Please use this identifier to cite or link to this item: http://hdl.handle.net/10362/182736
Title: The bHLH transcription factor OsPRI1 activates the Setaria viridis PEPC1 promoter in rice
Author: Carvalho, Pedro
Gomes, Célia
Gonçalves, Ivan
Lourenço, Tiago F.
Vlad, Daniela
Langdale, Jane A.
Saibo, Nelson J.M.
Keywords: C photosynthesis
cell-specific gene expression
phosphoenolpyruvate carboxylase
rice
transcriptional regulation
Physiology
Plant Science
Issue Date: 7-Feb-2024
Abstract: Photosynthetic efficiency is reduced by the dual role of Rubisco, which acts either as a carboxylase or as an oxygenase, the latter leading to photorespiration. C4 photosynthesis evolved as a carbon-concentrating mechanism to reduce photorespiration. To engineer C4 into a C3 plant, it is essential to understand how C4 genes, such as phosphoenolpyruvate carboxylase (PEPC1), are regulated to be expressed at high levels and in a cell-specific manner. Yeast one-hybrid screening was used to show that OsPRI1, a rice bHLH transcription factor involved in iron homeostasis, binds to the Setaria viridis PEPC1 promoter. This promoter drives mesophyll-specific gene expression in rice. The role of OsPRI1 in planta was characterized using a rice line harbouring SvPEPC1pro::GUS. We show that OsPRI1 activates the S. viridis PEPC1 promoter by binding to an N-box in the proximal promoter, and that GUS activity is highly reduced in SvPEPC1pro::GUS lines when OsPRI1 is mutated. Cross-species comparisons showed that the SvPRI1 homolog binds to the SvPEPC1 promoter but the maize ZmPRI1 does not bind to the ZmPEPC1 promoter. Our results suggest that elements of the iron homeostasis pathway were co-opted to regulate PEPC1 gene expression during the evolution of some but not all C4 species.
Description: Funding Information: The authors would like to acknowledge Dr Steve Kelly and Dr David Emms for help using OrthoFinder. The authors would like to thank Dr Bruno Catarino for insights into the work. The authors would like to acknowledge the Protein purification services of the ITQB for assistance in recombinant protein purification. This work was funded by Fundação para a Ciência e a Tecnologia (Portugal) through the R&D unit ‘GREEN-IT Bioresources for Sustainability’ (UIDB/04551/2020 & UIDP/04551/2020) and the fellowships to PC (PD/BD/128403/2017) and CG (2020.08000.BD), and CEEC contract to TFL (through Scientific Employment Stimulus contract (CEECIND/03641/2017)). It was also supported by the European Union project 3 to 4 (Grant agreement no.: 289582). Funding Information: The authors would like to acknowledge Dr Steve Kelly and Dr David Emms for help using OrthoFinder. The authors would like to thank Dr Bruno Catarino for insights into the work. The authors would like to acknowledge the Protein purification services of the ITQB for assistance in recombinant protein purification. This work was funded by Fundação para a Ciência e a Tecnologia (Portugal) through the R&D unit ‘GREEN‐IT Bioresources for Sustainability’ (UIDB/04551/2020 & UIDP/04551/2020) and the fellowships to PC (PD/BD/128403/2017) and CG (2020.08000.BD), and CEEC contract to TFL (through Scientific Employment Stimulus contract (CEECIND/03641/2017)). It was also supported by the European Union project 3 to 4 (Grant agreement no.: 289582). Publisher Copyright: © 2024 The Authors. New Phytologist © 2024 New Phytologist Foundation.
Peer review: yes
URI: http://hdl.handle.net/10362/182736
DOI: https://doi.org/10.1111/nph.19556
ISSN: 0028-646X
Appears in Collections:Home collection (ITQB)

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