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The α isoform of topoisomerase II is required for hypercompaction of mitotic chromosomes in human cells.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Farr, Christine J 
Antoniou-Kourounioti, Melissa 
Mimmack, Michael L 
Volkov, Arsen 
Porter, Andrew CG 

Abstract

As proliferating cells transit from interphase into M-phase, chromatin undergoes extensive reorganization, and topoisomerase (topo) IIα, the major isoform of this enzyme present in cycling vertebrate cells, plays a key role in this process. In this study, a human cell line conditional null mutant for topo IIα and a derivative expressing an auxin-inducible degron (AID)-tagged version of the protein have been used to distinguish real mitotic chromosome functions of topo IIα from its more general role in DNA metabolism and to investigate whether topo IIβ makes any contribution to mitotic chromosome formation. We show that topo IIβ does contribute, with endogenous levels being sufficient for the initial stages of axial shortening. However, a significant effect of topo IIα depletion, seen with or without the co-depletion of topo IIβ, is the failure of chromosomes to hypercompact when delayed in M-phase. This requires much higher levels of topo II protein and is impaired by drugs or mutations that affect enzyme activity. A prolonged delay at the G2/M border results in hyperefficient axial shortening, a process that is topo IIα-dependent. Rapid depletion of topo IIα has allowed us to show that its function during late G2 and M-phase is truly required for shaping mitotic chromosomes.

Description

Keywords

Antigens, Neoplasm, Catalytic Domain, Cell Line, Chromosomes, Human, DNA Topoisomerases, Type II, DNA-Binding Proteins, G2 Phase, Humans, Mitosis, Mutation, Protein Isoforms, Quinolines, Thiazoles

Journal Title

Nucleic Acids Res

Conference Name

Journal ISSN

0305-1048
1362-4962

Volume Title

42

Publisher

Oxford University Press (OUP)
Sponsorship
Cancer Research Uk (None)