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LcNAC13 与 LcR1MYB1 互作,共同调控荔枝果实成熟过程中花色苷生物合成相关基因。

LcNAC13 Physically Interacts with LcR1MYB1 to Coregulate Anthocyanin Biosynthesis-Related Genes during Litchi Fruit Ripening.

机构信息

Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou 510650, China.

Key Laboratory of Post-Harvest Handling of Fruits, Ministry of Agriculture, Guangzhou 510650, China.

出版信息

Biomolecules. 2019 Apr 4;9(4):135. doi: 10.3390/biom9040135.

Abstract

Anthocyanin accumulation is crucial for the development of quality for most fruit. The mechanism underlying the regulation of anthocyanin biosynthesis by transcription factors in litchi fruit remains largely unknown. In this study, we isolated one NAC (NAM, ATAF1/2 and CUC2) TF gene, . Expression of was upregulated as ripening proceeded, followed by the accumulation of anthocyanins. Electrophoretic mobility shift assay (EMSA) and transient expression assay showed that LcNAC13 could negatively regulate the expression of anthocyanin biosynthesis-related genes, including , , , , , and . Furthermore, LcR1MYB1, as one R1-MYB type MYB, was identified to physically interact with LcNAC13 and reverse the effect of LcNAC13. Taken together, these results suggested that LcNAC13 and LcR1MYB1 may act together to antagonistically regulate anthocyanin biosynthesis during litchi fruit ripening, which helps to provide new insights into the regulatory networks of anthocyanin biosynthesis.

摘要

花色苷积累对大多数水果的品质发育至关重要。荔枝果实中转录因子调控花色苷生物合成的机制在很大程度上尚不清楚。本研究中,我们分离得到一个 NAC(NAM、ATAF1/2 和 CUC2)TF 基因 。随着果实成熟, 的表达上调,随后花色苷积累。电泳迁移率变动分析(EMSA)和瞬时表达分析表明,LcNAC13 可以负调控花色苷生物合成相关基因的表达,包括 、 、 、 、 和 。此外,作为 R1-MYB 型 MYB 之一的 LcR1MYB1 被鉴定与 LcNAC13 发生物理互作,并逆转 LcNAC13 的作用。综上所述,这些结果表明 LcNAC13 和 LcR1MYB1 可能在荔枝果实成熟过程中共同作用,拮抗调控花色苷生物合成,这有助于深入了解花色苷生物合成的调控网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d18/6523642/662796435590/biomolecules-09-00135-g001.jpg

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