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Phosphatidylserine synthase regulates cellular homeostasis through distinct metabolic mechanisms.
Yang, Xiao; Liang, Jingjing; Ding, Long; Li, Xia; Lam, Sin-Man; Shui, Guanghou; Ding, Mei; Huang, Xun.
Afiliación
  • Yang X; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
  • Liang J; University of Chinese Academy of Sciences, Beijing, China.
  • Ding L; School of Life Sciences, Shandong First Medical University & Shandong Academy of Medical Sciences, TaiAn, China.
  • Li X; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
  • Lam SM; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
  • Shui G; University of Chinese Academy of Sciences, Beijing, China.
  • Ding M; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
  • Huang X; LipidAll Technologies Co., Ltd. Changzhou, China.
PLoS Genet ; 15(12): e1008548, 2019 12.
Article en En | MEDLINE | ID: mdl-31869331
ABSTRACT
Phosphatidylserine (PS), synthesized in the endoplasmic reticulum (ER) by phosphatidylserine synthase (PSS), is transported to the plasma membrane (PM) and mitochondria through distinct routes. The in vivo functions of PS at different subcellular locations and the coordination between different PS transport routes are not fully understood. Here, we report that Drosophila PSS regulates cell growth, lipid storage and mitochondrial function. In pss RNAi, reduced PS depletes plasma membrane Akt, contributing to cell growth defects; the metabolic shift from phospholipid synthesis to neutral lipid synthesis results in ectopic lipid accumulation; and the reduction of mitochondrial PS impairs mitochondrial protein import and mitochondrial integrity. Importantly, reducing PS transport from the ER to PM by loss of PI4KIIIα partially rescues the mitochondrial defects of pss RNAi. Together, our results uncover a balance between different PS transport routes and reveal that PSS regulates cellular homeostasis through distinct metabolic mechanisms.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilserinas / Membrana Celular / CDPdiacilglicerol-Serina O-Fosfatidiltransferasa / Proteínas de Drosophila / Drosophila melanogaster / Retículo Endoplásmico / CDP-Diacilglicerol-Inositol 3-Fosfatidiltransferasa Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilserinas / Membrana Celular / CDPdiacilglicerol-Serina O-Fosfatidiltransferasa / Proteínas de Drosophila / Drosophila melanogaster / Retículo Endoplásmico / CDP-Diacilglicerol-Inositol 3-Fosfatidiltransferasa Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2019 Tipo del documento: Article País de afiliación: China