Assessment of the flowering genetic regulatory network in tropical orchids with different lifeforms

ABSTRACT: The reproductive transition in angiosperms includes morphological changes when a vegetative shoot apical meristem (VM) forming leaves, becomes an inflorescence meristem (IM) that forms bracts and flowers. This process is controlled in monocots, like Oryza sativa, by a Genetic Regulatory Network (GRN) that includes promoters like Heading date 3a (Hd3a) (FLOWERING LOCUS T-FT), Heading date 1 (Hd1) (CONSTANS-CO), FLOWERING LOCUS D (OsFD1) and 14–3–3 proteins that activate floral meristem identity genes. Repressors involved in the maintenance of the vegetative phases include TERMINAL FLOWER LOCUS 1 (TFL1) and OsMADS55 (AGAMOUS Like24/SHORT VEGETATIVE PHASE). Additionally, FLOWERING LOCUS C (FLC) and VERNALIZATION 2 (VRN2) are important in Poales species that respond to cold. Although flowering mechanisms have been studied in detail in monocot model species, little is known about how the same process occurs in orchids with different habits colonizing different niches. Terrestrial and epiphytic orchids vary in meristem hierarchies and the development of storage organs. We performed a comprehensive analysis of the morpho-anatomical changes from VM to IM in the terrestrial orchid Epidendrum fimbriatum with nearly continuous flowering all year long in cloud Andean forests. Using the landmarks for reproductive transition we performed comparative transcriptomic analyses in VM versus IM. We used a differential expression gene approach between those stages, and we found 40 DEGs between VM and IM involved in reproductive transition. Furthermore, we used a targeted search to isolate more than 30 orthologs from the canonical flowering GRN in parallel to the DEGs. In addition, we corroborated the results from our RNAseq data with spatio-temporal expression analyses using in situ hybridization and by protein-protein interaction studies using yeast two hybrid experiments. We are currently comparing these results with experiments performed in orchids with seasonal flowering, including Cattleya trianae, an orchid with storage organs and epiphytic habit, and Elleanthus aurantiacus with terrestrial habit and lacking storage organs. Our results allow us to re-evaluate the flowering GRN in orchids when compared to the model species O. sativa and other Poaceae. In general, we have found evidence for: 1) high duplication rates for flowering integrators in orchids but a low percentage of homologs transcriptionally active; 2) the retention of canonical flowering integrators, at the expense of low expression, the loss of key protein interactions and possibly pseudogenization of some homologs; and 3) changes in the transcriptomic profiles in different orchids according to their habits.

• Autores: Mafrigal Bedoya, Yesenia; Pabón Mora, Natalia; Scanlon, Michael; Bemer, Marian; Alzate Restrepo, Juan Fernando
• Tipo de recurso: http://purl.org/coar/resource_type/c_5794
• Fecha de publicación: 2023
• Institución: Universidad de Antioquia
• Repositorio: Repositorio UdeA
• Idioma: eng
• OAI Identifier: oai:bibliotecadigital.udea.edu.co:10495/36147
• Acceso en línea: https://hdl.handle.net/10495/36147
• Palabra clave: Orchidaceae; RNA-Seq; Orquídeas; Orchids; Floración; Flowering; Evo Devo; http://aims.fao.org/aos/agrovoc/c_2992
• Rights: openAccess
• License: https://creativecommons.org/licenses/by-nc-sa/4.0/