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2025年5月6日 星期二
  2017, Vol. 25 Issue (12): 1950-1960    
  研究论文与报告 本期目录 | 过刊浏览 | 高级检索 |
丝瓜WRKY转录因子基因的分离与褐变分析
刘建汀1,朱海生1,温庆放2,王彬3,张前荣1,陈敏氡1,林珲2,薛珠政3
1. 福建省农业科学院作物研究所
2.
3. 福建省农业科学院 作物研究所/福建省农业科学院蔬菜研究中心/福建省蔬菜工程技术研究中心
Isolation and Browning Analysis of WRKY Transcription Factor Gene of Luff (Luffa cylindrical)
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摘要 WRKY转录因子是一类发现于高等植物中的转录因子超家族。许多研究表明,WRKY转录因子在植物生物和非生物胁迫中起作用,但是这些研究主要集中在拟南芥(Arabidopsis thaliana)等模式植物中,在甜瓜(Cucumis melo)及辣椒(Capsicum annuum)等蔬菜作物中也有报道,而丝瓜(Luffa cylindrical)WRKY转录因子在褐变中的研究还未见相关报道。前期利用转录组测序(RNA-seq)技术获得了鲜切丝瓜福丝3号果肉褐变前后转录组数据库,本研究从中筛选得到4个与植物WRKY转录因子蛋白一致性较高的Unigene序列。分析发现,4个丝瓜WRKY基因Unigene0018509、Unigene0021412、Unigene0025291和Unigene0034271均含1个完整的开放读码框(ORF),序列全长分别为2 189、1 990、2 365和2 274 bp,GenBank登录号为:KY621843~KY621846。Wolf Psort预测显示,4个Unigene编码的WRKY蛋白均定位于细胞核中。系统进化和基因保守结构域分析表明,4个WRKY转录因子均含有1个保守的WRKY结构域,且锌指结构为C2H2型,属于第Ⅱ类WRKY蛋白家族。利用定量PCR技术分析了4个WRKY基因在丝瓜'福丝3号'不同组织(根、茎、叶、花和果肉)以及采后不同储藏时间下的表达情况,对4个WRKY基因在鲜切丝瓜果肉不同时间的表达模式与RNA-seq结果进行了分析。结果表明,4个丝瓜WRKY基因均具有组织表达特异性,且表达模式各不相同。4个WRKY基因在鲜切后q-PCR表达值与RNA-seq得到的表达量(fragments per kilobase million, FPKM)变化趋势基本一致,WRKY基因Unigene0018509、Unigene0021412和Unigene0025291在丝瓜鲜切后0~6 h内的表达量呈显著上调(P<0.05),Unigene0034271在0~3 h内上调表达,6 h出现下调表达。分析发现,4个WRKY基因在丝瓜采后不同储藏褐变时间内的表达趋势总体上调,但4个WRKY基因的表达模式不尽相同。该研究为进一步阐明丝瓜褐变调节机理和品种的选育提供理论依据。
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刘建汀
朱海生
温庆放
王彬
张前荣
陈敏氡
林珲
薛珠政
关键词 丝瓜转录组测序(RNA-seq)褐变WRKY表达分析    
Abstract:WRKY is a class of transcription factor superfamilies found in higher plants. Many studies have shown that WRKY transcription factors play a critical role in biotic and abiotic stress of plants. However, these studies are mainly concentrated in arabidopsis and other model plant species and also have been reported in melon(Cucumis melo) and pepper(Capsicum annuum) and other vegetable crops, while the research of WRKY transcription factor about browning from luffa (Luffa cylindrical) has not been reported in present. The transcriptome database of luffa Fushi-3 fresh-cut browning flesh were obtained by using the transcriptome sequencing (RNA-seq)technology in early , and a total of four Unigene sequences that shared high homology with WRKY protein were screened from the transcriptome databases in this study. Sequence analysis showed that full length of these four luffa WRKY genes (Unigene0018509, Unigene0021412, Unigene0025291 and Unigene0034271) were 2,189、1,990、2,365 and 2,274 bp, respectively, and they all contained an open reading frame(ORF), and the GenBank accession numbers were from KY621843 to KY621846. Wolf Psort prediction indicated that WRKY proteins encoded by the four Unigene were located in the nuclear. Gene phylogenetic analysis and conservative domains analysis showed that four luffa WRKY transcription factors all had a WRKY conserved domain and C2H2 type zinc finger, which suggested that these four WRKY protein were members of the second category of WRKY protein family. The expression levels of these four WRKY genes in different tissues (root, stem, leaf,flower and fruit) and different storage periods of postharvest flesh were analyzed by quantitative Real-time PCR, and the expression patterns and RNA-seq results of four WRKY genes during different time points of fresh-cut browning flesh have also been analyzed. The results showed that all of the four WRKY genes had the tissue-specific expression, and their expression patterns were different. The variation trends of these four WRKY genes on the expression of quantitative Real-time PCR and RNA-seq databases (i.e.,FPKM value) in luffa fresh-cut browning fruit were almost same, and the expression of Unigene0018509, Unigene0021412 and Unigene0025291 were significantly up-regulated from 0 h to 6 h after fresh-cut browning, and the expression of Unigene0034271 was up-regulated during 0 ~ 3 h and then decreased in 6 h. Overall, the expression trends of four WRKY genes were up-regulated in different postharvest and storage browning periods and their expression patterns were not the same. This study may provide a theoretical foundation for further expounding the luffa browning mechanism and breeding of varieties.
Key wordsLuffa    Transcriptome sequencing(RNA-seq)    Browning    WRKY    Expression analysis
收稿日期: 2017-06-07      出版日期: 2017-12-10
通讯作者: 朱海生     E-mail: zhs0246@163.com
引用本文:   
刘建汀 朱海生 温庆放 王彬 张前荣 陈敏氡 林珲 薛珠政. 丝瓜WRKY转录因子基因的分离与褐变分析[J]. , 2017, 25(12): 1950-1960.
链接本文:  
http://journal05.magtech.org.cn/Jwk_ny/CN/     或     http://journal05.magtech.org.cn/Jwk_ny/CN/Y2017/V25/I12/1950
 
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