Isolation of 10 Differentially Expressed cDNAs in Differentiated Neuro2a Cells Induced Through Controlled Expression of the GD3 Synthase Gene

Abstract: Recently, we showed that transfection of GD3 synthase cDNA into Neuro2a cells, a mouse neuroblastoma cell line, causes cell differentiation with neurite sprouting. In a search for the genes involved in this ganglioside‐induced Neuro2a differentiation, we used a tetracycline‐regulated GD3 synthase cDNA expression system combined with differential display PCRs to identify mRNAs that were differentially expressed at four representative time points during the process. We report here the identification of 10 mRNAs that are expressed highly at the Neuro2a differentiated stage. These cDNAs were named GDAP1–GDAP10 for (ganglioside‐induced differentiation‐associated protein) cDNAs. It is interesting that in retinoic acid‐induced neural differentiated mouse embryonic carcinoma P19 cells, GDAP mRNA expression levels were also up‐regulated (except that of GDAP3), ranging from three to > 10 times compared with nondifferentiated P19 cells. All the GDAP genes (except that of GDAP3) were developmentally regulated. The GDAP1, 2, 6, 8, and 10 mRNAs were expressed highly in the adult mouse brain, whereas all the other GDAP mRNAs were expressed in most tissues. Our results suggested that these GDAP genes might be involved in the signal transduction pathway that is triggered through the expression of a single sialyltransferase gene to induce neurite‐like differentiation of Neuro2a cells.

[1]  R. Proia,et al.  Embryonic Stem Cells with a Disrupted GD3 Synthase Gene Undergo Neuronal Differentiation in the Absence of b-Series Gangliosides* , 1998, The Journal of Biological Chemistry.

[2]  Y. Watanabe,et al.  Glycolipid sialyltransferases are enhanced during neural differentiation of mouse embryonic carcinoma cells, P19. , 1997, Biochemical and biophysical research communications.

[3]  S. Tsuji,et al.  Regulated expression system for GD3 synthase cDNA and induction of differentiation in Neuro2a cells. , 1997, Glycobiology.

[4]  P. Chambon A decade of molecular biology of retinoic acid receptors , 1996, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[5]  K. Takamiya,et al.  Heterogeneity in the Expression Pattern of Two Ganglioside Synthase Genes During Mouse Brain Development , 1996, Journal of neurochemistry.

[6]  S. Hakomori,et al.  Functional role of glycosphingolipids in cell recognition and signaling. , 1995, Journal of biochemistry.

[7]  T. Nishi,et al.  Induction of cholinergic differentiation with neurite sprouting by de novo biosynthesis and expression of GD3 and b-series gangliosides in Neuro2a cells. , 1994, The Journal of biological chemistry.

[8]  K. Takamiya,et al.  Isolation of GD3 synthase gene by expression cloning of GM3 alpha-2,8-sialyltransferase cDNA using anti-GD2 monoclonal antibody. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Y. Watanabe,et al.  Expression cloning of a CMP-NeuAc:NeuAc alpha 2-3Gal beta 1-4Glc beta 1-1'Cer alpha 2,8-sialyltransferase (GD3 synthase) from human melanoma cells. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[10]  T. Nishi,et al.  Expression cloning of a GM3-specific alpha-2,8-sialyltransferase (GD3 synthase). , 1994, The Journal of biological chemistry.

[11]  D. Gottlieb,et al.  From embryonal carcinoma cells to neurons: The P19 pathway , 1994, BioEssays : news and reviews in molecular, cellular and developmental biology.

[12]  R. Durbin,et al.  2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans , 1994, Nature.

[13]  Hermann Bujard,et al.  Control of gene activity in higher eukaryotic cells by prokaryotic regulatory elements , 1993 .

[14]  M. McBurney,et al.  P19 embryonal carcinoma cells. , 1993, The International journal of developmental biology.

[15]  P. Chambon,et al.  Multiplicity generates diversity in the retinoic acid signalling pathways. , 1992, Trends in biochemical sciences.

[16]  G L Gilliland,et al.  Combining experimental information from crystal and solution studies: joint X-ray and NMR refinement. , 1992, Science.

[17]  A. Pardee,et al.  Differential display of eukaryotic messenger RNA by means of the polymerase chain reaction. , 1992, Science.

[18]  M. Gossen,et al.  Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[19]  H. Rahmann,et al.  Gangliosides and neuronal differentiation , 1992, Neurochemistry International.

[20]  T. Seyfried,et al.  Ganglioside Composition of Normal and Mutant Mouse Embryos , 1989, Journal of neurochemistry.

[21]  T. Yamashita,et al.  A novel, carbohydrate signal-mediated cell surface protein phosphorylation: ganglioside GQ1b stimulates ecto-protein kinase activity on the cell surface of a human neuroblastoma cell line, GOTO. , 1988, Journal of biochemistry.

[22]  T. Yamashita,et al.  Synthetic Sialyl Compounds as Well as Natural Gangliosides Induce Neuritogenesis in a Mouse Neuroblastoma Cell Line (Neuro2a) , 1988, Journal of neurochemistry.

[23]  T. Seyfried Ganglioside abnormalities associated with failed neural differentiation in a T-locus mutant mouse embryo. , 1987, Developmental biology.

[24]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[25]  P. Arcari,et al.  The complete sequence of a full length cDNA for human liver glyceraldehyde-3-phosphate dehydrogenase: evidence for multiple mRNA species. , 1984, Nucleic acids research.

[26]  S. Tsuji,et al.  GQ1b, a bioactive ganglioside that exhibits novel nerve growth factor (NGF)-like activities in the two neuroblastoma cell lines. , 1983, Journal of biochemistry.

[27]  M. McBurney,et al.  Control of muscle and neuronal differentiation in a cultured embryonal carcinoma cell line , 1982, Nature.

[28]  A. Pardee,et al.  Analysis of altered gene expression by differential display. , 1995, Methods in enzymology.

[29]  E. Robertson Teratocarcinomas and embryonic stem cells : a practical approach , 1987 .