IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v4y2013i1d10.1038_ncomms2599.html
   My bibliography  Save this article

Topoisomerase IIα promotes activation of RNA polymerase I transcription by facilitating pre-initiation complex formation

Author

Listed:
  • Swagat Ray

    (School of Biological Sciences and the Centre for Cancer Research and Cell Biology, Queen’s University Belfast)

  • Tatiana Panova

    (School of Biological Sciences and the Centre for Cancer Research and Cell Biology, Queen’s University Belfast
    Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee)

  • Gail Miller

    (Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee)

  • Arsen Volkov

    (Gene Targeting Group, Centre for Haematology, Imperial College Faculty of Medicine, Du Cane Road, London W12 0NN, UK)

  • Andrew C. G. Porter

    (Gene Targeting Group, Centre for Haematology, Imperial College Faculty of Medicine, Du Cane Road, London W12 0NN, UK)

  • Jackie Russell

    (Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee)

  • Konstantin I. Panov

    (School of Biological Sciences and the Centre for Cancer Research and Cell Biology, Queen’s University Belfast
    Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee)

  • Joost C. B. M. Zomerdijk

    (Centre for Gene Regulation and Expression, College of Life Sciences, University of Dundee)

Abstract

Type II DNA topoisomerases catalyse DNA double-strand cleavage, passage and re-ligation to effect topological changes. There is considerable interest in elucidating topoisomerase II roles, particularly as these proteins are targets for anti-cancer drugs. Here we uncover a role for topoisomerase IIα in RNA polymerase I-directed ribosomal RNA gene transcription, which drives cell growth and proliferation and is upregulated in cancer cells. Our data suggest that topoisomerase IIα is a component of the initiation-competent RNA polymerase Iβ complex and interacts directly with RNA polymerase I-associated transcription factor RRN3, which targets the polymerase to promoter-bound SL1 in pre-initiation complex formation. In cells, activation of rDNA transcription is reduced by inhibition or depletion of topoisomerase II, and this is accompanied by reduced transient double-strand DNA cleavage in the rDNA-promoter region and reduced pre-initiation complex formation. We propose that topoisomerase IIα functions in RNA polymerase I transcription to produce topological changes at the rDNA promoter that facilitate efficient de novo pre-initiation complex formation.

Suggested Citation

  • Swagat Ray & Tatiana Panova & Gail Miller & Arsen Volkov & Andrew C. G. Porter & Jackie Russell & Konstantin I. Panov & Joost C. B. M. Zomerdijk, 2013. "Topoisomerase IIα promotes activation of RNA polymerase I transcription by facilitating pre-initiation complex formation," Nature Communications, Nature, vol. 4(1), pages 1-12, June.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2599
    DOI: 10.1038/ncomms2599
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms2599
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms2599?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    Citations

    Citations are extracted by the CitEc Project, subscribe to its RSS feed for this item.
    as


    Cited by:

    1. Zhi-Zhi Yang & Bing Yang & Haiyan Yan & Xingyu Ma & Bin Tian & Bingqi Zheng & Yong-Xian Chen & Yi-Ming Dong & Jinsi Deng & Ziling Zhan & Yanmei Shi & Jing Yuan Zhang & Daning Lu & Jie-Hua He & Yin Zha, 2025. "DCAF13-mediated K63-linked ubiquitination of RNA polymerase I promotes uncontrolled proliferation in Breast Cancer," Nature Communications, Nature, vol. 16(1), pages 1-19, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms2599. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.