Saito Makoto, Iestamantavicius Vytautas, Hess Daniel, Matthias Patrick
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Faculty of Sciences, University of Basel, Basel, Switzerland.
Methods Mol Biol. 2021;2209:217-234. doi: 10.1007/978-1-0716-0935-4_14.
Stress granules are dynamic structures that assemble in response to various forms of stress, such as heat shock or oxidative stress, among others. We had previously shown that the lysine deacetylase HDAC6 is required for the formation of stress granules, but the substrate important for this function was not known. We recently found that the RNA helicase DDX3X is a novel HDAC6 substrate, which is critical for the formation of stress granules. Through a series of detailed experiments, we showed that, upon stress, DDX3X becomes acetylated in an intrinsically disordered region; this alters its propensity to undergo phase separation and inhibits growth of the stress granules. HDAC6, by deacetylating DDX3X, allows maturation of the stress granules. This work identified acetylation of an RNA helicase as a critical regulator of the stress response. Here, we present methods to analyze the acetylation of DDX3X; these methods can be easily adapted to study the acetylation of other helicases, or other proteins.
应激颗粒是一种动态结构,可在诸如热休克或氧化应激等各种应激形式下组装形成。我们之前已经表明,赖氨酸脱乙酰酶HDAC6是应激颗粒形成所必需的,但对于该功能重要的底物尚不清楚。我们最近发现,RNA解旋酶DDX3X是一种新型的HDAC6底物,它对应激颗粒的形成至关重要。通过一系列详细实验,我们表明,在应激时,DDX3X在一个内在无序区域发生乙酰化;这改变了其发生相分离的倾向,并抑制应激颗粒的生长。HDAC6通过使DDX3X去乙酰化,使应激颗粒成熟。这项工作确定了RNA解旋酶的乙酰化是应激反应的关键调节因子。在这里,我们介绍分析DDX3X乙酰化的方法;这些方法可以很容易地适用于研究其他解旋酶或其他蛋白质的乙酰化。