Zhu Jiayi, Guo Xueying, Li Xin, Tang Dongqin
School of Design, Shanghai Jiao Tong University, Shanghai, China.
Instrumental Analysis Center, Shanghai Jiao Tong University, Shanghai, China.
Front Plant Sci. 2021 Nov 15;12:756300. doi: 10.3389/fpls.2021.756300. eCollection 2021.
is rich in flower colors with beautiful flower shapes and pleasant aroma. Flavonoids are vital to the color formation of its flowers. In this study, five cultivars with different flower colors were used to study on the level of accumulation of their flavonoids and expression of flavonoid-related genes and further explore new novel transcription factor (TF). Ultra-high-performance liquid chromatography and VION ion mobility quadrupole time-of-flight mass spectrometer (UPLC-Q-TOF-MS) were used to determine the flavonoids. Combined with transcriptome sequencing technology, the molecular mechanism of the flavonoid metabolism difference in was revealed. A total of 10 anthoxanthin components and 12 anthocyanin components were detected using UPLC-Q-TOF-MS. All six common anthocyanin aglycones in high plants, including cyanidin, delphinidin, petunidin, peonidin, malvidin, and pelargonidin, were detected in at first time in this study. In orange, yellow, and white cultivars, anthoxanthins gradually decreased with the opening of the petals, while in red and purple cultivars, anthoxanthins first increased and then decreased. No anthocyanin was detected in yellow and white cultivars, while anthocyanins increased with the opening of the petals and reached their maximum at the flowering stage (S3) in other three cultivars. The correlation analysis revealed that the color of petals was closely related to the composition and content of anthoxanthins and anthocyanins. Petals of five cultivars at S3 were then selected for transcriptome sequencing by using the Illumina Hiseq 4000 platform, and a total of 100,539 unigenes were obtained. There were totally 5,162 differentially expressed genes (DEGs) when the four colored cultivars were compared with the white cultivar at S3. Comparing all DEGs with gene ontology (GO), KEGG, and Pfam databases, it was found that the genes involved in the flavonoid biosynthesis pathway were significantly different. In addition, AP2, WRKY, and bHLH TF families ranked the top three among all differently expressed TFs in all DEGs. Quantitative real-time PCR (qRT-PCR) technology was used to analyze the expression patterns of the structural genes of flavonoid biosynthesis pathway in . The results showed that metabolic process was affected significantly by structural genes in this pathway, such as , , , , , and . Cluster analysis was performed by using all annotated WRKY and AP2 TFs and the above structural genes based on their relatively expression. Four novel candidate TFs of WRKY and AP2 family were screened. Their spatiotemporal expression patterns revealed that these four novel TFs may participate in the regulation of the flavonoid biosynthesis, thus controlling its color formation in petals.
花色丰富,花形优美,香气宜人。黄酮类化合物对其花朵的颜色形成至关重要。本研究选用了五个不同花色的品种,研究其黄酮类化合物的积累水平和黄酮类相关基因的表达,并进一步探索新的新型转录因子(TF)。采用超高效液相色谱和VION离子淌度四极杆飞行时间质谱仪(UPLC-Q-TOF-MS)测定黄酮类化合物。结合转录组测序技术,揭示了[品种名称]中黄酮类代谢差异的分子机制。使用UPLC-Q-TOF-MS共检测到10种黄酮醇成分和12种花青素成分。本研究首次在[品种名称]中检测到高等植物中所有六种常见的花青素苷元,包括矢车菊素、飞燕草素、矮牵牛素、芍药素、锦葵素和天竺葵素。在橙色、黄色和白色品种中,黄酮醇随着花瓣的开放逐渐减少,而在红色和紫色品种中,黄酮醇先增加后减少。在黄色和白色品种中未检测到花青素,而在其他三个品种中,花青素随着花瓣的开放而增加,并在开花期(S3)达到最大值。相关性分析表明,[品种名称]花瓣的颜色与黄酮醇和花青素的组成及含量密切相关。然后,使用Illumina Hiseq 4000平台对S3期五个品种的花瓣进行转录组测序,共获得100,539个单基因。当将四个有色品种与S3期的白色品种进行比较时,共有5162个差异表达基因(DEG)。将所有DEG与基因本体(GO)、KEGG和Pfam数据库进行比较,发现参与黄酮类生物合成途径的基因存在显著差异。此外,AP2、WRKY和bHLH转录因子家族在所有DEG中所有差异表达的转录因子中排名前三。采用定量实时PCR(qRT-PCR)技术分析了[品种名称]中黄酮类生物合成途径结构基因的表达模式。结果表明,该途径中的结构基因如[具体基因名称]等对代谢过程有显著影响。基于相对表达量,对所有注释的WRKY和AP2转录因子以及上述结构基因进行聚类分析。筛选出WRKY和AP2家族的四个新型候选转录因子。它们的时空表达模式表明,这四个新型转录因子可能参与黄酮类生物合成调控,从而控制[品种名称]花瓣的颜色形成。