Time-Series Transcriptomics Reveals That <i>AGAMOUS-LIKE22</i> Affects Primary Metabolism and Developmental Processes in Drought-Stressed Arabidopsis

Ulrike Bechtold(University of Essex), Christopher A. Penfold(University of Warwick), Dafyd J. Jenkins(University of Warwick), Roxane Legaie(University of Warwick), Jonathan D. Moore(University of Warwick), Tracy Lawson(University of Essex), Jack S. A. Matthews(University of Essex), Silvère Vialet‐Chabrand(University of Essex), Laura Baxter(University of Warwick), Sunitha Subramaniam(University of Essex), Richard Hickman(University of Warwick), Hannah Florance(University of Exeter), Christine Sambles(University of Exeter), Deborah L. Salmon(University of Exeter), Regina Feil(Max Planck Institute of Molecular Plant Physiology), Laura Bowden(University of Warwick), Claire Hill(University of Warwick), Neil R. Baker(University of Essex), John E. Lunn(Max Planck Institute of Molecular Plant Physiology), Bärbel Finkenstädt(University of Warwick), Andrew Mead(University of Warwick), Vicky Buchanan‐Wollaston(University of Warwick), Jim Beynon(University of Warwick), D.A.J. Rand(University of Warwick), David L. Wild(University of Warwick), Katherine Denby(University of Warwick), Sascha Ott(University of Warwick), Nicholas Smirnoff(University of Exeter), Philip M. Mullineaux(University of Essex)
The Plant Cell
February 1, 2016
Cited by 121Open Access
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Abstract

In Arabidopsis thaliana, changes in metabolism and gene expression drive increased drought tolerance and initiate diverse drought avoidance and escape responses. To address regulatory processes that link these responses, we set out to identify genes that govern early responses to drought. To do this, a high-resolution time series transcriptomics data set was produced, coupled with detailed physiological and metabolic analyses of plants subjected to a slow transition from well-watered to drought conditions. A total of 1815 drought-responsive differentially expressed genes were identified. The early changes in gene expression coincided with a drop in carbon assimilation, and only in the late stages with an increase in foliar abscisic acid content. To identify gene regulatory networks (GRNs) mediating the transition between the early and late stages of drought, we used Bayesian network modeling of differentially expressed transcription factor (TF) genes. This approach identified AGAMOUS-LIKE22 (AGL22), as key hub gene in a TF GRN. It has previously been shown that AGL22 is involved in the transition from vegetative state to flowering but here we show that AGL22 expression influences steady state photosynthetic rates and lifetime water use. This suggests that AGL22 uniquely regulates a transcriptional network during drought stress, linking changes in primary metabolism and the initiation of stress responses.


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