Otagaki S, Ogawa Y, Hibrand-Saint Oyant L, Foucher F, Kawamura K, Horibe T, Matsumoto S
Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya, Japan.
INRA, Institut de Recherche en Horticulture et Semences (INRA, AGROCAMPUS-OUEST) Université d'Angers, Beaucouzé, France.
Plant Biol (Stuttg). 2015 Jul;17(4):808-15. doi: 10.1111/plb.12299. Epub 2015 Jan 19.
Rose flowers have long delighted humans as ornamental plants. To improve the ornamental value of roses it is necessary to understand the regulatory mechanisms of flowering. We previously found that flowering time is controlled by three minor quantitative trait loci (QTLs) and a major QTL co-localised with RoFT. In this study, we isolated three RoFT alleles encoding completely identical amino acid sequences from the parents of a mapping population. Correlation analysis of the RoFT genotypes and flowering time phenotypes in the mapping population showed that the RoFT_f and RoFT_g alleles contribute to the early-flowering phenotype, while the RoFT_e allele contributes to the late-flowering phenotype. We developed two novel cleaved amplified polymorphic sequence (CAPS) markers based on the genomic sequences of the RoFT alleles and clearly showed that the relationship between RoFT genotype and flowering time was applicable to 12 of 13 cultivated roses grown at the Higashiyama Botanical Gardens, Japan. Allele-specific expression analysis using a reverse transcription CAPS assay suggested that these RoFT alleles are regulated differentially at the transcription level. Furthermore, transgenic Arabidopsis thaliana plants ectopically expressing the RoFT gene showed an early-flowering phenotype. Conversely, in roses, RoFT was continuously expressed after floral bud formation, and RoFT transcript accumulation reached its peak after that of the floral meristem identity gene RoAP1b. These data suggest that RoFT may be essential not only for floral transition but also for normal floral development and flowering in roses.
玫瑰作为观赏植物长期以来一直深受人们喜爱。为了提高玫瑰的观赏价值,有必要了解开花的调控机制。我们之前发现开花时间受三个微效数量性状位点(QTL)和一个与RoFT共定位的主效QTL控制。在本研究中,我们从一个作图群体的亲本中分离出三个编码完全相同氨基酸序列的RoFT等位基因。对作图群体中RoFT基因型和开花时间表型的相关性分析表明,RoFT_f和RoFT_g等位基因导致早花表型,而RoFT_e等位基因导致晚花表型。我们基于RoFT等位基因的基因组序列开发了两种新型酶切扩增多态性序列(CAPS)标记,并清楚地表明RoFT基因型与开花时间之间的关系适用于日本东山植物园种植的13种栽培玫瑰中的12种。使用逆转录CAPS分析的等位基因特异性表达分析表明,这些RoFT等位基因在转录水平上受到差异调控。此外,异位表达RoFT基因的转基因拟南芥植株表现出早花表型。相反,在玫瑰中,RoFT在花芽形成后持续表达,并且RoFT转录本积累在花分生组织特征基因RoAP1b之后达到峰值。这些数据表明,RoFT不仅可能对花的转变至关重要,而且对玫瑰的正常花发育和开花也至关重要。