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CYFIP2-containing WAVE complexes inhibit cell migration by a competition mechanism

View ORCID ProfileAnna Polesskaya, Arthur Boutillon, Sheng Yang, Yanan Wang, Stéphane Romero, Yijun Liu, Marc Lavielle, View ORCID ProfileSophie Vacher, View ORCID ProfileAnne Schnitzler, Nicolas Molinie, Nathalie Rocques, View ORCID ProfileArtem Fokin, Raphaël Guérois, View ORCID ProfileIvan Bièche, Baoyu Chen, Nicolas B. David, View ORCID ProfileAlexis M. Gautreau
doi: https://doi.org/10.1101/2020.07.02.184655
Anna Polesskaya
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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  • ORCID record for Anna Polesskaya
Arthur Boutillon
2INSERM U1182, CNRS UMR7645, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Sheng Yang
3Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA
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Yanan Wang
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Stéphane Romero
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Yijun Liu
3Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA
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Marc Lavielle
4INRIA Saclay & Center for Applied Mathematics (CMAP), Institut Polytechnique de Paris, 91120 Palaiseau, France
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  • For correspondence: Marc.Lavielle@inria.fr
Sophie Vacher
5Pharmacogenomics Unit, Department of Genetics, Institut Curie, 26 rue d’Ulm, 75005 Paris, France
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Anne Schnitzler
5Pharmacogenomics Unit, Department of Genetics, Institut Curie, 26 rue d’Ulm, 75005 Paris, France
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  • ORCID record for Anne Schnitzler
Nicolas Molinie
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Nathalie Rocques
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Artem Fokin
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Raphaël Guérois
6Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, University Paris-Saclay, CEA-Saclay, 91190 Gif-sur-Yvette, France
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Ivan Bièche
5Pharmacogenomics Unit, Department of Genetics, Institut Curie, 26 rue d’Ulm, 75005 Paris, France
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  • ORCID record for Ivan Bièche
Baoyu Chen
3Roy J. Carver Department of Biochemistry, Biophysics and Molecular Biology, Iowa State University, Ames, IA 50011, USA
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Nicolas B. David
2INSERM U1182, CNRS UMR7645, Institut Polytechnique de Paris, 91120 Palaiseau, France
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Alexis M. Gautreau
1CNRS UMR7654, Institut Polytechnique de Paris, 91120 Palaiseau, France
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  • ORCID record for Alexis M. Gautreau
  • For correspondence: alexis.gautreau@polytechnique.edu
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ABSTRACT

Branched actin networks polymerized by the Arp2/3 complex are critical for cell migration. The WAVE complex is the major Arp2/3 activator at the leading edge of migrating cells. However, multiple distinct WAVE complexes can be assembled in a cell, due to the combinatorial complexity of paralogous subunits. When systematically analyzing the contribution of each WAVE complex subunit to the metastasis-free survival of breast cancer patients, we found that overexpression of the CYFIP2 subunit was surprisingly associated with good prognosis. Gain and loss of function experiments in transformed and untransformed mammary epithelial cells, as well as in prechordal plate cells in gastrulating zebrafish embryos, revealed that lamellipodium protrusion and cell migration were always inversely related to CYFIP2 levels. The role of CYFIP2 was systematically opposite to the role of the paralogous subunit CYFIP1 or of the NCKAP1 subunit, which determines levels of WAVE complexes. CYFIP2 showed no difference from CYFIP1 in assembling WAVE complexes or binding to active RAC1. CYFIP2-containing WAVE complexes, however, were less able to activate the Arp2/3 complex in response to RAC1 binding. CYFIP1- and CYFIP2-containing WAVE complexes thus compete for active RAC1 and produce different outcomes. Therefore, cell migration, lamellipodium protrusion and Arp2/3 activity are controlled by relative levels of CYFIP1 and CYFIP2.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • ↵# co-second author

  • The new version of the manuscript contains novel data, obtained in a number of experiments, according to the Reviewers' suggestions (Fig.2A, Fig.5, Fig.6). Five new co-authors have now participated in the study. While all the previously obtained conclusions have been confirmed, we now present two novel functional assays in two distinct cell lines, as well as an in-depth analysis of the underlying mechanisms.

  • Abbreviations

    BIC
    Bayesian Information Criteria
    KD
    knock-down
    KO
    knock-out
    MFS
    metastasis-free survival
    RFS
    Relapse-free survival
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    CYFIP2-containing WAVE complexes inhibit cell migration by a competition mechanism
    Anna Polesskaya, Arthur Boutillon, Sheng Yang, Yanan Wang, Stéphane Romero, Yijun Liu, Marc Lavielle, Sophie Vacher, Anne Schnitzler, Nicolas Molinie, Nathalie Rocques, Artem Fokin, Raphaël Guérois, Ivan Bièche, Baoyu Chen, Nicolas B. David, Alexis M. Gautreau
    bioRxiv 2020.07.02.184655; doi: https://doi.org/10.1101/2020.07.02.184655
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    CYFIP2-containing WAVE complexes inhibit cell migration by a competition mechanism
    Anna Polesskaya, Arthur Boutillon, Sheng Yang, Yanan Wang, Stéphane Romero, Yijun Liu, Marc Lavielle, Sophie Vacher, Anne Schnitzler, Nicolas Molinie, Nathalie Rocques, Artem Fokin, Raphaël Guérois, Ivan Bièche, Baoyu Chen, Nicolas B. David, Alexis M. Gautreau
    bioRxiv 2020.07.02.184655; doi: https://doi.org/10.1101/2020.07.02.184655

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