牡丹PsAGL6基因克隆与表达分析
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国家自然科学基金(31600568);


Cloning and Expression Analysis of Transcription Factor Gene PsAGL6 in Tree Peony (Paeonia suffruticosa L.)
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    摘要:

    该研究在转录组数据分析基础上,通过RTPCR方法从牡丹(Paeonia suffruticosa. L) 品种 ‘洛阳红’中克隆AGL6基因,并分析了其在不同组织和花型中的表达模式。结果显示:(1)AGL6开放阅读框长度732 bp,编码244个氨基酸;结构域分析显示,该基因具有高度保守的MADS MEF2区、K区、AGL6 I与AGL6II 基序,归类于MADSbox基因家族,命名为PsAGL6,GenBank登录号为MF563611。(2)同源比对分析显示,牡丹PsAGL6与葡萄VvAGL6氨基酸序列相似度最高,达79%。(3)qRTPCR分析结果显示,PsAGL6在牡丹各器官中均有表达,但营养器官中表达量较低,花器官中表达量较高,其中以萼片最高,花瓣与雌蕊次之;对4种牡丹花型花瓣的表达分析显示,PsAGL6基因在不同花型花瓣中的表达量差异明显,且蔷薇型牡丹花瓣相对表达量最高。研究表明,AGL6基因参与牡丹花器官的形成,为深入研究花器官发育的分子机制提供了帮助。

    Abstract:

    In the basis of transcriptomic analysis,a novel AGL6 gene was cloned from Paeonia suffruticosa cultivar ‘Luoyanghong’ by RTPCR technique, which contained an open reading frame of 732 bp encoding a putative protein of 244 amino acids. (1) Protein sequence analysis showed that the gene have highly conserved MADS MEF2 Domain, K Domain, typical AGL6 I and AGL6II Motif,which belongs to the MADS box gene family and named as PsAGL6 (GenBank No: MF563611). (2) Homology analysis showed that PsAGL6 protein was high identity with VvAGL6 from Vitis vinifera (79%). (3) qRTPCR demonstrated that PsAGL6 was expressed in all tissues, little expression in vegetable tissues, but high expression in the floral organs. Expression of PsAGL6 was highest in sepal, petal and carpel followed. In petal of different flower type of 4 tree peony cultivars, qRTPCR results showed that the expression of PsAGL6 had significant difference between different cultivars. The expression of PsAGL6 was the highest in the flower type of rose. In conclusion, PsAGL6 gene involves the formation of floral organs. These results provided help for revealing the molecular mechanism of floral organ development.

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唐文龙,赵鹏飞,李永华,等.牡丹PsAGL6基因克隆与表达分析[J].西北植物学报,2018,38(3):439-444

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  • 在线发布日期: 2018-04-23
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