IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v4y2013i1d10.1038_ncomms3841.html
   My bibliography  Save this article

Stepwise histone modifications are mediated by multiple enzymes that rapidly associate with nascent DNA during replication

Author

Listed:
  • Svetlana Petruk

    (Thomas Jefferson University)

  • Kathryn L. Black

    (Thomas Jefferson University)

  • Sina K. Kovermann

    (University of British Columbia, 6270 University Boulevard)

  • Hugh W. Brock

    (University of British Columbia, 6270 University Boulevard)

  • Alexander Mazo

    (Thomas Jefferson University)

Abstract

The mechanism of epigenetic inheritance following DNA replication may involve dissociation of chromosomal proteins from parental DNA and reassembly on daughter strands in a specific order. Here we investigated the behaviour of different types of chromosomal proteins using newly developed methods that allow assessment of the assembly of proteins during DNA replication. Unexpectedly, most chromatin-modifying proteins tested, including methylases, demethylases, acetyltransferases and a deacetylase, are found in close proximity to PCNA or associate with short nascent DNA. Histone modifications occur in a temporal order following DNA replication, mediated by complex activities of different enzymes. In contrast, components of several major nucleosome-remodelling complexes are dissociated from parental DNA, and are later recruited to nascent DNA following replication. Epigenetic inheritance of gene expression patterns may require many aspects of chromatin structure to remain in close proximity to the replication complex followed by reassembly on nascent DNA shortly after replication.

Suggested Citation

  • Svetlana Petruk & Kathryn L. Black & Sina K. Kovermann & Hugh W. Brock & Alexander Mazo, 2013. "Stepwise histone modifications are mediated by multiple enzymes that rapidly associate with nascent DNA during replication," Nature Communications, Nature, vol. 4(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:4:y:2013:i:1:d:10.1038_ncomms3841
    DOI: 10.1038/ncomms3841
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms3841
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms3841?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
    ---><---

    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_ncomms3841. 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.