This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Majumder, S
Right arrow Articles by Besmer, P
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Majumder, S
Right arrow Articles by Besmer, P

 Previous Article  |  Next Article 

Mol Cell Biol. 1988 November; 8(11): 4896-4903

c-kit protein, a transmembrane kinase: identification in tissues and characterization.

S Majumder, K Brown, F H Qiu and P Besmer

Laboratory of Molecular Oncology, Memorial Sloan-Kettering Cancer Center, New York, New York.

ABSTRACT

The proto-oncogene c-kit encodes a transmembrane kinase which is related to the receptors for colony-stimulating factor type 1 and platelet-derived growth factor, as well as to the immunoglobulin superfamily. Antibodies specific for the kinase domain of the P80 gag-kit protein of the Hardy-Zuckerman 4 feline sarcoma virus were prepared. These kit-specific antibodies were used to identify and characterize the c-kit protein in cat brain tissue. The c-kit protein product displays an autophosphorylating activity in immune complex kinase assays, and, in turn, this activity was used to identify the c-kit protein in different tissues. In cat brain, a single 145-kilodalton (kDa) glycoprotein was detected. Its N-linked carbohydrates were found to be sensitive to digestion with the endoglycosidases (neuraminidase, endoglycosidase F, and endoglycosidase H), indicating hybrid and/or complex and high-mannose structures. A partial purification of the c-kit protein was achieved by wheat germ agglutinin affinity chromatography, and the autophosphorylating activity of the partially purified c-kit protein was characterized and found to be specific for tyrosine. The kit antibodies cross-react with the murine c-kit protein product, and variant c-kit proteins in different mouse tissues were identified, with sizes of about 145 kDa (brain), 160 kDa (spleen), and 150 kDa (testis).


Mol Cell Biol. 1988 November; 8(11): 4896-4903




This article has been cited by other articles:

