{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Dunkler A"],"funding":["Deutsche Forschungsgemeinschaft","Biotechnology and Biological Sciences Research Council"],"pagination":["e202006193"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7933982"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["220(5)"],"pubmed_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 th"],"journal":["The Journal of cell biology"],"pubmed_title":["Type V myosin focuses the polarisome and shapes the tip of yeast cells."],"pmcid":["PMC7933982"],"funding_grant_id":["BB/P006507/1","BB/P006507","BB/P01190X/1","Jo 187/8-1","BB/P01190X"],"pubmed_authors":["Dunkler A","Neller J","Goryachev AB","Kromer JM","Gronemeyer T","Johnsson N","Leda M"],"additional_accession":[]},"is_claimable":false,"name":"Type V myosin focuses the polarisome and shapes the tip of yeast cells.","description":"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 th","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 May","modification":"2026-05-09T01:15:37.18Z","creation":"2025-06-01T03:24:41.055Z"},"accession":"S-EPMC7933982","cross_references":{"pubmed":["33656555"],"doi":["10.1083/jcb.202006193"]}}