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Title: Topoisomerase II binds importin {alpha} isoforms and exportin/CRM1 but does not shuttle between the nucleus and cytoplasm in proliferating cells

Journal Article · · Experimental Cell Research
 [1];  [1];  [2];  [2];  [3];  [4];  [1]
  1. Division of Cancer Biology and Genetics, Cancer Research Institute, Queen's University, Kingston, ON, K7L 3N6 (Canada)
  2. Max Delbrueck Center for Molecular Medicine, Robert Roessle Str 10, 13125 Berlin (Germany)
  3. Department of Medical Microbiology, Immunology and Cell Biology, Southern Illinois University School of Medicine, Springfield, IL 62794 (United States)
  4. Department of Biopharmaceutical Sciences, University of Illinois at Chicago, Chicago, IL 60612 (United States)

Resistance to anticancer drugs that target DNA topoisomerase II (topo II) isoforms {alpha} and/or {beta} is associated with decreased nuclear and increased cytoplasmic topo II{alpha}. Earlier studies have confirmed that functional nuclear localization and export signal sequences (NLS and NES) are present in both isoforms. In this study, we show that topo II {alpha} and {beta} bind and are imported into the nucleus by importin {alpha}1, {alpha}3, and {alpha}5 in conjunction with importin {beta}. Topo II{alpha} also binds exportin/CRM1 in vitro. However, wild-type topo II{alpha} has only been observed in the cytoplasm of cells that are entering plateau phase growth. This suggests that topo II{alpha} may shuttle between the nucleus and the cytoplasm with the equilibrium towards the nucleus in proliferating cells but towards the cytoplasm in plateau phase cells. The CRM1 inhibitor Leptomycin B increases the nuclear localization of GFP-tagged topo II{alpha} with a mutant NLS, suggesting that its export is being inhibited. However, homokaryon shuttling experiments indicate that fluorescence-tagged wild-type topo II {alpha} and {beta} proteins do not shuttle in proliferating Cos-1 or HeLa cells. We conclude that topo II {alpha} and {beta} nuclear export is inhibited in proliferating cells so that these proteins do not shuttle.

OSTI ID:
20972115
Journal Information:
Experimental Cell Research, Vol. 313, Issue 3; Other Information: DOI: 10.1016/j.yexcr.2006.11.004; PII: S0014-4827(06)00462-9; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0014-4827
Country of Publication:
United States
Language:
English

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