IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0034261.html
   My bibliography  Save this article

PHYRN: A Robust Method for Phylogenetic Analysis of Highly Divergent Sequences

Author

Listed:
  • Gaurav Bhardwaj
  • Kyung Dae Ko
  • Yoojin Hong
  • Zhenhai Zhang
  • Ngai Lam Ho
  • Sree V Chintapalli
  • Lindsay A Kline
  • Matthew Gotlin
  • David Nicholas Hartranft
  • Morgen E Patterson
  • Foram Dave
  • Evan J Smith
  • Edward C Holmes
  • Randen L Patterson
  • Damian B van Rossum

Abstract

Both multiple sequence alignment and phylogenetic analysis are problematic in the “twilight zone” of sequence similarity (≤25% amino acid identity). Herein we explore the accuracy of phylogenetic inference at extreme sequence divergence using a variety of simulated data sets. We evaluate four leading multiple sequence alignment (MSA) methods (MAFFT, T-COFFEE, CLUSTAL, and MUSCLE) and six commonly used programs of tree estimation (Distance-based: Neighbor-Joining; Character-based: PhyML, RAxML, GARLI, Maximum Parsimony, and Bayesian) against a novel MSA-independent method (PHYRN) described here. Strikingly, at “midnight zone” genetic distances (∼7% pairwise identity and 4.0 gaps per position), PHYRN returns high-resolution phylogenies that outperform traditional approaches. We reason this is due to PHRYN's capability to amplify informative positions, even at the most extreme levels of sequence divergence. We also assess the applicability of the PHYRN algorithm for inferring deep evolutionary relationships in the divergent DANGER protein superfamily, for which PHYRN infers a more robust tree compared to MSA-based approaches. Taken together, these results demonstrate that PHYRN represents a powerful mechanism for mapping uncharted frontiers in highly divergent protein sequence data sets.

Suggested Citation

  • Gaurav Bhardwaj & Kyung Dae Ko & Yoojin Hong & Zhenhai Zhang & Ngai Lam Ho & Sree V Chintapalli & Lindsay A Kline & Matthew Gotlin & David Nicholas Hartranft & Morgen E Patterson & Foram Dave & Evan J, 2012. "PHYRN: A Robust Method for Phylogenetic Analysis of Highly Divergent Sequences," PLOS ONE, Public Library of Science, vol. 7(4), pages 1-13, April.
  • Handle: RePEc:plo:pone00:0034261
    DOI: 10.1371/journal.pone.0034261
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0034261
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0034261&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0034261?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
    ---><---

    References listed on IDEAS

    as
    1. Hiroyuki Watanabe & Joris Vriens & Jean Prenen & Guy Droogmans & Thomas Voets & Bernd Nilius, 2003. "Anandamide and arachidonic acid use epoxyeicosatrienoic acids to activate TRPV4 channels," Nature, Nature, vol. 424(6947), pages 434-438, July.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Annika Simon & Thomas Einem & Alexander Seidinger & Michaela Matthey & Laura Bindila & Daniela Wenzel, 2022. "The endocannabinoid anandamide is an airway relaxant in health and disease," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    2. Kirill D. Nadezhdin & Irina A. Talyzina & Aravind Parthasarathy & Arthur Neuberger & David X. Zhang & Alexander I. Sobolevsky, 2023. "Structure of human TRPV4 in complex with GTPase RhoA," Nature Communications, Nature, vol. 14(1), pages 1-11, December.
    3. Do Hoon Kwon & Feng Zhang & Brett A. McCray & Shasha Feng & Meha Kumar & Jeremy M. Sullivan & Wonpil Im & Charlotte J. Sumner & Seok-Yong Lee, 2023. "TRPV4-Rho GTPase complex structures reveal mechanisms of gating and disease," Nature Communications, Nature, vol. 14(1), pages 1-15, 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:plo:pone00:0034261. 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.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with 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: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    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.