PubMed Health⌕ Search

Biomedical subjects

W D Taylor

Publications and source records attributed to W D Taylor.

At least 19 recordsLinked to original sources
PubMed1992

Cell density dependence of ultraviolet light enhanced reactivation of Herpes simplex type I and the large plaque effect in C3H/10T1/2 mouse fibroblasts.

C3H/10T1/2 mouse fibroblasts were grown to different cell densities either by plating at low density and allowing different growth periods, or by plating at a series of increasing densities and allowing the same growth period. These plates were UV irradiated at 7.5 J/m2 or mock irradiated and 24 h later infected with UV-irradiated Herpes simplex type I virus which had been UV irradiated at 50 or 125 J/m2 or mock irradiated. The numbers and sizes of plaques were measured and these data used to calculate the extent of UV-enhanced host cell reactivation, the capacity enhancement, the large plaque effect (LPE) and the small plaque effect (SME). The influence of cell density on these phenomena was similar for both series of density experiments. Ultraviolet-enhanced host cell reactivation could be demonstrated only for cultures of lower density. The capacity of the cells for Herpes simplex type I virus decreased with cell density, but UV irradiated cells showed an increase in capacity with cell density. Plaque sizes decreased in all cases with cell density but the LPE and SPE were not significantly altered. The greatest variation in the above parameters occurred just as the cells were approaching confluence, where most host cell reactivation experiments are carried out. We conclude that the reproducibility of such experiments depends critically on cell density, a dependence which may be relevant to mechanistic interpretations of the UV-dependent phenomena.

Animals↗
PubMed1991

Ultraviolet light-induced plasmid-chromosome recombination in Escherichia coli: the role of recB and recF.

Bacterial host cells of different rec genotypes were used to investigate genetic requirements of ultraviolet light (UV)-induced homologous plasmid-chromosome recombination. Plasmid DNAs which contained a wt or mutant lacY gene were irradiated with UV prior to transformation into Escherichia coli host strains which contained the complementary lacY allele. Surviving transformants were screened to determine the directions of UV-induced recombinational exchange between the bacterial and plasmid lacY genes, by assaying lactose utilization. Nonreciprocal chromosome-to-plasmid recombination was 100% dependent on the recA gene and greater than 80% dependent on the recF gene, but not dependent upon the recB gene of E. coli. In contrast, reciprocal plasmid-chromosome recombination was strictly dependent on the recA gene, greatly dependent (approx. 80%) on the recF gene, and moderately dependent on the recB gene. Nonreciprocal plasmid-to-chromosome recombination was only induced at very low frequencies, and appeared to be moderately dependent on the recB gene, but not dependent on the recF gene. UV-induced plasmid-chromosome recombination appeared to proceed by a two-step mechanism. In this model, the initial step is recF-dependent, recB-independent, and either resolves to become a nonreciprocal chromosome-to-plasmid recombinant, or proceeds to the second step. The second step is moderately recB-dependent and results in the reciprocal exchange of plasmid-chromosome sequences.

Bacterial Proteins↗
PubMed1990

Recombination between irradiated shuttle vector DNA and chromosomal DNA in African green monkey kidney cells.

An autonomously replicating shuttle vector was used to investigate enhancement of plasmid-chromosome recombination in mammalian host cells by gamma irradiation and UV light. Sequences homologous to the shuttle vector were stably inserted into the genome of African green monkey kidney cells to act as the target substrate for these recombination events. The shuttle vector molecules were irradiated at various doses before transfection into the mammalian host cells that contained the stable insertions. The homologous transfer of the bacterial ampicillin resistance gene from the inserted sequences to replace a mutant ampicillin sensitivity gene on the shuttle vector was identified by the recovery of ampicillin-resistant plasmids after Hirt extraction and transformation into Escherichia coli host cells. Gamma irradiation increased homologous shuttle vector-chromosome recombination, whereas UV light did not increase the frequency of recombinant plasmids detected. Introducing specific double-strand breaks in the plasmid or prolonging the time of plasmid residence in the mammalian host cells also enhanced plasmid-chromosome recombination. In contrast, plasmid mutagenesis was increased by UV irradiation of the plasmid but did not change with time. The ampicillin-resistant recombinant plasmid molecules analyzed appeared to rise mostly from nonconservative exchanges that involved both homologous and possibly nonhomologous interactions with the host chromosome. The observation that similar recombinant structures were obtained from all the plasmid treatments and host cells used suggests a common mechanism for plasmid-chromosome recombination in these mammalian cells.

Animals↗
PubMed1990

Developmental factors and performance in remedial courses.

This study investigated the relations between various developmental factors and performance in remedial courses. The Iowa Developing Autonomy Inventory, Iowa Managing Emotions Inventory, and Iowa Developing Competency Inventory were administered to 231 students enrolled in a developmental studies program at a large state university (enrollment about 25,000). Regression analyses indicated that various developmental measures accounted for a small effect (amount of variance accounted for ranged from 2% to 7%) on performance in remedial courses. The percentage of variance accounted for by the three inventories was similar to what could be accounted for by more traditional measures of SAT scores and high-school grade point averages. The percentage of variance accounted for by traditional measures ranged from 2% to 10%.

