Centro de Genómica, Instituto Valenciano de Investigaciones Agrarias, Carretera Moncada-Náquera km 4.5, 46113 Moncada, Valencia, Spain.
BMC Plant Biol. 2010 Dec 15;10:276. doi: 10.1186/1471-2229-10-276.
External ripening in Citrus fruits is morphologically characterized by a colour shift from green to orange due to the degradation of chlorophylls and the accumulation of carotenoid pigments. Although numerous genes coding for enzymes involved in such biochemical pathways have been identified, the molecular control of this process has been scarcely studied. In this work we used the Citrus clementina mutants 39B3 and 39E7, showing delayed colour break, to isolate genes potentially related to the regulation of peel ripening and its physiological or biochemical effects.
Pigment analyses revealed different profiles of carotenoid and chlorophyll modification in 39B3 and 39E7 mutants. Flavedo from 39B3 fruits showed an overall delay in carotenoid accumulation and chlorophyll degradation, while the flavedo of 39E7 was devoid of the apocarotenoid β-citraurin among other carotenoid alterations. A Citrus microarray containing about 20,000 cDNA fragments was used to identify genes that were differentially expressed during colour change in the flavedo of 39B3 and 39E7 mutants respect to the parental variety. The results highlighted 73 and 90 genes that were respectively up- and down-regulated in both mutants. CcGCC1 gene, coding for a GCC type transcriptional factor, was found to be down-regulated. CcGCC1 expression was strongly induced at the onset of colour change in the flavedo of parental clementine fruit. Moreover, treatment of fruits with gibberellins, a retardant of external ripening, delayed both colour break and CcGCC1 overexpression.
In this work, the citrus fruit ripening mutants 39B3 and 39E7 have been characterized at the phenotypic, biochemical and transcriptomic level. A defective synthesis of the apocarotenoid β-citraurin has been proposed to cause the yellowish colour of fully ripe 39E7 flavedo. The analyses of the mutant transcriptomes revealed that colour change during peel ripening was strongly associated with a major mobilization of mineral elements and with other previously known metabolic and photosynthetic changes. The expression of CcGCC1 was associated with peel ripening since CcGCC1 down-regulation correlated with a delay in colour break induced by genetic, developmental and hormonal causes.
柑橘果实的外果皮成熟过程在形态上表现为果皮颜色从绿色转变为橙色,这是由于叶绿素的降解和类胡萝卜素色素的积累。尽管已经鉴定出许多编码参与这种生化途径的酶的基因,但对这个过程的分子控制研究甚少。在这项工作中,我们使用了外果皮成熟延迟的柑橘克莱门氏小柑橘突变体 39B3 和 39E7,来分离可能与果皮成熟调控及其生理或生化效应相关的基因。
色素分析显示 39B3 和 39E7 突变体的类胡萝卜素和叶绿素修饰存在不同的模式。39B3 果实的黄皮层显示出类胡萝卜素积累和叶绿素降解的整体延迟,而 39E7 的黄皮层除了其他类胡萝卜素改变外,还缺乏脱羧类胡萝卜素 β-柠乌素。使用包含约 20000 个 cDNA 片段的柑橘微阵列来鉴定在 39B3 和 39E7 突变体果皮颜色变化过程中差异表达的基因,这些基因与亲本品种进行比较。结果突出显示了在两个突变体中分别上调和下调的 73 和 90 个基因。编码 GCC 型转录因子的 CcGCC1 基因被发现下调。CcGCC1 表达在亲本克莱门氏小柑橘果实黄皮层颜色变化开始时强烈诱导。此外,用赤霉素处理果实,赤霉素是外果皮成熟的抑制剂,会延迟颜色变化和 CcGCC1 的过表达。
在这项工作中,对柑橘果实成熟突变体 39B3 和 39E7 进行了表型、生化和转录组学特征分析。提出了一种缺陷的脱羧类胡萝卜素 β-柠乌素的合成,可能导致完全成熟的 39E7 黄皮层呈现黄色。对突变体转录组的分析表明,果皮成熟过程中的颜色变化与大量矿质元素的动员以及其他先前已知的代谢和光合作用变化密切相关。CcGCC1 的表达与果皮成熟有关,因为 CcGCC1 的下调与遗传、发育和激素引起的颜色变化延迟相关。