycolysis. It is increasingly recognized that acetylation also regulates autophagy; for example, increasing the cellular acetylation level by treating cells with histone deacetylase (HDAC) inhibitors such as TSA can promote autophagy, and knockdown of the histone acetyltransferase KAT2B/p300 induces autophagy in nutrient-rich conditions. Our goal is to dissect the molecular mechanisms underlying the seemingly complicated role of acetylation in autophagy. We used Saccharomyces cerevisiae as a model organism because it can be genetically manipulated in a relatively easy and reliable way, allowing us to test the function of acetylases, deacetylases and acetylation sites on autophagy regulation in a "clean" system.
越来越多的证据表明,乙酰化在包括转录调控、DNA 损伤修复、细胞周期进程、衰老和糖酵解在内的各种生物过程中发挥着重要作用。人们越来越认识到,乙酰化也调节自噬;例如,通过用组蛋白去乙酰化酶 (HDAC) 抑制剂如 TSA 处理细胞来增加细胞内乙酰化水平可以促进自噬,并且在营养丰富的条件下敲低组蛋白乙酰转移酶 KAT2B/p300 可诱导自噬。我们的目标是剖析乙酰化在自噬中看似复杂的作用的分子机制。我们使用酿酒酵母作为模式生物,因为它可以通过相对简单可靠的方式进行遗传操作,使我们能够在“清洁”系统中测试乙酰转移酶、去乙酰化酶和自噬调节中的乙酰化位点的功能。