首页> 外文期刊>The Plant Cell >Reduced Biosynthesis of Digalactosyldiacylglycerol, a Major Chloroplast Membrane Lipid, Leads to Oxylipin Overproduction and Phloem Cap Lignification in Arabidopsis
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Reduced Biosynthesis of Digalactosyldiacylglycerol, a Major Chloroplast Membrane Lipid, Leads to Oxylipin Overproduction and Phloem Cap Lignification in Arabidopsis

机译:双半乳糖基二酰基甘油(一种主要的叶绿体膜脂质)的生物合成减少,导致拟南芥中的脂蛋白过度生产和韧皮部木质化。

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DIGALACTOSYLDIACYLGLYCEROL SYNTHASE1 (DGD1) is a chloroplast outer membrane protein responsible for the biosynthesis of the lipid digalactosyldiacylglycerol (DGDG) from monogalactosyldiacylglycerol (MGDG). The Arabidopsis thaliana dgd1 mutants have a greater than 90% reduction in DGDG content, reduced photosynthesis, and altered chloroplast morphology. However, the most pronounced visible phenotype is the extremely short inflorescence stem, but how deficient DGDG biosynthesis causes this phenotype is unclear. We found that, in dgd1 mutants, phloem cap cells were lignified and jasmonic acid (JA)-responsive genes were highly upregulated under normal growth conditions. The coronative insensitive1 dgd1 and allene oxide synthase dgd1 double mutants no longer exhibited the short inflorescence stem and lignification phenotypes but still had the same lipid profile and reduced photosynthesis as dgd1 single mutants. Hormone and lipidomics analyses showed higher levels of JA, JA-isoleucine, 12-oxo-phytodienoic acid, and arabidopsides in dgd1 mutants. Transcript and protein level analyses further suggest that JA biosynthesis in dgd1 is initially activated through the increased expression of genes encoding 13-lipoxygenases (LOXs) and phospholipase A-I gamma 3 (At1g51440), a plastid lipase with a high substrate preference for MGDG, and is sustained by further increases in LOX and allene oxide cyclase mRNA and protein levels. Our results demonstrate a link between the biosynthesis of DGDG and JA.
机译:DIGALACTOSYLDIACYLGLYCEROLSYNTHASE1(DGD1)是一种叶绿体外膜蛋白,负责从单半乳糖基二酰基甘油(MGDG)生物合成脂质二半乳糖基二酰基甘油(DGDG)。拟南芥dgd1突变体的DGDG含量降低了90%以上,光合作用降低,叶绿体形态发生了变化。但是,最明显的可见表型是非常短的花序茎,但尚不清楚DGDG生物合成不足如何导致该表型。我们发现,在dgd1突变体中,韧皮部帽细胞被木质化,而茉莉酸(JA)响应基因在正常生长条件下高度上调。加冕的不敏感1 dgd1和氧化烯合酶dgd1双突变体不再表现出短的花序茎和木质化表型,但仍具有与dgd1单突变体相同的脂质特征和降低的光合作用。激素和脂质组学分析显示dgd1突变体中JA,JA-异亮氨酸,12-氧代植物二烯酸和阿拉伯糖苷的含量较高。转录本和蛋白质水平分析进一步表明,dgd1中的JA生物合成最初是通过编码13-脂加氧酶(LOXs)和磷脂酶AIγ3(At1g51440)(一种对MGDG具有较高底物优先性的质体脂酶)的基因表达增加而被激活的。通过进一步增加LOX和氧化烯环化酶mRNA和蛋白质水平来维持。我们的结果证明了DGDG和JA的生物合成之间的联系。

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