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A novel role of the organizer gene Goosecoid as an inhibitor of Wnt/PCP-mediated convergent extension in Xenopus and mouse

  1. Author:
    Ulmer, Baerbel
    Tingler, Melanie
    Kurz, Sabrina
    Maerker, Markus
    Andre, Philipp
    Moench, Dina
    Campione, Marina
    Deissler, Kirsten
    Lewandoski, Mark
    Thumberger, Thomas
    Schweickert, Axel
    Fainsod, Abraham
    Steinbeisser, Herbert
    Blum, Martin
  2. Author Address

    Univ Hohenheim, Garbenstr 30, D-70599 Stuttgart, Germany.NCI, Canc & Dev Biol Lab, Genet Vertebrate Dev Sect, NIH, Frederick, MD 21702 USA.Hebrew Univ Jerusalem, Inst Med Res Israel Canada, Dept Dev Biol & Canc Res, IL-9112102 Jerusalem, Israel.Univ Heidelberg Hosp, Inst Human Genet, Neuenheimer Feld 366, D-69120 Heidelberg, Germany.Univ Med Ctr Hamburg Eppendorf, Cardiovasc Res Ctr, Dept Expt Pharmacol & Toxicol, D-20246 Hamburg, Germany.Univ Padua, CNR, Inst Neurosci, Dept Biomed Sci, I-35100 Padua, Italy.Heidelberg Univ, Ctr Organismal Studies COS Heidelberg, Neuenheimer Feld 230, D-69120 Heidelberg, Germany.
    1. Year: 2017
    2. Date: 2017-02-21
    3. Epub Date: 2017-02-21
  1. Journal: SCIENTIFIC REPORTS
  2. NATURE PUBLISHING GROUP,
    1. 7
  3. Type of Article: Article
  4. Article Number: 43010
  5. ISSN: 2045-2322
  1. Abstract:

    Goosecoid (Gsc) expression marks the primary embryonic organizer in vertebrates and beyond. While functions have been assigned during later embryogenesis, the role of Gsc in the organizer has remained enigmatic. Using conditional gain-of-function approaches in Xenopus and mouse to maintain Gsc expression in the organizer and along the axial midline, neural tube closure defects (NTDs) arose and dorsal extension was compromised. Both phenotypes represent convergent extension (CE) defects, arising from impaired Wnt/planar cell polarity (PCP) signaling. Dvl2 recruitment to the cell membrane was inhibited by Gsc in Xenopus animal cap assays and key Wnt/PCP factors (RhoA, Vangl2, Prickle, Wnt11) rescued Gsc-mediated NTDs. Re-evaluation of endogenous Gsc functions in MO-mediated gene knockdown frog and knockout mouse embryos unearthed PCP/CE-related phenotypes as well, including cartilage defects in Xenopus and misalignment of inner ear hair cells in mouse. Our results assign a novel function to Gsc as an inhibitor of Wnt/PCP-mediated CE. We propose that in the organizer Gsc represses CE as well: Gsc-expressing prechordal cells, which leave the organizer first, migrate and do not undergo CE like the Gsc-negative notochordal cells, which subsequently emerge from the organizer. In this model, Gsc provides a switch between cell migration and CE, i.e. cell intercalation.

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External Sources

  1. DOI: 10.1038/srep43010
  2. PMID: 28220837
  3. PMCID: PMC5318956
  4. WOS: 000394699000001

Library Notes

  1. Fiscal Year: FY2016-2017
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