Fan Zhiyi, Zhai Yanlei, Wang Yuan, Zhang Long, Song Miaoyu, Flaishman Moshe A, Ma Huiqin
College of Horticulture, China Agricultural University, Beijing, China.
Department of Fruit Tree Sciences, Agricultural Research Organization, The Volcani Center, Bet Dagan, Israel.
Front Plant Sci. 2022 Jul 14;13:948084. doi: 10.3389/fpls.2022.948084. eCollection 2022.
WD40 proteins serve as crucial regulators in a broad spectrum of plant developmental and physiological processes, including anthocyanin biosynthesis. However, in fig ( L.), neither the WD40 family nor any member involved in anthocyanin biosynthesis has been elucidated. In the present study, 204 genes were identified from the fig genome and phylogenetically classified into 5 clusters and 12 subfamilies. Bioinformatics analysis prediction localized 109, 69, and 26 FcWD40 proteins to the cytoplasm, nucleus and other cellular compartments, respectively. RNA-seq data mining revealed 127 s expressed at FPKM > 10 in fig fruit. Most of these genes demonstrated higher expression in the early stages of fruit development. FcWD40-97 was recruited according to three criteria: high expression in fig fruit, predicted nuclear localization, and closest clustering with TTG1s identified in other plants. , encoding 339 amino acids including 5 WD-repeat motifs, showed 88.01 and 87.94% amino acid sequence similarity to apple and peach TTG1, respectively. The gene is located on fig chromosome 4, and is composed of 1 intron and 2 exons. Promoter analysis revealed multiple light-responsive elements, one salicylic acid-responsive element, three methyl jasmonate-responsive elements, and one MYB-binding site involved in flavonoid biosynthesis gene regulation. FcWD40-97 was in the FPKM > 100 expression level group in fig fruit, and higher expression was consistently found in the peel compared to the flesh at the same development stages. Expression level did not change significantly under light deprivation, whereas in leaves and roots, its expression was relatively low. Transient expression verified FcWD40-97's localization to the nucleus. Yeast two-hybrid (Y2H) and biomolecular fluorescence complementation (BiFC) assays revealed that FcWD40-97 interacts with FcMYB114, FcMYB123, and FcbHLH42 proteins and , showing that FcWD40-97 functions as a member of the MYB-bHLH-WD40 (MBW) complex in anthocyanin-biosynthesis regulation in fig. We therefore renamed as . Our results provide the first systematic analysis of the family and identification of in fig pigmentation.
WD40蛋白在包括花青素生物合成在内的广泛植物发育和生理过程中起着关键调节作用。然而,在无花果(Ficus carica L.)中,WD40家族以及任何参与花青素生物合成的成员都尚未得到阐明。在本研究中,从无花果基因组中鉴定出204个基因,并通过系统发育分析将其分为5个簇和12个亚家族。生物信息学分析预测分别有109、69和26个FcWD40蛋白定位于细胞质、细胞核和其他细胞区室。RNA-seq数据挖掘显示,在无花果果实中,有127个基因的FPKM>10。这些基因中的大多数在果实发育早期表现出较高的表达。根据三个标准筛选出FcWD40-97:在无花果果实中高表达、预测的核定位以及与其他植物中鉴定出的TTG1s聚类最接近。该基因编码339个氨基酸,包括5个WD重复基序,与苹果和桃的TTG1氨基酸序列相似性分别为88.01%和87.94%。该基因位于无花果第4号染色体上,由1个内含子和2个外显子组成。启动子分析揭示了多个光响应元件、1个水杨酸响应元件、3个茉莉酸甲酯响应元件以及1个参与类黄酮生物合成基因调控的MYB结合位点。FcWD40-97在无花果果实中处于FPKM>100的表达水平组,并且在相同发育阶段,果皮中的表达始终高于果肉。在遮光条件下,其表达水平没有显著变化,而在叶片和根中,其表达相对较低。瞬时表达验证了FcWD40-97定位于细胞核。酵母双杂交(Y2H)和生物分子荧光互补(BiFC)分析表明,FcWD40-97与FcMYB114、FcMYB123和FcbHLH42蛋白相互作用,表明FcWD40-97在无花果花青素生物合成调控中作为MYB-bHLH-WD40(MBW)复合体的一员发挥作用。因此,我们将其重命名为FcTTG1。我们的结果首次对无花果WD40家族进行了系统分析,并鉴定了参与无花果色素沉着的FcTTG1。