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HD-ZIP IV 转录因子 GLABRA2 在蒺藜苜蓿种皮中原花青素生物合成中作为激活剂起作用。

The HD-ZIP IV transcription factor GLABRA2 acts as an activator for proanthocyanidin biosynthesis in Medicago truncatula seed coat.

机构信息

The Key Laboratory of Plant Development and Environmental Adaptation Biology, Ministry of Education, School of Life Science, Shandong University, Qingdao, 266237, P.R. China.

Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, 100193, P.R. China.

出版信息

Plant J. 2024 Sep;119(5):2303-2315. doi: 10.1111/tpj.16918. Epub 2024 Jul 11.

DOI:10.1111/tpj.16918
PMID:38990552
Abstract

Proanthocyanidins (PAs), a group of flavonoids, are found in leaves, flowers, fruits, and seed coats of many plant species. PAs are primarily composed of epicatechin units in the seed coats of the model legume species, Medicago truncatula. It can be synthesized from two separate pathways, the leucoanthocyanidin reductase (MtLAR) pathway and the anthocyanidin synthase (MtANS) pathway, which produce epicatechin through anthocyanidin reductase (MtANR). These pathways are mainly controlled by the MYB-bHLH-WD40 (MBW) ternary complex. Here, we characterize a class IV homeodomain-leucine zipper (HD-ZIP IV) transcription factor, GLABRA2 (MtGL2), which contributes to PA biosynthesis in the seed coat of M. truncatula. Null mutation of MtGL2 results in dark brown seed coat, which is accompanied by reduced PAs accumulation and increased anthocyanins content. The MtGL2 gene is predominantly expressed in the seed coat during the early stages of seed development. Genetic and molecular analyses indicate that MtGL2 positively regulates PA biosynthesis by directly activating the expression of MtANR. Additionally, our results show that MtGL2 is strongly induced by the MBW activator complexes that are involved in PA biosynthesis. Taken together, our results suggest that MtGL2 acts as a novel positive regulator in PA biosynthesis, expanding the regulatory network and providing insights for genetic engineering of PA production.

摘要

原花青素(PAs)是一组类黄酮,存在于许多植物物种的叶子、花朵、果实和种皮中。PAs 主要由模式豆科植物紫花苜蓿的种皮中的表儿茶素单元组成。它可以通过两个独立的途径合成,即无色儿茶素还原酶(MtLAR)途径和花色素苷合酶(MtANS)途径,这两种途径通过花色素苷还原酶(MtANR)产生表儿茶素。这些途径主要受 MYB-bHLH-WD40(MBW)三元复合物控制。在这里,我们描述了一个第四类同源域-亮氨酸拉链(HD-ZIP IV)转录因子 GLABRA2(MtGL2),它有助于紫花苜蓿种皮中的 PA 生物合成。MtGL2 的缺失突变导致种皮呈深棕色,同时伴随着 PA 积累减少和花青素含量增加。MtGL2 基因在种子发育的早期主要在种皮中表达。遗传和分子分析表明,MtGL2 通过直接激活 MtANR 的表达来正向调控 PA 生物合成。此外,我们的结果表明,MtGL2 强烈地被参与 PA 生物合成的 MBW 激活复合物诱导。总之,我们的结果表明,MtGL2 作为 PA 生物合成的一种新的正调控因子,扩展了调控网络,并为 PA 生产的遗传工程提供了见解。

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