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VqMYB154 promotes polygene expression and enhances resistance to pathogens in Chinese wild grapevine

机译:VQMYB154促进多基因表达增强了中国野生葡萄原体的病原体

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摘要

aVqMYB154 was screened from 106 MYB genes in Danfeng-2 leaves infected by U. necator artificial inoculation under field conditions. b–e Expression of MYB154 was determined by qRT-PCR. b Leaves of Danfeng-2 and (c) Cabernet Sauvignon were inoculated with U. necator and sampled at 0, 12, 24, 48, 72, 96, and 120 h. d Leaves of Danfeng-2 and (e) Cabernet Sauvignon were inoculated with Pst DC3000 and collected at 0, 24, 48, 72 h. Pst DC3000, Pst DC3000 infection; PM-Inoculation, U. necator infection; Mock, control treated with sterile water. f Leaves from Danfeng-2 were treated with 100 μM phytohormones, 1% (w/v) hydrogen peroxide, and 5 mM CaCl2. Leaves were collected at 0, 0.5, 1, 2, 6, and 10 h after spraying. Results are shown as the means (±SD) of three biological assays. Significance was determined with GraphPad Prism using one-way ANOVA with Fisher’s LSD test (*P < 0.05; **P < 0.01)
机译:一种VQMYB154从Danfeng-2叶中的106个MyB基因筛选,由U. Necator人工接种在现场条件下。通过QRT-PCR测定MyB154的B-E表达。 B丹峰-2和(c)赤霞珠的叶子用U. Necator接种,并在0,12,4,48,72,96和120小时采样。 D丹丰-2和(e)赤霞珠的叶子用PST DC3000接种,并在0,24,48,72小时内收集。 PST DC3000,PST DC3000感染; PM接种,U. Necator感染;用无菌水处理的模拟。丹风-2的叶子被100μm植物激素,1%(w / v)过氧化氢和5mM CaCl 2处理。在喷涂后在0,0.5,1,2,6和10h处收集叶子。结果显示为三种生物测定的平均值(±SD)。使用具有Fisher的LSD测试的单向ANOVA使用GraphPad Prism测定意义(* P <0.05; ** P <0.01)

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