Progresses in mitogen-activated protein kinase-activated protein kinases

被引:0
|
作者
Gong Xiao-Wei
Jiang Yong [1 ]
机构
[1] So Med Univ, Dept Pathophysiol, Guangzhou 510515, Peoples R China
[2] So Med Univ, Key Lab Prote Gongdong Prov, Guangzhou 510515, Peoples R China
关键词
MAPK-activated protein kinase; mitogen-activated protein kinase; signal transduction;
D O I
暂无
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
Mitogen-activated protein kinase (MAPK) signaling pathways are involved in multiple important cellular responses. To activate their downstream protein kinases by phosphorylation is a crucial manner for MAPK family members to fulfill their physiological functions. Downstream of MAPKs, there exist three structurally related MAPK-activated protein kinases (MAPKAPKs or MKs), i.e., MK2, MK3 and MK5. Once upon activated by MAPKs, MKs signal to different cellular targets, to regulate gene expression at the levels of transcription and translation, control cytoskeleton remodelling and cell cycle, and mediate cell migration and embryonic development. Recently, based on the gene knockout studies, the function divisions among different MK subfamily members are gradually clear, leading to tremendous advancements of our knowledge on MKs.
引用
收藏
页码:695 / 701
页数:7
相关论文
共 27 条
  • [1] MAPKAP kinase-2:: Three's company at the G2 checkpoint
    Abraham, RT
    [J]. MOLECULAR CELL, 2005, 17 (02) : 163 - 164
  • [2] Posttranslational regulation of tristetraprolin subcellular localization and protein stability by p38 mitogen-activated protein kinase and extracellular signal-regulated kinase pathways
    Brook, M
    Tchen, CR
    Santalucia, T
    McIlrath, J
    Arthur, JSC
    Saklatvala, J
    Clark, AR
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (06) : 2408 - 2418
  • [3] The Mnks are novel components in the control of TNFα biosynthesis and phosphorylate and regulate hnRNP A1
    Buxadé, M
    Parra, JL
    Rousseau, S
    Shpiro, N
    Marquez, R
    Morrice, N
    Bain, J
    Espel, E
    Proud, CG
    [J]. IMMUNITY, 2005, 23 (02) : 177 - 189
  • [4] MAPKAP kinase 2 phosphorylates tristetraprolin on in vivo sites including Ser178, a site required for 14-3-3 binding
    Chrestensen, CA
    Schroeder, MJ
    Shabanowitz, J
    Hunt, DF
    Pelo, JW
    Worthington, MT
    Sturgill, TW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) : 10176 - 10184
  • [5] p38 mitogen-activated protein kinase-dependent and -independent signaling of mRNA stability of AU-rich element-containing transcripts
    Frevel, MAE
    Bakheet, T
    Silva, AM
    Hissong, JG
    Khabar, KSA
    Williams, BRG
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (02) : 425 - 436
  • [6] MAPKAP kinases - MKs - two's company, three's a crowd
    Gaestel, M
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2006, 7 (02) : 120 - 130
  • [7] MAPKAP kinase 2-deficient mice are resistant to collagen-induced arthritis
    Hegen, Martin
    Gaestel, Matthias
    Nickerson-Nutter, Cheryl L.
    Lin, Lih-Ling
    Telliez, Jean-Baptiste
    [J]. JOURNAL OF IMMUNOLOGY, 2006, 177 (03): : 1913 - 1917
  • [8] Mitogen-activated protein kinase-activated protein kinase 2 regulates tumor necrosis factor mRNA stability and translation mainly by altering tristetraprolin expression, stability, and binding to adenine/uridine-rich element
    Hitti, E
    Iakovleva, T
    Brook, M
    Deppenmeier, S
    Gruber, AD
    Radzioch, D
    Clark, AR
    Blackshear, PJ
    Kotlyarov, A
    Gaestel, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (06) : 2399 - 2407
  • [9] MAPKAP kinase 2 is essential for LPS-induced TNF-α biosynthesis
    Kotlyarov, A
    Neininger, A
    Schubert, C
    Eckert, R
    Birchmeier, C
    Volk, HD
    Gaestel, M
    [J]. NATURE CELL BIOLOGY, 1999, 1 (02) : 94 - 97
  • [10] Distinct cellular functions of MK2
    Kotlyarov, A
    Yannoni, Y
    Fritz, S
    Laass, K
    Telliez, JB
    Pitman, D
    Lin, LL
    Gaestel, M
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (13) : 4827 - 4835