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Synergistic Binding of bHLH Transcription Factors to the Promoter of the Maize NADP-ME Gene Used in C(4) Photosynthesis Is Based on an Ancient Code Found in the Ancestral C(3) State

C(4) photosynthesis has evolved repeatedly from the ancestral C(3) state to generate a carbon concentrating mechanism that increases photosynthetic efficiency. This specialized form of photosynthesis is particularly common in the PACMAD clade of grasses, and is used by many of the world’s most produ...

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Detalles Bibliográficos
Autores principales: Borba, Ana Rita, Serra, Tânia S, Górska, Alicja, Gouveia, Paulo, Cordeiro, André M, Reyna-Llorens, Ivan, Kneřová, Jana, Barros, Pedro M, Abreu, Isabel A, Oliveira, Maria Margarida, Hibberd, Julian M, Saibo, Nelson J M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995220/
https://www.ncbi.nlm.nih.gov/pubmed/29659975
http://dx.doi.org/10.1093/molbev/msy060
Descripción
Sumario:C(4) photosynthesis has evolved repeatedly from the ancestral C(3) state to generate a carbon concentrating mechanism that increases photosynthetic efficiency. This specialized form of photosynthesis is particularly common in the PACMAD clade of grasses, and is used by many of the world’s most productive crops. The C(4) cycle is accomplished through cell-type-specific accumulation of enzymes but cis-elements and transcription factors controlling C(4) photosynthesis remain largely unknown. Using the NADP-Malic Enzyme (NADP-ME) gene as a model we tested whether mechanisms impacting on transcription in C(4) plants evolved from ancestral components found in C(3) species. Two basic Helix-Loop-Helix (bHLH) transcription factors, ZmbHLH128 and ZmbHLH129, were shown to bind the C(4)NADP-ME promoter from maize. These proteins form heterodimers and ZmbHLH129 impairs trans-activation by ZmbHLH128. Electrophoretic mobility shift assays indicate that a pair of cis-elements separated by a seven base pair spacer synergistically bind either ZmbHLH128 or ZmbHLH129. This pair of cis-elements is found in both C(3) and C(4) Panicoid grass species of the PACMAD clade. Our analysis is consistent with this cis-element pair originating from a single motif present in the ancestral C(3) state. We conclude that C(4) photosynthesis has co-opted an ancient C(3) regulatory code built on G-box recognition by bHLH to regulate the NADP-ME gene. More broadly, our findings also contribute to the understanding of gene regulatory networks controlling C(4) photosynthesis.