{"title":"Oligomerization-Mediated Phase-Separation in the Nucleoid-Associated Sensory Protein H-NS is Controlled by Ambient Cues","authors":"Bincy Lukose, Saloni Goyal, Athi N Naganathan","doi":"10.1101/2024.08.10.607472","DOIUrl":null,"url":null,"abstract":"H-NS, a nucleoid-associated protein (NAP) from enterobacteria, regulates gene expression by dynamically transducing environmental cues to conformational assembly and DNA binding. In this work, we show that H-NS from Escherichia coli, which can assemble into octameric and tetrameric oligomerization states, forms spontaneous micron-sized liquid-like condensates with DNA at sub-physiological concentrations in vitro. The heterotypic condensates are metastable at 298 K, partially solubilizing with time, while still retaining their liquid-like properties. The condensates display UCST-like phase behavior solubilizing at higher temperatures, but with a large decrease in droplet-assembly propensities at 310 K and also at higher ionic strength. Condensate formation can be tuned in a cyclic manner between 298 and 310 K with the extent of reversibility determined by the incubation time, highlighting strong hysteresis. An engineered phospho-mimetic variant (Y61E) of H-NS, which is dimeric and only weakly binds DNA, is unable to form condensates. The Y61E mutant solubilizes pre-formed H-NS condensates with DNA in a few minutes with nearly an order of magnitude speed-up in droplet dissolution at 310 K relative to 298 K, demonstrating rapid molecular transport between dilute and condensed phases. Our results establish that the oligomerization of H-NS is intrinsically tied not only to DNA binding but also its phase-separation tendencies, while showcasing the regulatable and programmable nature of heterotypic condensates formed by an archetypal NAP via multiple cues and their lifetimes.","PeriodicalId":501048,"journal":{"name":"bioRxiv - Biophysics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Biophysics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.10.607472","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
H-NS, a nucleoid-associated protein (NAP) from enterobacteria, regulates gene expression by dynamically transducing environmental cues to conformational assembly and DNA binding. In this work, we show that H-NS from Escherichia coli, which can assemble into octameric and tetrameric oligomerization states, forms spontaneous micron-sized liquid-like condensates with DNA at sub-physiological concentrations in vitro. The heterotypic condensates are metastable at 298 K, partially solubilizing with time, while still retaining their liquid-like properties. The condensates display UCST-like phase behavior solubilizing at higher temperatures, but with a large decrease in droplet-assembly propensities at 310 K and also at higher ionic strength. Condensate formation can be tuned in a cyclic manner between 298 and 310 K with the extent of reversibility determined by the incubation time, highlighting strong hysteresis. An engineered phospho-mimetic variant (Y61E) of H-NS, which is dimeric and only weakly binds DNA, is unable to form condensates. The Y61E mutant solubilizes pre-formed H-NS condensates with DNA in a few minutes with nearly an order of magnitude speed-up in droplet dissolution at 310 K relative to 298 K, demonstrating rapid molecular transport between dilute and condensed phases. Our results establish that the oligomerization of H-NS is intrinsically tied not only to DNA binding but also its phase-separation tendencies, while showcasing the regulatable and programmable nature of heterotypic condensates formed by an archetypal NAP via multiple cues and their lifetimes.
H-NS是一种来自肠杆菌的核团相关蛋白(NAP),它通过动态地将环境线索传递给构象组装和DNA结合来调节基因表达。在这项研究中,我们发现大肠杆菌的 H-NS 可以组装成八聚体和四聚体的寡聚状态,在体外亚生理浓度下与 DNA 自发形成微米大小的液态凝集物。这种异型凝聚物在 298 K 时是稳定的,随着时间的推移会部分溶解,但仍保持其液态特性。冷凝物显示出类似 UCST 的相行为,在较高温度下会发生溶解,但在 310 K 和较高离子强度下,液滴组装的倾向性会大幅下降。凝结物的形成可在 298 至 310 K 之间以循环方式进行调整,其可逆性程度由培养时间决定,突出显示了很强的滞后性。H-NS的一个工程磷酸化模拟变体(Y61E)是二聚体,只能与DNA微弱结合,无法形成凝结物。Y61E 突变体能在几分钟内溶解与 DNA 预先形成的 H-NS 凝聚物,在 310 K 温度下,液滴溶解速度比 298 K 温度下加快了近一个数量级,这表明稀释相和凝聚相之间的分子运输非常迅速。我们的研究结果证明,H-NS 的寡聚化不仅与 DNA 结合有内在联系,而且还与其相分离倾向有关,同时还展示了由典型 NAP 通过多种线索及其生命周期形成的异型凝聚物的可调节性和可编程性。