Ancient duons may underpin spatial patterning of gene expression in C<sub>4</sub> leaves.

Reyna-Llorens, Ivan; Burgess, Steven J; Reeves, Gregory; Singh, Pallavi; Stevenson, Sean R; Williams, Ben P; Stanley, Susan; Hibberd, Julian M · Proc Natl Acad Sci U S A · 2018

basic_science · Level V

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Abstract

If the highly efficient C<sub>4</sub> photosynthesis pathway could be transferred to crops with the C<sub>3</sub> pathway there could be yield gains of up to 50%. It has been proposed that the multiple metabolic and developmental modifications associated with C<sub>4</sub> photosynthesis are underpinned by relatively few master regulators that have allowed the evolution of C<sub>4</sub> photosynthesis more than 60 times in flowering plants. Here we identify a component of one such regulator that consists of a pair of <i>cis</i>-elements located in coding sequence of multiple genes that are preferentially expressed in bundle sheath cells of C<sub>4</sub> leaves. These motifs represent duons as they play a dual role in coding for amino acids as well as controlling the spatial patterning of gene expression associated with the C<sub>4</sub> leaf. They act to repress transcription of C<sub>4</sub> photosynthesis genes in mesophyll cells. These duons are also present in the C<sub>3</sub> model <i>Arabidopsis thaliana</i>, and, in fact, are conserved in all land plants and even some algae that use C<sub>3</sub> photosynthesis. C<sub>4</sub> photosynthesis therefore appears to have coopted an ancient regulatory code to generate the spatial patterning of gene expression that is a hallmark of C<sub>4</sub> photosynthesis. This intragenic transcriptional regulatory sequence could be exploited in the engineering of efficient photosynthesis of crops.

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