Movatterモバイル変換


[0]ホーム

URL:


Publisher LogoGenome Research

Skip to main page content

Advanced Search
  • AACR Annual Meeting

Chromodomains direct integration of retrotransposons to heterochromatin

  1. Xiang Gao1,3,
  2. Yi Hou1,
  3. Hirotaka Ebina2,
  4. Henry L. Levin2, and
  5. Daniel F. Voytas1,4
  1. 1 Department of Genetics, Development & Cell Biology, Iowa State University, Ames, Iowa 50011, USA;
  2. 2 Section on Eukaryotic Transposable Elements, Laboratory of Gene Regulation and Development, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA

Abstract

The enrichment of mobile genetic elements in heterochromatin may be due, in part, to targeted integration. The chromoviruses are Ty3/gypsy retrotransposons with chromodomains at their integrase C termini. Chromodomains are logical determinants for targeting to heterochromatin, because the chromodomain of heterochromatin protein 1 (HP1) typically recognizes histone H3 K9 methylation, an epigenetic mark characteristic of heterochromatin. We describe three groups of chromoviruses based on amino acid sequence relationships of their integrase C termini. Genome sequence analysis indicates that representative chromoviruses from each group are enriched in gene-poor regions of the genome relative to other retrotransposons, and when fused to fluorescent marker proteins, the chromodomains target proteins to specific subnuclear foci coincident with heterochromatin. The chromodomain of the fungal element, MAGGY, interacts with histone H3 dimethyl- and trimethyl-K9, and when the MAGGY chromodomain is fused to integrase of theSchizosaccharomyces pombe Tf1 retrotransposon, new Tf1 insertions are directed to sites of H3 K9 methylation. Repetitive sequences such as transposable elements trigger the RNAi pathway resulting in their epigenetic modification. Our results suggest a dynamic interplay between retrotransposons and heterochromatin, wherein mobile elements recognize heterochromatin at the time of integration and then perpetuate the heterochromatic mark by triggering epigenetic modification.

Footnotes

  • 3 Present address: Department of Biology, 1001 East Third Street, Indiana University, Bloomington, Indiana 47405, USA.

  • 4 Corresponding author.

    4 E-mailVoytas{at}iastate.edu; fax (515) 294-7155.

  • [Supplemental material is available online atwww.genome.org.]

  • Article published online before print. Article and publication date are athttp://www.genome.org/cgi/doi/10.1101/gr.7146408

    • Received September 16, 2007.
    • Accepted December 20, 2007.
  • Copyright © 2008, Cold Spring Harbor Laboratory Press
  • Add to CiteULikeCiteULike
  • Add to DeliciousDelicious
  • Add to DiggDigg
  • Add to FacebookFacebook
  • Add to Google+Google+
  • Add to RedditReddit
  • Add to TwitterTwitter

What's this?

« Previous |Next Article »Table of Contents

This Article

  1. Published in AdvanceFebruary 6, 2008, doi:10.1101/gr.7146408 Genome Res. 18: 359-369Copyright © 2008, Cold Spring Harbor Laboratory Press
  1. »AbstractFree
  2. Full TextFree
  3. Full Text (PDF)Free
  4. Supplemental Reseach Data
  5. Podcast

Article Category

Services

  1. Alert me when this article is cited
  2. Alert me if a correction is posted
  3. Similar articles in this journal
  4. Similar articles in Web of Science
  5. Article Metrics
  6. Similar articles in PubMed
  7. Download to citation manager
  8. Permissions

Citing Articles

  1. Load citing article information
  2. Citing articles via Web of Science
  3. Citing articles via Google Scholar

Google Scholar

  1. Articles by Gao, X.
  2. Articles by Voytas, D. F.
  3. Search for related content

PubMed/NCBI

  1. PubMed citation
  2. Articles by Gao, X.
  3. Articles by Voytas, D. F.

Share

    • Add to CiteULikeCiteULike
    • Add to DeliciousDelicious
    • Add to DiggDigg
    • Add to FacebookFacebook
    • Add to Google+Google+
    • Add to RedditReddit
    • Add to TwitterTwitter

    What's this?

Current Issue

  1. March 2025, 35 (3)
  1. Current Issue
  1. Alert me to new issues of Genome Research

Copyright © 2025 by Cold Spring Harbor Laboratory Press

  • Print ISSN:1088-9051
  • Online ISSN:1549-5469

[8]ページ先頭

©2009-2025 Movatter.jp