4.8 Article

Phytochrome-imposed oscillations in PIF3 protein abundance regulate hypocotyl growth under diurnal light/dark conditions in Arabidopsis

期刊

PLANT JOURNAL
卷 71, 期 3, 页码 390-401

出版社

WILEY-BLACKWELL
DOI: 10.1111/j.1365-313X.2012.04992.x

关键词

PIF3; hypocotyl elongation; short day; phytochrome-mediated degradation; transcriptional regulation; Arabidopsis

资金

  1. CSIC [Jae-Pre_08_01049, 2010ESTCSIC-12125]
  2. 'Comissionat per a Universitats i Recerca del Departament d'Innovacio, Universitats i Empresa' from the Generalitat de Catalunya
  3. Marie Curie International Reintegration Grant [PIRG06-GA-2009-256420, 046568]
  4. National Institutes of Health [GM-47475]
  5. Department of Energy [DEFG03-87ER13742]
  6. USDA Agricultural Research Service [5335-21000-027-00D]
  7. Spanish Ministerio de Ciencia e Innovacion [BIO2006-09254, BIO2009-07675]
  8. Generalitat de Catalunya [2009-SGR-206]

向作者/读者索取更多资源

Arabidopsis seedlings display rhythmic growth when grown under diurnal conditions, with maximal elongation rates occurring at the end of the night under short-day photoperiods. Current evidence indicates that this behavior involves the action of the growth-promoting bHLH factors PHYTOCHROME-INTERACTING FACTOR 4 (PIF4) and PHYTOCHROME-INTERACTING FACTOR 5 (PIF5) at the end of the night, through a coincidence mechanism that combines their transcriptional regulation by the circadian clock with control of protein accumulation by light. To assess the possible role of PIF3 in this process, we have analyzed hypocotyl responses and marker gene expression in pif single- and higher-order mutants. The data show that PIF3 plays a prominent role as a promoter of seedling growth under diurnal light/dark conditions, in conjunction with PIF4 and PIF5. In addition, we provide evidence that PIF3 functions in this process through its intrinsic transcriptional regulatory activity, at least in part by directly targeting growth-related genes, and independently of its ability to regulate phytochrome B (phyB) levels. Furthermore, in sharp contrast to PIF4 and PIF5, our data show that the PIF3 gene is not subject to transcriptional regulation by the clock, but that PIF3 protein abundance oscillates under diurnal conditions as a result of a progressive decline in PIF3 protein degradation mediated by photoactivated phyB, and consequent accumulation of the bHLH factor during the dark period. Collectively, the data suggest that phyB-mediated, post-translational regulation allows PIF3 accumulation to peak just before dawn, at which time it accelerates hypocotyl growth, together with PIF4 and PIF5, by directly regulating the induction of growth-related genes.

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