4.8 Article

CO interacts with JAZ repressors and bHLH subgroup IIId factors to negatively regulate jasmonate signaling in Arabidopsis seedlings

Journal

PLANT CELL
Volume 35, Issue 2, Pages 852-873

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/plcell/koac331

Keywords

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Funding

  1. National Natural Science Foundation of China [32100445, 31922009, 31870259, 32270613]
  2. Applied Basic Research Project of Yunnan Province [2019FI006, 202001AV070009, 202001AT070118, 202101AW070005]
  3. Youth Innovation Promotion Association of the of Chinese Academy of Sciences [Y201973, 2022399]
  4. Yunnan Revitalization Talent Support Program in Yunnan Province [YNWR-QNBJ-2018-075]
  5. CAS Light of West China Program

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The study reveals the important role of CONSTANS (CO) in mediating physiological responses other than flowering and explains the mechanism of its interaction with jasmonate signaling.
CONSTANS (CO) is a master flowering-time regulator that integrates photoperiodic and circadian signals in Arabidopsis thaliana. CO is expressed in multiple tissues, including young leaves and seedling roots, but little is known about the roles and underlying mechanisms of CO in mediating physiological responses other than flowering. Here, we show that CO expression is responsive to jasmonate. CO negatively modulated jasmonate-imposed root-growth inhibition and anthocyanin accumulation. Seedlings from co mutants were more sensitive to jasmonate, whereas overexpression of CO resulted in plants with reduced sensitivity to jasmonate. Moreover, CO mediated the diurnal gating of several jasmonate-responsive genes under long-day conditions. We demonstrate that CO interacts with JASMONATE ZIM-DOMAIN (JAZ) repressors of jasmonate signaling. Genetic analyses indicated that CO functions in a CORONATINE INSENSITIVE1 (COI1)-dependent manner to modulate jasmonate responses. Furthermore, CO physically associated with the basic helix-loop-helix (bHLH) subgroup IIId transcription factors bHLH3 and bHLH17. CO acted cooperatively with bHLH17 in suppressing jasmonate signaling, but JAZ proteins interfered with their transcriptional functions and physical interaction. Collectively, our results reveal the crucial regulatory effects of CO on mediating jasmonate responses and explain the mechanism by which CO works together with JAZ and bHLH subgroup IIId factors to fine-tune jasmonate signaling.

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