Abstract
Nuclear extracts of 3T6 mouse cells were able to assemble in vitro minichromosomes which displayed a 150‐bp periodicity. Activities of both DNA topoisomerases I and II were detected in these extracts. When a supercoiled pUC DNA was added, it was first relaxed in less than 3 min, then slowly supercoiled again in 1–4 h. Both reactions occurred either in the absence or the presence of added Mg2+ and/or ATP, they were not blocked by DNA topoisomerase II inhibitors and they were inhibited by an antiserum against DNA topoisomerase I and by camptothecin. These findings led us to propose that, under our in vitro assay conditions, chromatin assembly is mainly carried out by a DNA topoisomerase I. Copyright © 1989, Wiley Blackwell. All rights reserved
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CITATION STYLE
CÁCERES, J. F., BLANGY, D., & GLIKIN, G. C. (1989). Requirement of DNA topoisomerases for in vitro chromatin assembly by 3T6 mouse cell extracts. European Journal of Biochemistry, 181(2), 531–537. https://doi.org/10.1111/j.1432-1033.1989.tb14756.x
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