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Temperature is a crucial environmental cue that governs plant growth and adaptation in natural habitats. PHYTOCHROME INTERACTING FACTOR 4 (PIF4) functions as a central regulator promoting thermomorphogenesis in Arabidopsis. An understanding of its precise regulation is essential for optimal thermomorphogenic growth. Here, we identified two BBX proteins, BBX24 and BBX25, as novel components of the PIF4-mediated thermosensory pathway that promote growth at elevated temperatures. Single and double mutants of bbx24 and bbx25 exhibit moderate to strong temperature-insensitive hypocotyl and cotyledon growth. Elevated temperatures induce BBX24 and BBX25 mRNA expression and protein accumulation. Genetic and biochemical analyses reveal that BBX24 and BBX25 enhance PIF4-mediated thermosensory growth by counteracting ELF3, a key component of the evening complex. Whereas ELF3 represses BBX24 and BBX25 gene expression at low ambient temperatures during the evening, the inhibition of ELF3 activity under elevated temperatures increases BBX24 and BBX25 activity. Moreover, BBX24 and BBX25 suppress ELF3 function through direct physical interaction, likely relieving its repression of PIF4 and enhancing thermomorphogenesis. These findings identify the ELF3-BBX24/BBX25-PIF4 axis as a key regulatory module controlling plant growth and development in response to temperature cues.
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http://dx.doi.org/10.1016/j.xplc.2025.101391 | DOI Listing |
Plant Commun
July 2025
Department of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur 741246, West Bengal, India; Centre for Climate and Environmental Studies, Indian Institute of Science Education and Research Kolkata, Mohanpur 741246, West Bengal, India. Electronic address: ngsre
Temperature is a crucial environmental cue that governs plant growth and adaptation in natural habitats. PHYTOCHROME INTERACTING FACTOR 4 (PIF4) functions as a central regulator promoting thermomorphogenesis in Arabidopsis. An understanding of its precise regulation is essential for optimal thermomorphogenic growth.
View Article and Find Full Text PDFPlant Signal Behav
September 2020
Key Laboratory of Ecology and Environmental Science in Guangdong Higher Education, School of Life Science, South China Normal University, Guangzhou, China.
The B-box proteins (BBXs) are a family of zinc finger proteins containing one/two B-box domain(s), which play important roles in plant growth and development. Though the BBX family genes have been identified and named, no systematic study has taken on BBX family genes involved in the regulation of UV-B induced photomorphogenesis in . In our previous report, BBX24/STO was demonstrated to be a negative regulator in UV-B signaling pathway in .
View Article and Find Full Text PDFPlant Cell
April 2013
Environmental and Evolutionary Genomics Section, Institut de Biologie de l’Ecole, Normale Supérieure Paris, France.
Plant Signal Behav
August 2013
Department of Biological and Environmental Sciences; Gothenburg University; Gothenburg, Sweden; Current affiliation: Department of Biotechnology; National Institute of Technology; Durgapur, West Bengal, India.
BBX24 and BBX25 are two important transcriptional regulators, which regulate seedling photomorphogenesis in Arabidopsis. Very recently, we have shown that BBX24 and BBX25 negatively regulate the expression of BBX22, reducing the function of HY5, by physically interacting with its bZIP domain. (1) Furthermore, HY5 HOMOLOG, HYH, has been reported to heterodimerize with HY5 and enhances its photomorphogenic function in seedling de-etiolation by serving as coactivator.
View Article and Find Full Text PDFPlant Cell
April 2013
Department of Biological and Environmental Sciences, Gothenburg University, Gothenburg SE 40530, Sweden.
ELONGATED HYPOCOTYL5 (HY5) is a basic domain/leucine zipper (bZIP) transcription factor, central for the regulation of seedling photomorphogenesis. Here, we identified a B-BOX (BBX)-containing protein, BBX25/SALT TOLERANCE HOMOLOG, as an interacting partner of HY5, which has been previously found to physically interact with CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1). BBX25 physically interacts with HY5 both in vitro and in vivo.
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