4.8 Article

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

期刊

PLANT CELL
卷 28, 期 2, 页码 345-366

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OXFORD UNIV PRESS INC
DOI: 10.1105/tpc.15.00910

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资金

  1. UK Biotechnology and Biological Science Research Council (BBSRC) [BB/F005806/1]
  2. University of Essex
  3. NERC-CASE award [ENV-EATR-DTP: NE/L002582/1]
  4. BBSRC [BB/1001187_1]
  5. Max Planck Society
  6. Exeter Science Strategy funding
  7. Department for Environment, Food, and Rural Affairs through the NORNEX project
  8. Wellcome Trust
  9. BBSRC [BB/I020004/1, BB/F011652/1, BB/F005806/1, BB/F005822/1] Funding Source: UKRI
  10. EPSRC [EP/I036575/1] Funding Source: UKRI
  11. Biotechnology and Biological Sciences Research Council [BB/I020004/1, BB/F011652/1, BB/F005822/1, BB/F005806/1] Funding Source: researchfish
  12. Engineering and Physical Sciences Research Council [EP/I036575/1] Funding Source: researchfish

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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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