Achievement↗
PubMed1990

Homologous recombination and mutagenesis of gamma-irradiated plasmid DNA in Escherichia coli host cells.

Plasmid DNA was used to study gamma-radiation-induced recombination and mutagenesis in Escherichia coli host cells. Plasmid pBRP1, a derivative of pBR322 containing the lac operon of E. coli, was irradiated with 60Co gamma rays prior to transformation into E. coli strains of different recA and lac genotypes. Plasmid-chromosome recombination was assayed in lacY1 host cells, whereas plasmid mutagenesis was assayed in delta lac host cells lacking chromosomal sequences homologous to the plasmid. Both recombinant and mutant plasmids were identified by the phenotypic changes in lactose utilization, and confirmed by restriction analysis of isolated plasmids. Plasmid-chromosome recombination was induced to high levels (about 20% of survivors at 700 Gy) and was dependent on the host recA gene. Plasmid mutagenesis occurred at lower levels (about 1.5% of survivors at 600 Gy) and was relatively independent of the recA gene. Plasmid survival was unaffected by the presence or absence of host recA mutations or the potential for plasmid-chromosome recombination.

Cobalt Radioisotopes↗
PubMed1988

Expression of the rat growth hormone gene in transfected CV-1 cells.

Expression of the cloned rat growth hormone gene was studied in transfected CV-1 cells. Cell lines expressing rat growth hormone synthesized and secreted the 22 kilodalton form and the 20 kilodalton variant. The results confirm that the 20 kilodalton variant arises from an alternatively spliced mRNA rather than expression from a variant gene in rat. The 5' end of the mRNA from expressing cell lines was located upstream of the normal initiation site in rat. Transcription initiated within a 5' flanking AT rich sequence. Results presented indicate that transcription from normally silent promoter or promoter-like sequences dictated rat growth hormone gene expression in transfected cells. Finally, no hormone was expressed by CV-1 cells transfected with a plasmid containing the rat growth hormone gene in the same transcriptional reading frame as the neomycin resistance gene of pSV2neo indicating an effect of cloning orientation on expression in CV-1 cells.

Animals↗
PubMed1987

Alternative splicing model for the synthesis and secretion of the 20 kilodalton form of rat growth hormone.

The characterization of a 20 kilodalton (20 kD) variant of rat growth hormone is reported. The 20 kD variant from rat pituitary gland extracts was identified on Western immunoblots of polyacrylamide gels. It was also shown that pituitary tissue maintained in culture secretes the 20 kD form. A rat growth hormone cDNA fragment was used as a probe in S1 nuclease mapping experiments of rat pituitary poly (A) mRNA to detect the presence of two growth hormone mRNAs in the rat pituitary gland. The protected mRNAs correspond to the predicted sizes that would encode the 22 kD and 20 kD forms of growth hormone. The site of variation between the mRNAs maps to a potential alternative 3' splice site in the 5' end of exon 3 of the coding sequence. The results support the hypothesis that the 20 kD variant in rat is the product of an mRNA alternatively spliced in exon 3, as is the case for the human growth hormone.

Animals↗
PubMed1986

Reciprocal and non-reciprocal homologous recombination between Escherichia coli chromosomal DNA and ultraviolet light-irradiated plasmid DNA.

Plasmid DNA substrates were used to study ultraviolet (UV)-induced recombination events in Escherichia coli host cells. Plasmids derived from pBR322, containing all or part of the lac operon of E. coli, were irradiated with ultraviolet light before transformation into E. coli strains of different recA and lacY genotypes. Recombinational exchanges were identified by phenotypic changes in lactose utilization and were confirmed by restriction analysis of isolated plasmids. Ultraviolet-induced reciprocal plasmid-chromosome recombination occurred at a slightly higher frequency then non-reciprocal chromosome-to-plasmid recombination, and at a much higher frequency than non-reciprocal plasmid-to-chromosome recombination. These frequencies did not depend on segregative mechanisms. The asymmetry of non-reciprocal exchange was not due to the particular arrangement of wild-type and lacY1 alleles because the same results were observed when these were interchanged. The host recA gene was required for plasmid-chromosome recombination, and slightly enhanced plasmid survival. Evidence for plasmid replication prior to recombination was found in reciprocal recombinants, but rarely in the non-reciprocal recombinants analyzed. Irradiation of competent bacterial host cells prior to transformation did not effectively induce plasmid-chromosome recombination.

DNA, Bacterial↗
PubMed1985

Parvovirus infection in pigs with necrotic and vesicle-like lesions.

