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Biomedical subjects

R Baserga

Publications and source records attributed to R Baserga.

At least 235 records · Page 13Linked to original sources
PubMed1981

Characterization and biological activity of cloned simian virus 40 DNA fragments.

The biological activity of fragments of the SV40 genome was determined by manual microinjection of the fragments into the nuclei of mammalian cells. Fragments of the SV40 A gene (that codes for the T antigens) were obtained either directly by digestion with restriction endonucleases or after cloning into plasmid pBR322. Three different biological activities were studied: expression of T antigen, induction of cell DNA synthesis, and, in a few cases, reactivation of repressed ribosomal RNA genes. By using a number of fragments with deletions in the various portions of the SV40 A gene, we have been able to conclude that: 1) the sequences from 0.65 to 0.51 map units are not needed for the induction of cell DNA synthesis; 2) the sequences from 0.42 to 0.17 map units are not needed for the induction of cell DNA synthesis; and 3) the critical sequences for the induction of cell DNA synthesis, 0.51 to 0.42 map units, are different from those necessary for the reactivation of repressed ribosomal RNA genes (0.39-0.33 map units). These results indicate that the information for these two fundamental processes of cell proliferation resides in two separate and distinct domains of the SV40 A gene.

Animals↗
PubMed1981

The cell cycle.

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Animals↗
PubMed1981

Routine growth of cell lines in medium supplemented with milk instead of serum.

Several cell lines can be grown in media, supplemented with milk instead of serum. To obtain a good plating efficiency the medium containing milk must be supplemented with calf serum at a final concentration of 0.5%. The milk must be centrifuged before use to get rid of the fat and cellular debris. Using these precautions several monolayer cell lines can be grown routinely in milk supplemented media, just as well as in serum supplemented media. The economic advantages of using milk instead of serum are considerable.

Animals↗
PubMed1981

Identification of adenovirus 2 early genes required for induction of cellular DNA synthesis in resting hamster cells.

tsAF8 cells are temperature-sensitive (ts) mutants of BHK-21 cells that arrest at the nonpermissive temperature in the G1 phase of the cell cycle. When made quiescent by serum restriction, they can be stimulated to enter the S phase by 10% serum at 34 degrees C, but not at 40.6 degrees C. Infection by adenovirus type 2 or type 5 stimulates cellular DNA synthesis in tsAF8 cells at both 34 and 40.6 degrees C. Infection of these cells with deletion Ad5dl312, Ad5dl313, Ad2 delta p305, and Ad2+D1) and temperature-sensitive (H5ts125, H5ts36) mutants of adenovirus indicates that the expression of both early regions 1A and 2 is needed to induce quiescent tsAF8 cells to enter the S phase at the permissive temperature. This finding has been confirmed by microinjection of selected adenovirus DNA fragments into the nucleus of tsAF8 cells. In addition, we have shown that additional viral functions encoded by early regions 1B and 5 are required for the induction of cellular DNA synthesis at the nonpermissive temperature.

Adenoviruses, Human↗
PubMed1981

Induction of cellular deoxyribonucleic acid synthesis in butyrate-treated cells by simian virus 40 deoxyribonucleic acid.

Sodium butyrate (3 mM) inhibited the entry into the S phase of quiescent 3T3 cells stimulated by serum, but had no effect on the accumulation of cellular ribonucleic acid. Simian virus 40 infection or manual microinjection of cloned fragments from the simian virus 40 A gene caused quiescent 3T3 cells to enter the S phase even in the presence of butyrate. NGI cells, a line of 3T3 cells transformed by simian virus 40, grew vigorously in 3 mM butyrate. Homokaryons were formed between G1 and S-phase 3T3 cells, Butyrate inhibited the induction of deoxyribonucleic acid synthesis that usually occurs in B1 nuclei when G1 cells are fused with S-phase cells. However, when G1 3T3 cells were fused with exponentially growing NGI cells, the 3T3 nuclei were induced to enter deoxyribonucleic acid synthesis. In tsAF8 cells, a ribonucleic acid polymerase II mutant that stops in the G1 phase of the cell cycle, no temporal sequence was demonstrated between the butyrate block and the temperature-sensitive block. These results confirm previous reports that certain virally coded proteins can induce cell deoxyribonucleic acid synthesis in the absence of cellular functions that are required by serum-stimulated cells. Our interpretation of these data is that butyrate inhibited cell growth by inhibiting the expression of genes required for the G0 leads to G1 leads to S transition and that the product of the simian virus 40 A gene overrode this inhibition by providing all of the necessary functions for the entry into the S phase.

Animals↗
PubMed1980

Failure of accumulation of cellular RNA in hamster cells stimulated to synthesize DNA by infection with adenovirus 2.

