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乙烯反应因子 Pp4ERF24 和 Pp12ERF96 通过与 MYB114 互作调控‘红早酥’梨果实中蓝光诱导的花青苷合成。

Ethylene response factors Pp4ERF24 and Pp12ERF96 regulate blue light-induced anthocyanin biosynthesis in 'Red Zaosu' pear fruits by interacting with MYB114.

机构信息

Department of Horticulture, Zhejiang University, Hangzhou, 310058, Zhejiang, People's Republic of China.

The Key Laboratory of Horticultural Plant Growth, Development and Quality Improvement, The Ministry of Agriculture of China, Hangzhou, 310058, Zhejiang, People's Republic of China.

出版信息

Plant Mol Biol. 2019 Jan;99(1-2):67-78. doi: 10.1007/s11103-018-0802-1. Epub 2018 Dec 11.

Abstract

Pp4ERF24 and Pp12ERF96 fine tune blue light-induced anthocyanin biosynthesis via interacting with PpMYB114 and promoting the interaction between PpMYB114 and PpbHLH3, which enhances the expression of PpMYB114-induced PpUFGT. The red coloration of pear fruit is attributed to anthocyanin accumulation, which is transcriptionally regulated by the MYB-bHLH-WD40 complex. A number of ethylene response factors (ERF) have been identified to regulate anthocyanin biosynthesis in different plants. In pear, several ERF transcription factor genes were identified to be potentially involved in the light-induced anthocyanin biosynthesis according to transcriptome data. But the molecular mechanism of these ERFs underlying the regulation of anthocyanin accumulation is unknown. In this study, exposure of 'Red Zaosu' pear, a mutant of 'Zaosu' pear, to blue light significantly induced the anthocyanin accumulation by increasing the expression levels of anthocyanin biosynthetic genes. Gene expression analysis confirmed that the expression of Pp4ERF24 and Pp12ERF96 genes were up-regulated in the process of blue light-induced anthocyanin biosynthesis. Yeast two-hybrid and bimolecular fluorescence complementation assay revealed that Pp4ERF24 and Pp12ERF96 interacted with PpMYB114, but not with PpMYB10. Bimolecular fluorescence complementation assay demonstrated that the interaction between these two ERFs and PpMYB114 enhanced the interaction between PpMYB114 and PpbHLH3. Further analysis by dual luciferase assay verified that these two ERFs increased the up-regulation of PpMYB114-mediated PpUFGT expression. Furthermore, co-transformation of Pp12ERF96 with PpMYB114 and PpbHLH3 in tobacco leaves led to enhanced anthocyanin accumulation. Transient overexpression of Pp4ERF24 or Pp12ERF96 alone in 'Red Zaosu' pear fruit also induced anthocyanin biosynthesis in pear peel. Our findings provide insights into a mechanism involving the synergistic interaction of ERFs with PpMYB114 to regulate light-dependent coloration and anthocyanin biosynthesis in pear fruits.

摘要

Pp4ERF24 和 Pp12ERF96 通过与 PpMYB114 相互作用并促进 PpMYB114 与 PpbHLH3 之间的相互作用来微调蓝光诱导的花色素苷生物合成,从而增强 PpMYB114 诱导的 PpUFGT 的表达。梨果实的红色着色归因于花色素苷的积累,而花色素苷的转录调控是由 MYB-bHLH-WD40 复合物完成的。已经鉴定出许多乙烯响应因子(ERF)在不同植物中调节花色素苷生物合成。在梨中,根据转录组数据,已经鉴定出一些 ERF 转录因子基因可能参与光诱导的花色素苷生物合成。但是,这些 ERF 调节花色素苷积累的分子机制尚不清楚。在这项研究中,“红早酥”梨(“早酥”梨的突变体)暴露于蓝光下,通过增加花色素苷生物合成基因的表达水平,显著诱导花色素苷积累。基因表达分析证实,在蓝光诱导的花色素苷生物合成过程中,Pp4ERF24 和 Pp12ERF96 基因的表达上调。酵母双杂交和双分子荧光互补测定显示,Pp4ERF24 和 Pp12ERF96 与 PpMYB114 相互作用,但不与 PpMYB10 相互作用。双分子荧光互补测定表明,这两个 ERFs 与 PpMYB114 的相互作用增强了 PpMYB114 与 PpbHLH3 之间的相互作用。通过双荧光素酶测定进一步分析证实,这两个 ERF 增加了 PpMYB114 介导的 PpUFGT 表达的上调。此外,在烟草叶片中共同转化 Pp12ERF96 与 PpMYB114 和 PpbHLH3 导致果皮中花青素积累增强。单独瞬时过表达 Pp4ERF24 或 Pp12ERF96 在“红早酥”梨果实中也诱导了梨皮中的花色素苷生物合成。我们的研究结果提供了一种机制的见解,涉及 ERF 与 PpMYB114 的协同相互作用,以调节梨果实中光依赖性着色和花色素苷生物合成。

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