缺刻缘绿藻二酰甘油酰基转移酶2(DGAT2)的基因特性与功能鉴定

Q4 Environmental Science 水产学报 Pub Date : 2013-01-01 DOI:10.3724/SP.J.1231.2013.38654
房逢立, 吴洪, 周志刚
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Abstract

Acyl-CoA:diacylglycerol acyltransferase(DGAT;EC 2.3.1.20)is regarded as a key enzyme in triacylglycerol(TAG)biosynthesis of microalgae and other plants.In order to understand the biosynthesis of TAG in Myrmecia incisa,we found a putative full-length DGAT2 cDNA sequence in the homology search of a pyrosequencing transcriptome of this microalga.The full-length cDNA sequence was composed of 1 997 bp.It comprised a 44-bp 5′-untranslated region(UTR),a 897-bp 3′-UTR with a typical poly A tail,and a 1 056 bp open reading frame(ORF)encoding a 351-amino-acid protein with a putative molecular weight of 39.43 ku and pI at 9.46.Neighbor-Joining(NJ)phylogenetic tree inferred from the putative proteins of DGAT genes indicated that this gene belongs to DGAT2 gene family,significantly different from DGAT1 and DGAT3 families.Multiple sequence alignment of amino acids indicated that a conserved and characteristic sequence HPHG of the DGAT2's was present in this gene.Therefore,this gene was designated as MiDGAT2.Compared with the DNA sequence of MiDGAT2,it was found that its coding region was interrupted by 6 introns with all splicing sites well matching the GT-AG rule.In order to investigate the function of MiDGAT2,its open reading frame was amplified by RT-PCR and sub-cloned into the shuttle vector pYES2 to generate the recombinant vector pY-MiDGAT2.This recombinant plasmid was transformed into a TAG-defective mutant H1246 of Saccharomyces cerevisiae for expression by electroporation.The target gene integrated in the yeast genome was confirmed by sequencing and a transformant with pY-MiDGAT2 was screened out.This yeast transformant was cultured in SC medium with galactose as an inducer.Thin layer chromatogram(TLC)analysis of yeast lipids showed that the TAG-defective mutant H1246 transformed with MiDGAT2 could restore the ability to synthesize TAG,indicating that MiDGAT2 encodes a DGAT enzyme involved in the biosynthesis of TAG.When the yeast cells were stained with fluorescent dye Bodipy,it was found that lipid droplets were present in the TAG-defective mutant H1246 transformed with MiDGAT2,although the diameter of lipid droplets was smaller than that of wild type.
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缺刻缘绿藻二酰甘油酰基转移酶2(DGAT2)的基因特性与功能鉴定
酰基辅酶a:二酰基甘油酰基转移酶(diacylglycerol acyltransferase, DGAT;EC 2.3.1.20)是微藻等植物三酰基甘油(triacylglycerol, TAG)生物合成的关键酶。为了进一步了解切丝桃金娘(Myrmecia incisa)中TAG的生物合成过程,我们对切丝桃金娘(Myrmecia incisa)的焦磷酸测序转录组进行同源性搜索,发现了一个推测的DGAT2全长cDNA序列。全长cDNA序列为1 997 bp。它由一个44-bp的5 ' -未翻译区(UTR)、一个897-bp的典型聚a尾3 ' -未翻译区(UTR)和一个1 056 bp的开放阅读框(ORF)组成,编码一个351个氨基酸的蛋白,推测分子量为39.43 ku, pI为9.46。根据DGAT基因推定蛋白的邻居连接(NJ)系统发育树推断该基因属于DGAT2基因家族,与DGAT1和DGAT3家族有显著差异。多个氨基酸序列比对表明,该基因具有DGAT2的保守特征序列HPHG。因此,该基因被命名为MiDGAT2。与MiDGAT2的DNA序列比较,发现其编码区被6个内含子打断,所有剪接位点均符合GT-AG规则。为了研究MiDGAT2的功能,通过RT-PCR扩增其开放阅读框,并将其亚克隆到穿梭载体pYES2中,生成重组载体pY-MiDGAT2。将该重组质粒转化为酿酒酵母(Saccharomyces cerevisiae)的tag缺陷突变体H1246,通过电穿孔法表达。通过测序确认了整合到酵母基因组中的目的基因,并筛选出带有pY-MiDGAT2的转化体。以半乳糖为诱导剂,在SC培养基中进行酵母转化培养。酵母脂质薄层色谱(TLC)分析表明,经MiDGAT2转化的TAG缺陷突变体H1246可以恢复TAG合成能力,这表明MiDGAT2编码一种DGAT酶参与TAG的生物合成。用荧光染料Bodipy对酵母细胞进行染色,发现经MiDGAT2转化的tag缺陷突变体H1246中存在脂滴,尽管脂滴直径比野生型小。
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来源期刊
水产学报
水产学报 Environmental Science-Management, Monitoring, Policy and Law
CiteScore
1.40
自引率
0.00%
发文量
5213
期刊介绍: "Fisheries of" mainly reflects the results of scientific research and development of the direction of aquaculture for domestic and foreign academic exchanges Fisheries Service. Mainly basic research published in Fisheries, aquaculture and proliferation of fishing waters environmental protection, preservation of aquatic products processing and utilization, fishing equipment, and other aspects of mechanical papers, research briefings and reviewed.
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