AI Article Synopsis

  • - The study explores the MYB-bHLH-WD repeat (MBW) transcriptional complex in eggplant, focusing on its crucial role in regulating anthocyanin production during fruit development, using recent genomic data.
  • - Researchers confirmed the presence of key MBW complex members and identified a novel R3 MYB repressor (SmelMYBL1), which inhibits anthocyanin biosynthesis by competing with MYB activators for binding to bHLH proteins.
  • - Experimental techniques like qPCR and yeast assays were utilized to analyze the interactions among these proteins, demonstrating that the presence of SmelMYBL1 blocks anthocyanin accumulation when expressed alongside certain MBW components.

Article Abstract

Here we focus on the highly conserved MYB-bHLH-WD repeat (MBW) transcriptional complex model in eggplant, which is pivotal in the transcriptional regulation of the anthocyanin biosynthetic pathway. Through a genome-wide approach performed on the recently released Eggplant Genome (cv. 67/3) previously identified, and reconfirmed by us, members belonging to the MBW complex (SmelANT1, SmelAN2, SmelJAF13, SmelAN1) were functionally characterized. Furthermore, a regulatory R3 MYB type repressor (SmelMYBL1), never reported before, was identified and characterized as well. Through a qPCR approach, we revealed specific transcriptional patterns of candidate genes in different plant tissue/organs at two stages of fruit development. Two strategies were adopted for investigating the interactions of bHLH partners (SmelAN1, SmelJAF13) with MYB counterparts (SmelANT1, SmelAN2 and SmelMYBL1): Yeast Two Hybrid (Y2H) and Bimolecular Fluorescent Complementation (BiFC) in A. thaliana mesophylls protoplast. Agro-infiltration experiments highlighted that N. benthamiana leaves transiently expressing SmelANT1 and SmelAN2 showed an anthocyanin-pigmented phenotype, while their co-expression with SmelMYBL1 prevented anthocyanin accumulation. Our results suggest that SmelMYBL1 may inhibits the MBW complex via the competition with MYB activators for bHLH binding site, although this hypothesis requires further elucidation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7224497PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0232986PLOS

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