Fan Jilian, Yan Chengshi, Roston Rebecca, Shanklin John, Xu Changcheng
Bioscience Department, Brookhaven National Laboratory, Upton, New York 11973.
Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan 48824.
Plant Cell. 2014 Oct;26(10):4119-34. doi: 10.1105/tpc.114.130377. Epub 2014 Oct 7.
Triacylglycerol (TAG) metabolism is a key aspect of intracellular lipid homeostasis in yeast and mammals, but its role in vegetative tissues of plants remains poorly defined. We previously reported that PHOSPHOLIPID:DIACYLGLYCEROL ACYLTRANSFERASE1 (PDAT1) is crucial for diverting fatty acids (FAs) from membrane lipid synthesis to TAG and thereby protecting against FA-induced cell death in leaves. Here, we show that overexpression of PDAT1 enhances the turnover of FAs in leaf lipids. Using the trigalactosyldiacylglycerol1-1 (tgd1-1) mutant, which displays substantially enhanced PDAT1-mediated TAG synthesis, we demonstrate that disruption of SUGAR-DEPENDENT1 (SDP1) TAG lipase or PEROXISOMAL TRANSPORTER1 (PXA1) severely decreases FA turnover, leading to increases in leaf TAG accumulation, to 9% of dry weight, and in total leaf lipid, by 3-fold. The membrane lipid composition of tgd1-1 sdp1-4 and tgd1-1 pxa1-2 double mutants is altered, and their growth and development are compromised. We also show that two Arabidopsis thaliana lipin homologs provide most of the diacylglycerol for TAG synthesis and that loss of their functions markedly reduces TAG content, but with only minor impact on eukaryotic galactolipid synthesis. Collectively, these results show that Arabidopsis lipins, along with PDAT1 and SDP1, function synergistically in directing FAs toward peroxisomal β-oxidation via TAG intermediates, thereby maintaining membrane lipid homeostasis in leaves.
三酰甘油(TAG)代谢是酵母和哺乳动物细胞内脂质稳态的一个关键方面,但其在植物营养组织中的作用仍不清楚。我们之前报道过,磷脂:二酰甘油酰基转移酶1(PDAT1)对于将脂肪酸(FAs)从膜脂合成转向TAG从而保护叶片免受FA诱导的细胞死亡至关重要。在此,我们表明PDAT1的过表达增强了叶片脂质中FAs的周转。利用三半乳糖二酰甘油1-1(tgd1-1)突变体,该突变体显示出显著增强的PDAT1介导的TAG合成,我们证明糖依赖性1(SDP1)TAG脂肪酶或过氧化物酶体转运蛋白1(PXA1)的破坏会严重降低FA周转,导致叶片TAG积累增加至干重的9%,总叶片脂质增加3倍。tgd1-1 sdp1-4和tgd1-1 pxa1-2双突变体的膜脂组成发生改变,其生长和发育受到损害。我们还表明,两个拟南芥脂素同源物为TAG合成提供了大部分二酰甘油,它们功能的丧失显著降低了TAG含量,但对真核半乳糖脂合成只有轻微影响。总体而言,这些结果表明,拟南芥脂素与PDAT1和SDP1协同作用,通过TAG中间体将FAs导向过氧化物酶体β-氧化,从而维持叶片中的膜脂稳态。