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Type V myosin focuses the polarisome and shapes the tip of yeast cells.
Dünkler, Alexander; Leda, Marcin; Kromer, Jan-Michael; Neller, Joachim; Gronemeyer, Thomas; Goryachev, Andrew B; Johnsson, Nils.
Afiliação
  • Dünkler A; Institute of Molecular Genetics and Cell Biology, Department of Biology, Ulm University, Ulm, Germany.
  • Leda M; Centre for Synthetic and Systems Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh, UK.
  • Kromer JM; Institute of Molecular Genetics and Cell Biology, Department of Biology, Ulm University, Ulm, Germany.
  • Neller J; Institute of Molecular Genetics and Cell Biology, Department of Biology, Ulm University, Ulm, Germany.
  • Gronemeyer T; Institute of Molecular Genetics and Cell Biology, Department of Biology, Ulm University, Ulm, Germany.
  • Goryachev AB; Centre for Synthetic and Systems Biology, Institute of Cell Biology, University of Edinburgh, Edinburgh, UK.
  • Johnsson N; Institute of Molecular Genetics and Cell Biology, Department of Biology, Ulm University, Ulm, Germany.
J Cell Biol ; 220(5)2021 05 03.
Article em En | MEDLINE | ID: mdl-33656555
ABSTRACT
The polarisome is a cortical proteinaceous microcompartment that organizes the growth of actin filaments and the fusion of secretory vesicles in yeasts and filamentous fungi. Polarisomes are compact, spotlike structures at the growing tips of their respective cells. The molecular forces that control the form and size of this microcompartment are not known. Here we identify a complex between the polarisome subunit Pea2 and the type V Myosin Myo2 that anchors Myo2 at the cortex of yeast cells. We discovered a point mutation in the cargo-binding domain of Myo2 that impairs the interaction with Pea2 and consequently the formation and focused localization of the polarisome. Cells carrying this mutation grow round instead of elongated buds. Further experiments and biophysical modeling suggest that the interactions between polarisome-bound Myo2 motors and dynamic actin filaments spatially focus the polarisome and sustain its compact shape.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: J Cell Biol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Saccharomyces cerevisiae / Proteínas de Saccharomyces cerevisiae Idioma: En Revista: J Cell Biol Ano de publicação: 2021 Tipo de documento: Article