» Articles » PMID: 29149026

Non-Catalytic Roles of the Topoisomerase IIα C-Terminal Domain

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2017 Nov 18
PMID 29149026
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

DNA Topoisomerase IIα (Topo IIα) is a ubiquitous enzyme in eukaryotes that performs the strand passage reaction where a double helix of DNA is passed through a second double helix. This unique reaction is critical for numerous cellular processes. However, the enzyme also possesses a C-terminal domain (CTD) that is largely dispensable for the strand passage reaction but is nevertheless important for the fidelity of cell division. Recent studies have expanded our understanding of the roles of the Topo IIα CTD, in particular in mitotic mechanisms where the CTD is modified by Small Ubiquitin-like Modifier (SUMO), which in turn provides binding sites for key regulators of mitosis.

Citing Articles

Histone H3 tail modifications required for meiosis in .

Prichard A, Johansson M, Kirkpatrick D, Clarke D bioRxiv. 2024; .

PMID: 39713340 PMC: 11661218. DOI: 10.1101/2024.12.09.627563.


Structural and functional insights into the T-even type bacteriophage topoisomerase II.

Xin Y, Xian R, Yang Y, Cong J, Rao Z, Li X Nat Commun. 2024; 15(1):8719.

PMID: 39379365 PMC: 11461880. DOI: 10.1038/s41467-024-53037-3.


Bioinformatic Analysis of Topoisomerase IIα Reveals Interdomain Interdependencies and Critical C-Terminal Domain Residues.

Endsley C, Moore K, Townsley T, Durston K, Deweese J Int J Mol Sci. 2024; 25(11).

PMID: 38891861 PMC: 11172036. DOI: 10.3390/ijms25115674.


Aspergillus SUMOylation mutants exhibit chromosome segregation defects including chromatin bridges.

Zhang J, Qiu R, Bieger B, Oakley C, Oakley B, Egan M Genetics. 2023; 225(4).

PMID: 37724751 PMC: 10697819. DOI: 10.1093/genetics/iyad169.


The interplay between DNA topoisomerase 2α post-translational modifications and drug resistance.

Lotz C, Lamour V Cancer Drug Resist. 2022; 3(2):149-160.

PMID: 35582608 PMC: 9090595. DOI: 10.20517/cdr.2019.114.


References
1.
Winey M, Yarar D, Giddings Jr T, Mastronarde D . Nuclear pore complex number and distribution throughout the Saccharomyces cerevisiae cell cycle by three-dimensional reconstruction from electron micrographs of nuclear envelopes. Mol Biol Cell. 1997; 8(11):2119-32. PMC: 25696. DOI: 10.1091/mbc.8.11.2119. View

2.
Chang C, Goulding S, Earnshaw W, Carmena M . RNAi analysis reveals an unexpected role for topoisomerase II in chromosome arm congression to a metaphase plate. J Cell Sci. 2003; 116(Pt 23):4715-26. DOI: 10.1242/jcs.00797. View

3.
Rodriguez-Bravo V, Maciejowski J, Corona J, Buch H, Collin P, Kanemaki M . Nuclear pores protect genome integrity by assembling a premitotic and Mad1-dependent anaphase inhibitor. Cell. 2014; 156(5):1017-31. PMC: 3947552. DOI: 10.1016/j.cell.2014.01.010. View

4.
Agostinho M, Santos V, Ferreira F, Costa R, Cardoso J, Pinheiro I . Conjugation of human topoisomerase 2 alpha with small ubiquitin-like modifiers 2/3 in response to topoisomerase inhibitors: cell cycle stage and chromosome domain specificity. Cancer Res. 2008; 68(7):2409-18. DOI: 10.1158/0008-5472.CAN-07-2092. View

5.
Isik S, Sano K, Tsutsui K, Seki M, Enomoto T, Saitoh H . The SUMO pathway is required for selective degradation of DNA topoisomerase IIbeta induced by a catalytic inhibitor ICRF-193(1). FEBS Lett. 2003; 546(2-3):374-8. DOI: 10.1016/s0014-5793(03)00637-9. View