Division zone activity determines the potential of drought‐stressed maize leaves to resume growth after rehydration

Drought is one of the most devastating causes of yield losses in crops like maize, and the anticipated increases in severity and duration of drought spells due to climate change pose an imminent threat to agricultural productivity. To understand the drought response, phenotypic and molecular studies...

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Hauptverfasser: Van Hautegem, Tom, Takasaki, Hironori, Lorenzo, Christian, Demuynck, Kirin, Claeys, Hannes, Villers, Timothy, Sprenger, Heike, Debray, Kevin, Schaumont, Dries, Verbraeken, Lennart, Pevernagie, Julie, Merchie, Julie, Cannoot, Bernard, Aesaert, Stijn, Coussens, Griet, Yamaguchi‐Shinozaki, Kazuko, Nuccio, Michael L, Van Ex, Fred, Pauwels, Laurens, Jacobs, Thomas B, Ruttink, Tom, Inzé, Dirk, Nelissen, Hilde
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Sprache:eng
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Zusammenfassung:Drought is one of the most devastating causes of yield losses in crops like maize, and the anticipated increases in severity and duration of drought spells due to climate change pose an imminent threat to agricultural productivity. To understand the drought response, phenotypic and molecular studies are typically performed at a given time point after drought onset, representing a steady-state adaptation response. Because growth is a dynamic process, we monitored the drought response with high temporal resolution and examined cellular and transcriptomic changes after rehydration at 4 and 6 days after leaf four appearance. These data showed that division zone activity is a determinant for full organ growth recovery upon rehydration. Moreover, a prolonged maintenance of cell division by the ectopic expression of PLASTOCHRON1 extends the ability to resume growth after rehydration. The transcriptome analysis indicated that GROWTH-REGULATING FACTORS (GRFs) affect leaf growth by impacting cell division duration, which was confirmed by a prolonged recovery potential of the GRF1-overexpression line after rehydration. Finally, we used a multiplex genome editing approach to evaluate the most promising differentially expressed genes from the transcriptome study and as such narrowed down the gene space from 40 to seven genes for future functional characterization.
ISSN:0140-7791
1365-3040