Department of Systems Biology, Graduate School of Pharmaceutical Sciences, Kyoto University.
Biol Pharm Bull. 2024;47(3):600-605. doi: 10.1248/bpb.b23-00739.
Temperature-dependent translational control of the core clock gene Per2 plays an important role in establishing entrainment of the circadian clock to physiological body temperature cycles. Previously, we found an involvement of the phosphatidylinositol 3-kinase (PI3K) in causing Per2 protein expression in response to a warm temperature shift (WTS) within a physiological range (from 35 to 38.5 °C). However, signaling pathway mediating the Per2 protein expression in response to WTS is only sparsely understood. Additional factor(s) other than PI3K remains unknown. Here we report the identification of eukaryotic initiation factor 2α (eIF2α) kinases, protein kinase R (PKR) and PKR-like endoplasmic reticulum kinase (PERK), as a novel mediator of WTS-dependent Per2 protein expression. Canonically, eIF2α has been regarded as a major downstream target of PERK and PKR. However, we found that PERK and PKR mediate WTS response of Per2 in a manner not involving eIF2α. We observed that PERK and PKR serve as an upstream regulator of PI3K rather than eIF2α in the context of WTS-dependent Per2 protein expression. There have been studies reporting PI3K activation occurring depending on PERK and PKR, while its physiological contribution has remained elusive. Our finding therefore not only helps to enrich the knowledge of how WTS affects Per2 protein expression but also extends the region of cellular biology involving the PERK/PKR-mediated PI3K activation to include entrainment-mechanism of the circadian clock.
温度依赖的核心时钟基因 Per2 的翻译调控在使生物钟适应生理体温周期方面起着重要作用。先前,我们发现磷脂酰肌醇 3-激酶 (PI3K) 在生理范围内(35 至 38.5°C)的温热温度转换 (WTS) 中引起 Per2 蛋白表达的参与。然而,介导 WTS 下 Per2 蛋白表达的信号通路知之甚少。除了 PI3K 之外,其他额外的因素仍不清楚。在这里,我们报告鉴定出真核起始因子 2α (eIF2α) 激酶、蛋白激酶 R (PKR) 和内质网激酶样 PERK (PERK),作为 WTS 依赖性 Per2 蛋白表达的新介质。通常,eIF2α 被认为是 PERK 和 PKR 的主要下游靶标。然而,我们发现 PERK 和 PKR 以不涉及 eIF2α 的方式介导 WTS 响应的 Per2 蛋白表达。我们观察到 PERK 和 PKR 在 WTS 依赖性 Per2 蛋白表达的情况下作为 PI3K 的上游调节剂,而不是 eIF2α。已经有研究报道 PI3K 的激活取决于 PERK 和 PKR,但它的生理贡献仍然难以捉摸。因此,我们的发现不仅有助于丰富 WTS 如何影响 Per2 蛋白表达的知识,而且还将涉及 PERK/PKR 介导的 PI3K 激活的细胞生物学区域扩展到包括生物钟的驯化机制。