8 results on '"Falcone, G"'
Search Results
2. Delineating v-Src downstream effector pathways in transformed myoblasts
- Author
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Ciuffini, L, primary, Castellani, L, additional, Salvati, E, additional, Galletti, S, additional, Falcone, G, additional, and Alemà, S, additional
- Published
- 2007
- Full Text
- View/download PDF
3. v-Src inhibits myogenic differentiation by interfering with the regulatory network of muscle-specific transcriptional activators at multiple levels.
- Author
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Falcone G, Ciuffini L, Gauzzi MC, Provenzano C, Strano S, Gallo R, Castellani L, and Alemà S
- Subjects
- Animals, Base Sequence, Cell Division physiology, Cell Line, Transformed, DNA metabolism, DNA Primers, Mice, Muscle, Skeletal cytology, MyoD Protein metabolism, Oncogene Protein pp60(v-src) metabolism, Quail, Cell Differentiation physiology, Muscle, Skeletal metabolism, Oncogene Protein pp60(v-src) physiology, Trans-Activators metabolism
- Abstract
The conversion of skeletal myoblasts to terminally differentiated myocytes is negatively controlled by several growth factors and oncoproteins. In this study, we have investigated the molecular mechanisms by which v-Src, a prototypic tyrosine kinase, perturbs myogenesis in primary avian myoblasts and in established murine C2C12 satellite cells. We determined the expression levels of the cell cycle regulators pRb, cyclin D1 and D3 and cyclin-dependent kinase inhibitors p21 and p27 in v-Src-transformed myoblasts and found that, in contrast to myogenin, they are normally modulated by differentiative cues, implying that v-Src affects myogenesis independent of cell proliferation. We then examined the levels of expression, DNA-binding ability and transcription-activation potentials of myogenic regulatory factors in transformed myoblasts and in myotubes after reactivation of a temperature-sensitive allele of v-Src. Our results reveal two distinct potential modes of repression targeted to myogenic factors. On the one hand, we show that v-Src reversibly inhibits the expression of MyoD and myogenin in C2C12 cells and of myogenin in quail myoblasts. Remarkably, these loci become resistant to activation of the kinase in the postmitotic compartment. On the other hand, we demonstrate that v-Src efficiently inhibits muscle gene expression by repressing the transcriptional activity of myogenic factors without affecting MyoD DNA-binding activity. Indeed, forced expression of MyoD and myogenin allows terminal differentiation of transformed myoblasts. Finally, we found that ectopic expression of the coactivator p300 restores transcription from extrachromosomal muscle-specific promoters.
- Published
- 2003
- Full Text
- View/download PDF
4. Expression of RALT, a feedback inhibitor of ErbB receptors, is subjected to an integrated transcriptional and post-translational control.
- Author
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Fiorini M, Ballarò C, Sala G, Falcone G, Alemà S, and Segatto O
- Subjects
- Animals, Antineoplastic Agents, Hormonal pharmacology, Blotting, Northern, Carrier Proteins antagonists & inhibitors, Carrier Proteins genetics, Cell Cycle, Cell Division, Cell Transformation, Neoplastic, Cells, Cultured, Cysteine Proteinase Inhibitors pharmacology, Enzyme Activation, Epithelial Cells metabolism, Feedback, Physiological, Fibroblasts metabolism, Gene Expression Regulation, Humans, Mice, Mitogen-Activated Protein Kinases antagonists & inhibitors, Mitogen-Activated Protein Kinases metabolism, Mitogens pharmacology, Phosphorylation, Protein Binding, Proto-Oncogene Proteins c-raf genetics, Receptor, ErbB-2 chemistry, Receptor, ErbB-2 metabolism, Tamoxifen pharmacology, Tumor Suppressor Proteins, ras Proteins metabolism, src Homology Domains, Adaptor Proteins, Signal Transducing, Carrier Proteins metabolism, Protein Biosynthesis physiology, Proto-Oncogene Proteins c-raf metabolism, Receptor, ErbB-2 antagonists & inhibitors, Signal Transduction, Transcription, Genetic physiology
- Abstract
Over-expression studies have demonstrated that RALT (receptor associated late transducer) is a feedback inhibitor of ErbB-2 mitogenic and transforming signals. In growth-arrested cells, expression of endogenous RALT is induced by mitogenic stimuli, is high throughout mid to late G1 and returns to baseline as cells move into S phase. Here, we show that physiological levels of RALT effectively suppress ErbB-2 mitogenic signals. We also investigate the regulatory mechanisms that preside to the control of RALT expression. We demonstrate that pharmacological ablation of extracellular signal-regulated kinase (ERK) activation leads to blockade of RALT expression, unlike genetic and/or pharmacological interference with the activities of PKC, Src family kinases, p38 SAPK and PI-3K. Tamoxifen-dependent activation of an inducible Raf : ER chimera was sufficient to induce RALT expression. Thus, activation of the Ras-Raf-ERK pathway is necessary and sufficient to drive RALT expression. The RALT protein is labile and was found to accumulate robustly upon pharmacological inhibition of the proteasome. We were able to detect ubiquitin-conjugated RALT species in living cells, suggesting that ubiquitinylation targets RALT for proteasome-dependent degradation. Such an integrated transcriptional and post-translational control is likely to provide RALT with the ability to fluctuate timely in order to tune ErbB signals.
