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Light-mediated anthocyanin biosynthesis in rose petals involves a balanced regulatory module comprising transcription factors RhHY5, RhMYB114a, and RhMYB3b.

Yuhang YanJiaxing ZhaoShengnan LinMouliang LiJiayi LiuOlivier RaymondPhilippe VergneWeilong KongQuanshu WuXiaoni ZhangManzhu BaoMohammed BendahmaneXiaopeng Fu
Published in: Journal of experimental botany (2023)
Roses are significant botanical species with both ornamental and economic value, displaying diverse floral traits, particularly an extensive array of petal colors. The red pigmentation of rose petals is predominantly attributed to anthocyanin accumulation. However, the underlying regulatory mechanism of anthocyanin biosynthesis in roses remains elusive. This study presents a novel light-responsive regulatory module governing anthocyanin biosynthesis in rose petals, which involves the transcription factors RhHY5, RhMYB114a, and RhMYB3b. Under light conditions, RhHY5 represses RhMYB3b expression, and induces RhMYB114a expression that positively regulates anthocyanin biosynthesis in rose petals through the direct activation of anthocyanin structural genes via the MYB114a-bHLH3-WD40 complex. Notably, this function likely involves an interaction and synergy between RhHY5 and the MYB114a-bHLH3-WD40 complex. Additionally, RhMYB3b is activated by RhMYB114a to prevent excessive accumulation of anthocyanin. Conversely, in low light conditions, the degradation of RhHY5 leads to down-regulation of RhMYB114a and up-regulation of RhMYB3b, which in turn inhibits the expression of both RhMYB114a and anthocyanin structural genes. Additionally, RhMYB3b competes with RhMYB114a for binding to RhbHLH3 and the promoters of anthocyanin-related structural genes. Overall, our study uncovers a complex light-mediated regulatory network that governs anthocyanin biosynthesis in the rose, thereby advancing our understanding of the underlying molecular mechanisms of anthocyanin biosynthesis in rose flowers.
Keyphrases
  • transcription factor
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  • genome wide identification
  • genome wide
  • dna binding
  • cell wall
  • high resolution
  • mass spectrometry
  • binding protein
  • gene expression
  • drug delivery
  • weight loss
  • single molecule