4.7 Article

Defining the subcellular distribution and metabolic channeling of phosphatidylinositol

Journal

JOURNAL OF CELL BIOLOGY
Volume 219, Issue 3, Pages -

Publisher

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201906130

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Funding

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development Intramural Research Program
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development visiting fellowship
  3. Natural Sciences and Engineering Research Council of Canada Banting postdoctoral fellowship
  4. European Regional Development Fund (OP RDE, project Chemical biology for drugging undruggable targets ChemBioDrug) [CZ.02.1.01/0.0/0.0/16_019/0000729]
  5. Czech Academy of Sciences [RVO: 61388963]
  6. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [ZIAHD000196] Funding Source: NIH RePORTER

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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.

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