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拟南芥 FAD7 和 FAD8 质体去饱和酶在组织分布及对 JA 和 ABA 介导的冷胁迫或防御反应中的特异性贡献。

Tissue Distribution and Specific Contribution of Arabidopsis FAD7 and FAD8 Plastid Desaturases to the JA- and ABA-Mediated Cold Stress or Defense Responses.

机构信息

Department of Plant Nutrition, Estaci�n Experimental Aula Dei (EEAD-CSIC), Avda. Monta�ana 1005, Zaragoza, Spain.

School of Life Sciences, University of Warwick, Gibbet Hill Road, Coventry, UK.

出版信息

Plant Cell Physiol. 2019 May 1;60(5):1025-1040. doi: 10.1093/pcp/pcz017.

Abstract

To overcome the difficulties to analyze membrane desaturases at the protein level, transgenic Arabidopsis plants expressing the plastidial AtFAD7 and AtFAD8 ω-3 desaturases fused to green fluorescent protein, under the control of their endogenous promoters, were generated and their tissue relative abundance was studied. Gene expression, glucuronidase promoter activity, immunoblot and confocal microscopy analyses indicated that AtFAD7 is the major ω-3 desaturase in leaves when compared to AtFAD8. This higher abundance of AtFAD7 was consistent with its higher promoter activity and could be related with its specificity for the abundant leaf galactolipids. AtFAD7 was also present in roots but at much lower level than leaves. AtFAD8 expression and protein abundance in leaves was consistent with its lower promoter activity, suggesting that transcriptional control modulates the abundance of both desaturases in leaves. AtFAD7 protein levels increased in response to wounding but not to jasmonate (JA), and decreased upon abscisic acid (ABA) treatment. Conversely, AtFAD8 protein levels increased upon cold or JA exposure and decreased at high temperatures, but did not respond to ABA or wounding. These results indicated specific and non-redundant roles for the plastidial ω-3 desaturases in defense, temperature stress or phytohormone mediated responses and a tight coordination of their activities between biotic and abiotic stress signaling pathways. Our data suggested that transcriptional regulation was crucial for this coordination. Finally, bimolecular fluorescence complementation analysis showed that both AtFAD7 and AtFAD8 interact with the AtFAD6 ω-6 desaturase in vivo, suggesting that quaternary complexes are involved in trienoic fatty acid production within the plastid membranes.

摘要

为了克服在蛋白质水平上分析膜去饱和酶的困难,生成了表达质体来源的 AtFAD7 和 AtFAD8 ω-3 去饱和酶与绿色荧光蛋白融合的转基因拟南芥植物,其表达受内源启动子的控制,并研究了它们的组织相对丰度。基因表达、β-葡糖苷酸酶启动子活性、免疫印迹和共聚焦显微镜分析表明,与 AtFAD8 相比,AtFAD7 是叶片中主要的 ω-3 去饱和酶。AtFAD7 的这种更高丰度与其更高的启动子活性一致,并且可能与其对丰富的叶半乳糖脂的特异性有关。AtFAD7 也存在于根中,但水平远低于叶片。AtFAD8 在叶片中的表达和蛋白丰度与其较低的启动子活性一致,这表明转录调控调节了这两种去饱和酶在叶片中的丰度。AtFAD7 蛋白水平在受到伤害时增加,但不受茉莉酸(JA)的影响,而在受到脱落酸(ABA)处理时减少。相反,AtFAD8 蛋白水平在受到冷或 JA 暴露时增加,在高温时减少,但对 ABA 或伤害没有反应。这些结果表明质体 ω-3 去饱和酶在防御、温度应激或植物激素介导的反应中具有特定且不可替代的作用,并且它们的活性在生物和非生物应激信号通路之间得到紧密协调。我们的数据表明转录调控对于这种协调至关重要。最后,双分子荧光互补分析表明,AtFAD7 和 AtFAD8 均与质体来源的 AtFAD6 ω-6 去饱和酶在体内相互作用,这表明在质体膜内涉及四元复合物的三烯酸脂肪酸的产生。

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