Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima 739-8521, Japan.
Department of Life Sciences, Faculty of Agriculture, Kagawa University, Kagawa 761-0795, Japan.
Arch Biochem Biophys. 2018 Feb 15;640:83-92. doi: 10.1016/j.abb.2018.01.001. Epub 2018 Jan 6.
Intracellular signal transduction is built on the basis of the subtle balance between phosphorylation and dephosphorylation. Ca/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F/POPX2) and CaMKP-N (PPM1E/POPX1) are Ser/Thr phosphatases that belong to the PPM (protein phosphatase, Mg/Mn-dependent) family. The former was discovered in rat brain as a novel protein phosphatase regulating Ca/calmodulin-dependent protein kinases (CaMKs), whereas the latter was first identified in human cDNA databases using the rat CaMKP sequence. Subsequent studies have revealed that they are involved in various cellular functions through regulation of not only CaMKs but also other protein kinases such as AMP-activated protein kinase. Furthermore, accumulating evidence shows possible involvement of CaMKP and CaMKP-N in the pathogenesis of various diseases including cancer. Therefore, the biochemistry of CaMKP and CaMKP-N largely contributes to molecular medicine targeting these phosphatases. In this review, we summarized recent progress in the enzymology and biology of CaMKP and CaMKP-N. We also focused on etiology studies in which CaMKP and CaMKP-N are involved. Based on the emerging evidence, future perspectives of studies on these phosphatases and related issues to be elucidated are discussed.
细胞内信号转导是建立在磷酸化和去磷酸化之间微妙平衡的基础上的。钙/钙调蛋白依赖性蛋白激酶磷酸酶 (CaMKP/PPM1F/POPX2) 和 CaMKP-N (PPM1E/POPX1) 是丝氨酸/苏氨酸磷酸酶,属于 PPM(蛋白磷酸酶,Mg/Mn 依赖性)家族。前者作为一种新的调节钙/钙调蛋白依赖性蛋白激酶 (CaMKs) 的蛋白磷酸酶在大鼠脑中被发现,而后者最初是使用大鼠 CaMKP 序列在人类 cDNA 数据库中鉴定的。随后的研究表明,它们通过调节不仅 CaMKs 而且其他蛋白激酶(如 AMP 激活的蛋白激酶),参与各种细胞功能。此外,越来越多的证据表明 CaMKP 和 CaMKP-N 可能参与包括癌症在内的各种疾病的发病机制。因此,CaMKP 和 CaMKP-N 的生物化学在针对这些磷酸酶的分子医学中起着重要作用。在这篇综述中,我们总结了 CaMKP 和 CaMKP-N 的酶学和生物学的最新进展。我们还重点介绍了涉及 CaMKP 和 CaMKP-N 的病因学研究。基于新出现的证据,讨论了对这些磷酸酶及其相关问题的未来研究展望。