Physiological Laboratory for South China Fruits, College of Horticulture, South China Agricultural University, Guangzhou, China.
PLoS One. 2011 Apr 29;6(4):e19455. doi: 10.1371/journal.pone.0019455.
Litchi has diverse fruit color phenotypes, yet no research reflects the biochemical background of this diversity. In this study, we evaluated 12 litchi cultivars for chromatic parameters and pigments, and investigated the effects of abscisic acid, forchlorofenron (CPPU), bagging and debagging treatments on fruit coloration in cv. Feizixiao, an unevenly red cultivar. Six genes encoding chalcone synthase (CHS), chalcone isomerase (CHI), flavanone 3-hydroxylase (F3H), dihydroflavonol 4-reductase (DFR), anthocyanidin synthase (ANS) and UDP-glucose: flavonoid 3-O-glucosyltransferase (UFGT) were isolated from the pericarp of the fully red litchi cv. Nuomici, and their expression was analyzed in different cultivars and under the above mentioned treatments. Pericarp anthocyanin concentration varied from none to 734 mg m(-2) among the 12 litchi cultivars, which were divided into three coloration types, i.e. non-red ('Kuixingqingpitian', 'Xingqiumili', 'Yamulong'and 'Yongxing No. 2'), unevenly red ('Feizixiao' and 'Sanyuehong') and fully red ('Meiguili', 'Baila', Baitangying' 'Guiwei', 'Nuomici' and 'Guinuo'). The fully red type cultivars had different levels of anthocyanin but with the same composition. The expression of the six genes, especially LcF3H, LcDFR, LcANS and LcUFGT, in the pericarp of non-red cultivars was much weaker as compared to those red cultivars. Their expression, LcDFR and LcUFGT in particular, was positively correlated with anthocyanin concentrations in the pericarp. These results suggest the late genes in the anthocyanin biosynthetic pathway were coordinately expressed during red coloration of litchi fruits. Low expression of these genes resulted in absence or extremely low anthocyanin accumulation in non-red cultivars. Zero-red pericarp from either immature or CPPU treated fruits appeared to be lacking in anthocyanins due to the absence of UFGT expression. Among these six genes, only the expression of UFGT was found significantly correlated with the pericarp anthocyanin concentration (r = 0.84). These results suggest that UFGT played a predominant role in the anthocyanin accumulation in litchi as well as pericarp coloration of a given cultivar.
荔枝具有多种果实颜色表型,但尚无研究反映这种多样性的生化背景。在这项研究中,我们评估了 12 个荔枝品种的色度参数和色素,并研究了脱落酸、调吡咯烷(CPPU)、套袋和去袋处理对不均匀红品种妃子笑果实着色的影响。从完全红色荔枝品种 Nuomici 的果皮中分离出编码查尔酮合酶(CHS)、查尔酮异构酶(CHI)、黄烷酮 3-羟化酶(F3H)、二氢黄酮醇 4-还原酶(DFR)、花青素合酶(ANS)和 UDP-葡萄糖:类黄酮 3-O-葡萄糖基转移酶(UFGT)的 6 个基因,并分析了它们在不同品种和上述处理下的表达。12 个荔枝品种的果皮中花色苷浓度从无到 734mgm(-2)不等,可分为 3 种着色类型,即非红色(“魁星清田”、“兴秋梨”、“杨梅龙”和“永兴 2 号”)、不均匀红色(“妃子笑”和“三月红”)和完全红色(“美味梨”、“白蜡”、“白塘营”、“桂味”、“糯米糍”和“桂圆”)。完全红色类型的品种具有不同水平的花色苷,但组成相同。非红色品种果皮中 6 个基因(特别是 LcF3H、LcDFR、LcANS 和 LcUFGT)的表达明显弱于红色品种。它们的表达,特别是 LcDFR 和 LcUFGT,与果皮中花色苷浓度呈正相关。这些结果表明,在荔枝果实的红色着色过程中,花色苷生物合成途径的晚期基因协调表达。非红色品种这些基因表达水平较低,导致花色苷积累极少或不存在。未成熟或 CPPU 处理的果实中零红色果皮似乎由于 UFGT 表达缺失而缺乏花色苷。在这 6 个基因中,只有 UFGT 的表达与果皮花色苷浓度显著相关(r=0.84)。这些结果表明,UFGT 在荔枝中花色苷的积累以及特定品种果皮着色中起主要作用。