IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v11y2020i1d10.1038_s41467-020-14500-z.html
   My bibliography  Save this article

De novo emergence of adaptive membrane proteins from thymine-rich genomic sequences

Author

Listed:
  • Nikolaos Vakirlis

    (University of Dublin)

  • Omer Acar

    (University of Pittsburgh
    University of Pittsburgh)

  • Brian Hsu

    (University of California San Diego)

  • Nelson Castilho Coelho

    (University of Pittsburgh
    University of Pittsburgh)

  • S. Branden Van Oss

    (University of Pittsburgh
    University of Pittsburgh)

  • Aaron Wacholder

    (University of Pittsburgh
    University of Pittsburgh)

  • Kate Medetgul-Ernar

    (University of California San Diego)

  • Ray W. Bowman

    (University of Pittsburgh)

  • Cameron P. Hines

    (University of California San Diego)

  • John Iannotta

    (University of Pittsburgh
    University of Pittsburgh)

  • Saurin Bipin Parikh

    (University of Pittsburgh
    University of Pittsburgh)

  • Aoife McLysaght

    (University of Dublin)

  • Carlos J. Camacho

    (University of Pittsburgh)

  • Allyson F. O’Donnell

    (University of Pittsburgh
    University of Pittsburgh)

  • Trey Ideker

    (University of California San Diego)

  • Anne-Ruxandra Carvunis

    (University of Pittsburgh
    University of Pittsburgh)

Abstract

Recent evidence demonstrates that novel protein-coding genes can arise de novo from non-genic loci. This evolutionary innovation is thought to be facilitated by the pervasive translation of non-genic transcripts, which exposes a reservoir of variable polypeptides to natural selection. Here, we systematically characterize how these de novo emerging coding sequences impact fitness in budding yeast. Disruption of emerging sequences is generally inconsequential for fitness in the laboratory and in natural populations. Overexpression of emerging sequences, however, is enriched in adaptive fitness effects compared to overexpression of established genes. We find that adaptive emerging sequences tend to encode putative transmembrane domains, and that thymine-rich intergenic regions harbor a widespread potential to produce transmembrane domains. These findings, together with in-depth examination of the de novo emerging YBR196C-A locus, suggest a novel evolutionary model whereby adaptive transmembrane polypeptides emerge de novo from thymine-rich non-genic regions and subsequently accumulate changes molded by natural selection.

Suggested Citation

  • Nikolaos Vakirlis & Omer Acar & Brian Hsu & Nelson Castilho Coelho & S. Branden Van Oss & Aaron Wacholder & Kate Medetgul-Ernar & Ray W. Bowman & Cameron P. Hines & John Iannotta & Saurin Bipin Parikh, 2020. "De novo emergence of adaptive membrane proteins from thymine-rich genomic sequences," Nature Communications, Nature, vol. 11(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14500-z
    DOI: 10.1038/s41467-020-14500-z
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-020-14500-z
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-020-14500-z?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
    ---><---

    Citations

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


    Cited by:

    1. Rujia Chen & Ning Xiao & Yue Lu & Tianyun Tao & Qianfeng Huang & Shuting Wang & Zhichao Wang & Mingli Chuan & Qing Bu & Zhou Lu & Hanyao Wang & Yanze Su & Yi Ji & Jianheng Ding & Ahmed Gharib & Huixin, 2023. "A de novo evolved gene contributes to rice grain shape difference between indica and japonica," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    2. Junhui Peng & Li Zhao, 2024. "The origin and structural evolution of de novo genes in Drosophila," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    3. Bharat Ravi Iyengar & Anna Grandchamp & Erich Bornberg-Bauer, 2024. "How antisense transcripts can evolve to encode novel proteins," Nature Communications, Nature, vol. 15(1), pages 1-11, 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:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-14500-z. 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.