Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Institute of Biochemistry and Molecular Biology, College of Life Sciences, National Yang-Ming University, Taipei, Taiwan.
EMBO Rep. 2020 Jul 3;21(7):e48324. doi: 10.15252/embr.201948324. Epub 2020 Jun 2.
Nuclear accessibility of transcription factors controls gene expression, co-regulated by Ran-dependent nuclear localization and a competitive regulatory network. Here, we reveal that nuclear import factor-facilitated transcriptional repression attenuates ribosome biogenesis under chronic salt stress. Kap114p, one of the karyopherin-βs (Kap-βs) that mediates nuclear import of yeast TATA-binding protein (yTBP), exhibits a yTBP-binding affinity four orders of magnitude greater than its counterparts and suppresses binding of yTBP with DNA. Our crystal structure of Kap114p reveals an extensively negatively charged concave surface, accounting for high-affinity basic-protein binding. KAP114 knockout in yeast leads to a high-salt growth defect, with transcriptomic analyses revealing that Kap114p modulates expression of genes associated with ribosomal biogenesis by suppressing yTBP binding to target promoters, a trans-repression mechanism we attribute to reduced nuclear Ran levels under salinity stress. Our findings reveal that Ran integrates the nuclear transport pathway and transcription regulatory network, allowing yeast to respond to environmental stresses.
转录因子的核可及性控制基因表达,受 Ran 依赖性核定位和竞争性调控网络共同调节。在这里,我们揭示了核输入因子促进的转录抑制在慢性盐胁迫下减弱核糖体生物发生。Kap114p 是介导酵母 TATA 结合蛋白(yTBP)核输入的核孔蛋白-β(Kap-β)之一,与其他 Kap-β 相比,它表现出四数量级更高的 yTBP 结合亲和力,并抑制 yTBP 与 DNA 的结合。我们的 Kap114p 晶体结构揭示了一个广泛的带负电荷的凹面,解释了其与碱性蛋白的高亲和力结合。酵母中的 KAP114 敲除导致耐盐生长缺陷,转录组分析显示 Kap114p 通过抑制 yTBP 与靶启动子的结合来调节与核糖体生物发生相关的基因表达,这是一种反式抑制机制,我们归因于盐胁迫下核内 Ran 水平降低。我们的研究结果表明,Ran 整合了核转运途径和转录调控网络,使酵母能够对环境压力做出反应。