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Evolution of the C(4 )phosphoenolpyruvate carboxylase promoter of the C(4 )species Flaveria trinervia: the role of the proximal promoter region

BACKGROUND: The key enzymes of photosynthetic carbon assimilation in C(4 )plants have evolved independently several times from C(3 )isoforms that were present in the C(3 )ancestral species. The C(4 )isoform of phosphoenolpyruvate carboxylase (PEPC), the primary CO(2)-fixing enzyme of the C(4 )cycle,...

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Detalles Bibliográficos
Autores principales: Engelmann, Sascha, Zogel, Corinna, Koczor, Maria, Schlue, Ute, Streubel, Monika, Westhoff, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2241601/
https://www.ncbi.nlm.nih.gov/pubmed/18208593
http://dx.doi.org/10.1186/1471-2229-8-4
Descripción
Sumario:BACKGROUND: The key enzymes of photosynthetic carbon assimilation in C(4 )plants have evolved independently several times from C(3 )isoforms that were present in the C(3 )ancestral species. The C(4 )isoform of phosphoenolpyruvate carboxylase (PEPC), the primary CO(2)-fixing enzyme of the C(4 )cycle, is specifically expressed at high levels in mesophyll cells of the leaves of C(4 )species. We are interested in understanding the molecular changes that are responsible for the evolution of this C(4)-characteristic PEPC expression pattern, and we are using the genus Flaveria (Asteraceae) as a model system. It is known that cis-regulatory sequences for mesophyll-specific expression of the ppcA1 gene of F. trinervia (C(4)) are located within a distal promoter region (DR). RESULTS: In this study we focus on the proximal region (PR) of the ppcA1 promoter of F. trinervia and present an analysis of its function in establishing a C(4)-specific expression pattern. We demonstrate that the PR harbours cis-regulatory determinants which account for high levels of PEPC expression in the leaf. Our results further suggest that an intron in the 5' untranslated leader region of the PR is not essential for the control of ppcA1 gene expression. CONCLUSION: The allocation of cis-regulatory elements for enhanced expression levels to the proximal region of the ppcA1 promoter provides further insight into the regulation of PEPC expression in C(4 )leaves.