Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Department of Biology, Stanford University, Stanford, CA 94305, USA.
Cell. 2020 Mar 5;180(5):928-940.e14. doi: 10.1016/j.cell.2020.02.014. Epub 2020 Feb 27.
Covalent modifications to histones are essential for development, establishing distinct and functional chromatin domains from a common genetic sequence. Whereas repressed chromatin is robustly inherited, no mechanism that facilitates inheritance of an activated domain has been described. Here, we report that the Set3C histone deacetylase scaffold Snt1 can act as a prion that drives the emergence and transgenerational inheritance of an activated chromatin state. This prion, which we term [ESI] for expressed sub-telomeric information, is triggered by transient Snt1 phosphorylation upon cell cycle arrest. Once engaged, the prion reshapes the activity of Snt1 and the Set3C complex, recruiting RNA pol II and interfering with Rap1 binding to activate genes in otherwise repressed sub-telomeric domains. This transcriptional state confers broad resistance to environmental stress, including antifungal drugs. Altogether, our results establish a robust means by which a prion can facilitate inheritance of an activated chromatin state to provide adaptive benefit.
组蛋白的共价修饰对于发育至关重要,它将共同的遗传序列转化为具有独特功能的染色质结构域。虽然抑制性染色质能够稳定遗传,但目前尚未发现促进激活结构域遗传的机制。在这里,我们报告说组蛋白去乙酰化酶支架 Snt1 的 Set3C 可以作为一种朊病毒,驱动激活染色质状态的出现和跨代遗传。我们将这种朊病毒命名为表达端粒下信息的 [ESI],它是由细胞周期停滞时 Snt1 的短暂磷酸化触发的。一旦被触发,朊病毒就会重塑 Snt1 和 Set3C 复合物的活性,招募 RNA pol II 并干扰 Rap1 结合,从而激活原本受抑制的端粒下结构域中的基因。这种转录状态赋予了广泛的抗环境压力的能力,包括抗真菌药物。总之,我们的研究结果为朊病毒促进激活染色质状态的遗传提供了一种稳健的方法,从而带来适应性优势。