- Published
- 2002
- Full Text
- View/download PDF
5. Induction of telomerase activity in v-myc-transformed avian cells.
- Author
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Falchetti ML, Falcone G, D'Ambrosio E, Verna R, Alemà S, and Levi A
- Subjects
- Animals, Cell Line, Transformed, Chickens, Enzyme Induction, Humans, Neurons, Oncogene Protein p55(v-myc) genetics, Quail, Receptors, Estrogen genetics, Receptors, Estrogen metabolism, Oncogene Protein p55(v-myc) metabolism, Telomerase metabolism
- Abstract
Telomerase activity is detectable in the majority of tumors or immortalized cell lines, but is repressed in most normal human somatic cells. It is generally assumed that reactivation of telomerase prevents the erosion of chromosome ends which occurs in cycling cells and, hence, hinders cellular replicative senescence. Here, we show that the expression of v-Myc oncoprotein by retroviral infection of telomerase-negative embryonal quail myoblasts and chicken neuroretina cells is sufficient for reactivating telomerase activity, earlier than telomere shortening could occur. Furthermore, the use of a conditional v-Myc-estrogen receptor protein (v-MycER) causes estrogen-dependent expression of detectable levels of telomerase activity in recently infected chick embryo fibroblasts and neuroretina cells. We conclude that the high levels of telomerase activity in v-Myc-expressing avian cells are not the mere consequence of transformation or of a differentiative block, since v-Src tyrosine kinase, which prevents terminal differentiation and promotes cell transformation, fails to induce telomerase activity.
- Published
- 1999
- Full Text
- View/download PDF
6. Regulation of the tyrosine kinase substrate Eps8 expression by growth factors, v-Src and terminal differentiation.
- Author
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Gallo R, Provenzano C, Carbone R, Di Fiore PP, Castellani L, Falcone G, and Alemà S
- Subjects
- 3T3 Cells, Adaptor Proteins, Signal Transducing, Animals, Blood, Carcinogens pharmacology, Cell Line, Transformed, Cytoskeletal Proteins, Gene Expression Regulation genetics, Mice, Phosphorylation, Signal Transduction, Substrate Specificity, Tyrosine metabolism, Up-Regulation genetics, Cell Differentiation physiology, Gene Expression Regulation drug effects, Genes, src, Growth Substances pharmacology, Protein-Tyrosine Kinases metabolism, Proteins genetics
- Abstract
SH3-containing proteins are involved in signal transduction by a number of growth factor receptors and in the organization of the cytoskeleton. The recently identified Eps8 protein, which contains an SH3 domain, is coupled functionally and physically to the EGFR and is tyrosine phosphorylated by this receptor and other receptors as well. Here, we examined the regulation of eps8 expression in response to mitogenic or differentiative signals. We show that Eps8 is expressed at low levels in resting fibroblasts, but its expression is strongly induced during activation by serum, phorbol esters and the v-src oncogene. Conversely, expression of Eps8, but not of other EGFR substrates such as Shc or Eps15, is virtually extinguished in non-proliferating, terminally differentiated murine myogenic cells. The putative role of Eps8 protein as a v-Src substrate was analysed in murine fibroblasts and in quail myogenic cells expressing a temperature-sensitive variant of the tyrosine kinase. Tyrosine phosphorylation of Eps8 was detected only at the permissive temperature. A non-myristylated, transformation-defective mutant of v-Src did not phosphorylate Eps8, whereas it phosphorylated Shc. Together, these findings indicate that Eps8 may be a critical substrate of v-Src. They further establish Eps8 as an example of a signal transducer whose expression senses the balance between growth and differentiation and might, therefore, be involved in the determination of the phenotype.
