scholarly journals Ribonucleic acid synthesis in porphyric rat liver induced by 3,5-dicarbethoxy-1,4-dihydrocollidine

1973 ◽  
Vol 136 (1) ◽  
pp. 209-215 ◽  
Author(s):  
Hajime Nawata ◽  
Kenichi Kato
Keyword(s):  
Rat Liver ◽  
Liver Cell ◽  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Acid Synthesis ◽  
Rapid Decrease ◽  
Aminolaevulinic Acid ◽  
Induction Mechanism

1. Administration of 3,5-dicarbethoxy-1,4-dihydrocollidine to rats caused a marked increase in the activity of δ-aminolaevulinic acid synthetase as well as a slight net increase in RNA in the livers. 2. 3,5-Dicarbethoxy-1,4-dihydrocollidine primarily stimulated the synthesis of RNA in the nucleus of the liver cell. 3. The decrease in RNA synthesis after administration of this drug resulted in a rapid decrease in the activity of this induced enzyme. This was also confirmed by treatment with actinomycin D. 4. From kinetic experiments on synthesis of RNA and δ-aminolaevulinic acid synthetase in vivo the induction mechanism of this enzyme was discussed.

Hormone-induced differentiation of antheridial branches in Achlya ambisexualis: dependence on ribonucleic acid synthesis

1974 ◽  
Vol 20 (7) ◽  
pp. 977-980 ◽  
Author(s):  
David K. Horowitz ◽  
Peter J. Russell
Keyword(s):  
Sexual Differentiation ◽  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Steroid Hormone ◽  
Acid Synthesis ◽  
Aquatic Fungus ◽  
Induced Differentiation ◽  
Sexual Steroid ◽  
Achlya Ambisexualis

Sexual differentiation in male strains of the aquatic fungus Achlya ambisexualis Raper is induced by antheridiol, a sexual steroid hormone secreted by female strains. Antheridiol-induced initiation of the morphologically distinct antheridial branches in male Achlya is completely prevented when DNA-dependent RNA synthesis is inhibited by actinomycin D. In addition antheridial branch elongation is inhibited to a degree proportional to the concentration of actinomycin D added. Thus, evidence indicates that RNA synthesis is required for antheridiol-induced initiation of antheridial branching and that continued RNA synthesis is required for elongation of antheridial branches.

scholarly journals Decreased ribonucleic acid synthesis in isolated rat liver nuclei during starvation

1970 ◽  
Vol 120 (2) ◽  
pp. 381-384 ◽  
Author(s):  
D. Rickwood ◽  
H. G. Klemperer
Keyword(s):  
Rna Polymerase ◽  
Ammonium Sulphate ◽  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Acid Synthesis ◽  
Isolated Nuclei ◽  
Isolated Rat Liver ◽  
Liver Nuclei ◽  
Isolated Rat

1. Isolated nuclei from starved rats showed a lowered incorporation of [14C]UMP into RNA. 2. The Mg2+-dependent incorporation was decreased by 30% after 1 day of starvation, but incorporation in the presence of Mn2+ and ammonium sulphate decreased only after longer periods of starvation. 3. RNA synthesis by nuclei in the presence of excess of added RNA polymerase was unchanged after 1 day of starvation and was inhibited by 20% after 4 days. 4. The capacity of nuclei to bind actinomycin D was unchanged after 1 day and was decreased by 20% after 4 days of starvation.

GIBBERELLIN, AS A REGULATOR OF PROTEIN AND RIBONUCLEIC ACID SYNTHESIS DURING SENESCENCE IN LEAF CELLS OF TARAXACUM OFFICINALE

1966 ◽  
Vol 44 (6) ◽  
pp. 739-745 ◽  
Author(s):  
R. A. Fletcher ◽  
Daphne J. Osborne
Keyword(s):  
Leaf Senescence ◽  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Acid Synthesis ◽  
Taraxacum Officinale ◽  
Leaf Discs ◽  
Protein And Rna Synthesis ◽  
Chlorophyll Protein ◽  
Gibberellin Treatment

The addition of gibberellin A3 (GA) to leaf discs of Taraxacum officinale Weber retards their senescence and delays the decline in the levels of chlorophyll, protein, and RNA. Incorporation of 14C leucine and 14C adenine into protein and RNA respectively was increased by GA. This enhancement of protein and RNA synthesis did not occur if the discs were supplied with actinomycin D before treatment with gibberellin. If, however, actinomycin D was added after the gibberellin treatment then the stimulatory effect of the hormone was maintained. These results suggest that the retarding action of gibberellins on leaf senescence could be mediated through a regulation of RNA synthesis that is DNA dependent.

scholarly journals Effect of allylisopropylacetamide on Nuclear Ribonucleic Acid synthesis in rat liver

