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

Singh, Pallavi; Stevenson, Sean R; Dickinson, Patrick J; Reyna-Llorens, Ivan; Tripathi, Anoop; Reeves, Gregory; Schreier, Tina B; Hibberd, Julian M · Sci Adv · 2023

basic_science · Level V

Where this comes from

Abstract

C<sub>4</sub> photosynthesis has evolved by repurposing enzymes found in C<sub>3</sub> plants. Compared with the ancestral C<sub>3</sub> state, accumulation of C<sub>4</sub> cycle proteins is enhanced. We used de-etiolation of C<sub>4</sub> <i>Gynandropsis gynandra</i> and C<sub>3</sub> <i>Arabidopsis thaliana</i> to understand this process. C<sub>4</sub> gene expression and chloroplast biogenesis in <i>G. gynandra</i> were tightly coordinated. Although C<sub>3</sub> and C<sub>4</sub> photosynthesis genes showed similar induction patterns, in <i>G. gynandra</i>, C<sub>4</sub> genes were more strongly induced than orthologs from <i>A. thaliana</i>. 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<sub>4</sub> 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<sub>4</sub> photosynthesis genes in C<sub>4</sub> leaves is enhanced because modifications in cis allowed integration into ancestral transcriptional networks.

Medical subject headings