The SH3, HOOK and guanylate kinase-like domains of hDLG are important for its cytoplasmic localization

被引:12
|
作者
Kohu, K [1 ]
Ogawa, F [1 ]
Akiyama, T [1 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Dept Mol & Genet Informat, Bunkyo Ku, Tokyo 113, Japan
关键词
D O I
10.1046/j.1365-2443.2002.00555.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: hDLG, the human homologue of the Drosophila tumour suppressor dlg , functions as a scaffolding protein that facilitates the transmission of diverse downstream signals. hDLG possesses multiple protein-binding domains, including three PDZ domains, an SH3 domain, a HOOK domain and a guanylate kinase-like (GK) domain. Results: We studied the significance of the PDZ, SH3, HOOK and GK domains in the cytoplasmic localization of hDLG. We found that mutation of the SH3 or GK domain, but not the PDZ domain, resulted in a re-localization of hDLG to the nucleus. Furthermore, hDLG was found to possess a potential nuclear localization signal in the HOOK domain. Conclusion: These results suggest that the SH3, HOOK and GK domains of hDLG are important for its cytoplasmic localization.
引用
收藏
页码:707 / 715
页数:9
相关论文
共 50 条
  • [31] Meltrin α cytoplasmic domain interacts with SH3 domains of Src and Grb2 and is phosphorylated by v-Src
    Suzuki, A
    Kadota, N
    Hara, T
    Nakagami, Y
    Izumi, T
    Takenawa, T
    Sabe, H
    Endo, T
    ONCOGENE, 2000, 19 (51) : 5842 - 5850
  • [32] Short Linear Motifs recognized by SH2, SH3 and Ser/Thr Kinase domains are conserved in disordered protein regions
    Ren, Siyuan
    Uversky, Vladimir N.
    Chen, Zhengjun
    Dunker, A. Keith
    Obradovic, Zoran
    BMC GENOMICS, 2008, 9 (Suppl 2)
  • [33] Short Linear Motifs recognized by SH2, SH3 and Ser/Thr Kinase domains are conserved in disordered protein regions
    Siyuan Ren
    Vladimir N Uversky
    Zhengjun Chen
    A Keith Dunker
    Zoran Obradovic
    BMC Genomics, 9
  • [34] The C-terminal SH2/SH3 domains of Connexin 43 are pivotal for its migration enhancing activity
    Kiemer, F.
    Pohl, U.
    Pogoda, K.
    ACTA PHYSIOLOGICA, 2015, 213 : 150 - 150
  • [35] The HOOK-domain between the SH3 and the GK domains of Cavβ subunits contains key determinants controlling calcium channel inactivation
    Richards, Mark W.
    Leroy, Jerome
    Pratt, Wendy S.
    Dolphin, Annette C.
    CHANNELS, 2007, 1 (02) : 92 - 101
  • [36] Direct binding of C-terminal region of p130(Cas) to SH2 and SH3 domains of Src kinase
    Nakamoto, T
    Sakai, R
    Ozawa, K
    Yazaki, Y
    Hirai, H
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) : 8959 - 8965
  • [37] A CaVβSH3/guanylate kinase domain interaction regulates multiple properties of voltage-gated Ca2+ channels
    Takahashi, SX
    Miriyala, J
    Tay, LH
    Yue, DT
    Colecraft, HM
    JOURNAL OF GENERAL PHYSIOLOGY, 2005, 126 (04): : 365 - 377
  • [38] Formation of complexes between Ca2+•calmodulin and the synapse-associated protein SAP97 requires the SH3 domain-guanylate kinase domain-connecting HOOK region
    Paarmann, I
    Spangenberg, O
    Lavie, A
    Konrad, M
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (43) : 40832 - 40838
  • [39] Synapsin IIb interacts with the C-terminal SH2 and SH3 domains of PLCγ1 and inhibits its enzymatic activity
    Han, SJ
    Hong, SH
    Kim, CG
    Lee, JB
    Choi, DK
    Kim, KR
    Kim, CG
    CELL BIOLOGY INTERNATIONAL, 2004, 28 (12) : 943 - 948
  • [40] STAT5 activation by BCR/ABL is dependent on its intact SH3 and SH2 domains and is required for leukemogenesis.
    Nieborowska-Skorska, M
    Wasik, MA
    Salomoni, F
    Kitamura, T
    Calabretta, B
    Skorski, T
    BLOOD, 1998, 92 (10) : 91A - 91A