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园艺学报 ›› 2019, Vol. 46 ›› Issue (2): 317-329.doi: 10.16420/j.issn.0513-353x.2018-0441

• 研究论文 • 上一篇    下一篇

一个矮牵牛花器官发育突变体aps的表型鉴定及遗传分析

周 琴1,鲁 瑞1,张书婷1,包满珠1,刘国锋1,2,*   

  1. 1华中农业大学园艺林学学院,园艺植物生物学教育部重点实验室,武汉 430070;2广州市林业与园林科学研究院,广州 510405
  • 出版日期:2019-02-25 发布日期:2019-02-25
  • 基金资助:

    国家自然科学基金项目(31471914,31772345)

Phenotype Characterization and Genetic Analysis of a Floral Mutant aps in Petunia

ZHOU Qin1,LU Rui1,ZHANG Shuting1,BAO Manzhu1,and LIU Guofeng1,2,*   

  1. 1Key Laboratory of Horticulture Plant Biology,Ministry of Education,College of Horticulture and Forestry Sciences,Huazhong Agricultural University,Wuhan 430070,China;2Guangzhou Institute of Forestry and Landscape Architecture,Guangzhou 510405,China
  • Online:2019-02-25 Published:2019-02-25

摘要:

在利用矮牵牛W138株系构建突变体库的过程中,获得了一种花器官发育突变体,该突变体主要表现为花萼和花瓣发育异常,命名为aps(abnormal petals and sepals)。与正常W138植株相比,aps突变体最明显的表型是花冠开裂,通常为3裂,同时5个花萼中有2个出现部分瓣化。扫描电镜观察结果显示,突变体瓣化花萼的表皮细胞表现为正常花瓣的细胞形态。通过突变体自交、与正常姊妹株和矮牵牛W115株系杂交以及F1自交和回交等遗传分析发现,aps突变性状为单基因控制的隐性性状。qPCR分析结果表明,在突变体花萼中,3个B类基因(FBP1、PMADS1和PMADS2)和部分E类基因(FBP2、FBP4和FBP5)出现异位表达或表达量显著升高,而所有A类基因(FBP26、FBP29、PFG、AP2A、AP2B和AP2C)的表达量均明显下降,E类基因FBP9和FBP23的表达量也下调;突变体花瓣中,A类基因除FBP29不表达外,其他所有基因的表达量均显著增加,B类基因FBP1和PMADS2,E类基因FBP2、FBP5、FBP23和PMADS12的表达量上调;C类和D类基因的表达在突变体花萼和花瓣中没有明显变化,但在雄蕊和花柱中C类基因表达量明显下降,D类基因FBP7在子房中显著下调。aps突变体为研究矮牵牛花器官发育的调控机制及相关基因之间的调控关系提供了良好的材料。

关键词: 矮牵牛, 花器官, 发育, 突变体, 花萼瓣化, 花冠开裂, MADS-box

Abstract:

A floral mutant was obtained during the construction of a mutant library with Petunia hybrida W138 strain,which was mainly characterized by abnormal development of sepals and petals,and named as aps(abnormal petals and sepals). Compared with normal W138 plant(Wt),the most obvious phenotype of aps is its split corolla,usually with three lobes;simultaneously,two of five sepals in aps mutant are petaloid. Scanning electron microscopy(SEM)analysis indicated that the shape of epidermis cells in the petaloid sepals of aps plants was the same as that in petals of Wt plants. The genetic analysis by selfing,crossing,and backcrossing between aps and its normal sister plants or W115 suggested that the trait of aps is controlled by a single recessive gene. qPCR was used to analyze the expression of floral development related genes in four whorls of organs between aps and Wt flowers. The results showed that three B-class genes(FBP1,PMADS1 and PMADS2)and some E-class genes(FBP2,FBP4 and FBP5)was activated in petaloid sepals of aps mutants,however,the expression of all A-class genes including FBP26,FBP29,PEG,AP2A,AP2B and AP2C,as well as the E-class genes FBP9 and FBP23,are down-regulated in this whorl. In aps petals,except for FBP29 that is not expressed in petals,all other A-class genes are up-regulated,as are the B-class genes,FBP1 and PMADS2,and the E-class genes FBP2,FBP5,FBP23 and PMADS12. The expression of C- and D-class genes are not altered in sepals and petals of the mutants,but both C-class genes are downregulated in stamens and styles of aps plants,like the D-class gene FBP7 in ovaries. The characterization of aps mutant provides a good chance for studying the molecular regulation of floral organ development and for exploring the relationship of floral genes in petunia.

Key words: petunia, floral organ, development, mutant, petaloid sepal, split corolla, MADS-box

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