首页> 美国卫生研究院文献>Journal of Experimental Botany >Characterization of a canola C2 domain gene that interacts with PG an effector of the necrotrophic fungus Sclerotinia sclerotiorum
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Characterization of a canola C2 domain gene that interacts with PG an effector of the necrotrophic fungus Sclerotinia sclerotiorum

机译:芥菜油菜C2域基因的表征与PG坏死性真菌菌核盘菌的效应子。

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摘要

Sspg1d, one of endopolygalacturonases, is an important fungal effector secreted by the necrotrophic fungus Sclerotinia sclerotiorum during early infection. Using sspg1d as bait, a small C2 domain protein (designated as IPG-1) was identified by yeast two-hybrid screening of a canola cDNA library. Deletion analysis confirmed that the C-terminus of IPG-1 is responsible for its interaction with sspg1d in the yeast two-hybrid assay. The sspg1d/IPG-1 interaction was further confirmed in plant cells by a biomolecular fluorescence complementation (BiFC) assay. A transient expression assay showed that the IPG-1–GFP fusion protein was targeted to the plasma membrane and nucleus in onion epidermal cells. Following treatment with a Ca2+ ionophore, it was distributed throughout the cytosol. Real-time PCR assay demonstrated that IPG-1 was highly induced by Sclerotinia sclerotiorum in canola leaves and stems. Southern blot analysis indicated the presence of about five homologues of IPG-1 in the canola genome. Two additional members of the IPG-1gene family were isolated by RT-PCR. Their sequence similarity with IPG-1 is as high as 95%. However, they did not interact with sspg1d in the yeast two-hybrid assay. Possible roles of IPG-1 and its association with sspg1d in the defence signalling pathway were discussed.
机译:Sspg1d是一种内聚半乳糖醛酸酶,是早期感染时坏死性菌核盘菌菌核菌分泌的重要真菌效应物。使用sspg1d作为诱饵,通过双低油菜籽cDNA文库的酵母双杂交筛选确定了一个小的C2域蛋白(称为IPG-1)。缺失分析证实,IPG-1的C末端是其与酵母双杂交法中的sspg1d相互作用的原因。 sspg1d / IPG-1相互作用在植物细胞中通过生物分子荧光互补(BiFC)分析得到了进一步证实。瞬时表达分析表明,IPG-1–GFP融合蛋白靶向洋葱表皮细胞的质膜和细胞核。用Ca 2 + 离子载体处理后,它分布在整个细胞质中。实时荧光定量PCR检测表明,油菜菌核盘菌菌核菌在油菜叶片和茎中高度诱导了IPG-1的表达。 Southern印迹分析表明在低芥酸菜子基因组中存在约五个IPG-1同源物。通过RT-PCR分离了IPG-1基因家族的另外两个成员。它们与IPG-1的序列相似性高达95%。但是,它们在酵母双杂交检测中并未与sspg1d相互作用。讨论了IPG-1在防御信号通路中的可能作用及其与sspg1d的关系。

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