Genomic organization of the Shc-related phosphotyrosine adapters and characterization of the full-length Sck/ShcB: Specific association of p68-Sck/ShcB with pp135

被引:20
作者
Kojima, T
Yoshikawa, Y
Takada, S
Sato, M
Nakamura, T
Takahashi, N
Copeland, NG
Gilbert, DJ
Jenkins, NA
Mori, N
机构
[1] NILS, Dept Mol Genet Res, Morioka, Aichi 4748522, Japan
[2] NAIST, Dept Biosci, Takayama, Nara 6300101, Japan
[3] Kyoto Univ, Fac Sci, Ctr Dev Biol, Kyoto 6068224, Japan
[4] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Mammalian Genet Lab, Ft Detrick, MD 21702 USA
关键词
adapter; genome; N-Shc; phosphotyrosine; PTB; Sck; SH2; ShcB; ShcC; signal transduction; Src;
D O I
10.1006/bbrc.2001.5080
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
The She gene family is an emerging family, containing at least three members designated Shc/ShcA, Sck/Sli/ShcB, N-Shc/Rai/ShcC in mammals. In this study, we determined the genomic organization of the mouse She family. Coding regions of ShcA, B, and C each comprised 12 exons, spanned approximately 6, 20, and 65 kb, and located on chromosome 3, 10, and 13, respectively. Based on this genome analysis, we determined the full-length structure of mouse Sck/ShcB as a 68-kD protein. We found that the 68-kD full-length Sck/ShcB was more efficiently phosphorylated upon EGF treatment than the previously-analyzed CH2-deleted form. We also found that Sck specifically interacted with a 135-kD phosphoprotein (pp135) through its SH2 domain following membrane depolarization. The Sck-pp135 interaction was reduced by Src kinase inhibitors. These results suggest that Sck, but not N-Shc nor She, transmit signals in conjunction with pp135 following Src activation and/or calcium entry in the cell. (C) 2001 Academic Press.
引用
收藏
页码:1039 / 1047
页数:9
相关论文
共 33 条
  • [1] MAPPING OF MURINE FIBROBLAST GROWTH-FACTOR RECEPTORS REFINES REGIONS OF HOMOLOGY BETWEEN MOUSE AND HUMAN-CHROMOSOMES
    AVRAHAM, KB
    GIVOL, D
    AVIVI, A
    YAYON, A
    COPELAND, NG
    JENKINS, NA
    [J]. GENOMICS, 1994, 21 (03) : 656 - 658
  • [2] BUCHBERG AM, 1989, GENETICS, V122, P153
  • [3] Emerging roles for SH2/PTB-containing Shc adaptor proteins in the developing mammalian brain
    Cattaneo, E
    Pelicci, PG
    [J]. TRENDS IN NEUROSCIENCES, 1998, 21 (11) : 476 - 481
  • [4] The genes encoding the Eph-related receptor tyrosine kinase ligands LERK-1 (EPLG1, Epl1), LERK-3 (EPLG3, Epl3), and LERK-4 (EPLG4, EPl4) are clustered on human chromosome 1 and mouse chromosome 3
    Cerretti, DP
    Lyman, SD
    Kozlosky, CJ
    Copeland, NG
    Gilbert, DJ
    Jenkins, NA
    Valentine, V
    Kirstein, MN
    Shapiro, DN
    Morris, SW
    [J]. GENOMICS, 1996, 33 (02) : 277 - 282
  • [5] DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME
    COPELAND, NG
    JENKINS, NA
    [J]. TRENDS IN GENETICS, 1991, 7 (04) : 113 - 118
  • [6] A novel pathway from phosphorylation of tyrosine residues 239/240 of Shc, contributing to suppress apoptosis by IL-3
    Gotoh, N
    Tojo, A
    Shibuya, M
    [J]. EMBO JOURNAL, 1996, 15 (22) : 6197 - 6204
  • [7] Green EL, 1981, GENETICS PROBABILITY, P77
  • [8] Green MC., 1989, GENETIC VARIANTS STR, P12
  • [9] New role for Shc in activation of the phosphatidylinositol 3-kinase/Akt pathway
    Gu, HH
    Maeda, H
    Moon, JJ
    Lord, JD
    Yoakim, M
    Nelson, BH
    Neel, BG
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (19) : 7109 - 7120
  • [10] Characterization of human SHC p66 cDNA and its processed pseudogene mapping to Xq12-q13.1
    Harun, RB
    Smith, KK
    Leek, JP
    Markham, AF
    Norris, A
    Morrison, JFJ
    [J]. GENOMICS, 1997, 42 (02) : 349 - 352