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园艺学报 ›› 2016, Vol. 43 ›› Issue (2): 347-354.doi: 10.16420/j.issn.0513-353x.2015-0634

• 研究报告 • 上一篇    下一篇

凤丹(Paeonia ostii)脂肪酸去饱和酶基因PoFAD2的克隆及表达分析

宋淑香1,郭先锋1,2,*,马 燕1,李俊杰1,韩璐璐1   

  1. 1山东农业大学林学院,山东泰安 271018;2山东省城乡风景园林工程技术研究中心,山东泰安 271018
  • 出版日期:2016-02-25 发布日期:2016-02-25
  • 基金资助:
    山东省自然科学基金项目(ZR2014CM028)

Isolation and Expression Analysis of PoFAD2 Gene in Paeonia ostii

SONG Shu-xiang1,GUO Xian-feng1,2,*,MA Yan1,LI Jun-jie1,and HAN Lu-lu1   

  1. 1College of Forestry,Shandong Agricultural University,Tai’an,Shandong 271018,China;2Shandong Provincial Research Center of Landscape Engineering Technology for Urban and Rural,Tai’an,Shandong 271018,China
  • Online:2016-02-25 Published:2016-02-25

摘要: 以油用牡丹凤丹(Paeonia ostii T. Hong & J. X. Zhang)胚珠为试材,通过反转录PCR(reverse transcription PCR,RT-PCR)及RACE技术得到脂肪酸去饱和酶基因FAD2 的cDNA全长,命名为PoFAD2(GenBank注册号为KT153989)。该基因全长为1 695 bp,开放阅读框(open reading frame,ORF)为1 152 bp,编码383个氨基酸。系统发育树结果表明PoFAD2与芍药(P. lactiflora)FAD2具有最高的同源性,亲缘关系最近。此外,PoFAD2编码的氨基酸序列中存在3个高度保守的组氨酸簇及4个跨膜区,且含有Delta12-FADs的特异位点,这些结果表明,该基因属于脂肪酸去饱和酶家族。实时荧光定量PCR(real-time quantitative PCR,qRT-PCR)结果表明:PoFAD2在凤丹各组织中的表达差异较大,在茎、萼片、雄蕊及花瓣中几乎不表达,在叶片中极微弱表达,表达量仅为胚珠中的1/73,在芽及雌蕊中低表达,表达量约为胚珠中的1/10 ~ 1/12,而在胚珠中高表达;种子发育进程中,PoFAD2表达量呈现先急速上升之后迅速下降再回升的趋势,且于花后75 d出现表达量的最高峰。

关键词: 凤丹, FAD2基因, 基因克隆, 表达分析, 种子

Abstract: A fatty acid desaturase2(FAD2)gene,designated as PoFAD2,was isolated from the ovule of Paeonia ostii T. Hong & J. X. Zhang using reverse transcription PCR and RACE technology. The full-length cDNA was 1 695 bp with an open reading frame of 1 152 bp,encoding a putative protein of 383 amino acids. The phylogenetic tree analysis indicated that PoFAD2 had the highest similarity with FAD2 from P. lactiflora. In addition,the amino acid sequences encoded by PoFAD2 contained three highly conservative histidine clusters,four transmembrane domains and a specific hit of Delta12-FADs,which peculiarly belong to the family of fatty acids desaturase. Real-time quantitative PCR showed that PoFAD2 was differentially expressed in various tissues of P. ostii. It was barely expressed in stems,sepals,stamens or petals,weakly present in leaves(about one seventieth of ovules),moderately in buds and pistils(aboutone tenth of ovules),and extremely highly in ovules. This gene was therefore considered as seed specific. During seed development,PoFAD2 transcript in ovules rapidly increased and reached the highest level at 75 day after florescence,followed by a sharp decline and gradual recovery.

Key words: Paeonia ostii, PoFAD2, molecular cloning, expression analysis, seed

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