A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis

Lipid droplet (LD) utilization is an important cellular activity that regulates energy balance and release of lipid second messengers. Because fatty acids exhibit both beneficial and toxic properties, their release from LDs must be controlled. Here we demonstrate that yeast Sfh3, an unusual Sec14-li...

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Main Authors: Ren, J., Lin, C., Pathak, M., Temple, B., Nile, A., Mousely, Carl, Duncan, M., Eckert, D., Leiker, T., Ivanova, P., Myers, D., Murphy, R., Brown, H., Verdaasdonkf, J., Bloom, K., Ortlund, E., Neiman, A., Bankaitis, V.
Format: Journal Article
Published: American Society for Cell Biology 2014
Online Access:http://hdl.handle.net/20.500.11937/33506
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author Ren, J.
Lin, C.
Pathak, M.
Temple, B.
Nile, A.
Mousely, Carl
Duncan, M.
Eckert, D.
Leiker, T.
Ivanova, P.
Myers, D.
Murphy, R.
Brown, H.
Verdaasdonkf, J.
Bloom, K.
Ortlund, E.
Neiman, A.
Bankaitis, V.
author_facet Ren, J.
Lin, C.
Pathak, M.
Temple, B.
Nile, A.
Mousely, Carl
Duncan, M.
Eckert, D.
Leiker, T.
Ivanova, P.
Myers, D.
Murphy, R.
Brown, H.
Verdaasdonkf, J.
Bloom, K.
Ortlund, E.
Neiman, A.
Bankaitis, V.
author_sort Ren, J.
building Curtin Institutional Repository
collection Online Access
description Lipid droplet (LD) utilization is an important cellular activity that regulates energy balance and release of lipid second messengers. Because fatty acids exhibit both beneficial and toxic properties, their release from LDs must be controlled. Here we demonstrate that yeast Sfh3, an unusual Sec14-like phosphatidylinositol transfer protein, is an LD-associated protein that inhibits lipid mobilization from these particles. We further document a complex biochemical diversification of LDs during sporulation in which Sfh3 and select other LD proteins redistribute into discrete LD subpopulations. The data show that Sfh3 modulates the efficiency with which a neutral lipid hydrolase-rich LD subclass is consumed during biogenesis of specialized membrane envelopes that package replicated haploid meiotic genomes. These results present novel insights into the interface between phosphoinositide signaling and developmental regulation of LD metabolism and unveil meiosis-specific aspects of Sfh3 (and phosphoinositide) biology that are invisible to contemporary haploid-centric cell biological, proteomic, and functional genomics approaches.
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format Journal Article
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T08:32:54Z
publishDate 2014
publisher American Society for Cell Biology
recordtype eprints
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spelling curtin-20.500.11937-335062017-09-13T15:31:15Z A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis Ren, J. Lin, C. Pathak, M. Temple, B. Nile, A. Mousely, Carl Duncan, M. Eckert, D. Leiker, T. Ivanova, P. Myers, D. Murphy, R. Brown, H. Verdaasdonkf, J. Bloom, K. Ortlund, E. Neiman, A. Bankaitis, V. Lipid droplet (LD) utilization is an important cellular activity that regulates energy balance and release of lipid second messengers. Because fatty acids exhibit both beneficial and toxic properties, their release from LDs must be controlled. Here we demonstrate that yeast Sfh3, an unusual Sec14-like phosphatidylinositol transfer protein, is an LD-associated protein that inhibits lipid mobilization from these particles. We further document a complex biochemical diversification of LDs during sporulation in which Sfh3 and select other LD proteins redistribute into discrete LD subpopulations. The data show that Sfh3 modulates the efficiency with which a neutral lipid hydrolase-rich LD subclass is consumed during biogenesis of specialized membrane envelopes that package replicated haploid meiotic genomes. These results present novel insights into the interface between phosphoinositide signaling and developmental regulation of LD metabolism and unveil meiosis-specific aspects of Sfh3 (and phosphoinositide) biology that are invisible to contemporary haploid-centric cell biological, proteomic, and functional genomics approaches. 2014 Journal Article http://hdl.handle.net/20.500.11937/33506 10.1091/mbc.E13-11-0634 American Society for Cell Biology unknown
spellingShingle Ren, J.
Lin, C.
Pathak, M.
Temple, B.
Nile, A.
Mousely, Carl
Duncan, M.
Eckert, D.
Leiker, T.
Ivanova, P.
Myers, D.
Murphy, R.
Brown, H.
Verdaasdonkf, J.
Bloom, K.
Ortlund, E.
Neiman, A.
Bankaitis, V.
A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title_full A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title_fullStr A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title_full_unstemmed A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title_short A phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
title_sort phosphatidylinositol transfer protein integrates phosphoinositide signaling with lipid droplet metabolism to regulate a developmental program of nutrient stress–induced membrane biogenesis
url http://hdl.handle.net/20.500.11937/33506