Delayed inhibition of DNA synthesis in mouse jejunum by low doses of Actinomycin D

1966 ◽  
Vol 68 (2) ◽  
pp. 177-184 ◽  
Author(s):  
Renato Baserga ◽  
Richard D. Estensen ◽  
Robert O. Petersen
1966 ◽  
Vol 22 (5) ◽  
pp. 294-295 ◽  
Author(s):  
H. Rothstein ◽  
J. Fortin ◽  
D. Sonneborn

1971 ◽  
Vol 49 (2) ◽  
pp. 498-506 ◽  
Author(s):  
V. L. Rudick

Changes in the levels of DNA and RNA syntheses have been studied in unagitated cultures of Acanthamoeba castellanii during the phases of logarithmic multiplication (LM) and population growth deceleration (PGD). Pulse-labeling experiments show that the rate of DNA synthesis decreases at the same time that DNA per cell is known to drop by 50%. The drop in DNA content has been explained by demonstrating with hydroxyurea that the majority of LM amebas can replicate once when DNA synthesis is inhibited and, therefore, must be in G2, whereas the PGD amebas cannot multiply in the presence of inhibitor and, therefore, must be in G1. The inhibition of DNA synthesis in LM or PGD cells has been shown to induce encystment. The rate of RNA synthesis, as illustrated by pulse-labeling experiments, increases 25% in late LM-early PGD while RNA per cell increases 75%. The rate of synthesis then decreases 65%. The majority of accumulated RNA has been demonstrated to be ribosomal by disc electrophoresis. By using actinomycin D at different stages during the RNA build-up, the ability of the amebas to encyst has been shown to depend on the presence of this RNA. The observations on DNA and RNA are discussed with respect to the occurrence of cysts in the cultures during PGD.


Genetics ◽  
1973 ◽  
Vol 73 (4) ◽  
pp. 583-596
Author(s):  
B K Vig

ABSTRACT Glycine max (soybean) is the only known higher plant with a definitely established occurrence of somatic crossing over. This material lends itself to the analysis of somatic crossing over, gross chromosomal aberrations and mutations, all of which may be induced by the same treatment of the mutagen given to seeds. This is made possible because gene Y11 for chlorophyll development in the variety L65-1237 is incompletely dominant over its allele y11, so that twin or double spots composed of a dark green (Y 11 Y 11)and a yellow (Y 11 Y 11) component can be observed adjacent to and as mirror images of each other on the light green Y 11 Y 11 leaves in the areas of complementary exchange for these genes. Lack of growth of either component of this double spot as well as several types of chromosomal disturbances give rise to single spots resembling phenotypes of Y 11 Y 11 or Y 11 Y 11 leaves. Point mutations can be studied by looking for green sectors originating from Y 11 Y 11 genotype on the Y 11 Y 11 plants. Seeds obtained from heterozygous plants were treated with caffeine, cytosine arabinoside, actinomycin D and 5-fluoro-deoxyuridine, all known inhibitors of DNA synthesis, and puromycin, an inhibitor of synthesis of proteins. The treatments with caffeine and actinomycin D increased the frequency of somatic crossing over as measured by the frequency of double spots on Y 11 Y 11 leaves, but cytosine arabinoside, 5-fluorodeoxyuridine and puromycin did not. Thus somatic crossing over was induced only by those chemicals which are known to allow rejoining of chromosomes, thereby suggesting a correlation between the two phenomena. These observations indicate that it is not the mere inhibition of DNA synthesis, but some rather more specific event in DNA repair which is responsible for complementary exchanges. Some of these results differ from studies carried out with fungi. The main effect of all chemicals tested, except caffeine and actinomycin D, was inferred to be the production of deletions in Y 11 Y 11 plants which raised the frequency of single (dark green or yellow) spots relative to the doubles. Caffeine was the only chemical which constantly increased the frequency of specific point mutations. In the control material, the great majority of spots are found on the upper surface of the leaf. This picture could not be changed in any of the treated materials, thus indicating uniform resistance of spongy mesophyll tissue to the mutagens applied.


1992 ◽  
Vol 267 (2) ◽  
pp. 691-694 ◽  
Author(s):  
V J LaMorte ◽  
P K Goldsmith ◽  
A M Spiegel ◽  
J L Meinkoth ◽  
J R Feramisco

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