Transient expression of high molecular weight, heat sensitive, trypsin-resistant form of tyrosinase in B-16 melanoma cells.

High molecular weight forms of tyrosinase have been found to be expressed during spontaneous remelanization of the amelanotic B-16 melanoma cells in culture as well as in melanotic tumors formed from amelanotic melanoma cells grown in C57BL/6J mice. Overnight extraction of the crude melanosomal fractions from such tumors and cultured melanoma cells reveal the presence of an additional DOPA-MBTH positive band well below the stacking gel. This band has been found to be alpha-PEP7 (antibody specific for tyrosinase) positive and alpha-PEP1 (antibody specific for TRP-1) negative on Western blot analysis. Heat treatment at 60 degrees C for 60 min results in the loss of this band and considerable loss of activity of the melanosomal extract. Trypsin treatment of these melanosomal extracts resulted in a minor change in the mobility of the high molecular weight band. SDS-PAGE under reduced conditions followed by Western blotting revealed that the high molecular weight band was lost and not detected by alpha-PEP7 or alpha-PEP1. These findings indicate that high molecular weight, heat sensitive and trypsin resistant forms of tyrosinase are transiently expressed in B-16 melanoma cells and tumors that are initiating remelanization following phenotypic drift towards the amelanotic state.

[1]  C. Garbe,et al.  Incomplete expression of the tyrosinase gene family (tyrosinase, TRP-1, and TRP-2) in human malignant melanoma cells in vitro. , 1995, Pigment cell research.

[2]  F. Solano,et al.  Effect of detergents and endogenous lipids on the activity and properties of tyrosinase and its related proteins. , 1995, Biochimica et biophysica acta.

[3]  S. Orlow,et al.  High-molecular-weight forms of tyrosinase and the tyrosinase-related proteins: evidence for a melanogenic complex. , 1994, The Journal of investigative dermatology.

[4]  K. Urabe,et al.  A new enzymatic function in the melanogenic pathway. The 5,6-dihydroxyindole-2-carboxylic acid oxidase activity of tyrosinase-related protein-1 (TRP1). , 1994, The Journal of biological chemistry.

[5]  F. Solano,et al.  Improved tyrosinase activity stains in polyacrylamide electrophoresis gels. , 1993, Pigment cell research.

[6]  F. Solano,et al.  Preparation of purified tyrosinase devoid of dopachrome tautomerase from mammalian malignant melanocytes. , 1993, Pigment cell research.

[7]  R. Halaban Molecular correlates in the progression of normal melanocytes to melanomas. , 1993, Seminars in cancer biology.

[8]  N. Copeland,et al.  A second tyrosinase‐related protein, TRP‐2, maps to and is mutated at the mouse slaty locus. , 1992, The EMBO journal.

[9]  V. Hearing,et al.  Enzymatic control of pigmentation in mammals , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[10]  G. Schütz,et al.  Functional analysis of alternatively spliced tyrosinase gene transcripts. , 1988, The EMBO journal.

[11]  F. Solano,et al.  Assays for mammalian tyrosinase: a comparative study. , 1988, Pigment cell research.

[12]  S. Pomerantz,et al.  Regulation of tyrosinase in human melanocytes grown in culture , 1983, The Journal of cell biology.

[13]  J. Pawelek,et al.  Mammalian tyrosinase catalyzes three reactions in the biosynthesis of melanin. , 1982, Science.

[14]  V. Hearing,et al.  Mammalian tyrosinase: isozymic forms of the enzyme. , 1981, The International journal of biochemistry.

[15]  V. Hearing,et al.  Mammalian tyrosinase. Structural and functional interraltionship of isozymes. , 1978, Biochimica et biophysica acta.

[16]  E. Delain,et al.  Ultrastructure of spontaneously differentiated human malignant melanocytes cultured from primary tumors. , 1977, Journal of the National Cancer Institute.

[17]  W. C. Quevedo,et al.  Action of Trypsin and Detergents on Tyrosinase of Normal and Malignant Melanocytes 1 , 1975, Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine.

[18]  J. Pawelek,et al.  Genetic control of melanization: isolation and analysis of amelanotic variants from cultured melanotic melanoma cells. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[19]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.

[20]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.