Regulation of glucosylceramide synthase and sphingolipid remodeling in the plant response to phosphate deficiency

Bao Yang, Yan Peng, Guo Zhang, Ruifan Liu, Simin Hao, Yi Ren, Shaoping Lu, Xuemin Wang, Liang Guo
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Abstract

Sphingolipids are important and abundant lipids in the plasma membrane, and their homeostasis plays a key role in plant growth, development, and stress responses. We previously found that non-specific phospholipase C4 (NPC4) hydrolyzes sphingophospholipids upon phosphate starvation. Here, we defined the downstream steps of sphingolipid remodeling by identifying glucosylceramide synthase (GCS) and its regulatory mechanisms in Arabidopsis thaliana. Phosphate deficiency induces the expression of GCS, and the encoded GCS enzyme mediates glucosylceramide biosynthesis. Down-regulation of GCS severely affects sphingolipid homeostasis and hinders plant growth under phosphate starvation. Accordingly, GCS over-expression promotes sphingolipid remodeling to maintain plant growth. In addition, PHOSPHATE STARVATION RESPONSE1 (PHR1), a key regulator of phosphate homeostasis, directly affects the expression of NPC4 and GCS to regulate sphingolipid remodeling during phosphate starvation. Together, these results identify the PHR1–NPC4–GCS module as a regulatory mechanism that fine-tunes sphingolipid homeostasis and reveal the importance of sphingolipid homeostasis in the plant response to phosphate deficiency.
植物对磷酸盐缺乏反应中葡萄糖神经酰胺合成酶和鞘脂重塑的调控
鞘脂是质膜中含量丰富的重要脂类,其稳态在植物生长发育和逆境反应中起着关键作用。我们之前发现非特异性磷脂酶C4 (NPC4)在磷酸盐饥饿时水解鞘磷脂。本研究通过鉴定拟南芥中葡萄糖神经酰胺合成酶(GCS)及其调控机制,确定了鞘脂重塑的下游步骤。磷酸缺乏诱导GCS的表达,编码的GCS酶介导糖基神经酰胺的生物合成。GCS的下调严重影响鞘脂稳态,阻碍植物在磷酸盐饥饿条件下的生长。因此,GCS过表达促进鞘脂重塑以维持植物生长。此外,磷酸盐饥饿反应1 (PHR1)是磷酸盐稳态的关键调控因子,可直接影响NPC4和GCS的表达,调节磷酸盐饥饿时鞘脂重塑。总之,这些结果确定了PHR1-NPC4-GCS模块作为微调鞘脂稳态的调节机制,并揭示了鞘脂稳态在植物对磷酸盐缺乏反应中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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