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Defining the subcellular distribution and metabolic channeling of phosphatidylinositol
Phosphatidylinositol (PI) is an essential structural component of eukaryotic membranes that also serves as the common precursor for polyphosphoinositide (PPIn) lipids. Despite the recognized importance of PPIn species for signal transduction and membrane homeostasis, there is still a limited underst...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054996/ https://www.ncbi.nlm.nih.gov/pubmed/32211894 http://dx.doi.org/10.1083/jcb.201906130 |
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author | Pemberton, Joshua G. Kim, Yeun Ju Humpolickova, Jana Eisenreichova, Andrea Sengupta, Nivedita Toth, Daniel J. Boura, Evzen Balla, Tamas |
author_facet | Pemberton, Joshua G. Kim, Yeun Ju Humpolickova, Jana Eisenreichova, Andrea Sengupta, Nivedita Toth, Daniel J. Boura, Evzen Balla, Tamas |
author_sort | Pemberton, Joshua G. |
collection | PubMed |
description | Phosphatidylinositol (PI) is an essential structural component of eukaryotic membranes that also serves as the common precursor for polyphosphoinositide (PPIn) lipids. Despite the recognized importance of PPIn species for signal transduction and membrane homeostasis, there is still a limited understanding of the relationship between PI availability and the turnover of subcellular PPIn pools. To address these shortcomings, we established a molecular toolbox for investigations of PI distribution within intact cells by exploiting the properties of a bacterial enzyme, PI-specific PLC (PI-PLC). Using these tools, we find a minor presence of PI in membranes of the ER, as well as a general enrichment within the cytosolic leaflets of the Golgi complex, peroxisomes, and outer mitochondrial membrane, but only detect very low steady-state levels of PI within the plasma membrane (PM) and endosomes. Kinetic studies also demonstrate the requirement for sustained PI supply from the ER for the maintenance of monophosphorylated PPIn species within the PM, Golgi complex, and endosomal compartments. |
format | Online Article Text |
id | pubmed-7054996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70549962020-09-02 Defining the subcellular distribution and metabolic channeling of phosphatidylinositol Pemberton, Joshua G. Kim, Yeun Ju Humpolickova, Jana Eisenreichova, Andrea Sengupta, Nivedita Toth, Daniel J. Boura, Evzen Balla, Tamas J Cell Biol Tools Phosphatidylinositol (PI) is an essential structural component of eukaryotic membranes that also serves as the common precursor for polyphosphoinositide (PPIn) lipids. Despite the recognized importance of PPIn species for signal transduction and membrane homeostasis, there is still a limited understanding of the relationship between PI availability and the turnover of subcellular PPIn pools. To address these shortcomings, we established a molecular toolbox for investigations of PI distribution within intact cells by exploiting the properties of a bacterial enzyme, PI-specific PLC (PI-PLC). Using these tools, we find a minor presence of PI in membranes of the ER, as well as a general enrichment within the cytosolic leaflets of the Golgi complex, peroxisomes, and outer mitochondrial membrane, but only detect very low steady-state levels of PI within the plasma membrane (PM) and endosomes. Kinetic studies also demonstrate the requirement for sustained PI supply from the ER for the maintenance of monophosphorylated PPIn species within the PM, Golgi complex, and endosomal compartments. Rockefeller University Press 2020-02-18 /pmc/articles/PMC7054996/ /pubmed/32211894 http://dx.doi.org/10.1083/jcb.201906130 Text en This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Tools Pemberton, Joshua G. Kim, Yeun Ju Humpolickova, Jana Eisenreichova, Andrea Sengupta, Nivedita Toth, Daniel J. Boura, Evzen Balla, Tamas Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title | Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title_full | Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title_fullStr | Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title_full_unstemmed | Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title_short | Defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
title_sort | defining the subcellular distribution and metabolic channeling of phosphatidylinositol |
topic | Tools |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054996/ https://www.ncbi.nlm.nih.gov/pubmed/32211894 http://dx.doi.org/10.1083/jcb.201906130 |
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