Laboratory of Molecular Radiology, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Department of Dermatology, Graduate School of Medicine, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Sci Rep. 2019 Nov 5;9(1):16010. doi: 10.1038/s41598-019-52435-8.
Serine-threonine kinase 38 (STK38) is a member of the protein kinase A (PKA)/PKG/PKC-family implicated in the regulation of cell division and morphogenesis. However, the molecular mechanisms underlying STK38 stability remain largely unknown. Here, we show that treatment of cells with either heat or the calcium ionophore A23187 induced STK38 degradation. The calpain inhibitor calpeptin suppressed hyperthermia-induced degradation or the appearance of A23187-induced cleaved form of STK38. An in vitro cleavage assay was then used to demonstrate that calpain I directly cleaves STK38 at the proximal N-terminal region. Deletion of the N-terminal region of STK38 increased its stability against hyperthermia. We further demonstrated that the MAPKK kinase (MAP3K) MEKK2 prevented both heat- and calpain-induced cleavage of STK38. MEKK2 knockdown enhanced hyperthermia-induced degradation of STK38. We performed an in vitro MEKK2 assay and identified the key regulatory site in STK38 phosphorylated by MEKK2. Experiments with a phosphorylation-defective mutant demonstrated that phosphorylation of Ser 91 is important for STK38 stability, as the enzyme is susceptible to degradation by the calpain pathway unless this residue is phosphorylated. In summary, we demonstrated that STK38 is a calpain substrate and revealed a novel role of MEKK2 in the process of STK38 degradation by calpain.
丝氨酸/苏氨酸激酶 38(STK38)是蛋白激酶 A(PKA)/PKG/PKC 家族的成员,参与细胞分裂和形态发生的调节。然而,STK38 稳定性的分子机制在很大程度上仍然未知。在这里,我们表明,用热或钙离子载体 A23187 处理细胞会诱导 STK38 降解。钙蛋白酶抑制剂 calpeptin 抑制热诱导的降解或 A23187 诱导的 STK38 裂解形式的出现。然后进行体外切割试验,证明钙蛋白酶 I 直接在近端 N 端区域切割 STK38。STK38 的 N 端区域缺失增加了其对热的稳定性。我们进一步证明,MAPKK 激酶(MAP3K)MEKK2 可防止 STK38 被热和钙蛋白酶诱导的切割。MEKK2 的敲低增强了热诱导的 STK38 降解。我们进行了体外 MEKK2 测定,并鉴定了 MEKK2 磷酸化的 STK38 的关键调节位点。用磷酸化缺陷突变体进行的实验表明,Ser 91 的磷酸化对 STK38 的稳定性很重要,因为除非该残基被磷酸化,否则该酶易受钙蛋白酶途径的降解。总之,我们证明 STK38 是钙蛋白酶的底物,并揭示了 MEKK2 在钙蛋白酶介导的 STK38 降解过程中的新作用。