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DGAT1 and PDAT1 Acyltransferases Have Overlapping Functions in Arabidopsis Triacylglycerol Biosynthesis and Are Essential for Normal Pollen and Seed Development

机译:DGAT1和PDAT1酰基转移酶在拟南芥三酰基甘油生物合成中具有重叠功能,对于正常的花粉和种子发育至关重要

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Triacylglycerol (TAG) biosynthesis is a principal metabolic pathway in most organisms, and TAG is the major form of carbon storage in many plant seeds. Acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) is the only acyltransferase enzyme that has been confirmed to contribute to TAG biosynthes is in Arabidopsis thaliana seeds. However,dgat1 null mutants display only a 20 to 40% decrease in seed oil content. To determine whether other enzymes contribute to TAG synthesis, candidate genes were expressed in TAG-deficient yeast, candidate mutants were crossed with the dgat1-1 mutant, and target genes were suppressed by RNA interference (RNAi). An in vivo role for phospholipid:diacylglycerol acyltransferase 1 (PDAT1;At5g13640) in TAG synthesis was revealed in this study. After failing to obtain double homozygous plants from crossing dgat1-1 and pdat1-2, further investigation showed that the dgat1-1 pdat1-2 double mutation resulted in sterile pollen that lacked visible oil bodies. RNAi silencing of PDAT1 in adgat1-1 background or DGAT1 in pdat1-1 background resulted in 70 to 80% decreases in oil content per seed and in disruptions of embryo development. These results establish in vivo involvement of PDAT1 in TAG biosynthesis, rule out major contributions by other candidate enzymes, and indicate that PDAT1 and DGAT1 have over lapping functions that are essential for normal pollen and seed development of Arabidopsis
机译:在大多数生物中,三酰基甘油(TAG)的生物合成是主要的代谢途径,而TAG是许多植物种子中碳储存的主要形式。乙酰辅酶A:二酰基甘油酰基转移酶1(DGAT1)是唯一被证实有助于拟南芥种子中TAG生物合成的酰基转移酶。但是,dgat1 null突变体显示种子油含量仅降低20%至40%。为了确定其他酶是否有助于TAG合成,在TAG缺陷型酵母中表达候选基因,将候选突变体与dgat1-1突变体杂交,并通过RNA干扰(RNAi)抑制目标基因。在这项研究中揭示了磷脂:二酰基甘油酰基转移酶1(PDAT1; At5g13640)在TAG合成中的体内作用。在无法从dgat1-1和pdat1-2杂交获得双重纯合植物后,进一步的研究表明dgat1-1 pdat1-2双重突变导致无菌花粉缺乏可见的油体。 adgat1-1背景中PDAT1或pdat1-1背景中DGAT1的RNAi沉默导致每粒种子含油量降低70%至80%,并破坏了胚胎发育。这些结果建立了PDAT1在TAG生物合成中的体内参与,排除了其他候选酶的主要贡献,并表明PDAT1和DGAT1具有对正常花粉和拟南芥种子发育必不可少的重叠功能。

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