- Published
- 1997
- Full Text
- View/download PDF
7. Transformation of NIH3T3 cells by Rous sarcoma virus occurs with high efficiency in the absence of proviral rearrangements or amplification.
- Author
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Falcone G, Provenzano C, Alemà S, and Tatò F
- Subjects
- 3T3 Cells, Animals, Mice, Oncogene Protein pp60(v-src) analysis, Avian Sarcoma Viruses genetics, Cell Transformation, Neoplastic, Cell Transformation, Viral, Gene Amplification, Gene Rearrangement, Genes, src, Proviruses genetics
- Abstract
NIH3T3 cells could be transformed by a mammaltropic strain of Rous sarcoma virus (RSV) with an efficiency 10(3) times greater than that observed in Balb/c 3T3 cells or other mammalian cell lines and almost identical to that of chick embryo fibroblasts. In infected NIH3T3 cells a single, properly integrated, provirus was sufficient to induce focus formation; moreover, kinase activity of pp60v-src and tyrosine phosphorylation of cellular proteins could be detected very soon after infection in the majority of cells. On the other hand, in transformed foci from RSV-infected Balb/c 3T3 cells both rearrangements and amplification of proviral sequences were frequently detected. Accordingly, expression of pp60v-src and ensuing tyrosine phosphorylation of cellular proteins occurred, at high levels, only in a minority of the infected cells. Furthermore, by using a murine retrovirus carrying the v-src oncogene and an independent selectable marker, we found that Balb/c 3T3 cells were transformed with a 100-fold lower efficiency than NIH3T3 cells, yet the majority of infected untransformed Balb/c 3T3 cells expressed active pp60v-src. These findings are consistent with the existence in most mammalian cell lines of a major restriction to v-src-induced transformation, operating at the level of proviral expression, that is apparently absent in NIH3T3 cells.
- Published
- 1992
8. Differential influence of adjacent normal cells on the proliferation of mammalian cells transformed by the viral oncogenes myc, ras and src.
- Author
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Bignami M, Rosa S, La Rocca SA, Falcone G, and Tatò F
- Subjects
- Animals, Carcinogens pharmacology, Cell Line, Genes, ras, Mice, Phorbol Esters pharmacology, RNA, Messenger genetics, Cell Adhesion, Cell Division, Cell Transformation, Viral drug effects, Oncogenes
- Abstract
We investigated the role of adjacent normal cells in the modulation of focal outgrowth of mammalian fibroblasts transformed by different viral oncogenes (myc, src and ras). NIH3T3 cells transformed by these three oncogenes were derived by transfection or infection and showed comparable cloning efficiencies in semi-solid medium. However, upon replating in liquid medium a small number of transformed cells together with a vast excess of normal mouse embryo fibroblasts C3H10T1/2, ras- and src-transformed cells were able to overgrow the monolayer and formed distinct foci, whereas myc-transformed cells lacked this ability. Conditioned medium from normal cells did not affect the proliferation of myc-transformed cells at clonal density. Addition of phorbol ester tumour promoters, either at the time of plating or as late as after one week, efficiently rescued focus formation by myc-transformed cells. In contrast, when myc-transformed cells were cultivated alone, their clone size and cloning efficiency were slightly reduced by the addition of tumour promoters. These results indicate that cell-cell contacts between transformed cells and adjacent normal cells specifically inhibit the growth of myc- but not of ras- or src-transformed cells. The ability of tumour promoters and phospholipase-C to rescue the focus forming ability of myc-transformed cells is consistent with the possibility that activation of protein-kinase C is involved in the clonal expansion of 'suppressed' myc-bearing cells.
- Published
- 1988
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