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丛枝菌根真菌分泌物依赖于细胞质 Ca(2+)增加激活植物细胞中的 MAP 激酶。

AM fungal exudates activate MAP kinases in plant cells in dependence from cytosolic Ca(2+) increase.

机构信息

DiVaPRA, Patologia Vegetale, Università degli Studi di Torino, Via L. da Vinci, 44, 10095 Grugliasco (TO), Italy.

出版信息

Plant Physiol Biochem. 2011 Sep;49(9):963-9. doi: 10.1016/j.plaphy.2011.04.008. Epub 2011 Apr 23.

Abstract

The molecular dialogue occurring prior to direct contact between the fungal and plant partners of arbuscular-mycorrhizal (AM) symbioses begins with the release of fungal elicitors, so far only partially identified chemically, which can activate specific signaling pathways in the host plant. We show here that the activation of MAPK is also induced by exudates of germinating spores of Gigaspora margarita in cultured cells of the non-leguminous species tobacco (Nicotiana tabacum), as well as in those of the model legume Lotus japonicus. MAPK activity peaked about 15 min after the exposure of the host cells to the fungal exudates (FE). FE were also responsible for a rapid and transient increase in free cytosolic Ca(2+) in Nicotiana plumbaginifolia and tobacco cells, and pre-treatment with a Ca(2+)-channel blocker (La(3+)) showed that in these cells, MAPK activation was dependent on the cytosolic Ca(2+) increase. A partial dependence of MAPK activity on the common Sym pathway could be demonstrated for a cell line of L. japonicus defective for LjSym4 and hence unable to establish an AM symbiosis. Our results show that MAPK activation is triggered by an FE-induced cytosolic Ca(2+) transient, and that a Sym genetic determinant acts to modulate the intensity and duration of this activity.

摘要

在丛枝菌根(AM)共生中真菌和植物伙伴直接接触之前发生的分子对话,始于真菌激发子的释放,这些激发子到目前为止仅部分从化学上进行了鉴定,它们可以激活宿主植物中的特定信号通路。我们在这里表明,MAPK 的激活也被大团囊霉发芽孢子的分泌物(FE)在非豆科物种烟草(Nicotiana tabacum)的培养细胞以及模式豆科植物百脉根(Lotus japonicus)的培养细胞中诱导。暴露于真菌分泌物(FE)后,宿主细胞的 MAPK 活性在约 15 分钟时达到峰值(FE)。FE 还导致Nicotiana plumbaginifolia 和烟草细胞中游离胞质 Ca(2+)的快速和短暂增加,并且用 Ca(2+)通道阻滞剂(La(3+))预处理表明,在这些细胞中,MAPK 激活依赖于胞质 Ca(2+)的增加。对于LjSym4 缺陷的百脉根细胞系(无法建立 AM 共生),MAPK 活性的部分依赖于常见的 Sym 途径可以证明。我们的结果表明,MAPK 激活是由 FE 诱导的胞质 Ca(2+)瞬变触发的,并且 Sym 遗传决定因素可调节该活性的强度和持续时间。

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