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Centromere DNA decatenation depends on cohesin removal and is required for mammalian cell division
Journal article   Open access   Peer reviewed

Centromere DNA decatenation depends on cohesin removal and is required for mammalian cell division

Lily Hui-Ching Wang, Bernd Mayer, Olaf Stemmann and Erich A. Nigg
Journal of Cell Science, Vol.123(5), pp.806-813
01/03/2010

Abstract

Cohesin NoCut PICH Spindle-assembly checkpoint Topoisomerase-II
Sister chromatid cohesion is mediated by DNA catenation and proteinaceous cohesin complexes. The recent visualization of PICH (Plk1-interacting checkpoint helicase)-coated DNA threads in anaphase cells raises new questions as to the role of DNA catenation and its regulation in time and space. In the present study we show that persistent DNA catenation induced by inhibition of Topoisomerase-IIα can contribute to sister chromatid cohesion in the absence of cohesin complexes and that resolution of catenation is essential for abscission. Furthermore, we use an in vitro chromatid separation assay to investigate the temporal and functional relationship between cohesin removal and Topoisomerase-IIα-mediated decatenation. Our data suggest that centromere decatenation can occur only after separase activation and cohesin removal, providing a plausible explanation for the persistence of centromere threads after anaphase onset.
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https://doi.org/10.1242/jcs.058255View
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