Exaptation of ancestral cell-identity networks enables C4 photosynthesis
Joseph Swift,
Leonie H. Luginbuehl (),
Lei Hua,
Tina B. Schreier,
Ruth M. Donald,
Susan Stanley,
Na Wang,
Travis A. Lee,
Joseph R. Nery,
Joseph R. Ecker () and
Julian M. Hibberd ()
Additional contact information
Joseph Swift: Salk Institute for Biological Studies
Leonie H. Luginbuehl: University of Cambridge
Lei Hua: University of Cambridge
Tina B. Schreier: University of Cambridge
Ruth M. Donald: University of Cambridge
Susan Stanley: University of Cambridge
Na Wang: University of Cambridge
Travis A. Lee: Salk Institute for Biological Studies
Joseph R. Nery: Salk Institute for Biological Studies
Joseph R. Ecker: Salk Institute for Biological Studies
Julian M. Hibberd: University of Cambridge
Nature, 2024, vol. 636, issue 8041, 143-150
Abstract:
Abstract C4 photosynthesis is used by the most productive plants on the planet, and compared with the ancestral C3 pathway, it confers a 50% increase in efficiency1. In more than 60 C4 lineages, CO2 fixation is compartmentalized between tissues, and bundle-sheath cells become photosynthetically activated2. How the bundle sheath acquires this alternate identity that allows efficient photosynthesis is unclear. Here we show that changes to bundle-sheath gene expression in C4 leaves are associated with the gain of a pre-existing cis-code found in the C3 leaf. From single-nucleus gene-expression and chromatin-accessibility atlases, we uncover DNA binding with one finger (DOF) motifs that define bundle-sheath identity in the major crops C3 rice and C4 sorghum. Photosynthesis genes that are rewired to be strongly expressed in the bundle-sheath cells of C4 sorghum acquire cis-elements that are recognized by DOFs. Our findings are consistent with a simple model in which C4 photosynthesis is based on the recruitment of an ancestral cis-code associated with bundle-sheath identity. Gain of such elements harnessed a stable patterning of transcription factors between cell types that are found in both C3 and C4 leaves to activate photosynthesis in the bundle sheath. Our findings provide molecular insights into the evolution of the complex C4 pathway, and might also guide the rational engineering of C4 photosynthesis in C3 crops to improve crop productivity and resilience3,4.
Date: 2024
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DOI: 10.1038/s41586-024-08204-3
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