Regulation of a ras-related protein during development of Dictyostelium discoideum

Recent work has shown that DNA sequences related to the mammalian ras proto-oncogenes are highly conserved in eucaryotic evolution. A monoclonal antibody (Y13-259) to mammalian p21ras specifically precipitated a 23,000-molecular-weight protein (p23) from lysates of Dictyostelium discoideum amoebae. Tryptic peptide analysis indicated that D. discoideum p23 was closely related in its primary structure to mammalian p21ras. p23 was apparently derived by post-translational modification of a 24,000-molecular-weight primary gene product. The amount of p23 was highest in growing amoebae, but declined markedly with the onset of differentiation such that by fruiting body formation there was less than 10% of the amoeboid level. The rate of p23 synthesis dropped rapidly during aggregation, rose transiently during pseudoplasmodial formation, and then declined during the terminal stages of differentiation. There was, therefore, a strong correlation between the expression of the ras-related protein p23 and cell proliferation of D. discoideum.

[1]  D. Goeddel,et al.  Comparative biochemical properties of normal and activated human ras p21 protein , 1984, Nature.

[2]  E. Scolnick,et al.  Requirement of either of a pair of ras-related genes of Saccharomyces cerevisiae for spore viability , 1984, Nature.

[3]  M. Wigler,et al.  Genes in S. cerevisiae encoding proteins with domains homologous to the mammalian ras proteins , 1984, Cell.

[4]  P. Maness,et al.  pp60c-src is developmentally regulated in the neural retina , 1984, Cell.

[5]  H. E. Gray,et al.  Cell-cycle control of c-myc but not c-ras expression is lost following chemical transformation , 1984, Cell.

[6]  E. Scolnick,et al.  Saccharomyces cerevisiae synthesizes proteins related to the p21 gene product of ras genes found in mammals , 1984, Molecular and cellular biology.

[7]  E. Scolnick,et al.  ras-Related gene sequences identified and isolated from Saccharomyces cerevisiae , 1983, Nature.

[8]  M. Wigler,et al.  Structure and activation of the human N-ras gene , 1983, Cell.

[9]  I. Verma,et al.  Transcription of c-onc genes c-rasKi and c-fms during mouse development , 1983, Molecular and cellular biology.

[10]  T. Pawson,et al.  Mapping of multiple phosphorylation sites within the structural and catalytic domains of the Fujinami avian sarcoma virus transforming protein , 1983, Journal of Virology.

[11]  C. Petropoulos,et al.  Expression of a cellular oncogene during liver regeneration. , 1983, Science.

[12]  J. Bishop Cellular oncogenes and retroviruses. , 1983, Annual review of biochemistry.

[13]  Jonathan A. Cooper,et al.  The transforming proteins of Rous sarcoma virus, Harvey sarcoma virus and Abelson virus contain tightly bound lipid , 1982, Cell.

[14]  D. Lowy,et al.  Comparative biochemical properties of p21 ras molecules coded for by viral and cellular ras genes , 1982, Journal of virology.

[15]  I. Verma,et al.  Differential expression of cellular oncogenes during pre- and postnatal development of the mouse , 1982, Nature.

[16]  T. Y. Shih,et al.  Characterization of the phosphorylation sites and the surrounding amino acid sequences of the p21 transforming proteins coded for by the Harvey and Kirsten strains of murine sarcoma viruses. , 1982, The Journal of biological chemistry.

[17]  E. Scolnick,et al.  Monoclonal antibodies to the p21 products of the transforming gene of Harvey murine sarcoma virus and of the cellular ras gene family , 1982, Journal of virology.

[18]  D. Lowy,et al.  Tumorigenic transformation of mammalian cells induced by a normal human gene homologous to the oncogene of Harvey murine sarcoma virus , 1982, Nature.

[19]  M. Shibuya,et al.  Cellular Sequences Related to Three New onc Genes of Avian Sarcoma Virus (fps, yes, and ros) and Their Expression in Normal and Transformed Cells , 1982, Journal of virology.

[20]  E. Scolnick,et al.  Identification of a precursor in the biosynthesis of the p21 transforming protein of harvey murine sarcoma virus , 1982, Journal of virology.

[21]  R. Weinberg,et al.  DNA sequences homologous to vertebrate oncogenes are conserved in Drosophila melanogaster. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[22]  M. Gonda,et al.  Analysis of two divergent rat genomic clones homologous to the transforming gene of Harvey murine sarcoma virus. , 1981, Proceedings of the National Academy of Sciences of the United States of America.

[23]  H. Lodish,et al.  Complexity of nuclear and polysomal RNAs in growing Dictyostelium discoideum cells. , 1980, Developmental biology.

[24]  T. Pawson,et al.  env Gene of Rous sarcoma virus: identification of the gene product by cell-free translation , 1980, Journal of virology.

[25]  A. Durston,et al.  The spatial pattern of DNA synthesis in Dictyostelium discoideum slugs. , 1978, Experimental cell research.

[26]  C. Town,et al.  The role of cyclic nucleotides and cell agglomeration in postaggregative enzyme synthesis in Dictyostelium discoideum. , 1978, Developmental biology.

[27]  J. Ashworth,et al.  The cell cycle and its relationship to development in Dictyostelium discoideum. , 1978, Developmental biology.

[28]  H. Pelham,et al.  An efficient mRNA-dependent translation system from reticulocyte lysates. , 1976, European journal of biochemistry.

[29]  Jerome B. Zeldis,et al.  Dictyostelium Discoideum: A Developmental System , 1976, The Yale Journal of Biology and Medicine.

[30]  M. Sussman Chapter 14 Biochemical and Genetic Methods in the Study of Cellular Slime Mold Development , 1966 .

[31]  M. Sussman,et al.  Metabolism of major cell components during slime mold morphogenesis. , 1961, Biochimica et biophysica acta.