Department of Biological Sciences, University of Naples Federico II, via Mezzocannone 8, 80134 Naples, Italy.
Mol Biol Rep. 2013 May;40(5):3523-35. doi: 10.1007/s11033-012-2426-x. Epub 2013 Jan 1.
According to the ABCDE model of flower development, the C- and D- class MADS box genes are involved in the formation of male and female reproductive organs (fused to form the column in orchids) and in ovule maturation (triggered by fertilization in orchids). In the present study, we report the isolation of the Orchis italica genes OitaAG and OitaSTK, homologs of the C-class AGAMOUS and the D-class SEEDSTICK genes of Arabidopsis, respectively. Analysis of their expression profiles reveals high levels of mRNA in columns and ovaries, particularly after pollination. However, weak expression is also detectable in the inner tepals (OitaAG) and the lip and root (OitaSTK). This expression profile is only partially overlapping with those reported in other orchid species and may be the consequence of a different evolutionary history of these functional gene classes in orchids. The genomic characterization of the OitaAG and OitaSTK genes shows that a high number of traces of mobile elements are present in introns and could have contributed to the size expansion of some of them (e.g., intron 2 and 3 of OitaAG and intron 3, 4 and 5 of OitaSTK). Nucleotide sequences of intron 1 of the OitaSTK gene and other STK-like genes do not share regulatory motifs, whereas sequence comparison of intron 2 of the OitaAG gene with that of intron 2 of other AG-like genes reveals, for the first time in an orchid species, the presence of conserved cis-regulatory boxes and binding sites for transcription factors that positively (e.g., LEAFY and WUSCHEL) or negatively (e.g., BELLRINGER) regulate the expression of the AG homologs in dicots and monocots.
根据花发育的 ABCDE 模型,C 类和 D 类 MADS 盒基因参与雄性和雌性生殖器官的形成(融合形成兰花的柱)和胚珠成熟(在兰花中由受精触发)。在本研究中,我们报告了 Orchis italica 基因 OitaAG 和 OitaSTK 的分离,它们分别是拟南芥 C 类 AGAMOUS 和 D 类 SEEDSTICK 基因的同源物。对其表达谱的分析表明,在柱和卵巢中 mRNA 水平较高,特别是在授粉后。然而,在内轮花被(OitaAG)和唇和根(OitaSTK)中也可以检测到较弱的表达。这种表达谱与其他兰花物种报道的表达谱部分重叠,可能是这些功能基因类在兰花中不同进化历史的结果。OitaAG 和 OitaSTK 基因的基因组特征表明,大量的移动元件痕迹存在于内含子中,这可能导致其中一些内含子的大小扩大(例如,OitaAG 的内含子 2 和 3 以及 OitaSTK 的内含子 3、4 和 5)。OitaSTK 基因内含子 1 的核苷酸序列和其他 STK 样基因没有共享调节基元,而 OitaAG 基因内含子 2 的序列与其他 AG 样基因的内含子 2 的序列比较首次揭示了在兰花物种中,保守的顺式调节盒和转录因子结合位点的存在,这些转录因子正向(例如,LEAFY 和 WUSCHEL)或负向(例如,BELLRINGER)调节双子叶植物和单子叶植物中 AG 同源物的表达。