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一种R2R3-MYB抑制转录因子对香蕉中花青素的生物合成起负调控作用。

, an R2R3-MYB Repressor Transcription Factor, Negatively Regulates the Biosynthesis of Anthocyanin in Banana.

作者信息

Deng Gui-Ming, Zhang Sen, Yang Qiao-Song, Gao Hui-Jun, Sheng Ou, Bi Fang-Cheng, Li Chun-Yu, Dong Tao, Yi Gan-Jun, He Wei-Di, Hu Chun-Hua

机构信息

Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences/Key Laboratory of South Subtropical Fruit Biology and Genetic Resource Utilization (Ministry of Agriculture and Rural Affairs)/Guangdong Province Key Laboratory of Tropical and Subtropical Fruit Tree Research, Guangzhou, China.

Key Laboratory of Horticultural Plant Biology of the Ministry of Education, College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Wuhan, China.

出版信息

Front Plant Sci. 2021 Jan 7;11:600704. doi: 10.3389/fpls.2020.600704. eCollection 2020.

Abstract

Anthocyanins spatiotemporally accumulate in certain tissues of particular species in the banana plant, and MYB transcription factors (TFs) serve as their primary regulators. However, the precise regulatory mechanism in banana remains to be determined. Here, we report the identification and characterization of , an R2R3-MYB repressor TF, characterized by the presence of EAR (ethylene-responsive element binding factor-associated amphiphilic repression) and TLLLFR motifs. expression was induced by the accumulation of anthocyanins. Transgenic banana plants overexpressing displayed a significant reduction in anthocyanin compared to wild type. Consistent with the above results, metabolome results showed that there was a decrease in all three identified cyanidins and one delphinidin, the main anthocyanins that determine the color of banana leaves, whereas both transcriptome and reverse transcription-quantitative polymerase chain reaction analysis showed that many key anthocyanin synthesis structural genes and TF regulators were downregulated in overexpressors. Furthermore, dual-luciferase assays showed that was able to bind to the , , , and promoters, leading to inhibition of their expression. Yeast two-hybrid analysis verified that MaMYB4 did not interact with bHLH, which ruled out the possibility that MaMYB4 could be incorporated into the MYB-bHLH-WD40 complex. Our results indicated that acts as a repressor of anthocyanin biosynthesis in banana, likely due to a two-level repression mechanism that consists of reduced expression of anthocyanin synthesis structural genes and the parallel downregulation of to interfere with the proper assembly of the MYB-bHLH-WD40 activation complex. To the best of our knowledge, this is the first MYB TF that regulates anthocyanin synthesis that was identified by genetic methods in bananas, which will be helpful for manipulating anthocyanin coloration in banana programs in the future.

摘要

花青素在香蕉植株特定物种的某些组织中进行时空积累,而MYB转录因子是其主要调节因子。然而,香蕉中精确的调控机制仍有待确定。在此,我们报告了一种R2R3-MYB抑制转录因子的鉴定和特性,其特征在于存在EAR(乙烯响应元件结合因子相关两亲性抑制)和TLLLFR基序。该基因的表达受花青素积累的诱导。与野生型相比,过表达该基因的转基因香蕉植株的花青素含量显著降低。与上述结果一致,代谢组学结果显示,在决定香蕉叶色的主要花青素中,三种已鉴定的花青素和一种飞燕草色素的含量均有所下降,而转录组和逆转录定量聚合酶链反应分析均表明,在过表达植株中,许多关键的花青素合成结构基因和转录因子调节因子均下调。此外,双荧光素酶检测表明,该基因能够与相关启动子结合,从而抑制其表达。酵母双杂交分析证实,MaMYB4不与bHLH相互作用,这排除了MaMYB4可被纳入MYB-bHLH-WD40复合体的可能性。我们的结果表明,MaMYB4在香蕉中作为花青素生物合成的抑制因子,可能是由于一种两级抑制机制,该机制包括花青素合成结构基因表达的降低以及相关基因的平行下调,以干扰MYB-bHLH-WD40激活复合体的正确组装。据我们所知,这是通过遗传方法在香蕉中鉴定出的第一个调节花青素合成的MYB转录因子,这将有助于未来在香蕉项目中调控花青素的着色。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09fd/7817548/1c9db8b433d1/fpls-11-600704-g001.jpg

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