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Omega-3 fatty acid desaturase gene family from two ω-3 sources Salvia hispanica and Perilla frutescens: Cloning characterization and expression

机译:来自两个ω-3来源丹参和紫苏的ω-3脂肪酸去饱和酶基因家族:克隆表征和表达

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摘要

Omega-3 fatty acid desaturase (ω-3 FAD, D15D) is a key enzyme for α-linolenic acid (ALA) biosynthesis. Both chia (Salvia hispanica) and perilla (Perilla frutescens) contain high levels of ALA in seeds. In this study, the ω-3 FAD gene family was systematically and comparatively cloned from chia and perilla. Perilla FAD3, FAD7, FAD8 and chia FAD7 are encoded by single-copy (but heterozygous) genes, while chia FAD3 is encoded by 2 distinct genes. Only 1 chia FAD8 sequence was isolated. In these genes, there are 1 to 6 transcription start sites, 1 to 8 poly(A) tailing sites, and 7 introns. The 5’UTRs of PfFAD8a/b contain 1 to 2 purine-stretches and 2 pyrimidine-stretches. An alternative splice variant of ShFAD7a/b comprises a 5’UTR intron. Their encoded proteins harbor an FA_desaturase conserved domain together with 4 trans-membrane helices and 3 histidine boxes. Phylogenetic analysis validated their identity of dicot microsomal or plastidial ω-3 FAD proteins, and revealed some important evolutionary features of plant ω-3 FAD genes such as convergent evolution across different phylums, single-copy status in algae, and duplication events in certain taxa. The qRT-PCR assay showed that the ω-3 FAD genes of two species were expressed at different levels in various organs, and they also responded to multiple stress treatments. The functionality of the ShFAD3 and PfFAD3 enzymes was confirmed by yeast expression. The systemic molecular and functional features of the ω-3 FAD gene family from chia and perilla revealed in this study will facilitate their use in future studies on genetic improvement of ALA traits in oilseed crops.
机译:Omega-3脂肪酸去饱和酶(ω-3FAD,D15D)是α-亚麻酸(ALA)生物合成的关键酶。奇亚(Salvia hispanica)和紫苏(Perilla frutescens)的种子中都含有高水平的ALA。在这项研究中,ω-3FAD基因家族被系统地和比较地从正大和紫苏中克隆。紫苏FAD3,FAD7,FAD8和chia FAD7由单拷贝(但杂合)基因编码,而chia FAD3由2个不同的基因编码。仅分离了1个Chia FAD8序列。在这些基因中,有1至6个转录起始位点,1至8个poly(A)拖尾位点和7个内含子。 PfFAD8a / b的5'UTR包含1-2个嘌呤伸展和2个嘧啶伸展。 ShFAD7a / b的另一个剪接变体包含5’UTR内含子。他们编码的蛋白质带有一个FA_desaturase保守结构域,以及4个跨膜螺旋和3个组氨酸盒。系统发育分析验证了双子叶植物微粒体或质体ω-3FAD蛋白的身份,并揭示了植物ω-3FAD基因的一些重要进化特征,例如跨不同门的趋同进化,藻类的单拷贝状态以及某些分类群中的重复事件。 。 qRT-PCR分析表明,两个物种的ω-3FAD基因在不同器官中的表达水平不同,并且它们也对多种胁迫处理产生响应。通过酵母表达证实了ShFAD3和PfFAD3酶的功能。这项研究揭示了来自正大和紫苏的ω-3FAD基因家族的系统性分子和功能特征,将有助于它们用于油料作物ALA性状遗传改良的未来研究中。

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