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Coevolution of Domain Interactions in the Chloroplast TGD1 2 3 Lipid Transfer Complex Specific to Brassicaceae and Poaceae Plants

机译:十字花科和禾本科植物特有的叶绿体TGD1、2、3脂质转移复合体中域相互作用的共同演化

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摘要

The import of lipids into the chloroplast is essential for photosynthetic membrane biogenesis. This process requires an ABC transporter in the inner envelope membrane with three subunits, TRIGALACTOSYLDIACYLGLYCEROL (TGD) 1, 2, and 3, named after the oligogalactolipids that accumulate in the respective Arabidopsis thaliana mutants. Unlike Arabidopsis, in the model grass Brachypodium distachyon, chloroplast lipid biosynthesis is largely dependent on imported precursors, resulting in a characteristic difference in chloroplast lipid acyl composition between the two plants. Accordingly, Arabidopsis is designated as a 16:3 (acyl carbons:double bounds) plant and Brachypodium as an 18:3 plant. Repression of TGD1 (BdTGD1) in Brachypodium affected growth without triggering oligogalactolipid biosynthesis. Moreover, expressing BdTGD1 in the Arabidopsis tgd1-1 mutant restored some phenotypes but did not reverse oligogalactolipid biosynthesis. A 27-amino acid loop (L45) is solely responsible for the incomplete functioning of BdTGD1 in Arabidopsis tgd1-1. Coevolutionary analysis and coimmunoprecipitation assays showed that the TGD1 L45 loop interacts with the mycobacterial cell entry domain of TGD2. To explain the observed differences in oligogalactolipid biosynthesis between the two species, we suggest that excess monogalactosyldiacylglycerol derived from chloroplast-derived precursors in Arabidopsis tgd1-1 is converted into oligogalactolipids, a process absent from Brachypodium with reduced TGD1 levels, which assembles monogalactosyldiacylglycerol exclusively from imported precursors.
机译:脂质向叶绿体中的导入对于光合膜生物发生至关重要。此过程需要在内膜膜中有一个ABC转运蛋白,该转运蛋白具有三个亚单位TRIGALACTOSYLDIACYLGLYCEROL(TGD)1、2和3,它们以在各自拟南芥突变体中积累的寡半乳糖脂命名。与拟南芥不同,在模型草短枝曲霉中,叶绿体脂质的生物合成很大程度上依赖于进口的前体,从而导致两种植物之间叶绿体脂质酰基组成的特征差异。因此,拟南芥被指定为16:3(酰基碳:双键)植物,而短梗植物被指定为18:3植物。在水曲霉中抑制TGD1(BdTGD1)会影响生长,而不会触发寡半乳糖脂的生物合成。此外,在拟南芥tgd1-1突变体中表达BdTGD1恢复了一些表型,但没有逆转寡半乳糖脂的生物合成。一个27个氨基酸的环(L45)完全负责拟南芥tgd1-1中BdTGD1的不完全功能。协同进化分析和免疫沉淀试验表明,TGD1 L45环与TGD2的分枝杆菌细胞进入结构域相互作用。为了解释观察到的两个物种之间的寡半乳糖脂生物合成差异,我们建议将拟南芥tgd1-1中叶绿体衍生的前体衍生的过量单半乳糖基二酰基甘油转化为寡半乳糖脂,短孢子虫不存在降低TGD1含量的过程,该过程仅由进口的半乳糖基糖脂组装而成前体。

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