Biochemical characterisation of elsamicin and other coumarin-related antitumour agents as potent inhibitors of human topoisomerase II

1993 ◽  
Vol 29 (14) ◽  
pp. 1985-1991 ◽  
Author(s):  
Aurelio Lorico ◽  
Byron H. Long
Author(s):  
Jason R. Swedlow ◽  
Neil Osheroff ◽  
Tim Karr ◽  
John W. Sedat ◽  
David A. Agard

DNA topoisomerase II is an ATP-dependent double-stranded DNA strand-passing enzyme that is necessary for full condensation of chromosomes and for complete segregation of sister chromatids at mitosis in vivo and in vitro. Biochemical characterization of chromosomes or nuclei after extraction with high-salt or detergents and DNAse treatment showed that topoisomerase II was a major component of this remnant, termed the chromosome scaffold. The scaffold has been hypothesized to be the structural backbone of the chromosome, so the localization of topoisomerase II to die scaffold suggested that the enzyme might play a structural role in the chromosome. However, topoisomerase II has not been studied in nuclei or chromosomes in vivo. We have monitored the chromosomal distribution of topoisomerase II in vivo during mitosis in the Drosophila embryo. This embryo forms a multi-nucleated syncytial blastoderm early in its developmental cycle. During this time, the embryonic nuclei synchronously progress through 13 mitotic cycles, so this is an ideal system to follow nuclear and chromosomal dynamics.


1980 ◽  
Vol 77 ◽  
pp. 85-89 ◽  
Author(s):  
Jean-François Labarre ◽  
Francois Lahana ◽  
Françoise Sournies ◽  
Suzy Cros ◽  
Georgette François
Keyword(s):  

2006 ◽  
Vol 128 (05) ◽  
Author(s):  
S Albrich ◽  
E Bremer ◽  
M Schmidt ◽  
A Victor ◽  
S Gebhard ◽  
...  

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