XAANTAL2 (AGL14) Is an Important Component of the Complex Gene Regulatory Network that Underlies Arabidopsis Shoot Apical Meristem Transitions

In Arabidopsis thaliana, multiple genes involved in shoot apical meristem (SAM) transitions have been characterized, but the mechanisms required for the dynamic attainment of vegetative, inflorescence, and floral meristem (VM, IM, FM) cell fates during SAM transitions are not well understood. Here w...

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Veröffentlicht in:Molecular plant 2015-05, Vol.8 (5), p.796-813
Hauptverfasser: Pérez-Ruiz, Rigoberto V., García-Ponce, Berenice, Marsch-Martínez, Nayelli, Ugartechea-Chirino, Yamel, Villajuana-Bonequi, Mitzi, de Folter, Stefan, Azpeitia, Eugenio, Dávila-Velderrain, José, Cruz-Sánchez, David, Garay-Arroyo, Adriana, Sánchez, María de la Paz, Estévez-Palmas, Juan M., Álvarez-Buylla, Elena R.
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Sprache:eng
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Zusammenfassung:In Arabidopsis thaliana, multiple genes involved in shoot apical meristem (SAM) transitions have been characterized, but the mechanisms required for the dynamic attainment of vegetative, inflorescence, and floral meristem (VM, IM, FM) cell fates during SAM transitions are not well understood. Here we show that a MADS-box gene, XAANTAL2 (XAL2/AGL14), is necessary and sufficient to induce flowering, and its regulation is important in FM maintenance and determinacy. xal2 mutants are late flowering, particularly under short-day (SD) condition, while XAL2 overexpressing plants are early flowering, but their flowers have vegetative traits. Interestingly, inflorescences of the latter plants have higher expression levels of LFY, AP1, and TFL1 than wild-type plants. In addition we found that XAL2 is able to bind the TFL1 regulatory regions. On the other hand, the basipetal carpels of the 35S::XAL2 lines lose determinacy and maintain high levels of WUS expression under SD condition. To provide a mechanistic explanation for the complex roles of XAL2 in SAM transitions and the apparently paradoxical phenotypes of XAL2 and other MADS-box (SOC1, AGL24) overexpressors, we conducted dynamic gene regulatory network (GRN) and epigenetic landscape modeling. We uncovered a GRN module that underlies VM, IM, and FM gene configurations and transition patterns in wild-type plants as well as loss and gain of function lines characterized here and previously. Our approach thus provides a novel mechanistic framework for understanding the complex basis of SAM development. We provide functional evidence showing the role of XAANTAL2 in the regulation of flowering transition and FM determinacy. We then integrate experimental data using gene regulatory network and epigenetic landscape models to provide a mechanistic explanation of the apparently paradoxical FM and IM phenotypes of XAL2 and other MADS-box (SOC1, AGL24) overexpression lines.
ISSN:1674-2052
1752-9867
DOI:10.1016/j.molp.2015.01.017