This study was conducted to breed interspecific hybrids by crossing between Asiatic hybrids for the purpose of cut flower or pot plant. According to results of reciprocal crossing between L. davidii and ‘Conception’, flower color of F1 appears nearer to that of each male parent but they seemed to be influenced by L. davidii which has side-facing flower position. The characteristic traits of F1 hybrids obtained from the cross between ‘Tresor’ and ‘Black Out’ is related to female parent ‘Tresor’. Whereas in a cross between ‘Navidad’ and ‘Hironde’, a progeny 122611-4 has the petal spot characteristic similar to the female Asiatic hybrid ‘Navidad’ and male parent ‘Gironde’ influence on the petal color. F1 hybrid cross ‘Gironde × Red Sensation’ showed parental flower color expression contribution. In addition ‘Gironde’ as parent contributed extensively in imparting flower color in the resulting hybrids. In the above statements, F1 progenies were more than 40cm in height and the plant height of their parents was over 70cm. Therefore, it is considered that their F1 progenies are not short if parents have a long plant height. In ‘Kotnali × Tiny Bee’ progenies, 112061-1 progeny expressed orange flower color similar to female while 112061-2 showed yellow flower color same as male. Plant height was 27.7cm and 22.4cm close to 35.0cm of male parent ‘Tiny Bee’. F1 hybrid of ‘Matrix × Holebibi’ expressed three flower color all of parents. It was dwarf and distinguishable as compared to parental phenotype. Therefore, it is concluded that for potted lily flower development carrying dwarf plant height and intermediate morphological traits Asiatic hybrids plays an important role such as ‘Tiny Bee’ and ‘Matrix’.

Anthocyanins are the major pigments contributing to flower coloration. A 1584 bp 5’ upstream sequence of ALCHS2 gene was isolated from Acapulco lily (Lilium Oriental hybrid cv. Acapulco). Computer-based analyses (GeneScan, AtPAN) predicted a CAATBOX1 and putative transcription factor-binding sites, including tissue-specific elements. When gALCHS7 promoter–gus fusion was introduced to petunia (‘Dream Red’), all ten putative transgenic plants showed localized GUS activity in the anther, but five of them also showed weak GUS activity in the ovule. No distinctive signal in the leaf and petal was detected in the same stage. To clearly determine the operation of the promotor region, anther and ovule tissues of transgenic line 6 were fixed in paraffin for dark-field analysis. At 1 cm length of floral bud, a GUS signal was not observed in the anther, but weak expression was observed in the ovule. Before anthesis, GUS protein was highly expressed in the pollen, endothecium, and epidermis. Fluorometric GUS assays of individual organs taken from four transgenic plants demonstrated that all lines showed high GUS activity in the anther compared to 35S CaMV promoter (pBI1 121), except line 34. Using the truncated promoters by cis-acting elements, we found that minimal region (gALCHS7-7, 270 bp) displayed GUS expression only in the anther, though at weaker activity than in the original promoter.