Porcine parvovirus was isolated from many visceral organs and also from the brain, serum and skin specimens of swine with vesicular-like conditions. Severe lesions were reported to have occurred in the mouth, on the tongue and snout, on the coronary band and in the interdigital spaces. Also, parvoviral antigens were demonstrated, by immunofluorescence, in the outer layers of hair follicles in skin adjacent to coronary band lesions.

Animals↗
PubMed1984

The fate and impact of oil and oil-dispersant mixtures in freshwater pond ecosystems: introduction.

Oil and oil-dispersant mixtures were added to the surface waters of a series of man-made ponds. The fate of the oil and dispersant (Norman Wells crude and Corexit 9527 respectively) were studied as well as the impact of the added chemicals on the ponds' ecosystems. Elements of the ecosystems studied include bacteria, fungi, phytoplankton, periphyton , proto- and mesozooplankton , zoobenthos and surface insects. In addition a number of water quality parameters were regularly monitored. Comparisons were made between oil-treated and control ponds, as well as oil-dispersant treated and oil and/or control ponds. This paper describes the experimental set up and provides a summary of the findings reported in the following five papers.

Animals↗
PubMed1984

Impact of oil and oil-dispersant mixtures on the fauna of freshwater ponds.

In a series of 5 artificial ponds, one was treated with a nomial concentration of 100 ppm of crude oil, two others were treated with a nominal 100 ppm of oil and 20 ppm of dispersant. Mesozooplankton populations were reduced in the oil-treated pond relative to the control pond, and eliminated in the oil-dispersant ponds. This condition persisted until the following year when the mesozooplankton was similar in all ponds. The protozooplankton experienced species shifts with Halteria and Strobilidium being eliminated initially in all treated ponds, but Halteria was collected in samples the following spring. Other protozoans such as thecamoebae increased in the treated ponds, while others, like zooflagellates , did not appear to be affected by the chemicals. Zoobenthos was affected by treatment, with the number of different types being reduced. The zoobenthos had recovered in one of the treated ponds the following spring, and that in the other treated ponds were recovering. Surface insects were eliminated after treatment, but recolonized during the next spring. Nekton were initially reduced by treatment. The population changes are discussed with respect to the fate of oil.

Animals↗
PubMed1984

Diffusion of a small molecule in the cytoplasm of mammalian cells.

Electron spin resonance was used to measure the diffusion of a small (Mr 170) spin label in the aqueous cytoplasm of mammalian cells. Translational and rotational motion were determined from the same spectra. Based on measurements made in model systems, it was hypothesized that calculations of the apparent viscosity from either rotational or translational motion would distinguish between the effects of cytoplasmic viscosity or cytoplasmic structure on diffusion. The diffusion coefficient calculated from spin label collision frequency, averaged 3.3 X 10(-6) cm2/sec in several cell lines. It was greater in growing cells and in cells treated with cytochalasin B than in quiescent cells. The viscosity of the cytoplasm calculated from the translational diffusion coefficient or the rotational correlation time was 2.0-3.0 centipoise (1 P = 0.1 Pa X sec), about 2-3 times that of the spin label in water. Therefore, over the dimensions measured by the technique, 50-100 A, solvent viscosity appears to be the major determinant of particle movement in cells under physiological conditions. However, when cells were subjected to hypertonic conditions, the translational motion decreased by 67%, while the rotational motion changed less than 20%. These data suggested that the decrease in cell volume under hypertonic conditions was accompanied by an increase in cytoplasmic barriers and a decrease in the spacing between existing components. In addition, a comparison of reported values for diffusion of a variety of molecules in water and in cells indicates that cytoplasmic structure plays an important role in the diffusion of proteins such as bovine serum albumin.

Animals↗
PubMed1984

Stimulation of recombination between homologous sequences on plasmid DNA and chromosomal DNA in Escherichia coli by N-acetoxy-2-acetylaminofluorene.

A plasmid containing a wild-type lac operon and a tetracycline-resistance gene was covalently modified by N-acetoxy-2-acetylaminofluorene and used to transform two series of Lac- Escherichia coli cell types. Each set contained wild-type and repair-deficient mutants. One set of cells contained a lacY mutation and the other a deletion of the entire lac operon. Survival and mutagenesis of the plasmid were measured as a function of the N-acetoxy-2-acetylaminofluorene concentration. The results indicate that when no homologous sequences are present in the chromosomal DNA, mutations occur at a low frequency: at 10% survival the frequency was 1-2 X 10(-4) mutants per transformant. When homologous sequences, the lacY allele, are present in the chromosomal DNA, Lac- plasmids are found at a high frequency in a recA-dependent, lexA-independent fashion: at 10% survival the frequency was 5-10 X 10(-2) mutants per transformant. Southern blot analysis of the restriction enzyme profiles of the resulting plasmid and host-cell DNA sequences showed recombinational transfer of host sequences to the N-acetoxy-2-acetylamino-fluorene-treated plasmid had occurred. When the host chromosomes contained Lac+ homologous sequences no mutants were found, indicating that the results were not caused by error-prone recombination.

2-Acetylaminofluorene↗