Differential expression and characterization of proto-oncogene product Ha-Ras GTPase in camel tissues

被引:0
作者
NurEKamal, MSA [1 ]
Raza, H [1 ]
Qureshi, MM [1 ]
Jaffer, U [1 ]
Ijaz, MK [1 ]
机构
[1] HH SHAIKH RES CTR RACING CAMELS, DIV INFECT DIS, AL AIN, U ARAB EMIRATES
关键词
Ha-Ras; G protein; GAP; immunocharacterization; fusion protein;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Pas proto-oncogene product is known to be involved in transducing signals for growth, differentiation and oncogenesis in mammalian cells. Using a monoclonal antibody to human Ha-Ras, a camel homolog of Ha-Ras protein having an apparent molecular mass of 21 kDa was identified. The expression level of Ha-Ras protein in various tissues of camel was compared with that of mouse tissues. In camel it was found that expression of Ha-Ras protein was highest in the kidney and moderate in the liver. Expression of Ha-Ras in camel lung, testis, spleen, heart, brain, intestine and muscle was found to be very low. While Ha-Ras expression in mouse was found to be highest in the intestine. A moderate expression of Ha-Ras was found in mouse testis, kidney and heart. The kidney tissue extract of camel was immunoprecipitated using the same human Ha-Ras antibody. Biochemical characterization of the immunoprecipitate revealed that like most other G proteins, the camel homolog of Ras is a GTPase. The GTPase activity was found to be stimulated specifically by recombinant human Ras GAP p120 and neurofibromin. It suggests that both camel and human share the same Ras mediated growth signaling process and that human Ras GAP might be able to complement camel Ras GAP function. Camel homolog of Raf-1 and MAP kinase (member of Ras signaling pathway) were also identified by immunoblot. This is the first demonstration showing the existence of a Ras mediated growth signal transduction pathway in camel.
引用
收藏
页码:47 / 52
页数:6
相关论文
共 36 条
  • [21] MORII N, 1991, J BIOL CHEM, V266, P7646
  • [22] MORII N, 1993, J BIOL CHEM, V268, P27160
  • [23] NICE EC, 1992, J BIOL CHEM, V267, P1546
  • [24] NUREKAMAL MSA, 1993, J BIOL CHEM, V268, P22331
  • [25] NUREKAMAL MSA, 1992, J BIOL CHEM, V267, P1415
  • [26] THE ROLE OF GLN61 AND GLU63 OF RAS GTPASES IN THEIR ACTIVATION BY NF1 AND RAS GAP
    NUREKAMAL, MSA
    MARUTA, H
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (12) : 1437 - 1442
  • [27] RAC MEDIATES GROWTH FACTOR-INDUCED ARACHIDONIC-ACID RELEASE
    PEPPELENBOSCH, MP
    QIU, RG
    DEVRIESSMITS, AMM
    TERTOOLEN, LGJ
    DELAAT, SW
    MCCORMICK, F
    HALL, A
    SYMONS, MH
    BOS, JL
    [J]. CELL, 1995, 81 (06) : 849 - 856
  • [28] PURIFICATION OF A PLASMA MEMBRANE-ASSOCIATED GTPASE-ACTIVATING PROTEIN-SPECIFIC FOR RAP1/KREV-1 FROM HL60 CELLS
    POLAKIS, PG
    RUBINFELD, B
    EVANS, T
    MCCORMICK, F
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (01) : 239 - 243
  • [29] STRUCTURE AND BIOLOGICAL-ACTIVITY OF V-RAF, A UNIQUE ONCOGENE TRANSDUCED BY A RETROVIRUS
    RAPP, UR
    GOLDSBOROUGH, MD
    MARK, GE
    BONNER, TI
    GROFFEN, J
    REYNOLDS, FH
    STEPHENSON, JR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (14): : 4218 - 4222
  • [30] THE SMALL GTP-BINDING PROTEIN RAC REGULATES GROWTH-FACTOR INDUCED MEMBRANE RUFFLING
    RIDLEY, AJ
    PATERSON, HF
    JOHNSTON, CL
    DIEKMANN, D
    HALL, A
    [J]. CELL, 1992, 70 (03) : 401 - 410