C 4 gene induction during de-etiolation evolved through changes in cis to allow integration with ancestral C 3 gene regulatory networks

Author:

Singh Pallavi1ORCID,Stevenson Sean R.1ORCID,Dickinson Patrick J.1ORCID,Reyna-Llorens Ivan1ORCID,Tripathi Anoop1ORCID,Reeves Gregory1ORCID,Schreier Tina B.1ORCID,Hibberd Julian M.1ORCID

Affiliation:

1. Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge CB2 3EA, UK.

Abstract

C 4 photosynthesis has evolved by repurposing enzymes found in C 3 plants. Compared with the ancestral C 3 state, accumulation of C 4 cycle proteins is enhanced. We used de-etiolation of C 4 Gynandropsis gynandra and C 3 Arabidopsis thaliana to understand this process. C 4 gene expression and chloroplast biogenesis in G. gynandra were tightly coordinated. Although C 3 and C 4 photosynthesis genes showed similar induction patterns, in G. gynandra , C 4 genes were more strongly induced than orthologs from A. thaliana . In vivo binding of TGA and homeodomain as well as light-responsive elements such as G- and I-box motifs were associated with the rapid increase in transcripts of C 4 genes. Deletion analysis confirmed that regions containing G- and I-boxes were necessary for high expression. The data support a model in which accumulation of transcripts derived from C 4 photosynthesis genes in C 4 leaves is enhanced because modifications in cis allowed integration into ancestral transcriptional networks.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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