IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v5y2014i1d10.1038_ncomms4419.html
   My bibliography  Save this article

Trunk cleavage is essential for Drosophila terminal patterning and can occur independently of Torso-like

Author

Listed:
  • Michelle A. Henstridge

    (School of Biological Sciences, Monash University)

  • Travis K. Johnson

    (School of Biological Sciences, Monash University
    Monash University)

  • Coral G. Warr

    (School of Biological Sciences, Monash University)

  • James C. Whisstock

    (Monash University
    Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Monash University)

Abstract

Terminal patterning in Drosophila is governed by a localized interaction between the Torso kinase (Tor) and its ligand Trunk (Trk). Currently, it is proposed that Trk must be cleaved in order to bind Tor, and that these proteolytic events are controlled by secretion of Torso-like (Tsl) only at the embryo poles. However, controversy surrounds these ideas since neither cleaved Trk nor a protease that functions in terminal patterning have been identified. Here we show that Trk is cleaved multiple times in vivo and that these proteolytic events are essential for its function. Unexpectedly, however, the Trk cleavage patterns we observe are unaltered in tsl-null mutants. One explanation for these data is that the influence of Tsl on localized Trk cleavage at the embryo poles is subtle and cannot be readily detected. Alternatively, we favour a scenario where Tsl functions post proteolytic processing of Trk to control localized terminal patterning.

Suggested Citation

  • Michelle A. Henstridge & Travis K. Johnson & Coral G. Warr & James C. Whisstock, 2014. "Trunk cleavage is essential for Drosophila terminal patterning and can occur independently of Torso-like," Nature Communications, Nature, vol. 5(1), pages 1-7, May.
  • Handle: RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms4419
    DOI: 10.1038/ncomms4419
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/ncomms4419
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/ncomms4419?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:5:y:2014:i:1:d:10.1038_ncomms4419. 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.