Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Horticulture Department, College of Agriculture and Biotechnology, Zhejiang University, Zijingang Campus, Hangzhou, 310058, China.
The New Zealand Institute for Plant & Food Research Limited (Plant & Food Research) Palmerston North, Private Bag 11600, Palmerston North, 4442, New Zealand.
New Phytol. 2022 Jul;235(2):630-645. doi: 10.1111/nph.18122. Epub 2022 Apr 22.
Anthocyanins are visual cues for pollination and seed dispersal. Fruit containing anthocyanins also appeals to consumers due to its appearance and health benefits. In kiwifruit (Actinidia spp.) studies have identified at least two MYB activators of anthocyanin, but their functions in fruit and the mechanisms by which they act are not fully understood. Here, transcriptome and small RNA high-throughput sequencing were used to comprehensively identify contributors to anthocyanin accumulation in kiwifruit. Stable overexpression in vines showed that both 35S::MYB10 and MYB110 can upregulate anthocyanin biosynthesis in Actinidia chinensis fruit, and that MYB10 overexpression resulted in anthocyanin accumulation which was limited to the inner pericarp, suggesting that repressive mechanisms underlie anthocyanin biosynthesis in this species. Furthermore, motifs in the C-terminal region of MYB10/110 were shown to be responsible for the strength of activation of the anthocyanic response. Transient assays showed that both MYB10 and MYB110 were not directly cleaved by miRNAs, but that miR828 and its phased small RNA AcTAS4-D4(-) efficiently targeted MYB110. Other miRNAs were identified, which were differentially expressed between the inner and outer pericarp, and cleavage of SPL13, ARF16, SCL6 and F-box1, all of which are repressors of MYB10, was observed. We conclude that it is the differential expression and subsequent repression of MYB activators that is responsible for variation in anthocyanin accumulation in kiwifruit species.
花色苷是传粉和种子传播的视觉线索。含有花色苷的果实因其外观和健康益处也吸引了消费者。在猕猴桃(Actinidia spp.)研究中,已经鉴定出至少两种花色苷的 MYB 激活剂,但它们在果实中的功能及其作用机制尚不完全清楚。在这里,通过转录组和小 RNA 高通量测序,全面鉴定了猕猴桃花色苷积累的贡献者。在葡萄藤中的稳定过表达表明,35S::MYB10 和 MYB110 都可以上调中华猕猴桃果实中花色苷的生物合成,并且 MYB10 的过表达导致花色苷的积累仅限于内果皮,这表明在该物种中花色苷生物合成存在抑制机制。此外,还表明 MYB10/110 中 C 端区域的基序负责激活花色苷反应的强度。瞬时测定表明,MYB10 和 MYB110 都不会被 miRNAs 直接切割,但 miR828 和其相移的小 RNA AcTAS4-D4(-) 可以有效地靶向 MYB110。还鉴定了其他 miRNA,它们在内外果皮之间存在差异表达,并且观察到 SPL13、ARF16、SCL6 和 F-box1 的切割,所有这些都是 MYB10 的抑制剂。我们得出的结论是,花色苷积累的变化是由 MYB 激活剂的差异表达和随后的抑制所导致的。