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    黄笛, 孙明, 袁存权, 程堂仁, 王佳, 张启翔. 春黄菊族部分植物CYC2d同源基因的分离与功能初步分析[J]. 北京林业大学学报, 2017, 39(4): 63-71. DOI: 10.13332/j.1000-1522.20170003
    引用本文: 黄笛, 孙明, 袁存权, 程堂仁, 王佳, 张启翔. 春黄菊族部分植物CYC2d同源基因的分离与功能初步分析[J]. 北京林业大学学报, 2017, 39(4): 63-71. DOI: 10.13332/j.1000-1522.20170003
    HUANG Di, SUN Ming, YUAN Cun-quan, CHENG Tang-ren, WANG Jia, ZHANG Qi-xiang. Isolation and functional analysis of CYC2d orthologous genes from several plants of the tribe Anthemideae[J]. Journal of Beijing Forestry University, 2017, 39(4): 63-71. DOI: 10.13332/j.1000-1522.20170003
    Citation: HUANG Di, SUN Ming, YUAN Cun-quan, CHENG Tang-ren, WANG Jia, ZHANG Qi-xiang. Isolation and functional analysis of CYC2d orthologous genes from several plants of the tribe Anthemideae[J]. Journal of Beijing Forestry University, 2017, 39(4): 63-71. DOI: 10.13332/j.1000-1522.20170003

    春黄菊族部分植物CYC2d同源基因的分离与功能初步分析

    Isolation and functional analysis of CYC2d orthologous genes from several plants of the tribe Anthemideae

    • 摘要: CYC同源基因作为控制花瓣对称性形成的关键基因,在菊科头状花序中主要调控着舌状花(两侧对称)的生长发育。菊科植物中舌状花的有或无及其分子调控机制和演化过程一直备受关注。本研究从花型不同的川甘亚菊、戈壁短舌菊和神农香菊中分别同源克隆了转录因子基因CYC2d。3个序列与菊花CmCYC2d基因氨基酸序列的比对结果显示其同源性均超过90%,且均含有保守的TCP和R结构域。半定量RT-qPCR结果显示,CYC2d在地被菊品种‘毛香玉’幼嫩花序中的表达量最高,而在川甘亚菊和戈壁短舌菊中的表达量非常微弱。因此,进一步通过实时荧光定量检测了CmCYC2d在‘毛香玉’6个发育时期舌状花和管状花中的表达情况,结果表明, CmCYC2d各个时期管状花中的表达量均很低,而在相应时期舌状花中的表达均很丰富。在不同花型的杂交F1代优株中,CmCYC2d也主要在不同位置的舌状花中高表达。通过农杆菌转化重组质粒pSUPER1300-CmCYC2d-GFP在烟草表皮细胞瞬时表达,亚细胞定位结果显示其定位于表皮细胞核。分别在野生型拟南芥和tcp1突变体(SALK-022364)中过表达CmCYC2d基因的结果表明,转基因阳性株系的营养生长受到抑制,花期延迟,花瓣大小和排列均发生了变化,使原本辐射对称的花瓣呈现两侧对称的趋势。从研究结果可知, 转录因子基因CmCYC2d对菊花舌状花的发育有重要调控作用。本研究为菊科舌状花演化的分子调控机制研究奠定了基础。

       

      Abstract: As the important gene of regulating flower symmetry, cyc-like proteins have been shown to mainly regulate the identity and development of ray floret (bilaterally symmetrical) in Asteraceae. The presence or absence of ray floret in Asteraceae and its molecular regulation mechanism as well as the evolutionary process have been highly concerned. Orthologous genes of CYC2d from Ajania potaninii, Brachanthemum titovii and Chrysanthemum indicum var. aromaticum were obtained by homology-based cloning. Their sequence alignment and conserved motif analysis were performed with the amino sequence of CmCYC2d, respectively. The results showed that their homology was more than 90% and all these proteins contained the conserved TCP and R domains. Furthermore, according to the result of semi-quantitative RT-PCR assay, CYC2d was strongly expressed in the young inflorescence of the groundcover chrysanthemum 'Mao xiangyu', while slightly expressed in that of A.potaninii and B.titovii. Therefore, the transcription levels of CmCYC2d were examined in ray and disc florets of 'Mao xiangyu' at six developing stages using quantitative real-time PCR. The results indicated that it was weakly expressed in disc florets of all stages, while highly expressed in ray florets of the corresponding stages. Moreover, in three F1 progenies with various whorls of ray florets, the CmCYC2d was expressed at much higher levels in ray florets of different whorls than in disc florets. The recombinant plasmid pSUPER1300-CmCYC2d-GFP was transiently expressed into the epidermal cells of Nicotiana benthamiana by agrobacterium-mediated transformation, and subcellular localization analysis revealed that the CmCYC2d protein mainly localized into the nucleus of epidermal cells. Furthermore, CmCYC2d was overexpressed in wild type Arabidopsis and the TCP1 mutant used the floral-dip method. The results showed that the vegetative growth and the flowering time of the positive transgenic lines were repressed and postponed. Moreover, the size and arrangement of the petals seemed to be changed, making the petal arrangement showed bilateral symmetry from original radial symmetry. These results indicate that the transcription factor CmCYC2d is essential in regulating ray floret identity in chrysanthemum. Our study lays a foundation for the research of molecular mechanisms for the evolutionary process of ray floret in Asteraceae.

       

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