Time-Series Transcriptomics Reveals That AGAMOUS-LIKE22 Affects Primary Metabolism and Developmental Processes in Drought-Stressed Arabidopsis
Author(s) -
Ulrike Bechtold,
Christopher A. Penfold,
Dafyd J. Jenkins,
Roxane Legaie,
Jonathan D. Moore,
Tracy Lawson,
Jack S. A. Matthews,
Silvère VialetChabrand,
Laura Baxter,
Sunitha Subramaniam,
Richard Hickman,
Hannah Florance,
Christine Sambles,
Deborah L. Salmon,
Regina Feil,
Laura Bowden,
Claire Hill,
Neil R. Baker,
John E. Lunn,
Bärbel Finkenstädt,
Andrew Mead,
Vicky BuchananWollaston,
Jim Bey,
D.A.J. Rand,
David L. Wild,
Katherine Denby,
Sascha Ott,
Nicholas Smirnoff,
Philip M. Mullineaux
Publication year - 2016
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.15.00910
Subject(s) - biology , transcriptome , abscisic acid , arabidopsis , gene , gene regulatory network , agamous , gene expression , arabidopsis thaliana , secondary metabolism , mads box , transcription factor , genetics , microbiology and biotechnology , mutant , biosynthesis
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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