4.7 Article

Comparative transcriptomic analysis identifies KcMYB1 as a R2R3-MYB anthocyanin activator in Kadsura coccinea

期刊

PLANT SCIENCE
卷 324, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.plantsci.2022.111458

关键词

Anthocyanin; Kadsura coccinea; Fruit color; KcMYB1; Activator

资金

  1. Guangxi Natural Science Foundation Project [GuikeAD20238034]
  2. Xinglin' Youth Talent of Guangxi University of Chinese Medicine Project Fund [2022C031]
  3. Youth Innovation Research Team Project Fund [2018QT001]
  4. Special Fund for Introducing Scientific and Technological Talents of Guangdong Academy of Agricultural Sciences [R2020YJ-YB3003]

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This study investigated the molecular mechanisms of fruit color formation in different cultivars of Kadsura coccinea. Metabolomics and transcriptomics analysis revealed differential anthocyanin accumulation levels and gene expression patterns between the cultivars. A key anthocyanin activator, KcMYB1, was identified and found to be closely related to anthocyanin accumulation.
Fruit color, as an important appearance attribute, is crucial for attracting consumers. However, the underlying mechanism regulating mature fruit color formation in Kadsura coccinea remains unclear. Here, a comprehensive metabolomics and transcriptomics analysis was performed to investigate the molecular mechanisms of anthocyanin accumulation between two K. coccinea cultivars with different mature fruit colors-Dahong No. 1 ' (red) and Jinhu' (yellow). Targeted metabolomic analysis revealed high anthocyanin levels, most of which were cyanidin and delphinidin derivatives, in Dahong No. 1 ' mature fruit peel. The SNP analysis indicated that the two different cultivars had similar genetic background. Moreover, comparative transcriptomic analysis demonstrated that differentially expressed genes (DEGs) were related to flavonoid biosynthesis and metabolic process in the two K. coccinea cultivars. Gene expression profiling data showed that the structural and regulatory genes associated with anthocyanin biosynthesis were significantly upregulated in Dahong No. 1 ' mature fruit peel, which was verified by quantitative real-time polymerase chain reaction (qRT-PCR). Notably, the key anthocyanin activator KcMYB1 was identified, which was significantly upregulated in Dahong No. 1 ' compared with Jinhu'. We further confirmed that KcMYB1 actively regulated the accumulation of anthocyanin by ectopic expression in vivo. Furthermore, allelic constitution of KcMYB1 in K. coccinea were investigated. The present study can provide insights for understanding the regulatory mechanisms of anthocyanin differential accumulation in the mature fruits of K. coccinea.

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