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Effects of neocarzinostatin on chromatin in HeLa S3 nuclei

TA Beerman, G Mueller and H Grimmond

Neocarzinostatin solubilizes chromatin from HeLa S3 nuclei by introducing strand scissions in linker regions. Multimeric nucleosome patterns are seen on both native and denaturing gel analysis. The mechanism of drug action differs from the type of chromatin digestion seen with micrococcal enzyme in that DNA damage occurs through single- strand breaks and less acid-soluble material is produced. In addition, drug-induced release of soluble chromatin from the nuclei is not very dependent upon the addition of EDTA. The monomer repeat size is larger than that found for micrococcal enzyme and contains linker regions that are partially single-stranded. Core histone proteins as well as histone H1 do not appear to be altered by drug action, although there is clear evidence that DNA damage can occur in nucleosome cores. The chromophore portion of the drug degrades chromatin as effectively as the holoantibiotic.

Volume 23, Issue 2, pp. 493-499, 03/01/1983
Copyright © 1983 by American Society for Pharmacology and Experimental Therapeutics




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J. Bacteriol.Home page
B. Heyd, G. Lerat, E. Adjadj, P. Minard, and M. Desmadril
Reinvestigation of the Proteolytic Activity of Neocarzinostatin
J. Bacteriol., April 1, 2000; 182(7): 1812 - 1818.
[Abstract] [Full Text]




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Copyright © 1983 by the American Society for Pharmacology and Experimental Therapeutics