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首页> 外文期刊>Plant Molecular Biology >Specific induction of TaAAPT1, an ER- and Golgi-localized ECPT-type aminoalcoholphosphotransferase, results in preferential accumulation of the phosphatidylethanolamine membrane phospholipid during cold acclimation in wheat
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Specific induction of TaAAPT1, an ER- and Golgi-localized ECPT-type aminoalcoholphosphotransferase, results in preferential accumulation of the phosphatidylethanolamine membrane phospholipid during cold acclimation in wheat

机译:TaAAPT1(ER和高尔基体定位的ECPT型氨基醇磷酸转移酶)的特异性诱导导致小麦冷驯化过程中磷脂酰乙醇胺膜磷脂的优先积累

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摘要

Cold acclimation requires substantial alteration in membrane property. In contrast to well-documented fatty acid unsaturation during cold acclimation, changes in phospholipid biosynthesis during cold acclimation are less understood. Here, we isolated and characterized two aminoalcoholphosphotransferase (AAPT) cDNAs, TaAAPT1 and TaAAPT2, from wheat. AAPTs utilize diacylglycerols and CDP-choline/ethanolamine as substrates and catalyze the final step of the CDP-choline/ethanolamine pathway for phosphatidylcholine (PC)/phosphatidylethanolamine (PE) synthesis, respectively. Functionality of TaAAPT1 and TaAAPT2 was demonstrated by heterologous expression in a yeast cpt1Δ ept1Δ double mutant that lacks both AAPT activities. Detailed characterization of AAPT activities from the transformed mutant cells indicated that TaAAPT1 is an ECPT-type enzyme with higher ethanolamine phosphotransferase (EPT) activity than choline phosphotransferase (CPT) activity, while TaAAPT2 is a CEPT-type with the opposite substrate preference. Transient expression of GFP-fused TaAAPT1 and TaAAPT2 proteins in wheat and onion cells indicated they are localized to both the endoplasmic reticulum and Golgi apparatus, suggesting that the final synthesis of PE and PC via the CDP-choline/ethanolamine pathway occurs in these organella. Quantitative PCR analyses revealed that TaAAPT1 expression is strongly induced by cold, while TaAAPT2 was constitutively expressed at lower levels. Measurement of phospholipid content in wheat leaves indicated that PE is more prominently increased in response to cold than PC and accordingly PE/PC ratio increased from 0.385 to 0.530 during 14 days of cold acclimation. Together, these data suggested that an increase in the PE/PC ratio during cold acclimation is regulated at the final step of the biosynthetic pathway. Keywords Cold acclimation - PE - PC - Phospholipid - Endoplasmic reticulum - Golgi apparatus
机译:冷驯化要求膜特性发生重大变化。与文献证明的冷驯化过程中的脂肪酸不饱和度相反,人们对冷驯化过程中磷脂生物合成的变化了解较少。在这里,我们从小麦中分离并鉴定了两个氨基醇磷酸转移酶(AAPT)cDNA TaAAPT1和TaAAPT2。 AAPT利用二酰基甘油和CDP-胆碱/乙醇胺作为底物,并催化CDP-胆碱/乙醇胺途径的最后一步分别用于磷脂酰胆碱(PC)/磷脂酰乙醇胺(PE)的合成。 TaAAPT1和TaAAPT2的功能通过酵母cpt1Δept1Δ双重突变体的异源表达得到证实,该突变体均缺乏AAPT活性。来自转化的突变细胞的AAPT活性的详细表征表明,TaAAPT1是一种ECPT型酶,其乙醇胺磷酸转移酶(EPT)活性高于胆碱磷酸转移酶(CPT)活性,而TaAAPT2是具有相反底物偏好的CEPT型酶。 GFP融合的TaAAPT1和TaAAPT2蛋白在小麦和洋葱细胞中的瞬时表达表明它们位于内质网和高尔基体中,表明通过CDP-胆碱/乙醇胺途径进行的PE和PC的最终合成发生在这些细胞器中。定量PCR分析显示,寒冷会强烈诱导TaAAPT1表达,而TaAAPT2则以较低水平组成性表达。小麦叶片中磷脂含量的测量表明,在寒冷条件下,PE在PC响应中比PC显着增加,并且在冷适应14天后,PE / PC比从0.385升高到0.530。总之,这些数据表明,在冷驯化过程中,PE / PC比的增加在生物合成途径的最后一步受到调节。关键词冷驯化-PE-PC-磷脂-内质网-高尔基体

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