Cyclamen persicum Mill. is a major product of Japan's horticultural industry, with tens of millions of potted plants sold each winter. For many years, a number of popular cyclamen cultivars have been produced by crosshybridization and mutation breeding techniques. In cyclamen, as in many horticultural plants, modification of the flower shape is important for improving the commercial value. However, there is not much natural flower shape variation in cyclamen, and moreover, developing new cyclamen breeds requires immense effort because of its complicated patterns of inheritance. Recently, molecular breeding techniques have been applied to solve this problem. These methods can be used to more directly produce new phenotypes with target characteristics. We have succeeded in demonstrating that the introduction of a chimeric cyclamen TCP (TEOSINTE BRANCHED1, CYCLOIDEA and PCF) repressor in the genome of cyclamen produces ruffled flowers with a high ornamental value (Tanaka et al. 2011). To continue to develop this field, it is important to determine genetic information and elucidate the exact mechanisms regulating flower formation in cyclamen.Cyclamen flowers, like those of many flowering plants, consist of four whorls. In the outermost whorl, there is a calyx consisting of five sepals. In whorl 2, there is a corolla consisting of five petals, with five stamens attached by short filaments in whorl 3. Whorl 4, in the center of the flower, contains one pistil with five fused carpels ( Figure 2A; Grey-Wilson 2002). Despite the commercial importance of cyclamen, molecular analysis of its flower architecture has not been completely performed, making effective molecular breeding of this plant impossible. Generally, the specification of floral organ identity is explained according to the classical ABC model (Coen and Meyerowitz 1991, Irish 2010). In this model, the interaction of three transcription factor classes affects the identity of an individual floral organ in each of the four whorls. Class-A genes alone contribute to sepal development in whorl 1, class-A and -B genes together lead to petal formation in whorl 2, class-B and -C genes combine in function to specify stamens in whorl 3, and class-C genes alone specify carpel identities in whorl 4. Following the recognition of class-D and -E genes, this model was extended to become the ABCDE model. In this extended model, class-D function genes required for ovule development were included based on studies of petunias (Angenent and Colombo 1996;Colombo et al. 1995;Theissen et al. 2000;Pinyopich et al. 2003). In addition, class-E genes have been identified
Identification and expression analysis of the Cyclamen persicum MADS-box gene familyYuri Tanaka, Tomomichi Yamamura, Teruhiko Terakawa* Central Research Laboratories, Hokko Chemical Industry Co., Ltd., Atsugi, Kanagawa 243-0023, Japan * E-mail: terakawa-t@hokkochem.co.jp Tel: ϩ81-46-228-5881 Fax: ϩ81-46-228-0164Received November 11, 2010; accepted February 1, 2011 (Edited by N. Mitsuda) Abstract Molecular analysis of c...