The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasis

Danny Mollerup Sørensen; Henrik Waldal Holen; Jesper Torbøl Pedersen; Helle Juel Martens; Daniele Silvestro; Lyubomir Dimitrov Stanchev; Sara Rute Costa; Thomas Günther Pomorski; Rosa Laura López-Marqués; Michael Palmgren

doi:10.1091/mbc.e18-06-0365

The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasis

Danny Mollerup Sørensen, Henrik Waldal Holen, Jesper Torbøl Pedersen, Helle Juel Martens, Daniele Silvestro, Lyubomir Dimitrov Stanchev, Sara Rute Costa, Thomas Günther Pomorski, Rosa Laura López-Marqués, Michael Palmgren^*

^*Corresponding author af dette arbejde

14 Citationer (Scopus)

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Abstract

P5A ATPases are expressed in the endoplasmic reticulum (ER) of all eukaryotic cells, and their disruption results in severe ER stress. However, the function of these ubiquitous membrane proteins, which belong to the P-type ATPase superfamily, is unknown. We purified a functional tagged version of the Saccharomyces cerevisiae P5A ATPase Spf1p and observed that the ATP hydrolytic activity of the protein is stimulated by phosphatidylinositol 4-phosphate (PI4P). Furthermore, SPF1 exhibited negative genetic interactions with SAC1, encoding a PI4P phosphatase, and with OSH1 to OSH6, encoding Osh proteins, which, when energized by a PI4P gradient, drive export of sterols and lipids from the ER. Deletion of SPF1 resulted in increased sensitivity to inhibitors of sterol production, a marked change in the ergosterol/lanosterol ratio, accumulation of sterols in the plasma membrane, and cytosolic accumulation of lipid bodies. We propose that Spf1p maintains cellular sterol homeostasis by influencing the PI4P-induced and Osh-mediated export of sterols from the ER.

Originalsprog	Engelsk
Tidsskrift	Molecular Biology of the Cell
Vol/bind	30
Udgave nummer	9
Sider (fra-til)	1069-1084
ISSN	1059-1524
DOI	https://doi.org/10.1091/mbc.e18-06-0365
Status	Udgivet - 15 apr. 2019

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10.1091/mbc.e18-06-0365Licens: CC BY-NC-SA

The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasisForlagets udgivne version, 2,35 MBLicens: CC BY-NC-SA

http://europepmc.org/articles/pmc6724510?pdf=renderLicens: CC BY-NC-SA

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Sørensen, D. M., Holen, H. W., Pedersen, J. T., Martens, H. J., Silvestro, D., Stanchev, L. D., Costa, S. R., Pomorski, T. G., López-Marqués, R. L., & Palmgren, M. (2019). The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasis. Molecular Biology of the Cell, 30(9), 1069-1084. https://doi.org/10.1091/mbc.e18-06-0365

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title = "The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasis",

abstract = "P5A ATPases are expressed in the endoplasmic reticulum (ER) of all eukaryotic cells, and their disruption results in severe ER stress. However, the function of these ubiquitous membrane proteins, which belong to the P-type ATPase superfamily, is unknown. We purified a functional tagged version of the Saccharomyces cerevisiae P5A ATPase Spf1p and observed that the ATP hydrolytic activity of the protein is stimulated by phosphatidylinositol 4-phosphate (PI4P). Furthermore, SPF1 exhibited negative genetic interactions with SAC1, encoding a PI4P phosphatase, and with OSH1 to OSH6, encoding Osh proteins, which, when energized by a PI4P gradient, drive export of sterols and lipids from the ER. Deletion of SPF1 resulted in increased sensitivity to inhibitors of sterol production, a marked change in the ergosterol/lanosterol ratio, accumulation of sterols in the plasma membrane, and cytosolic accumulation of lipid bodies. We propose that Spf1p maintains cellular sterol homeostasis by influencing the PI4P-induced and Osh-mediated export of sterols from the ER.",

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AU - Sørensen, Danny Mollerup

AU - Holen, Henrik Waldal

AU - Pedersen, Jesper Torbøl

AU - Martens, Helle Juel

AU - Silvestro, Daniele

AU - Stanchev, Lyubomir Dimitrov

AU - Costa, Sara Rute

AU - Pomorski, Thomas Günther

AU - López-Marqués, Rosa Laura

AU - Palmgren, Michael

PY - 2019/4/15

Y1 - 2019/4/15

N2 - P5A ATPases are expressed in the endoplasmic reticulum (ER) of all eukaryotic cells, and their disruption results in severe ER stress. However, the function of these ubiquitous membrane proteins, which belong to the P-type ATPase superfamily, is unknown. We purified a functional tagged version of the Saccharomyces cerevisiae P5A ATPase Spf1p and observed that the ATP hydrolytic activity of the protein is stimulated by phosphatidylinositol 4-phosphate (PI4P). Furthermore, SPF1 exhibited negative genetic interactions with SAC1, encoding a PI4P phosphatase, and with OSH1 to OSH6, encoding Osh proteins, which, when energized by a PI4P gradient, drive export of sterols and lipids from the ER. Deletion of SPF1 resulted in increased sensitivity to inhibitors of sterol production, a marked change in the ergosterol/lanosterol ratio, accumulation of sterols in the plasma membrane, and cytosolic accumulation of lipid bodies. We propose that Spf1p maintains cellular sterol homeostasis by influencing the PI4P-induced and Osh-mediated export of sterols from the ER.

AB - P5A ATPases are expressed in the endoplasmic reticulum (ER) of all eukaryotic cells, and their disruption results in severe ER stress. However, the function of these ubiquitous membrane proteins, which belong to the P-type ATPase superfamily, is unknown. We purified a functional tagged version of the Saccharomyces cerevisiae P5A ATPase Spf1p and observed that the ATP hydrolytic activity of the protein is stimulated by phosphatidylinositol 4-phosphate (PI4P). Furthermore, SPF1 exhibited negative genetic interactions with SAC1, encoding a PI4P phosphatase, and with OSH1 to OSH6, encoding Osh proteins, which, when energized by a PI4P gradient, drive export of sterols and lipids from the ER. Deletion of SPF1 resulted in increased sensitivity to inhibitors of sterol production, a marked change in the ergosterol/lanosterol ratio, accumulation of sterols in the plasma membrane, and cytosolic accumulation of lipid bodies. We propose that Spf1p maintains cellular sterol homeostasis by influencing the PI4P-induced and Osh-mediated export of sterols from the ER.

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The P5A ATPase Spf1p is stimulated by phosphatidylinositol 4-phosphate and influences cellular sterol homeostasis

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