IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v507y2014i7490d10.1038_nature12931.html
   My bibliography  Save this article

SRA- and SET-domain-containing proteins link RNA polymerase V occupancy to DNA methylation

Author

Listed:
  • Lianna M. Johnson

    (Cell and Developmental Biology, University of California at Los Angeles)

  • Jiamu Du

    (Structural Biology Program, Memorial Sloan-Kettering Cancer Center)

  • Christopher J. Hale

    (Cell and Developmental Biology, University of California at Los Angeles)

  • Sylvain Bischof

    (Cell and Developmental Biology, University of California at Los Angeles)

  • Suhua Feng

    (Cell and Developmental Biology, University of California at Los Angeles
    Howard Hughes Medical Institute, University of California at Los Angeles)

  • Ramakrishna K. Chodavarapu

    (Cell and Developmental Biology, University of California at Los Angeles)

  • Xuehua Zhong

    (Cell and Developmental Biology, University of California at Los Angeles
    Present address: Wisconsin Institute for Discovery, Laboratory of Genetics, University of Wisconsin, Madison, Wisconsin 53706, USA.)

  • Giuseppe Marson

    (Structural Biology Program, Memorial Sloan-Kettering Cancer Center)

  • Matteo Pellegrini

    (Cell and Developmental Biology, University of California at Los Angeles)

  • David J. Segal

    (University of California at Davis)

  • Dinshaw J. Patel

    (Structural Biology Program, Memorial Sloan-Kettering Cancer Center)

  • Steven E. Jacobsen

    (Cell and Developmental Biology, University of California at Los Angeles
    Howard Hughes Medical Institute, University of California at Los Angeles)

Abstract

In Arabidopsis, the RNA-directed DNA methylation pathway is important for establishing and maintaining DNA methylation — here Pol V is shown to depend on SUVH2 and SUVH9, where both of these proteins are proposed to bind specifically to methylated DNA to recruit Pol V, providing a self-reinforcing loop mechanism for maintenance of RNA-directed DNA methylation.

Suggested Citation

  • Lianna M. Johnson & Jiamu Du & Christopher J. Hale & Sylvain Bischof & Suhua Feng & Ramakrishna K. Chodavarapu & Xuehua Zhong & Giuseppe Marson & Matteo Pellegrini & David J. Segal & Dinshaw J. Patel , 2014. "SRA- and SET-domain-containing proteins link RNA polymerase V occupancy to DNA methylation," Nature, Nature, vol. 507(7490), pages 124-128, March.
  • Handle: RePEc:nat:nature:v:507:y:2014:i:7490:d:10.1038_nature12931
    DOI: 10.1038/nature12931
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/nature12931
    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/nature12931?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.

    Citations

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


    Cited by:

    1. Hong-Wei Zhang & Kun Huang & Zhan-Xi Gu & Xiao-Xian Wu & Jia-Wei Wang & Yu Zhang, 2023. "A cryo-EM structure of KTF1-bound polymerase V transcription elongation complex," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    2. Zheng Li & Ming Wang & Zhenhui Zhong & Javier Gallego-Bartolomé & Suhua Feng & Yasaman Jami-Alahmadi & Xinyi Wang & James Wohlschlegel & Sylvain Bischof & Jeff A. Long & Steven E. Jacobsen, 2023. "The MOM1 complex recruits the RdDM machinery via MORC6 to establish de novo DNA methylation," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
    3. Yinwen Zhang & Hosung Jang & Rui Xiao & Ioanna Kakoulidou & Robert S. Piecyk & Frank Johannes & Robert J. Schmitz, 2021. "Heterochromatin is a quantitative trait associated with spontaneous epiallele formation," Nature Communications, Nature, vol. 12(1), pages 1-13, 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:nature:v:507:y:2014:i:7490:d:10.1038_nature12931. 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.