Department of Postharvest Science of Fresh Produce, Agricultural Research Organization (ARO), the Volcani Center, PO Box 6, Bet Dagan 50250, Israel.
J Exp Bot. 2010 Mar;61(5):1523-35. doi: 10.1093/jxb/erq017. Epub 2010 Mar 3.
Six MaMADS-box genes have been cloned from the banana fruit cultivar Grand Nain. The similarity of these genes to tomato LeRIN is low and neither MaMADS2 nor MaMADS1 complement the tomato rin mutation. Nevertheless, the expression patterns, specifically in fruit and the induction during ripening and in response to ethylene and 1-MCP, suggest that some of these genes may participate in ripening. MaMADS1, 2, and 3, are highly expressed in fruit only, while the others are expressed in fruit as well as in other organs. Moreover, the suites of MaMADS-box genes and their temporal expression differ in peel and pulp during ripening. In the pulp, the increase in MaMADS2, 3, 4, and 5 expression preceded an increase in ethylene production, but coincides with the CO(2) peak. However, MaMADS1 expression in pulp coincided with ethylene production, but a massive increase in its expression occurred late during ripening, together with a second wave in the expression of MaMADS2, 3, and 4. In the peel, on the other hand, an increase in expression of MaMADS1, 3, and to a lesser degree also of MaMADS4 and 2 coincided with an increase in ethylene production. Except MaMADS3, which was induced by ethylene in pulp and peel, only MaMADS4, and 5 in pulp and MaMADS1 in peel were induced by ethylene. 1-MCP applied at the onset of the increase in ethylene production, increased the levels of MaMADS4 and MaMADS1 in pulp, while it decreased MaMADS1, 3, 4, and 5 in peel, suggesting that MaMADS4 and MaMADS1 are negatively controlled by ethylene at the onset of ethylene production only in pulp. Only MaMADS2 is neither induced by ethylene nor by 1-MCP, and it is expressed mainly in pulp. Our results suggest that two independent ripening programs are employed in pulp and peel which involve the activation of mainly MaMADS2, 4, and 5 and later on also MaMADS1 in pulp, and mainly MaMADS1, and 3 in peel. Hence, our results are consistent with MaMADS2, a SEP3 homologue, acting in the pulp upstream of the increase in ethylene production similarly to LeMADS-RIN.
从香蕉果实品种大蕉中克隆了 6 个 MaMADS-box 基因。这些基因与番茄 LeRIN 的相似性较低,MaMADS2 和 MaMADS1 都不能互补番茄 rin 突变。然而,这些基因的表达模式,特别是在果实中的表达以及在成熟过程中的诱导和对乙烯和 1-MCP 的反应,表明其中一些基因可能参与了成熟过程。MaMADS1、2 和 3 仅在果实中高度表达,而其他基因则在果实和其他器官中表达。此外,在成熟过程中,果皮和果肉中 MaMADS-box 基因的组合及其时空表达不同。在果肉中,MaMADS2、3、4 和 5 的表达增加先于乙烯生成的增加,但与 CO2 峰值同时发生。然而,MaMADS1 在果肉中的表达与乙烯生成同时发生,但在成熟过程中晚期其表达大量增加,同时 MaMADS2、3 和 4 的表达也出现第二次增加。另一方面,在果皮中,MaMADS1、3 的表达增加,程度较小的还有 MaMADS4 和 2 的表达增加,与乙烯生成的增加同时发生。除了在果肉和果皮中被乙烯诱导的 MaMADS3 之外,只有 MaMADS4 和 5 在果肉中,MaMADS1 在果皮中被乙烯诱导。1-MCP 在乙烯生成增加开始时应用,增加了果肉中 MaMADS4 和 MaMADS1 的水平,而降低了果皮中 MaMADS1、3、4 和 5 的水平,表明只有在果肉中,MaMADS4 和 MaMADS1 仅在乙烯生成开始时才受乙烯的负调控。只有 MaMADS2 既不受乙烯也不受 1-MCP 诱导,主要在果肉中表达。我们的结果表明,在果肉和果皮中采用了两种独立的成熟程序,主要涉及 MaMADS2、4 和 5 的激活,随后也涉及 MaMADS1 在果肉中的激活,以及主要涉及 MaMADS1 和 3 在果皮中的激活。因此,我们的结果与 SEP3 同源物 MaMADS2 一致,类似于 LeMADS-RIN,它在乙烯生成增加之前在果肉中起作用。