IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v449y2007i7165d10.1038_nature06256.html
   My bibliography  Save this article

Regulation of cell cycle progression and gene expression by H2A deubiquitination

Author

Listed:
  • Heui-Yun Joo

    (University of Alabama at Birmingham, Kaul Human Genetics Building 402A, 720 South 20th Street, Birmingham, Alabama 35294, USA)

  • Ling Zhai

    (University of Alabama at Birmingham, Kaul Human Genetics Building 402A, 720 South 20th Street, Birmingham, Alabama 35294, USA)

  • Chunying Yang

    (University of Alabama at Birmingham, Kaul Human Genetics Building 402A, 720 South 20th Street, Birmingham, Alabama 35294, USA)

  • Shuyi Nie

    (University of Alabama at Birmingham, MCLM 360, Birmingham, Alabama 35294-0005, USA)

  • Hediye Erdjument-Bromage

    (Molecular Biology Program, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA)

  • Paul Tempst

    (Molecular Biology Program, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, New York 10021, USA)

  • Chenbei Chang

    (University of Alabama at Birmingham, MCLM 360, Birmingham, Alabama 35294-0005, USA)

  • Hengbin Wang

    (University of Alabama at Birmingham, Kaul Human Genetics Building 402A, 720 South 20th Street, Birmingham, Alabama 35294, USA)

Abstract

An enzyme, Ubp-M, is identified that removes the ubiquitin modification from histone H2A. Depletion of Ubp-M leads to slower cell growth and abnormal chromosome segregation in mitosis. In addition, depletion of Ubp-M causes defects in development and dysregulation of Hox gene expression.

Suggested Citation

  • Heui-Yun Joo & Ling Zhai & Chunying Yang & Shuyi Nie & Hediye Erdjument-Bromage & Paul Tempst & Chenbei Chang & Hengbin Wang, 2007. "Regulation of cell cycle progression and gene expression by H2A deubiquitination," Nature, Nature, vol. 449(7165), pages 1068-1072, October.
  • Handle: RePEc:nat:nature:v:449:y:2007:i:7165:d:10.1038_nature06256
    DOI: 10.1038/nature06256
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature06256
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/nature06256?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
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    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:nature:v:449:y:2007:i:7165:d:10.1038_nature06256. 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.