Expression of genes involved in proanthocyanidin biosynthesis during fruit development in a Chinese pollination-constant, nonastringent (PCNA) persimmon, 'Luo Tian Tian Shi'

• Published in: Journal of the American Society for Horticultural Science Vol. 130; no. 6; pp. 830 - 835
• Main Authors: Ikegami, A, Yonemori, K, Kitajima, A, Sato, A, Yamada, M
• Format: Journal Article
• Language: English
• Published: 01-11-2005
• Subjects: alcohol oxidoreductases; anthocyanidin reductase; chemical constituents of plants; dihydroflavonol reductase; Diospyros kaki; flavonol 3-hydroxylase; fruiting; gene expression; genes; messenger RNA; naringenin-chalcone synthase; nonastringent persimmons; nucleic acid hybridization; oxidoreductases; persimmons; phenylalanine ammonia-lyase; proanthocyanidins; China
• ISSN: 0003-1062; 2327-9788
• DOI: 10.21273/jashs.130.6.830

Expression patterns of the genes involved in condensed tannin (CT) biosynthesis during fruit development was investigated in a Chinese pollination-constant, nonastringent (PCNA) persimmon (Diospyros kaki Thunb.) 'Luo Tian Tian Shi'. The transcript levels of phenylalanine ammonia-lyase (PAL) and dihydroflavonol reductase (DFR) in 'Luo Tian Tian Shi' were detected at high levels throughout the fruit growth. Chalcone synthase (CHS) and flavonol 3-hydroxylase (F3H) also continued to be transcribed during fruit growth, although their levels decreased earlier than PAL and DFR. In contrast, expression levels of these genes declined into undetectable levels at an early stage of fruit development in Japanese PCNA persimmon. In addition, anthocyanidin reductase (ANR), which encodes a key enzyme of the proanthocyanidin biosynthesis, was transcribed at high levels in 'Luo Tian Tian Shi' during fruit growth, but not in Japanese PCNA persimmon. By contrast, the expression of D. kaki serine carboxypeptidase-like protein 1 (DkSCPL1) that was obtained from suppression subtractive hybridization (SSH) analysis between artificially astringency-removed fruit and astringent fruit in a different experiment, declined earlier than the other flavonoid biosynthesis genes in 'Luo Tian Tian Shi', coincident with the termination of the tannin cell development. In the F1 progeny of the cross between 'Luo Tian Tian Shi' and Japanese PCNA 'Taishu', similar expression patterns were obtained among segregated PCNA and astringent offspring. These results indicate that Chinese PCNA is different from Japanese PCNA in expression of the genes involved in CT biosynthesis. In conclusion, we clarified that expression of the genes (PAL to ANR, but not SCPL) involved in flavonoid biosynthesis was continuous in the Chinese PCNA cultivar, despite the termination of tannin cell development.