The Ste20 group kinases as regulators of MAP kinase cascades

被引:537
作者
Dan, I [1 ]
Watanabe, NM
Kusumi, A
机构
[1] Nagoya Univ, Dept Biol Sci, Chikusa Ku, Nagoya, Aichi 4648602, Japan
[2] Japan Sci & Technol Corp, ERATO, Kusumi Membrane Organizer Project, Naka Ku, Nagoya, Aichi 4648012, Japan
关键词
D O I
10.1016/S0962-8924(01)01980-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ste20p (sterile 20 protein) is a putative yeast mitogen-activated protein kinase kinase kinase kinase (MAP4K) involved in the mating pathway. Its homologs in mammals, Drosophila, Caenorhabditis elegans and other organisms make up a large emerging group of protein kinases including 28 members in human. The Ste20 group kinases are further divided into the p21-activated kinase (PAK) and germinal center kinase (GCK) families. They are characterized by the presence of a conserved kinase domain and a noncatalytic region of great structural diversity that enables the kinases to interact with various signaling molecules and regulatory proteins of the cytoskeleton. This review describes the phylogenetic relationships of the Ste20 group kinases based on discussions with many researchers in this field. With the newly established phylogenetic relationships, crucial arguments can be advanced regarding the functions of these kinases as upstream activators of the MAPK pathways and possible activity as MAP4Ks. Their involvement in apoptosis, morphogenesis and cytoskeletal rearrangements is also discussed.
引用
收藏
页码:220 / 230
页数:11
相关论文
共 84 条
  • [61] Cloning and characterization of a human STE20-like protein kinase with unusual cofactor requirements
    Schinkmann, K
    Blenis, J
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (45) : 28695 - 28703
  • [62] p21-activated kinase 1 phosphorylates the death agonist Bad and protects cells from apoptosis
    Schürmann, A
    Mooney, AF
    Sanders, LC
    Sells, MA
    Wang, HG
    Reed, JC
    Bokoch, GM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (02) : 453 - 461
  • [63] Emerging from the PAK: The p21-activated protein kinase family
    Sells, MA
    Chernoff, J
    [J]. TRENDS IN CELL BIOLOGY, 1997, 7 (04) : 162 - 167
  • [64] Identification of two essential phosphorylated threonine residues in the catalytic domain of Mekk1 - Indirect activation by Pak3 and protein kinase C
    Siow, YL
    Kalmar, GB
    Sanghera, JS
    Tai, G
    Oh, SS
    Pelech, SL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (12) : 7586 - 7594
  • [65] Nck recruitment to Eph receptor, EphB1/ELK, couples ligand activation to c-Jun kinase
    Stein, E
    Huynh-Do, U
    Lane, AA
    Cerretti, DP
    Daniel, TO
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (03) : 1303 - 1308
  • [66] The Drosophila Ste20-related kinase misshapen is required for embryonic dorsal closure and acts through a JNK MAPK module on an evolutionarily conserved signaling pathway
    Su, YC
    Treisman, JE
    Skolnik, EY
    [J]. GENES & DEVELOPMENT, 1998, 12 (15) : 2371 - 2380
  • [67] NIK is a new Ste20-related kinase that binds NCK and MEKK1 and activates the SAPK/JNK cascade via a conserved regulatory domain
    Su, YC
    Han, JH
    Xu, SC
    Cobb, M
    Skolnik, EY
    [J]. EMBO JOURNAL, 1997, 16 (06) : 1279 - 1290
  • [68] The Ste20 kinase misshapen regulates both photoreceptor axon targeting and dorsal closure, acting downstream of distinct signals
    Su, YC
    Maurel-Zaffran, C
    Treisman, JE
    Skolnik, EY
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (13) : 4736 - 4744
  • [69] Regulation of the protein kinase Raf-1 by oncogenic Ras through phosphatidylinositol 3-kinase, Cdc42/Rac and Pak
    Sun, HY
    King, AJ
    Diaz, HB
    Marshall, MS
    [J]. CURRENT BIOLOGY, 2000, 10 (05) : 281 - 284
  • [70] TAK1 participates in c-Jun N-terminal kinase signaling during Drosophila development
    Takatsu, Y
    Nakamura, M
    Stapleton, M
    Danos, MC
    Matsumoto, K
    O'Connor, MB
    Shibuya, H
    Ueno, N
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (09) : 3015 - 3026