Key Laboratory of Tropical Crop Biotechnology, Ministry of Agriculture, Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Sciences, Haikou, 571101, Hainan, China.
Plant Cell Rep. 2012 Feb;31(2):369-78. doi: 10.1007/s00299-011-1172-1. Epub 2011 Oct 19.
To investigate the regulation of 14-3-3 proteins in banana (Musa acuminata L. AAA group, cv. Brazilian) fruit postharvest ripening, four cDNAs encoding 14-3-3 proteins were isolated from banana and designated as Ma-14-3-3a, Ma-14-3-3c, Ma-14-3-3e, and Ma-14-3-3i, respectively. Amino acid sequence alignment showed that the four 14-3-3 proteins shared a highly conserved core structure and variable C-terminal as well as N-terminal regions with 14-3-3 proteins from other plant species. Phylogenetic analysis revealed that the four 14-3-3 genes belong to the non-ε groups. They were differentially and specifically expressed in various tissues. Real-time RT-PCR analysis indicated that these four genes function differentially during banana fruit postharvest ripening. Three genes, Ma-14-3-3a, Ma-14-3-3c, and Ma-14-3-3e, were significantly induced by exogenous ethylene treatment. However, gene function differed in naturally ripened fruits. Ethylene could induce Ma-14-3-3c expression during postharvest ripening, but expression patterns of Ma-14-3-3a and Ma-14-3-3e suggest that these two genes appear to be involved in regulating ethylene biosynthesis during fruit ripening. No obvious relationship emerged between Ma-14-3-3i expression in naturally ripened and 1-MCP (1-methylcyclopropene)-treated fruit groups during fruit ripening. These results indicate that the 14-3-3 proteins might be involved in various regulatory processes of banana fruit ripening. Further studies will mainly focus on revealing the detailed biological mechanisms of these four 14-3-3 genes in regulating banana fruit postharvest ripening.
为了研究香蕉(Musa acuminata L. AAA 组,cv. Brazilian)果实采后成熟过程中 14-3-3 蛋白的调控作用,从香蕉中分离并分别命名为 Ma-14-3-3a、Ma-14-3-3c、Ma-14-3-3e 和 Ma-14-3-3i 的四个 cDNA 编码 14-3-3 蛋白。氨基酸序列比对表明,这四种 14-3-3 蛋白具有高度保守的核心结构,以及可变的 C 端和 N 端区域,与其他植物物种的 14-3-3 蛋白相似。系统进化分析表明,这四个 14-3-3 基因属于非-ε 组。它们在不同组织中表现出差异和特异性表达。实时 RT-PCR 分析表明,这四个基因在香蕉果实采后成熟过程中发挥不同的功能。三个基因,Ma-14-3-3a、Ma-14-3-3c 和 Ma-14-3-3e,在外源乙烯处理下显著诱导表达。然而,在自然成熟果实中基因功能不同。乙烯可以在采后成熟过程中诱导 Ma-14-3-3c 的表达,但 Ma-14-3-3a 和 Ma-14-3-3e 的表达模式表明,这两个基因可能参与调节果实成熟过程中的乙烯生物合成。在自然成熟和 1-MCP(1-甲基环丙烯)处理的果实组中,Ma-14-3-3i 的表达之间没有明显的关系。这些结果表明,14-3-3 蛋白可能参与了香蕉果实成熟的各种调控过程。进一步的研究将主要集中在揭示这四个 14-3-3 基因在调节香蕉果实采后成熟过程中的详细生物学机制上。