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首页> 外文期刊>Plant physiology >Abscisic acid and stress signals induce viviparous1 expression in seed and vegetative tissues of maize
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Abscisic acid and stress signals induce viviparous1 expression in seed and vegetative tissues of maize

机译:脱落酸和胁迫信号诱导玉米种子和营养组织中viviparous1表达

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摘要

Viviparous1 (Vp1) encodes a B3 domain-containing transcription factor that is a key regulator of seed maturation in maize (Zea mays). However, the mechanisms of Vp1 regulation are not well understood. To examine physiological factors that may regulate Vp1 expression, transcript levels were monitored in maturing embryos placed in culture under different conditions. Expression of Vp1 decreased after culture in hormone-free medium, but was induced by salinity or osmotic stress. Application of exogenous abscisic acid (ABA) also induced transcript levels within 1 h in a dose-dependent manner. The Vp1 promoter fused to beta-glucuronidase or green fluorescent protein reproduced the endogenous Vp1 expression patterns in transgenic maize plants and also revealed previously unknown expression domains of Vp1. The Vp1 promoter is active in the embryo and aleurone cells of developing seeds and, upon drought stress, was also found in phloem cells of vegetative tissues, including cobs, leaves, and stems. Sequence analysis of the Vp1 promoter identified a potential ABA-responsive complex, consisting of an ACGT-containing ABA response element (ABRE) and a coupling element 1-like motif. Electrophoretic mobility shift assay confirmed that the ABRE and putative coupling element 1 components specifically bound proteins in embryo nuclear protein extracts. Treatment of embryos in hormone-free Murashige and Skoog medium blocked the ABRE-protein interaction, whereas exogenous ABA or mannitol treatment restored this interaction. Our data support a model for a VP1-dependent positive feedback mechanism regulating Vp1 expression during seed maturation.
机译:Viviparous1(Vp1)编码含有B3结构域的转录因子,该因子是玉米(Zea mays)种子成熟的关键调节剂。但是,对Vp1调节的机制还不甚了解。为了检查可能调节Vp1表达的生理因素,在不同条件下放置在培养物中的成熟胚中监测了转录水平。在无激素的培养基中培养后,Vp1的表达下降,但由盐度或渗透压诱导。外源脱落酸(ABA)的应用还可以在1小时内以剂量依赖的方式诱导转录水平。与β-葡糖醛酸糖苷酶或绿色荧光蛋白融合的Vp1启动子在转基因玉米植物中复制了内源性Vp1表达模式,并且还揭示了以前未知的Vp1表达域。 Vp1启动子在发育中的种子的胚胎和糊粉细胞中具有活性,并且在干旱胁迫下,还在营养组织(包括穗轴,叶和茎)的韧皮部细胞中发现。 Vp1启动子的序列分析确定了一种潜在的ABA反应复合物,该复合物由含ACGT的ABA反应元件(ABRE)和偶联元件1样基序组成。电泳迁移率变动分析证实了ABRE和推定的偶联元件1组分特异性结合了胚胎核蛋白提取物中的蛋白。在无激素的Murashige和Skoog培养基中处理胚胎可阻断ABRE蛋白相互作用,而外源ABA或甘露醇治疗可恢复这种相互作用。我们的数据支持在种子成熟过程中调节Vp1表达的VP1依赖性正反馈机制模型。

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