Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/119851
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Type: Journal article
Title: Evolution of chloroplast retrograde signaling facilitates green plant adaptation to land
Author: Zhao, C.
Wang, Y.
Chan, K.
Marchant, D.
Franks, P.
Randall, D.
Tee, E.
Chen, G.
Ramesh, S.
Phua, S.
Zhang, B.
Hills, A.
Dai, F.
Xue, D.
Gilliham, M.
Tyerman, S.
Nevo, E.
Wu, F.
Zhang, G.
Wong, G.
et al.
Citation: Proceedings of the National Academy of Sciences of the United States of America, 2019; 116(11):5015-5020
Publisher: National Academy of Sciences of the United States of America
Issue Date: 2019
ISSN: 0027-8424
1091-6490
Statement of
Responsibility: 
Chenchen Zhao, Yuanyuan Wang, Kai Xun Chan, D. Blaine Marchant, Peter J. Franks, David Randall, Estee E. Tee, Guang Chen, Sunita Ramesh, Su Yin Phua, Ben Zhang, Adrian Hills, Fei Dai, Dawei Xue, Matthew Gilliham, Steve Tyerman, Eviatar Nevo, Feibo Wu, Guoping Zhang, Gane K.-S. Wong, James H. Leebens-Mack, Michael Melkonian, Michael R. Blatt, Pamela S. Soltis, Douglas E. Soltis, Barry J. Pogson, and Zhong-Hua Chen
Abstract: Chloroplast retrograde signaling networks are vital for chloroplast biogenesis, operation, and signaling, including excess light and drought stress signaling. To date, retrograde signaling has been considered in the context of land plant adaptation, but not regarding the origin and evolution of signaling cascades linking chloroplast function to stomatal regulation. We show that key elements of the chloroplast retrograde signaling process, the nucleotide phosphatase (SAL1) and 3'-phosphoadenosine-5'-phosphate (PAP) metabolism, evolved in streptophyte algae-the algal ancestors of land plants. We discover an early evolution of SAL1-PAP chloroplast retrograde signaling in stomatal regulation based on conserved gene and protein structure, function, and enzyme activity and transit peptides of SAL1s in species including flowering plants, the fern Ceratopteris richardii, and the moss Physcomitrella patens Moreover, we demonstrate that PAP regulates stomatal closure via secondary messengers and ion transport in guard cells of these diverse lineages. The origin of stomata facilitated gas exchange in the earliest land plants. Our findings suggest that the conquest of land by plants was enabled by rapid response to drought stress through the deployment of an ancestral SAL1-PAP signaling pathway, intersecting with the core abscisic acid signaling in stomatal guard cells.
Keywords: Comparative genomics; water stress; green plant evolution; signal transduction; stomata
Rights: Copyright © 2019 the Author(s). Published by PNAS. This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).
RMID: 0030108875
DOI: 10.1073/pnas.1812092116
Grant ID: http://purl.org/au-research/grants/arc/DE1401011143
http://purl.org/au-research/grants/arc/CE140100008
http://purl.org/au-research/grants/arc/DP150104007
Appears in Collections:Agriculture, Food and Wine publications

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