1975 ◽  
Vol 147 (1) ◽  
pp. 185-186 ◽  
Author(s):  
M K Sardana ◽  
M R Satyanarayana Rao ◽  
G Padmanaban
Keyword(s):  
Rat Liver ◽  
Enzyme Induction ◽  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Acid Synthesis ◽  
Potent Inducer

The porphyrogenic drug allylisopropylacetamide, a potent inducer of delta-aminolaevulinate synthetase, specifically increases nucleoplasmic RNA synthesis in rat liver. The drug-mediated increase in nucleoplasmic RNA synthesis is blocked by cycloheximide and haemin, which also inhibit the enzyme induction.

scholarly journals Studies of the ethylation of rat liver transfer ribonucleic acid after administration of l-ethionine

1972 ◽  
Vol 128 (1) ◽  
pp. 59-68 ◽  
Author(s):  
A. E. Pegg
Keyword(s):  
Rat Liver ◽  
Ribonucleic Acid ◽  
Major Part ◽  
Actinomycin D ◽  
Major Product ◽  
The Other ◽  
Methyl Donor ◽  
Principal Product

1. The ethylated nucleosides present in tRNA isolated from the livers of rats treated with 0.5g of l-ethionine/kg body wt. were investigated. Evidence that this tRNA contained N2-ethylguanine, N2N2-diethylguanine, N2-ethyl-N2-methylguanine, 7-ethylguanine, two ethylated pyrimidines and ethylated ribose groups was obtained. 2. Ethylation of bacterial tRNA was catalysed by extracts containing tRNA methylases prepared from rat liver by using S-adenosyl-l-ethionine as an ethyl donor, but the rate of ethylation was 20 times less than the rate of methylation with S-adenosyl-l-methionine as a methyl donor. 3. The principal product of such ethylation in vitro was N2-ethylguanine and traces of the other ethylated guanines and pyrimidines found in tRNA isolated from rats treated with ethionine in vivo were also found. 1-Ethyladenine was not formed, although 1-methyl-adenine is a major product of methylation of bacterial tRNA by these extracts, and 1-ethyladenine was not present in the rat liver tRNA isolated from ethionine-treated animals. 4. After injection of actinomycin D (15mg/kg body wt.) or l-methionine (1.0g/kg body wt.) before the ethionine, ethylation of tRNA was diminished by about 80% but not completely abolished. Administration of 1-aminocyclopentanecarboxylic acid (2.5g/kg body wt.) to inhibit the formation of S-adenosyl-l-ethionine inhibited ethylation of tRNA by 44%. 5. These results suggest that not all of the ethylation of tRNA that occurs in the livers of rats treated with ethionine is mediated by the action of tRNA methylases acting with S-adenosyl-l-ethionine as a substrate, but that this pathway does occur and accounts for a major part of the observed ethylation. 6. The results are discussed with reference to ethionine-induced hepatocarcinogenesis.

scholarly journals Effect of chloramphenicol on ribonucleic acid synthesis in liver cells in suspension

1965 ◽  
Vol 97 (1) ◽  
pp. 67-73 ◽  
Author(s):  
ST Jacob ◽  
PM Bhargava
Keyword(s):  
Rat Liver ◽  
Liver Cell ◽  
Ribonucleic Acid ◽  
Acid Synthesis ◽  
Inhibitory Effect ◽  
Cell Suspensions ◽  
Perfused Rat Liver ◽  
Tissue Slices ◽  
Hepatic Cells ◽  
Liver Homogenates

1. Chloramphenicol has a stimulatory effect on the incorporation of radioactive phosphate into the RNA of perfused rat-liver slices, whole liver homogenates or the liver-cell suspensions, and no effect on the incorporation of [(14)C]adenine and [(14)C]uracil into the RNA of the tissue slices. 2. Chloramphenicol completely inhibits the incorporation of labelled adenine and uracil into the RNA of the cell suspensions, or into the RNA of homogenates derived from the whole liver tissues. 3. Chloramphenicol has at most a slight inhibitory effect on the transport of labelled adenine or uracil in the hepatic cells in suspension; in the slices, the transport of these bases is not inhibited at all. 4. The above observations indicate that: (a) unlike the tissue slices, hepatic cells in suspension are permeable to chloramphenicol; (b) in the presence of chloramphenicol, for reasons that are not clear, the conversion of the base into the appropriate nucleotide does not proceed.

