Gene expression underlying floral epidermal specialization in Aristolochia fimbriata (Aristolochiaceae)

Harold Suárez-Baron, Juan F. Alzate, Favio González, Soraya Pelaz, Barbara A. Ambrose, Natalia Pabón-Mora

Producción: Contribución a una revistaArtículorevisión exhaustiva

5 Citas (Scopus)

Resumen

Background and Aims: The epidermis constitutes the outermost tissue of the plant body. Although it plays major structural, physiological and ecological roles in embryophytes, the molecular mechanisms controlling epidermal cell fate, differentiation and trichome development have been scarcely studied across angiosperms, and remain almost unexplored in floral organs. Methods: In this study, we assess the spatio-temporal expression patterns of GL2, GL3, TTG1, TRY, MYB5, MYB6, HDG2, MYB106-like, WIN1 and RAV1-like homologues in the magnoliid Aristolochia fimbriata (Aristolochiaceae) by using comparative RNA-sequencing and in situ hybridization assays. Key Results: Genes involved in Aristolochia fimbriata trichome development vary depending on the organ where they are formed. Stem, leaf and pedicel trichomes recruit most of the transcription factors (TFs) described above. Conversely, floral trichomes only use a small subset of genes including AfimGL2, AfimRAV1-like, AfimWIN1, AfimMYB106-like and AfimHDG2. The remaining TFs, AfimTTG1, AfimGL3, AfimTRY, AfimMYB5 and AfimMYB6, are restricted to the abaxial (outer) and the adaxial (inner) pavement epidermal cells. Conclusions: We re-evaluate the core genetic network shaping trichome fate in flowers of an early-divergent angiosperm lineage and show a morphologically diverse output with a simpler genetic mechanism in place when compared to the models Arabidopsis thaliana and Cucumis sativus. In turn, our results strongly suggest that the canonical trichome gene expression appears to be more conserved in vegetative than in floral tissues across angiosperms.

Idioma originalInglés
Páginas (desde-hasta)749-764
Número de páginas16
PublicaciónAnnals of Botany
Volumen127
N.º6
DOI
EstadoPublicada - 07 may. 2021
Publicado de forma externa

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