  • Bougherara, H., Subra, F., Crepin, R., Tauc, P., Auclair, C., Poul, M.-A. (2009). The Aberrant Localization of Oncogenic Kit Tyrosine Kinase Receptor Mutants Is Reversed on Specific Inhibitory Treatment. Mol Cancer Res 7: 1525-1533 [Abstract] [Full Text]  
  • Xiang, Z., Kreisel, F., Cain, J., Colson, A., Tomasson, M. H. (2007). Neoplasia Driven by Mutant c-KIT Is Mediated by Intracellular, Not Plasma Membrane, Receptor Signaling. Mol. Cell. Biol. 27: 267-282 [Abstract] [Full Text]  
  • Cervello, I., Martinez-Conejero, J.A., Horcajadas, J.A., Pellicer, A., Simon, C. (2007). Identification, characterization and co-localization of label-retaining cell population in mouse endometrium with typical undifferentiated markers. Hum Reprod 22: 45-51 [Abstract] [Full Text]  
  • Tkaczyk, C., Horejsi, V., Iwaki, S., Draber, P., Samelson, L. E., Satterthwaite, A. B., Nahm, D.-H., Metcalfe, D. D., Gilfillan, A. M. (2004). NTAL phosphorylation is a pivotal link between the signaling cascades leading to human mast cell degranulation following Kit activation and Fc{epsilon}RI aggregation. Blood 104: 207-214 [Abstract] [Full Text]  
  • Miliaras, D, Karasavvidou, F, Papanikolaou, A, Sioutopoulou, D (2004). KIT expression in fetal, normal adult, and neoplastic renal tissues. J. Clin. Pathol. 57: 463-466 [Abstract] [Full Text]  
  • Fiorentini, G., Rossi, S., Lanzanova, G., Bernardeschi, P., Dentico, P., De Giorgi, U. (2003). Potential use of imatinib mesylate in ocular melanoma and liposarcoma expressing immunohistochemical c-KIT (CD117). Ann Oncol 14: 805-805 [Full Text]  
  • Hashimoto, K., Matsumura, I., Tsujimura, T., Kim, D.-K., Ogihara, H., Ikeda, H., Ueda, S., Mizuki, M., Sugahara, H., Shibayama, H., Kitamura, Y., Kanakura, Y. (2003). Necessity of tyrosine 719 and phosphatidylinositol 3'-kinase-mediated signal pathway in constitutive activation and oncogenic potential of c-kit receptor tyrosine kinase with the Asp814Val mutation. Blood 101: 1094-1102 [Abstract] [Full Text]  
  • Scappini, B., Onida, F., Kantarjian, H. M., Dong, L., Verstovsek, S., Keating, M. J., Beran, M. (2001). Effects of Signal Transduction Inhibitor 571 in Acute Myelogenous Leukemia Cells. Clin. Cancer Res. 7: 3884-3893 [Abstract] [Full Text]  
  • Ikuno, Y., Leong, F.-L., Kazlauskas, A. (2000). Attenuation of Experimental Proliferative Vitreoretinopathy by Inhibiting the Platelet-Derived Growth Factor Receptor. IOVS 41: 3107-3116 [Abstract] [Full Text]  
  • Tsujimura, T., Hashimoto, K., Kitayama, H., Ikeda, H., Sugahara, H., Matsumura, I., Kaisho, T., Terada, N., Kitamura, Y., Kanakura, Y. (1999). Activating Mutation in the Catalytic Domain of c-kit Elicits Hematopoietic Transformation by Receptor Self-Association Not at the Ligand-Induced Dimerization Site. Blood 93: 1319-1329 [Abstract] [Full Text]  
  • Gentry,, P. C., Smith,, G. W., Leighr, D. R., Bao, B., Smith, M. F. (1998). Ontogeny of Stem Cell Factor Receptor (c-kit) Messenger Ribonucleic Acid in the Ovine Corpus Luteum. Biol. Reprod. 59: 983-990 [Abstract] [Full Text]  
  • Kozlowski, M., Larose, L., Lee, F., Le, D. M., Rottapel, R., Siminovitch, K. A. (1998). SHP-1 Binds and Negatively Modulates the c-Kit Receptor by Interaction with Tyrosine 569 in the c-Kit Juxtamembrane Domain. Mol. Cell. Biol. 18: 2089-2099 [Abstract] [Full Text]  
  • Lyman, S. D., Jacobsen, S. E. W. (1998). c-kit Ligand and Flt3 Ligand: Stem/Progenitor Cell Factors With Overlapping Yet Distinct Activities. Blood 91: 1101-1134 [Full Text]  
  • Amsterdam, A., Selvaraj, N. (1997). Control of Differentiation, Transformation, and Apoptosis in Granulosa Cells by Oncogenes, Oncoviruses, and Tumor Suppressor Genes. Endocr. Rev. 18: 435-461 [Abstract] [Full Text]  
  • Moriyama, Y., Tsujimura, T., Hashimoto, K., Morimoto, M., Kitayama, H., Matsuzawa, Y., Kitamura, Y., Kanakura, Y. (1996). Role of Aspartic Acid 814 in the Function and Expression of c-kit Receptor Tyrosine Kinase. J. Biol. Chem. 271: 3347-3350 [Abstract] [Full Text]  
  • Lodish, H.F., Hilton, D.J., Klingmuller, U., Watowich, S.S., Wu, H. (1995). The Erythropoietin Receptor: Biogenesis, Dimerization, and Intracellular Signal Transduction. Cold Spring Harb Symp Quant Biol 60: 93-104 [Abstract]  
  • Duttlinger, R, Manova, K, Chu, T., Gyssler, C, Zelenetz, A., Bachvarova, R., Besmer, P (1993). W-sash affects positive and negative elements controlling c-kit expression: ectopic c-kit expression at sites of kit-ligand expression affects melanogenesis. Development 118: 705-717 [Abstract]  
  • Tan, J., Nocka, K, Ray, P, Traktman, P, Besmer, P (1990). The dominant W42 spotting phenotype results from a missense mutation in the c-kit receptor kinase. Science 247: 209-212 [Abstract]  
  • Nocka, K, Majumder, S, Chabot, B, Ray, P, Cervone, M, Bernstein, A, Besmer, P (1989). Expression of c-kit gene products in known cellular targets of W mutations in normal and W mutant mice--evidence for an impaired c-kit kinase in mutant mice.. Genes Dev. 3: 816-826 [Abstract]