JrATHB-12 mediates JrMYB113 and JrMYB27 to control the different types of red walnut1

IF 4.6 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Integrative Agriculture Pub Date : 2024-03-04 DOI:10.1016/j.jia.2024.03.015
Haifeng Xu, Guifang Wang, Xinying Ji, Kun Xiang, Tao Wang, Meiyong Zhang, Guangning Shen, Rui Zhang, Junpei Zhang, Xin Chen
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Abstract

Red walnut has broad market prospects because it is richer in anthocyanin than ordinary walnut. However, the anthocyanin biosynthetic mechanism of red walnut is still unknown. We studied two types of red walnut, called red walnut 1 (R1), with a red pericarp and seed coat, and red walnut 2 (R2), with a red seed coat only. R1 mostly contained cyanidin-3-O-galactoside, while R2 contained a certain amount of each of cyanidin-3-O-galactoside, cyanidin-3-O-arabinoside, and cyanidin-3-O-glucoside. The (LOC109007163) and (LOC109010746), encoding genes of leucoanthocyanidin dioxygenase/anthocyanidin synthase (LDOX/ANS), were preliminarily appraised as crucial genes for anthocyanin biosynthesis in R1 and R2, respectively. The MYB differential genes analysis showed that and are specifically expressed in the red parts of R1 and R2, respectively, and are regarded as candidate regulatory genes. Ectopic expression in and transient injection in walnut showed that both MYB27 and MYB113, located in the nucleus, promoted anthocyanin accumulation, MYB27 promoted the expression, and MYB113 promoted the expressions of and . Yeast one-hybrid and electrophoretic mobility shift assays showed that MYB27 could only bind the promoter, while MYB113 could bind the promoters of and . In addition, we also identified an HD-Zip transcription factor ATHB-12, which is specifically expressed in the pericarp. After silencing the expression of , the R2 pericarp turned red, and the expression increased. Further experiments showed that ATHB-12 could specifically interact with MYB113 and bind to its promoter. This suggests that MYB27 controls R1 coloration by regulating , while MYB113 controls R2 coloration by regulating and , but the ATHB-12 can specifically bind and inhibit the of R2 pericarp so that it becomes unpigmented. This study reveals the anthocyanin biosynthesis mechanisms in different types of red walnut and provides a scientific basis for the selection and breeding of red walnut varieties.
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JrATHB-12 介导 JrMYB113 和 JrMYB27 控制不同类型的红核桃1
由于红核桃比普通核桃富含花青素,因此具有广阔的市场前景。然而,红核桃的花青素生物合成机制尚不清楚。我们对两种红核桃进行了研究,一种称为红核桃 1(R1),其果皮和种皮均为红色;另一种称为红核桃 2(R2),其种皮仅为红色。R1 主要含有青花素-3-O-半乳糖苷,而 R2 则含有一定量的青花素-3-O-半乳糖苷、青花素-3-O-阿拉伯糖苷和青花素-3-O-葡萄糖苷。经初步鉴定,R1 和 R2 中的白花青素二氧酶/花青素合成酶(LDOX/ANS)编码基因(LOC109007163)和(LOC109010746)分别是花青素生物合成的关键基因。MYB 差异基因分析表明,和分别在 R1 和 R2 的红色部分特异表达,被认为是候选调控基因。在核桃中异位表达和瞬时注射表明,位于细胞核中的 MYB27 和 MYB113 都能促进花青素的积累,其中 MYB27 能促进 和 的表达,而 MYB113 能促进 和 的表达。 酵母单杂交和电泳迁移实验表明,MYB27 只能与 和 的启动子结合,而 MYB113 能与 和 的启动子结合。 此外,我们还发现了一个 HD-Zip 转录因子 ATHB-12,它在果皮中特异表达。沉默 ATHB-12 的表达后,R2 果皮变红,表达量增加。进一步的实验表明,ATHB-12能与MYB113发生特异性相互作用,并与其启动子结合。这表明,MYB27 通过调节 和 来控制 R1 的着色,而 MYB113 则通过调节 和 来控制 R2 的着色,但 ATHB-12 能特异性地与 R2 果皮的启动子结合并抑制它,从而使 R2 果皮不着色。该研究揭示了不同类型红核桃的花青素生物合成机制,为红核桃品种的选育提供了科学依据。
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来源期刊
Journal of Integrative Agriculture
Journal of Integrative Agriculture AGRICULTURE, MULTIDISCIPLINARY-
CiteScore
7.90
自引率
4.20%
发文量
4817
审稿时长
3-6 weeks
期刊介绍: Journal of Integrative Agriculture publishes manuscripts in the categories of Commentary, Review, Research Article, Letter and Short Communication, focusing on the core subjects: Crop Genetics & Breeding, Germplasm Resources, Physiology, Biochemistry, Cultivation, Tillage, Plant Protection, Animal Science, Veterinary Science, Soil and Fertilization, Irrigation, Plant Nutrition, Agro-Environment & Ecology, Bio-material and Bio-energy, Food Science, Agricultural Economics and Management, Agricultural Information Science.
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