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Analyses of the floral organ morphogenesis and the differentially expressed genes of an apetalous flower mutant in Brassica napus

机译:甘蓝型油菜花器官突变体花器官形态发生和差异表达基因分析

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摘要

The floral organ morphogenesis of the apetalous flower mutant Apet33-10 in Brassica napus was investigated and the result showed that all the floral organ morphogenesis was normal except that petal primordium was not observed during flower development. Eighteen genes were found to be down regulated in early floral buds (less than 200 μm in length) of Apet33-10 at the stage of floral organ initiation by means of suppressive subtraction hybridization (SSH) and RT-PCR. These genes were involved in petal identity, calcium iron signal transduction, mRNA processing, protein synthesis and degradation, construction of cytoskeleton, hydrogen transportation, nucleic acid binding, alkaloid biosynthesis and unknown function. Three overall coding region cDNAs of APETALA3 (AP3) gene, BnAP3-2, BnAP3-3 and BnAP3-4 were obtained by RT-PCR, respectively. Real-time quantitative PCR analysis showed that the expression ratio among BnAP3-2, BnAP3-3 and BnAP3-4 was 3.67:3.68:1 in early floral buds of wild type Pet33-10. The expression level of BnAP3-2, BnAP3-3 and BnAP3-4 in early floral buds of Apet33-10 was down-regulated to 36.6, 28.3 and 66.8% with the comparison of that of wild type, respectively, and the overall expression level of AP3 genes in apetalous mutant amounted to 45.0% of that in wild type. The difference in the expression level of each AP3 gene in stamen between apetalous and wild type lines was not significant. It is suggested that lower abundant expression of AP3 genes during the early flower development might be enough for stamen primordium initiation, but not enough for petal primordium initiation in the apetalous line Apet33-10.
机译:研究了甘蓝型油菜花瓣状花突变体Apet33-10的花器官形态发生,结果表明,除未见花瓣原基外,所有花器官形态均正常。发现通过抑制性扣除杂交(SSH)和RT-PCR技术,在花器官启动阶段,Apet33-10的早期花蕾(长度小于200μm)中的十八个基因被下调。这些基因参与了花瓣鉴定,钙铁信号转导,mRNA加工,蛋白质合成和降解,细胞骨架的构建,氢转运,核酸结合,生物碱生物合成和未知功能。通过RT-PCR分别获得了APETALA3(AP3)基因的三个总编码区cDNA,即BnAP3-2,BnAP3-3和BnAP3-4。实时定量PCR分析显示,在野生型Pet33-10的早期花芽中,BnAP3-2,BnAP3-3和BnAP3-4之间的表达比为3.67:3.68:1。与野生型相比,Apet33-10早期花芽中BnAP3-2,BnAP3-3和BnAP3-4的表达水平分别下调至36.6、28.3和66.8%。花瓣状突变体中AP3基因的表达量为野生型的45.0%。花瓣型和野生型之间,每个AP3基因在雄蕊中的表达水平差异不显着。提示在花瓣发育早期,AP3基因较低的丰度表达可能足以启动雄蕊原基,但不足以刺激花瓣Apet33-10中的花瓣原基。

著录项

  • 来源
    《Plant Cell Reports》 |2008年第1期|9-20|共12页
  • 作者单位

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

    Key Laboratory of Ministry of Education for Bio-resources and Eco-environment College of Life Science Sichuan University Chengdu 610064 People’s Republic of China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Brassica n napus; Apetalous mutant; Floral buds; Suppressive subtraction hybridization; Real-time quantitative PCR;

    机译:甘蓝型油菜;花瓣突变体;花芽;抑制性减法杂交;实时定量PCR;

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