Singlet oxygen- and EXECUTER1-mediated signaling is initiated in grana margins and depends on the protease FtsH2

Formation of singlet oxygen (¹O₂) has been implicated with damaging photosystem II (PSII) that needs to undergo continuous repair to maintain photosynthetic electron transport. In addition to its damaging effect, ¹O₂ has also been shown to act as a signal that triggers stress acclimation and an enha...

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Published inProceedings of the National Academy of Sciences - PNAS Vol. 113; no. 26; pp. E3792 - E3800
Main Authors Wang, Liangsheng, (王良省), Kim, Chanhong, Xu, Xia, Piskurewicz, Urszula, Dogra, Vivek, Singh, Somesh, Mahler, Hanno, Apel, Klaus
Format Journal Article
LanguageEnglish
Published United States National Academy of Sciences 28.06.2016
SeriesPNAS Plus
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Summary:Formation of singlet oxygen (¹O₂) has been implicated with damaging photosystem II (PSII) that needs to undergo continuous repair to maintain photosynthetic electron transport. In addition to its damaging effect, ¹O₂ has also been shown to act as a signal that triggers stress acclimation and an enhanced stress resistance. A signaling role of ¹O₂ was first documented in the fluorescent (flu) mutant of Arabidopsis. It strictly depends on the chloroplast protein EXECUTER1 (EX1) and happens under nonphotoinhibitory light conditions. Under severe light stress, signaling is initiated independently of EX1 by ¹O₂ that is thought to be generated at the acceptor side of active PSII within the core of grana stacks. The results of the present study suggest a second source of ¹O₂ formation in grana margins close to the site of chlorophyll synthesis where EX1 is localized and the disassembly of damaged and reassembly of active PSII take place. The initiation of ¹O₂ signaling in grana margins depends on EX1 and the ATP-dependent zinc metalloprotease FtsH. As FtsH cleaves also the D1 protein during the disassembly of damaged PSII, EX1- and ¹O₂-mediated signaling seems to be not only spatially but also functionally associated with the repair of PSII.
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3Present address: Department of Plant Biology, University of Geneva, CH 1211 Geneva, Switzerland.
Author contributions: L.W., C.K., U.P., and K.A. designed research; L.W., C.K., X.X., U.P., V.D., S.S., and H.M. performed research; L.W., C.K., U.P., V.D., S.S., and K.A. analyzed data; and K.A. wrote the paper.
Edited by Robert Haselkorn, University of Chicago, Chicago, IL, and approved May 10, 2016 (received for review March 8, 2016)
2Present address: Grape Genetics Research Unit, US Department of Agriculture–Agricultural Research Service (USDA–ARS), Cornell University, Geneva, NY 14456.
1L.W. and C.K. contributed equally to this work.
ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.1603562113