SRC64 regulates the localization of a tec-family kinase required for Drosophila ring canal growth

被引:67
作者
Guarnieri, DJ
Dodson, GS
Simon, MA [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
D O I
10.1016/S1097-2765(00)80082-9
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
Mutation of the Src64 gene of Drosophila results in ovarian ring canal defects and reduced female fertility. We used a dosage-sensitive modifier screen to search for downstream components of the SRC64 signaling pathway. We show that mutations affecting Tec29, an essential gene encoding a member of the Tec family of protein tyrosine kinases, dominantly enhance the Src64 ring canal phenotype. Loss of Tec29 function in the female germline results in a phenotype strikingly similar to that caused by the loss of Src64 function. In each case, the ring canals are reduced in size and phosphotyrosine content. We further demonstrate that TEC29 localizes to the ring canal, and this subcellular localization requires Src64 function. These data suggest that TEC29 is a downstream target of SRC64, and that regulating TEC29 localization during ring canal growth may be a crucial SRC64 function.
引用
收藏
页码:831 / 840
页数:10
相关论文
共 60 条
  • [11] Gibson S, 1996, J IMMUNOL, V156, P2716
  • [12] Functional LCK is required for optimal CD28-mediated activation of the TEC family tyrosine kinase EMT/ITK
    Gibson, S
    August, A
    Branch, D
    Dupont, B
    Mills, GB
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (12) : 7079 - 7083
  • [13] PRIMARY SEQUENCE AND DEVELOPMENTAL EXPRESSION OF A NOVEL DROSOPHILA-MELANOGASTER SRC GENE
    GREGORY, RJ
    KAMMERMEYER, KL
    VINCENT, WS
    WADSWORTH, SG
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (06) : 2119 - 2127
  • [14] TXK, A NOVEL HUMAN TYROSINE KINASE EXPRESSED IN T-CELLS SHARES SEQUENCE IDENTITY WITH TEC FAMILY KINASES AND MAPS TO 4P12
    HAIRE, RN
    OHTA, Y
    LEWIS, JE
    FU, SM
    KROISEL, P
    LITMAN, GW
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (06) : 897 - 901
  • [15] THE PROTEIN-KINASE FAMILY - CONSERVED FEATURES AND DEDUCED PHYLOGENY OF THE CATALYTIC DOMAINS
    HANKS, SK
    QUINN, AM
    HUNTER, T
    [J]. SCIENCE, 1988, 241 (4861) : 42 - 52
  • [16] Lck phosphorylates the activation loop tyrosine of the Itk kinase domain and activates Itk kinase activity
    Heyeck, SD
    Wilcox, HM
    Bunnell, SC
    Berg, LJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (40) : 25401 - 25408
  • [17] Tec family protein-tyrosine kinases and pleckstrin homology domains in mast cells
    Kawakami, Y
    Yao, LB
    Han, W
    Kawakami, T
    [J]. IMMUNOLOGY LETTERS, 1996, 54 (2-3) : 113 - 117
  • [18] TYROSINE PHOSPHORYLATION AND ACTIVATION OF BRUTON TYROSINE KINASE UPON FC-EPSILON-RI CROSS-LINKING
    KAWAKAMI, Y
    YAO, LB
    MIURA, T
    TSUKADA, S
    WITTE, ON
    KAWAKAMI, T
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (08) : 5108 - 5113
  • [19] Characterization of the pleckstrin homology domain of Btk as an inositol polyphosphate and phosphoinositide binding domain
    Kojima, T
    Fukuda, M
    Watanabe, Y
    Hamazato, F
    Mikoshiba, K
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 236 (02) : 333 - 339
  • [20] Transphosphorylation of Bruton's tyrosine kinase on tyrosine 551 is critical for B cell antigen receptor function
    Kurosaki, T
    Kurosaki, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) : 15595 - 15598