Ramírez-Ramírez Jessica A, Madrigal Yesenia, Alzate Juan F, Pabón-Mora Natalia
Facultad de Ciencias Exactas y Naturales, Instituto de Biología, Universidad de Antioquia, Medellín, Colombia.
Centro Nacional de Secuenciación Genómica, Sede de Investigación Universitaria, Departamento de Microbiología y Parasitología, Facultad de Medicina, Universidad de Antioquia, Medellín, Colombia.
Cells Dev. 2021 Dec;168:203755. doi: 10.1016/j.cdev.2021.203755. Epub 2021 Nov 8.
In angiosperms the reproductive transition results in the transformation of a vegetative apical meristem (SAM) into an inflorescence meristem (IM), capable of forming floral meristems (FM). Two key players in the flowering transition are AGAMOUS-like 24 (AGL24) and SHORT VEGETATIVE PHASE (SVP). They are eudicot MADS-box paralogs performing opposite roles, as AGL24 positively regulates flowering while SVP represses the reproductive transition in Arabidopsis. We confirm that the Arabidopsis functional reference cannot be readily extrapolated to all eudicots as there are additional duplications of AGL24 in early divergent eudicots and core eudicots with significant sequence variation. In addition, we found that in monocots, two additional independent duplication events have resulted in at least three clades of AGL24/SVP homologs, some only found in Orchidaceae. Protein sequence analyses and comparative evolutionary rates point to higher rates of relaxed negative selection in the Core Eudicot AGL24 B and the Orch SVP-like B clades, in eudicots and monocots respectively. On the other hand, expression data points to plesiomorphic pleiotropic roles of AGL24/SVP genes likely similar to SVP core eudicot genes, and the acquisition of new roles as flowering positive regulators in Core Eudicot AGL24 A genes. Our research presents evidence on the diversification and recruitment of AGL24/SVP homologs in flowering transition in orchids. Although, broad expression of most copies does not allow to determine if they act as flowering repressors or promoters, the restricted expression of some homologs in the SAM suggests putative roles in maintaining the vegetative phase. If so studying in detail the function of AGL24/SVP homologs in orchids is critical to identify putative flowering repressors in a lineage where other canonical repressors remain elusive.
在被子植物中,生殖转变导致营养顶端分生组织(SAM)转变为花序分生组织(IM),后者能够形成花分生组织(FM)。开花转变中的两个关键因子是类AGAMOUS 24(AGL24)和短营养期(SVP)。它们是真双子叶植物MADS-box旁系同源基因,发挥相反的作用,因为AGL24正向调节开花,而SVP在拟南芥中抑制生殖转变。我们证实,拟南芥的功能参考不能轻易外推到所有真双子叶植物,因为在早期分化的真双子叶植物和核心真双子叶植物中存在AGL24的额外复制,且序列差异显著。此外,我们发现,在单子叶植物中,另外两个独立的复制事件导致了至少三个AGL24/SVP同源基因分支,有些仅在兰科植物中发现。蛋白质序列分析和比较进化速率表明,在核心真双子叶植物AGL24 B分支和单子叶植物的兰花SVP-like B分支中,分别存在更高的松弛负选择率。另一方面,表达数据表明AGL24/SVP基因可能具有与SVP核心真双子叶植物基因相似的原始多效性作用,以及在核心真双子叶植物AGL24 A基因中作为开花正向调节因子获得的新作用。我们的研究提供了关于兰花开花转变中AGL24/SVP同源基因多样化和招募的证据。尽管大多数拷贝的广泛表达无法确定它们是作为开花抑制因子还是促进因子起作用,但一些同源基因在SAM中的受限表达表明它们在维持营养期方面可能具有作用。如果是这样,详细研究兰花中AGL24/SVP同源基因的功能对于在一个其他经典抑制因子仍然难以捉摸的谱系中鉴定推定的开花抑制因子至关重要。