Fruit Research Institute, Fujian Academy of Agricultural Sciences, Fuzhou, Fujian 350013, China.
Fruit Research Institute, Fujian Academy of Agricultural Sciences, Fuzhou, Fujian 350013, China.
Gene. 2018 Nov 15;676:202-213. doi: 10.1016/j.gene.2018.07.039. Epub 2018 Jul 17.
Jaboticaba is a grape-like fruit that accumulates high levels of anthocyanins in the peel and is proposed as a good source of functional pigments. However, the molecular mechanisms underlying anthocyanin accumulation in jaboticaba peel remains to be elucidated. In this study, we employed RNA-seq technique to compare the transcriptomic differences between green-colored and black-colored jaboticaba peels. Over 5 million high-quality reads were assembled into 62,190 unigenes with an average length of 737 bp, 29,320 (47.15%) of them were annotated by public databases. 2152 unigenes were found to be differentially expressed (830 upregulated and 1322 downregulated). Gene ontology analysis and pathway enrichment annotation revealed that 18 differentially expressed genes encode phenylalanine ammonialyase, 4-coumaroyl:CoA-ligase, chalcone synthase, flavanone 3-hydroxylase, flavonoid 3'-hydroxylase, anthocyanidin synthase, UDP-glucose: flavonoid 3-O-glucosyltransferase, glutathione S-transferase, Cytochrome b5 were associated with anthocyanin biosynthesis. Additionally, 54 differentially expressed transcription factors were identified. Furthermore, the expression of genes involved in biosynthesis and signal transduction of ethylene and abscisic acid were negatively and positively correlated with that of anthocyanin pathway genes and anthocyanin accumulation, respectively. Quantitative reverse transcription PCR analysis of candidate genes showed trends similar to those in the RNA-seq analysis. McMYB, a homolog of AtMYB113, induced anthocyanin accumulation in tobacco leaves when co-infiltrated PsbHLH3. These results will contribute to further understanding of the molecular mechanisms regulating anthocyanin accumulation in jaboticaba peel.
嘉宝果是一种类似于葡萄的果实,其果皮中积累了大量的花色苷,被认为是功能性色素的良好来源。然而,嘉宝果皮中花色苷积累的分子机制尚不清楚。在这项研究中,我们采用 RNA-seq 技术比较了绿色和黑色嘉宝果皮之间的转录组差异。超过 500 万个高质量的读数组装成 62190 个 unigenes,平均长度为 737bp,其中 29320 个(47.15%)被公共数据库注释。发现 2152 个 unigenes差异表达(830 个上调,1322 个下调)。GO 分析和通路富集注释表明,18 个差异表达基因编码苯丙氨酸解氨酶、4-香豆酰辅酶 A 连接酶、查尔酮合酶、黄烷酮 3-羟化酶、黄酮 3'-羟化酶、花青素合酶、UDP-葡萄糖:黄酮 3-O-葡萄糖基转移酶、谷胱甘肽 S-转移酶、细胞色素 b5 与花色苷生物合成有关。此外,鉴定出 54 个差异表达的转录因子。此外,乙烯和脱落酸生物合成和信号转导相关基因的表达与花色苷途径基因和花色苷积累呈负相关和正相关。候选基因的定量 RT-PCR 分析显示与 RNA-seq 分析趋势相似。与 AtMYB113 同源的 McMYB 与 PsbHLH3 共浸润时诱导烟草叶片中花色苷的积累。这些结果将有助于进一步了解调控嘉宝果皮中花色苷积累的分子机制。