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紫肉甘薯及其黄肉突变体的比较转录组分析为块根中花青素生物合成相关转录因子提供了见解。

Comparative transcriptome analysis of purple-fleshed sweet potato and its yellow-fleshed mutant provides insight into the transcription factors involved in anthocyanin biosynthesis in tuberous root.

作者信息

Dong Wen, Tang Linfei, Peng Yali, Qin Yuzhi, Lin Yuan, Xiong Xingyao, Hu Xinxi

机构信息

Hunan Provincial Engineering Research Center for Potatoes, College of Horticulture, Hunan Agricultural University, Changsha, China.

Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences, Shenzhen, China.

出版信息

Front Plant Sci. 2022 Aug 8;13:924379. doi: 10.3389/fpls.2022.924379. eCollection 2022.

Abstract

In various plant species, many transcription factors (TFs), such as MYB, bHLH, and WD40, have been identified as regulators of anthocyanin biosynthesis in underground organs. However, the regulatory elements of anthocyanin biosynthesis in the tuberous roots of sweet potato have not been elucidated yet. Here, we selected the purple-fleshed sweet potato cultivar "Zhezi1" (ZZ ) and its spontaneous yellow-fleshed mutant "Xinli" (XL ) to investigate the regulatory mechanism of the anthocyanin biosynthesis in the tuberous roots of sweet potato. By analyzing the genotype in ZZ and XL , we found that the , a MYB TF involved in anthocyanin biosynthesis, was missing in the XL genome, which might lead to an extreme decrease in anthocyanins in XL . A comparative transcriptome analysis of ZZ and XL was conducted to find the TFs involved in anthocyanin biosynthesis in ZZ and XL . The anthocyanin structural genes were significantly enriched among the differentially expressed genes. Moreover, one MYB activator (), one bHLH (), three WRKY activator candidates (, , and ), and two MYB repressors ( and ) were highly expressed in ZZ accompanied with anthocyanin structural genes. We also tested the expression of these TFs in six purple- and two orange-fleshed sweet potato cultivars. Interestingly, most of these TFs were significantly positively correlated with anthocyanin contents in these cultivars. The function of the anthocyanin biosynthesis repression of and was verified through transient co-transformation with into tobacco leaves. Further functional verification of the above TFs was conducted by Y2H, BiFC, and dual-luciferase assays. These tests showed that the MYB-bHLH-WD40/MYB-bHLH-WD40-WRKY complex activated the promoter of anthocyanin structural gene and promoters for , , and , indicating reinforcement and feedback regulation to maintain the level of anthocyanin accumulation in the tuberous roots of purple-fleshed sweet potato. These results may provide new insights into the regulatory mechanism of anthocyanin biosynthesis and accumulation in underground organs of sweet potatoes.

摘要

在多种植物物种中,许多转录因子(TFs),如MYB、bHLH和WD40,已被确定为地下器官中花青素生物合成的调节因子。然而,甘薯块根中花青素生物合成的调控元件尚未阐明。在此,我们选择了紫肉甘薯品种“浙紫1号”(ZZ)及其自发黄肉突变体“新丽”(XL),以研究甘薯块根中花青素生物合成的调控机制。通过分析ZZ和XL的基因型,我们发现参与花青素生物合成的MYB转录因子在XL基因组中缺失,这可能导致XL中花青素极度减少。对ZZ和XL进行了比较转录组分析,以找出参与ZZ和XL中花青素生物合成的转录因子。花青素结构基因在差异表达基因中显著富集。此外,一个MYB激活因子()、一个bHLH()、三个WRKY激活候选因子(、和)以及两个MYB抑制因子(和)在ZZ中与花青素结构基因一起高表达。我们还检测了这些转录因子在六个紫肉和两个橙肉甘薯品种中的表达。有趣的是,这些转录因子中的大多数与这些品种中的花青素含量显著正相关。通过与在烟草叶片中瞬时共转化,验证了和对花青素生物合成的抑制功能。通过酵母双杂交(Y2H)、双分子荧光互补(BiFC)和双荧光素酶测定对上述转录因子进行了进一步的功能验证。这些试验表明,MYB-bHLH-WD40/MYB-bHLH-WD40-WRKY复合物激活了花青素结构基因的启动子以及、和的启动子,表明存在增强和反馈调节,以维持紫肉甘薯块根中花青素的积累水平。这些结果可能为甘薯地下器官中花青素生物合成和积累的调控机制提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b0f/9393619/a4502659425d/fpls-13-924379-g001.jpg

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