4.7 Article

PeMYB4L interacts with PeMYC4 to regulate anthocyanin biosynthesis in Phalaenopsis orchid

Journal

PLANT SCIENCE
Volume 324, Issue -, Pages -

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.plantsci.2022.111423

Keywords

PeMYB4L; Anthocyanin; VIGS; Phalaenopsis; MYB-bHLH; PeCHS

Funding

  1. National Key Research and Development Program [2018YFD1000404]
  2. Science and Technology Commission of Shanghai Municipality [18DZ2283500]
  3. Shanghai Engineering Research Center of Plant Germplasm Resources [17DZ2252700]

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In this study, a novel R2R3-MYB transcription factor, PeMYB4L, was identified to promote anthocyanin accumulation in Phalaenopsis spp. flowers. It was found that PeMYB4L can directly regulate the expression of the Phalaenopsis spp. chalcone synthase gene through MYBST1 binding site. In addition, the MYB-bHLH complex formed by PeMYC4 and PeMYB4L attenuated the expression of the Phalaenopsis spp. chalcone synthase gene and weakened anthocyanin production, revealing a novel regulatory model.
Phalaenopsis spp., one genus of Orchidaceae, have become very popular worldwide for their fascinating flowers with various colors and pigmentation patterns. Several R2R3-MYB transcription factors have been reported to function in anthocyanin accumulation in Phalaenopsis spp. However, its molecular mechanism underlying the detailed regulatory pathway remains poorly understood. In this study, we identified a novel subgroup 2 R2R3-MYB transcription factor PeMYB4L, the expression profile of which was concomitant with red color formation in Phalaenopsis spp. flowers. Virus-induced gene silencing (VIGS) and transient overexpression assay verified that PeMYB4L promotes anthocyanin accumulation in flower tissues. In addition, PeMYB4L could directly regulates the expression of Phalaenopsis spp. chalcone synthase gene (PeCHS) through MYBST1 (GGATA) binding site. It's interesting that the basic-helix-loop-helix (bHLH) protein PeMYC4 shows opposite expression pattern from PeMYB4L in anthocyanin accumulation. Furthermore, PeMYC4 was verified to form MYB-bHLH complex with PeMYB4L, and attenuated the expression of PeCHS and weakened anthocyanin production, indicating a novel regulatory model of MYB-bHLH complex. Our findings uncover the detailed regulatory pathway of MYB-bHLH, and might provide a new insight into the complicated anthocyanin pigmentation in Phalaenopsis spp.

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