AF8 cells are temperature-sensitive mutants of the cell cycle derived from baby hamster kidney (BHK) cells which arrest in the G1 phase when incubated at the nonpermissive temperature. RNA accumulation was studied in these cells by flow cytofluorimetry following serum stimulation or adenovirus 2 infection. Serum stimulation caused an increase in the amount of RNA per cell, which reached a maximum in S and G2 cells, as repeatedly reported in the literature. However, adenovirus 2 infection caused a fraction of cells to enter S phase without any concomitant increase in the amount of RNA per cell.

Adenoviruses, Human↗
PubMed1980

The narrow gauge.

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Educational Measurement↗
PubMed1980

Changes in RNA polymerase II in a cell cycle-specific temperature-sensitive mutant of hamster cells.

tsAF8 cells are a temperature-sensitive mutant of BHK cells that arrest at the nonpermissive temperature in the G1 phase of the cell cycle. The activity of solubilized RNA polymerase II and its ability to bine [3H]-gamma-amanitin decrease in tsAF8 cells at 40.6 degrees, with a half-life of approximately 10 hr. No appreciable changes occur in these two parameters in tsAF8 cells at 34 degrees or in BHK cells at either 34 degrees or 40.6 degrees. Protein synthesis is not appreciably affected for at least 24 hr after tsAF8 cells are shifted to 40.6 degrees. These results indicate that in tsAF8 cells at the nonpermissive temperature, there is a defect in either the synthesis, the assembly, or the stability of RNA polymerase II, and that the loss of RNA polymerase II molecules is not due to widespread cellular damage.

Amanitins↗
PubMed1980

Reactivation of G0 nuclei by S-phase cells.

tsAF8 cells are a temperature sensitive (ts) mutant of BHK that arrest in G1 at the nonpermissive temperature or after serum deprivation. G0 tsAF8 were fused by polyethylene glycol with other G0 tsAF8 cells, and the fusion products were incubated at the nonpermissive temperature. The homokaryons were incapable of entering S phase under these conditions. However, when S phase tsAF8 cells were fused with G0 tsAF8 cells, both nuclei in the homokaryons entered S phase, even when the fusion products were incubated at the nonpermissive temperature. In addition S phase tsAF8 cells, if fused with chick erythrocytes, can reactivate the chick nucleus, even if the heterokaryons are placed at nonpermissive temperature. Therefore S phase information of tsAF8 can induce DNA synthesis, after fusion, in mammalian G0 AF8 cells and chick erythrocytes even when the homokaryons or heterokaryons are incubated at the nonpermissive temperature.

Animals↗
PubMed1980

Reactivation of ribosomal RNA genes in human-mouse hybrid cells by 12-O-tetradecanoylphorbol 13-acetate.

The effect of the potent tumor promoter 12-O-tetradecanoylphorbol 13-acetate (TPA) on the expression of rRNA genes was studied in human greater than mouse hybrid cells (55-54 cells). These hybrids retain the rRNA genes of both parent species but express only human rRNA. 55-54 cells were treated with either TPA (1-100 nM), phorbol (0.01-1 micro M) or phorbol 13,20-diacetate (0.01-1 micro M). After 24 hr the cells were harvested and the extracted rRNA was analyzed by agarose/2.4% polyacrylamide gel electrophoresis. The results show that only the TPA-treated hybrid cells synthesized both human and mouse 28S rRNA. Untreated cells and cells treated with phorbol or phorbol 13,20-diacetate synthesized only human 28S rRNA. The reactivation of silent rRNA genes by TPA was not restricted to mouse rRNA genes. In mouse-human hybrids in which both human and mouse rRNA genes are present but only the mouse genes are expressed, TPA treatment led to reactivation of the silent human rRNA genes. Although tumor promoters are generally believed to alter gene expression, we have found a specific gene whose transcription is modified by treatment with TPA.

Animals↗
PubMed1980

Increase in cellular RNA in cells infected with DNA oncogenic viruses.

The amount of RNA per cell has been measured by flow microfluorometry in cultured cells stimulated by serum or infected with DNA oncogenic viruses (SV40, polyoma virus, and adenovirus). While all four agents stimulate, although to a different extent, cellular DNA synthesis in quiescent cells, the accumulation of cellular RNA varies. Serum, SV40, and polyoma virus cause a marked increase in total cellular RNA that is already apparent in G1 cells before entry into S. On the other hand, adenovirus 2, while capable of stimulating cellular DNA synthesis, fails to detectably increase the amount of RNA per cell. These results suggest that adenovirus 2 may act on quiescent cells through mechanisms different from those of serum, SV40, or polyoma virus.

Acridines↗
PubMed1980

Control of cell proliferation in transformed cells.

We have presented evidence that T-ag of SV40 reactivates silent rRNA genes. Since rRNA synthesis correlates with growth rates, it is conceivable that T-ag may stimulate cell proliferation by acting on rRNA genes. In SV40-transformed, T-positive cells, this would and does result in continuous cell proliferation, beyond the limits of that in normal cells.

Animals↗