Mitotic chromosomes are compacted laterally by KIF4 and condensin and axially by topoisomerase IIα

Author:

Samejima Kumiko1,Samejima Itaru1,Vagnarelli Paola1,Ogawa Hiromi1,Vargiu Giulia1,Kelly David A.1,de Lima Alves Flavia1,Kerr Alastair1,Green Lydia C.2,Hudson Damien F.2,Ohta Shinya1,Cooke Carol A.3,Farr Christine J.4,Rappsilber Juri15,Earnshaw William C.1

Affiliation:

1. Wellcome Trust Centre for Cell Biology, University of Edinburgh, King’s Buildings, Edinburgh EH9 3JR, Scotland, UK

2. Murdoch Childrens Research Institute, Royal Children’s Hospital, Melbourne, Victoria 3052, Australia

3. Neurology-Peripheral Nerve Division, Johns Hopkins University, Pathology-537, Baltimore, MD 21287

4. Department of Genetics, University of Cambridge, Cambridge CB2 3EH, England, UK

5. Department of Biotechnology, Technische Universität Berlin, 13353 Berlin, Germany

Abstract

Mitotic chromosome formation involves a relatively minor condensation of the chromatin volume coupled with a dramatic reorganization into the characteristic “X” shape. Here we report results of a detailed morphological analysis, which revealed that chromokinesin KIF4 cooperated in a parallel pathway with condensin complexes to promote the lateral compaction of chromatid arms. In this analysis, KIF4 and condensin were mutually dependent for their dynamic localization on the chromatid axes. Depletion of either caused sister chromatids to expand and compromised the “intrinsic structure” of the chromosomes (defined in an in vitro assay), with loss of condensin showing stronger effects. Simultaneous depletion of KIF4 and condensin caused complete loss of chromosome morphology. In these experiments, topoisomerase IIα contributed to shaping mitotic chromosomes by promoting the shortening of the chromatid axes and apparently acting in opposition to the actions of KIF4 and condensins. These three proteins are major determinants in shaping the characteristic mitotic chromosome morphology.

Publisher

Rockefeller University Press

Subject

Cell Biology

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