Department of Agricultural, Forest and Food Sciences, Plant Genetics and Breeding, University of Torino, Grugliasco (TO), Italy.
CREA, Research Centre for Genomics and Bioinformatics, Montanaso Lombardo (LO), Italy.
PLoS One. 2020 May 14;15(5):e0232986. doi: 10.1371/journal.pone.0232986. eCollection 2020.
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.
在这里,我们重点关注茄子中高度保守的 MYB-bHLH-WD 重复(MBW)转录复合物模型,该模型在花色苷生物合成途径的转录调控中起着关键作用。通过对最近发布的茄子基因组(cv. 67/3)进行全基因组分析,我们以前鉴定并重新确认了属于 MBW 复合物的成员(SmelANT1、SmelAN2、SmelJAF13、SmelAN1)。此外,还鉴定并表征了一个以前从未报道过的调节性 R3 MYB 型抑制剂(SmelMYBL1)。通过 qPCR 方法,我们揭示了候选基因在果实发育两个阶段不同植物组织/器官中的特定转录模式。采用两种策略研究 bHLH 伴侣(SmelAN1、SmelJAF13)与 MYB 对应物(SmelANT1、SmelAN2 和 SmelMYBL1)的相互作用:在拟南芥叶肉原生质体中进行酵母双杂交(Y2H)和双分子荧光互补(BiFC)。农杆菌浸润实验表明,瞬时表达 SmelANT1 和 SmelAN2 的 N. benthamiana 叶片表现出花色苷着色表型,而它们与 SmelMYBL1 的共表达则阻止了花色苷的积累。我们的结果表明,SmelMYBL1 可能通过与 MYB 激活子竞争 bHLH 结合位点来抑制 MBW 复合物,尽管这一假设需要进一步阐明。