Functions and dysfunctions of Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F) and CaMKP-N/PPM1E

被引:16
|
作者
Ishida, Atsuhiko [1 ]
Sueyoshi, Noriyuki [2 ]
Kameshita, Isamu [2 ]
机构
[1] Hiroshima Univ, Grad Sch Integrated Arts & Sci, Lab Mol Brain Sci, Higashihiroshima 7398521, Japan
[2] Kagawa Univ, Fac Agr, Dept Life Sci, Miki, Kagawa 7610795, Japan
关键词
Binding protein; Cell signaling; Disorder; Metastasis; microRNA; Negative regulation; CAMKP-N; POPX2; CANCER; IDENTIFICATION; LOCALIZATION; ACTIVATION; ASSAY; PROTOCADHERIN-GAMMA-C5; PHOSPHORYLATION; EXPRESSION;
D O I
10.1016/j.abb.2018.01.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular signal transduction is built on the basis of the subtle balance between phosphorylation and dephosphorylation. Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F/POPX2) and CaMKP-N (PPM1E/POPX1) are Ser/Thr phosphatases that belong to the PPM (protein phosphatase, Mg2+/Mn2+-dependent) family. The former was discovered in rat brain as a novel protein phosphatase regulating Ca2+/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.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 50 条
  • [1] Phosphorylation and activation of nuclear Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP-N/PPM1E) by Ca2+/calmodulin-dependent protein kinase I (CaMKI)
    Onouchi, Takashi
    Sueyoshi, Noriyuki
    Ishida, Atsuhiko
    Kameshita, Isamu
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2012, 422 (04) : 703 - 709
  • [2] An Active C-Terminally Truncated Form of Ca2+/Calmodulin-Dependent Protein Kinase Phosphatase-N (CaMKP-N/PPM1E)
    Ishida, Atsuhiko
    Tsumura, Kumiko
    Oue, Megu
    Takenaka, Yasuhiro
    Shigeri, Yasushi
    Goshima, Naoki
    Ishihara, Yasuhiro
    Hirano, Tetsuo
    Baba, Hiromi
    Sueyoshi, Noriyuki
    Kameshita, Isamu
    Yamazaki, Takeshi
    BIOMED RESEARCH INTERNATIONAL, 2013, 2013
  • [3] Inhibitors of the Ca2+/calmodulin-dependent protein kinase phosphatase family (CaMKP and CaMKP-N)
    Sueyoshi, Noriyuki
    Takao, Toshihiko
    Nimura, Takaki
    Sugiyama, Yasunorl
    Numano, Takamasa
    Shigeri, Yasushi
    Taniguchi, Takanobu
    Kameshita, Isamu
    Ishida, Atsuhiko
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 363 (03) : 715 - 721
  • [4] Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F) interacts with neurofilament L and inhibits its filament association
    Ozaki, Hana
    Katoh, Tsuyoshi
    Nakagawa, Ryoko
    Ishihara, Yasuhiro
    Sueyoshi, Noriyuki
    Kameshita, Isamu
    Taniguchi, Takanobu
    Hirano, Tetsuo
    Yamazaki, Takeshi
    Ishida, Atsuhiko
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 477 (04) : 820 - 825
  • [5] Regulation of Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP/PPM1F) by protocadherin-γC5 (Pcdh-γC5)
    Onouchi, Takashi
    Kishino-Kaneko, Yoshimi
    Kameshita, Isamu
    Ishida, Atsuhiko
    Sueyoshi, Noriyuki
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2015, 585 : 109 - 120
  • [6] CaM kinase phosphatase (CaMKP/PPM1F/POPX2) is specifically inactivated through gallate-mediated protein carbonylation
    Akizuki, Kazutoshi
    Ishikawa, Shun
    Obatake, Rika
    Ozaki, Hana
    Shimoda, Nao
    Nehira, Tatsuo
    Yamazaki, Takeshi
    Kinumi, Tomoya
    Osawa, Jin
    Sueyoshi, Noriyuki
    Kameshita, Isamu
    Shigeri, Yasushi
    Ishida, Atsuhiko
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2022, 720
  • [7] Regulation of Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP) by oxidation/reduction at Cys-359
    Baba, Hiromi
    Sueyoshi, Noriyuki
    Shigeri, Yasushi
    Ishida, Atsuhiko
    Kameshita, Isamu
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2012, 526 (01) : 9 - 15
  • [8] Functional processing of nuclear Ca2+/calmodulin-dependent protein kinase phosphatase (CaMKP-N): Evidence for a critical role of proteolytic processing in the regulation of its catalytic activity, subcellular localization and substrate targeting in vivo
    Sueyoshi, Noriyuki
    Nimura, Takaki
    Onouchi, Takashi
    Baba, Hiromi
    Takenaka, Shinobu
    Ishida, Atsuhiko
    Kameshita, Isamu
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2012, 517 (01) : 43 - 52
  • [9] Ppm1E is an in cellulo AMP-activated protein kinase phosphatase
    Voss, Martin
    Paterson, James
    Kelsall, Ian R.
    Martin-Granados, Cristina
    Hastie, C. James
    Peggie, Mark W.
    Cohen, Patricia T. W.
    CELLULAR SIGNALLING, 2011, 23 (01) : 114 - 124
  • [10] Ca2+/calmodulin-dependent protein kinase kinase β phosphorylation of Sirtuin 1 in endothelium is atheroprotective
    Wen, Liang
    Chen, Zhen
    Zhang, Fan
    Cui, Xiaopei
    Sun, Wei
    Geary, Greg G.
    Wang, Yinsheng
    Johnson, David A.
    Zhu, Yi
    Chien, Shu
    Shyy, John Y. -J.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (26) : E2420 - E2427