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Construction of efficient and effective transformation vectors for palmitoyl-acyl carrier protein thioesterase gene silencing in oil palm

机译:油棕棕榈酰基-酰基载体蛋白硫酯酶基因沉默的高效转化载体的构建

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摘要

Palm oil obtained from E. guineensis Jacq. Tenera is known to have about 44% of palmitic acid (C16:0). Palmitoyl-Acyl Carrier Protein Thioesterase (PATE) is one of the key enzymes involved in plastidial fatty acid biosynthesis; and it determines the level of the C16:0 assimilation in oilseeds. This enzyme's activity in oil palm is responsible for high (> 44 % in E. guineensis Jacq. Tenera and 25 % in E. oleifera) content of C16:0 in its oil. By post-transcriptional PATE gene silencing, C16:0 content can be minimized for nutritional value improvement of the palm oil. The objective of this study was the construction of novel transformation vectors for PATE gene silencing. Six different transformation vectors targeted against PATE gene were constructed using 619 bp long PATE gene (5' region) fragment (from GenBank ). In one set of three transformation vectors, PATE gene fragment was fused with CaMV 35S promoter in antisense, intron-spliced inverted repeat (ISIR), and inverted repeat (IR) orientations to generate antisense mRNA and hair-pin RNAs (hpRNA). In another set of three transformation vectors with same design, CaMV 35S was replaced with Oil palm mesocarp tissue-specific promoter (MSP). The expression cassette of antisense, ISIR, and IR of PATE gene fragments were constructed in primary cloning vector, pHANNIBAL or its derivative/s. Finally, all 6 expression cassettes were sub-cloned into pCAMBIA 1301 which contains the Hygromycinr and the GUS reporter genes for transformant selection and transformation detection respectively. The results of the RE analyses of the constructs and sequence analyses of PATE and MSP shows and confirms the orientation, size and locations of all the components from constructs. We hypothesize that 4 (pISIRPATE-PC, pIRPATE-PC, pMISIRPATE-PC and pMIRPATE-PC) out of 6 transformation vectors constructed in this study will be efficient and effective in palmitoyl-ACP thioesterase gene silencing in oil palm.AbbreviationsantiPATE - Antisense Palmitoyl-acyl carrier protein thioesterase, BCV - Binary cloning vector, cDNA - Complementary deoxyribonucleic acid, hpRNA - hair-pin RNA, ihpRNA - intron containing hair-pin RNA, IR - inverted repeat, ISIR - intron-spliced inverted repeat, MCS - Multiple cloning site, MSP - Oil palm mesocarp tissue-specific promoter,nt - Nucleotide/s,PATE - Palmitoyl-acyl carrier protein thioesterase,PCR - Polymerase chain reaction,PCV - Primary cloning vector,pDNA - Plasmid deoxyribonucleic acid,PTGS - Post-transcriptional gene silencing,RE - Restriction enzyme.
机译:棕榈油获自E. guineensis Jacq。已知特内拉氏菌具有约44%的棕榈酸(C16:0)。棕榈酰-酰基载体蛋白硫酯酶(PATE)是参与质体脂肪酸生物合成的关键酶之一;它确定了油料种子中C16:0同化的水平。该酶在油棕中的活性导致其油中C16:0的含量较高(在E. guineensis Jacq。Tenera中大于44%,在E. oleifera中为25%)。通过转录后PATE基因沉默,可使C16:0含量降至最低,从而提高棕榈油的营养价值。这项研究的目的是构建用于PATE基因沉默的新型转化载体。使用619 bp长的PATE基因(5'区)片段(来自GenBank)构建了六种针对PATE基因的不同转化载体。在一组三个转化载体中,将PATE基因片段与CaMV 35S启动子以反义,内含子剪接的反向重复(ISIR)和反向重复(IR)方向融合,以生成反义mRNA和发夹RNA(hpRNA)。在具有相同设计的另一组三个转化载体中,将CaMV 35S替换为油棕中果皮组织特异性启动子(MSP)。在原代克隆载体pHANNIBAL或其衍生物中构建了PATE基因片段的反义,ISIR和IR表达盒。最后,将所有6个表达盒亚克隆到pCAMBIA 1301中,其中包含潮霉素和GUS报道基因,分别用于转化子选择和转化检测。对构建体进行RE分析的结果以及PATE和MSP的序列分析结果显示并确认了构建体中所有组件的方向,大小和位置。我们假设在这项研究中构建的6种转化载体中的4种(pISIRPATE-PC,pIRPATE-PC,pMISIRPATE-PC和pMIRPATE-PC)在油棕中的棕榈酰-ACP硫酯酶基因沉默中将是有效和有效的。 -酰基载体蛋白硫酯酶,BCV-二进制克隆载体,cDNA-互补脱氧核糖核酸,hpRNA-发夹RNA,ihpRNA-含有发夹RNA的内含子,IR-反向重复ISIR-内含子拼接的反向重复,MCS-多个克隆位点,MSP-油棕中果皮组织特异性启动子,nt-核苷酸,PATE-棕榈酰基酰基载体蛋白硫酯酶,PCR-聚合酶链反应,PCV-主要克隆载体,pDNA-质粒脱氧核糖核酸,PTGS-转录后基因沉默,RE-限制酶。

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