ULTRASTRUCTURAL EVIDENCE FOR THE STIMULATION OF NUCLEAR RIBONUCLEIC ACID SYNTHESIS BY OESTRADIOL-17β IN THE VAGINAL EPITHELIUM OF THE OVARIECTOMIZED MOUSE

1970 ◽  
Vol 47 (2) ◽  
pp. 143-NP ◽  
Author(s):  
IRINA POLLARD
Keyword(s):  
Ribonucleic Acid ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Control Level ◽  
Staining Technique ◽  
Acid Synthesis ◽  
Vaginal Epithelium ◽  
Ovariectomized Mouse ◽  
Ultrastructural Evidence ◽  
Stimulation Of

SUMMARY The cytochemical nature of the ultrastructural nucleolar transformation previously observed in the vaginal epithelium of the ovariectomized mouse after local application of oestradiol-17β was investigated using a recently developed ultrastructural staining technique. Oestradiol treatment induced ribonucleic acid (RNA) synthesis, especially in the nucleolus but also in the nuclear chromatic region and ribosomes. Actinomycin D administered simultaneously with oestradiol reduced the oestrogen-induced nucleolar response to the control level. These findings are discussed with special reference to the mode of action of oestrogens.

scholarly journals Ribonucleic acid synthesis in vitro in primary spermatocytes isolated from rat testis

1977 ◽  
Vol 168 (1) ◽  
pp. 23-31 ◽  
Author(s):  
J. Anton Grootegoed ◽  
Anne H. Grollé-Hey ◽  
Focko F. G. Rommerts ◽  
Henk J. Van Der Molen
Keyword(s):  
Electrophoretic Mobility ◽  
Rna Synthesis ◽  
Actinomycin D ◽  
Marked Change ◽  
Acid Synthesis ◽  
Specific Pattern ◽  
28S Rrna ◽  
Phenol Extraction

The incorporation of [3H]uridine into RNA was studied quantitatively (by incorporation of [3H]uridine into acid-precipitable material) and qualitatively (by phenol extraction and electrophoretic separation of RNA in polyacrylamide gels) in preparations enriched in primary spermatocytes, obtained from testes of rats 26 or 32 days old. The rate of incorporation of [3H]uridine into RNA of isolated spermatocytes was constant during the first 8h of incubation, after which it decreased, but the decreased rate of incorporation was not reflected in a marked change in electrophoretic profiles of labelled RNA. In isolated spermatocytes, [3H]uridine was incorporated mainly into heterogeneous RNA with a low electrophoretic mobility. Most of this RNA was labile, as shown when further RNA synthesis was inhibited with actinomycin D. Spermatocytes in vivo also synthesized heterogeneous RNA with a low electrophoretic mobility. A low rate of incorporation of [3H]uridine into rRNA of isolated spermatocytes was observed. The cleavage of 32S precursor rRNA to 28S rRNA was probably retarded in spermatocytes in vitro as well as in vivo. RNA synthesis by preparations enriched in early spermatids or Sertoli cells was qualitatatively different from RNA synthesis by the spermatocyte preparations. It is concluded that isolated primary spermatocytes maintain a specific pattern of RNA synthesis, which resembles RNA synthesis in spermatocytes in vivo. Therefore isolated spermatocytes of the rat can be used for studying the possible regulation of RNA synthesis during the meiotic prophase.

Effect of Some Metabolic Inhibitors on Vinblastine-Induced Ribosomal-Granular Material Complexes

1971 ◽  
Vol 29 ◽  
pp. 548-549
Author(s):  
Awtar Krishan ◽  
Dora Hsu
Keyword(s):  
Granular Material ◽  
Rna Synthesis ◽  
Culture Medium ◽  
Actinomycin D ◽  
Metabolic Inhibitors ◽  
Protein And Rna Synthesis ◽  
Apparent Reduction ◽  
Plant Alkaloids ◽  
In Cells

Cells exposed to antitumor plant alkaloids, vinblastine and vincristine sulfate have large proteinacious crystals and complexes of ribosomes, helical polyribosomes and electron-dense granular material (ribosomal complexes) in their cytoplasm, Binding of H3-colchicine by the in vivo crystals shows that they contain microtubular proteins. Association of ribosomal complexes with the crystals suggests that these structures may be interrelated.In the present study cultured human leukemic lymphoblasts (CCRF-CEM), were incubated with protein and RNA-synthesis inhibitors, p. fluorophenylalanine, puromycin, cycloheximide or actinomycin-D before the addition of crystal-inducing doses of vinblastine to the culture medium. None of these compounds could completely prevent the formation of the ribosomal complexes or the crystals. However, in cells pre-incubated with puromycin, cycloheximide, or actinomycin-D, a reduction in the number and size of the ribosomal complexes was seen. Large helical polyribosomes were absent in the ribosomal complexes of cells treated with puromycin, while in cells exposed to cycloheximide, there was an apparent reduction in the number of ribosomes associated with the ribosomal complexes (Fig. 2).

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