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      Extracellular vesicles secreted by Saccharomyces cerevisiae are involved in cell wall remodelling

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          Abstract

          Extracellular vesicles (EVs) are membranous vesicles that are released by cells. In this study, the role of the Endosomal Sorting Complex Required for Transport (ESCRT) machinery in the biogenesis of yeast EVs was examined. Knockout of components of the ESCRT machinery altered the morphology and size of EVs as well as decreased the abundance of EVs. In contrast, strains with deletions in cell wall biosynthesis genes, produced more EVs than wildtype. Proteomic analysis highlighted the depletion of ESCRT components and enrichment of cell wall remodelling enzymes, glucan synthase subunit Fks1 and chitin synthase Chs3, in yeast EVs. Interestingly, EVs containing Fks1 and Chs3 rescued the yeast cells from antifungal molecules. However, EVs from fks1∆ or chs3∆ or the vps23chs3∆ double knockout strain were unable to rescue the yeast cells as compared to vps23∆ EVs. Overall, we have identified a potential role for yeast EVs in cell wall remodelling.

          Abstract

          Kening Zhao et al. show that yeast extracellular vesicles are depleted of ESCRT proteins but enriched with Fks1 and Chs3. The toxic effect of antifungal agents can be diminished by exposure to the Fks1- and Chs3- rich extracellular vesicles, suggesting a role for yeast extracellular vesicles in cell wall remodelling.

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          Most cited references31

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          Exosomes: secreted vesicles and intercellular communications

          Exosomes are small membrane vesicles of endocytic origin secreted by most cell types, and are thought to play important roles in intercellular communications. Although exosomes were originally described in 1983, interest in these vesicles has really increased dramatically in the last 3 years, after the finding that they contain mRNA and microRNA. This discovery sparked renewed interest for the general field of membrane vesicles involved in intercellular communications, and research on these structures has grown exponentially over the last few years, probing their composition and function, as well as their potential value as biomarkers.
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            Vesiclepedia 2019: a compendium of RNA, proteins, lipids and metabolites in extracellular vesicles

            Abstract Extracellular vesicles (EVs) are membranous vesicles that are released by both prokaryotic and eukaryotic cells into the extracellular microenvironment. EVs can be categorised as exosomes, ectosomes or shedding microvesicles and apoptotic bodies based on the mode of biogenesis. EVs contain biologically active cargo of nucleic acids, proteins, lipids and metabolites that can be altered based on the precise state of the cell. Vesiclepedia (http://www.microvesicles.org) is a web-based compendium of RNA, proteins, lipids and metabolites that are identified in EVs from both published and unpublished studies. Currently, Vesiclepedia contains data obtained from 1254 EV studies, 38 146 RNA entries, 349 988 protein entries and 639 lipid/metabolite entries. Vesiclepedia is publicly available and allows users to query and download EV cargo based on different search criteria. The mode of EV isolation and characterization, the biophysical and molecular properties and EV-METRIC are listed in the database aiding biomedical scientists in assessing the quality of the EV preparation and the corresponding data obtained. In addition, FunRich-based Vesiclepedia plugin is incorporated aiding users in data analysis.
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              The emerging shape of the ESCRT machinery.

              The past two years have seen an explosion in the structural understanding of the endosomal sorting complex required for transport (ESCRT) machinery that facilitates the trafficking of ubiquitylated proteins from endosomes to lysosomes via multivesicular bodies (MVBs). A common organization of all ESCRTs is a rigid core attached to flexibly connected modules that recognize other components of the MVB pathway. Several previously unsuspected key links between multiple ESCRT subunits, phospholipids and ubiquitin have now been elucidated, which, together with the detailed morphological analyses of ESCRT-depletion phenotypes, provide new insights into the mechanism of MVB biogenesis.
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                Author and article information

                Contributors
                M.Anderson@latrobe.edu.au
                S.Mathivanan@latrobe.edu.au
                Journal
                Commun Biol
                Commun Biol
                Communications Biology
                Nature Publishing Group UK (London )
                2399-3642
                9 August 2019
                9 August 2019
                2019
                : 2
                : 305
                Affiliations
                [1 ]ISNI 0000 0001 2342 0938, GRID grid.1018.8, Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science, , La Trobe University, ; Melbourne, VIC 3086 Australia
                [2 ]ISNI 0000 0001 2342 0938, GRID grid.1018.8, Department of Computer Science and Information Technology, , La Trobe University, ; Melbourne, VIC 3086 Australia
                [3 ]ISNI 0000000403978434, GRID grid.1055.1, Cancer Research Division, , Peter MacCallum Cancer Centre, ; Melbourne, VIC 3000 Australia
                [4 ]ISNI 0000 0001 2179 088X, GRID grid.1008.9, Sir Peter MacCallum Department of Oncology, , University of Melbourne, ; Melbourne, VIC 3010 Australia
                [5 ]ISNI 0000 0001 2179 088X, GRID grid.1008.9, Bio21 Institute, , University of Melbourne, ; Melbourne, VIC 3010 Australia
                [6 ]ISNI 0000 0004 1936 7304, GRID grid.1010.0, ARC Centre of Excellence in Plant Cell Walls and Adelaide Glycomics, , The University of Adelaide, Waite Campus, ; Urrbrae, SA 5064 Australia
                Author information
                http://orcid.org/0000-0002-9717-7560
                http://orcid.org/0000-0002-0421-3957
                http://orcid.org/0000-0002-9119-7173
                http://orcid.org/0000-0003-4421-3609
                http://orcid.org/0000-0002-8257-5128
                Article
                538
                10.1038/s42003-019-0538-8
                6688994
                31428693
                db7163f3-3fe0-4e9b-b925-61faf6a09530
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 July 2018
                : 2 July 2019
                Funding
                Funded by: Australian Research Council (DE150101777)
                Categories
                Article
                Custom metadata
                © The Author(s) 2018

                proteomics,biotechnology,escrt,fungal biology
                proteomics, biotechnology, escrt, fungal biology

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