Endosomal vesicle fusion machinery is involved with the contractile vacuole in Dictyostelium discoideum.


Journal

Journal of cell science
ISSN: 1477-9137
Titre abrégé: J Cell Sci
Pays: England
ID NLM: 0052457

Informations de publication

Date de publication:
15 01 2023
Historique:
received: 02 08 2022
accepted: 13 12 2022
pubmed: 23 12 2022
medline: 20 1 2023
entrez: 22 12 2022
Statut: ppublish

Résumé

Contractile vacuoles (CVs), enigmatic osmoregulatory organelles, share common characteristics, such as a requirement for RAB11 and high levels of V-ATPase. These commonalities suggest a conserved evolutionary origin for the CVs with implications for understanding of the last common ancestor of eukaryotes and eukaryotic diversification more broadly. A taxonomically broader sampling of CV-associated machinery is required to address this question further. We used a transcriptomics-based approach to identify CV-associated gene products in Dictyostelium discoideum. This approach was first validated by assessing a set of known CV-associated gene products, which were significantly upregulated following hypo-osmotic exposure. Moreover, endosomal and vacuolar gene products were enriched in the upregulated gene set. An upregulated SNARE protein (NPSNB) was predominantly plasma membrane localised and enriched in the vicinity of CVs, supporting the association with this organelle found in the transcriptomic analysis. We therefore confirm that transcriptomic approaches can identify known and novel players in CV function, in our case emphasizing the role of endosomal vesicle fusion machinery in the D. discoideum CV and facilitating future work to address questions regarding the deep evolution of eukaryotic organelles.

Identifiants

pubmed: 36546731
pii: 286683
doi: 10.1242/jcs.260477
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. Published by The Company of Biologists Ltd.

Déclaration de conflit d'intérêts

Competing interests The authors declare no competing or financial interests.

Auteurs

Paul T Manna (PT)

Institute of Neuroscience and Physiology, Department of Physiology, University of Gothenburg, Gothenburg, Box 430, 405 30, Sweden.
Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Alberta, T6G 2G3, Canada.

Lael D Barlow (LD)

Department of Biological Sciences, University of Alberta, Edmonton, Alberta, T6G 2E9, Canada.
Division of Biological Chemistry and Drug Discovery, School of Life, Sciences, University of Dundee, Dundee DD1 5EH, UK.

Inmaculada Ramirez-Macias (I)

Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Alberta, T6G 2G3, Canada.
Microbiology Unit, University Hospital Virgen de las Nieves, Granada 18014, Spain.
Instituto de Investigación Biosanitaria ibs, Granada, 18012, Spain.

Emily K Herman (EK)

Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Alberta, T6G 2G3, Canada.
Department of Agricultural, Food and Nutritional Science, Faculty of Agricultural, Life and Environmental Sciences, University of Alberta, Edmonton, Alberta, T6G 1C9, Canada.

Joel B Dacks (JB)

Division of Infectious Diseases, Department of Medicine, University of Alberta, Edmonton, Alberta, Alberta, T6G 2G3, Canada.
Department of Biological Sciences, University of Alberta, Edmonton, Alberta, T6G 2E9, Canada.
Centre for Life's Origins and Evolution, Department of Genetics, Evolution, and Environment, University of College London, London WC1E 6BT, UK.

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