IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v2y2011i1d10.1038_ncomms1328.html
   My bibliography  Save this article

Intron retention in the Drosophila melanogaster Rieske iron sulphur protein gene generated a new protein

Author

Listed:
  • Alisson M. Gontijo

    (Instituto de Neurociencias de Alicante, CSIC-UMH, Sant Joan d'Alacant)

  • Veronica Miguela

    (Instituto de Neurociencias de Alicante, CSIC-UMH, Sant Joan d'Alacant)

  • Michael F. Whiting

    (Brigham Young University)

  • R.C. Woodruff

    (Bowling Green State University)

  • Maria Dominguez

    (Instituto de Neurociencias de Alicante, CSIC-UMH, Sant Joan d'Alacant)

Abstract

Genomes can encode a variety of proteins with unrelated architectures and activities. It is known that protein-coding genes of de novo origin have significantly contributed to this diversity. However, the molecular mechanisms and evolutionary processes behind these originations are still poorly understood. Here we show that the last 102 codons of a novel gene, Noble, assembled directly from non-coding DNA following an intronic deletion that induced alternative intron retention at the Drosophila melanogaster Rieske Iron Sulphur Protein (RFeSP) locus. A systematic analysis of the evolutionary processes behind the origin of Noble showed that its emergence was strongly biased by natural selection on and around the RFeSP locus. Noble mRNA is shown to encode a bona fide protein that lacks an iron sulphur domain and localizes to mitochondria. Together, these results demonstrate the generation of a novel protein at a naturally selected site.

Suggested Citation

  • Alisson M. Gontijo & Veronica Miguela & Michael F. Whiting & R.C. Woodruff & Maria Dominguez, 2011. "Intron retention in the Drosophila melanogaster Rieske iron sulphur protein gene generated a new protein," Nature Communications, Nature, vol. 2(1), pages 1-12, September.
  • Handle: RePEc:nat:natcom:v:2:y:2011:i:1:d:10.1038_ncomms1328
    DOI: 10.1038/ncomms1328
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms1328
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms1328?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:2:y:2011:i:1:d:10.1038_ncomms1328. 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.