State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
University of Chinese Academy of Sciences, Beijing, China.
PLoS Genet. 2019 Dec 23;15(12):e1008548. doi: 10.1371/journal.pgen.1008548. eCollection 2019 Dec.
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.
磷脂酰丝氨酸(PS)由内质网(ER)中的磷脂酰丝氨酸合成酶(PSS)合成,通过不同的途径运输到质膜(PM)和线粒体。PS 在不同亚细胞位置的体内功能以及不同 PS 运输途径之间的协调尚不完全清楚。在这里,我们报告果蝇 PSS 调节细胞生长、脂质储存和线粒体功能。在 pss RNAi 中,PS 的减少会耗尽质膜中的 Akt,导致细胞生长缺陷;从磷脂合成到中性脂质合成的代谢转变导致异位脂质积累;线粒体 PS 的减少会损害线粒体蛋白的输入和线粒体的完整性。重要的是,通过丧失 PI4KIIIα 减少 ER 到 PM 的 PS 转运部分挽救了 pss RNAi 的线粒体缺陷。总之,我们的研究结果揭示了不同 PS 运输途径之间的平衡,并表明 PSS 通过不同的代谢机制调节细胞内稳态。