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首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Identification and subcellular localisation of Sl;INT7: A novel tomato (Solanum lycopersicum Mill.) fruit ripening-related and stress-inducible gene
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Identification and subcellular localisation of Sl;INT7: A novel tomato (Solanum lycopersicum Mill.) fruit ripening-related and stress-inducible gene

机译:; Sl; INT7的鉴定和亚细胞定位:一种新型番茄(Solanum lycopersicum Mill。)果实成熟相关和胁迫诱导基因

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The key step in ethylene (C2H4) signalling during tomato fruit ripening is initialized via the direct interaction between C2H4 and specialized membrane-bound receptors, including Never-Ripe (NR), which is strongly induced during ripening. In order to identify novel ripening-related C2H4-dependent components, a yeast two-hybrid interaction screen has previously been employed, in which AIR cDNA has been used as bait. This screen has identified a clone corresponding to interacting protein 7 (Sl;INT7), through its specific and strong interaction with the NR receptor (L Alexander, Z. Lin, R. Hackett, I. Wilson and D. Grierson, unpublished work). In this work, our objective was to identify the corresponding NR-interacting gene and subsequently characterize its expression response to various stress treatments, as well as unravelling its subcellular location in the cell. By sequencing and plant database interrogation, SI;INT7 was found to be a small gene with an open reading frame (ORF) of similar to 243 bb encoding a protein composed of 77 aa that shares no sequence homology with any known gene. Notably, northern analyses demonstrated that Sl;INT7 gene expression is up-regulated in response to various stress signalling molecules such as salicylic acid (SA), abscissic acid, jasmonic acid, nitric oxide (NO) and salt, implicating Sl;INT7 in biotic and abiotic stress signalling transduction responses. To gain more insight into the possible function of Sl:IN77, a construct in which SI;INT7 is C-terminally fused to the green fluorescent protein (GFP) was generated. Subsequently, 35S::Sl;INT7::GFP-containing constructs were transiently expressed in both tobacco leaves and onion peels via microprojectiles bombardment. Subsequently, confocal laser microscopic examination of bombarded tobacco and onion tissues revealed that the expression of GFP-Sl;INT7 was observed predominantly in the plasma membrane, compared to the location throughout the cell observed with the control GFP construct alone. These results are discussed in the light of our present knowledge of C2H4-mediated control over fruit ripening and degree of cross-talk with other stress signalling pathways. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
机译:番茄果实成熟过程中乙烯(C2H4)信号传导的关键步骤是通过C2H4与特定膜结合受体(包括Never-Ripe(NR))之间的直接相互作用而初始化的,该受体在成熟过程中被强烈诱导。为了鉴定新的与成熟相关的C2H4依赖性成分,以前已采用酵母双杂交相互作用筛选,其中AIR cDNA已用作诱饵。该筛选通过与NR受体的特异性强相互作用而鉴定出了与相互作用蛋白7(S1; INT7)相对应的克隆(L Alexander,Z.Lin,R.Hackett,I.Wilson和D.Grierson,未发表的著作) 。在这项工作中,我们的目标是鉴定相应的NR相互作用基因,并随后表征其对各种胁迫处理的表达反应,并揭示其在细胞中的亚细胞位置。通过测序和植物数据库询问,发现SI; INT7是一个小基因,其开放阅读框(ORF)与243 bb相似,编码一个由77个氨基酸组成的蛋白质,该蛋白质与任何已知基因没有序列同源性。值得注意的是,Northern分析表明,Sl; INT7基因表达响应各种胁迫信号分子(例如水杨酸(SA),脱落酸,茉莉酸,一氧化氮(NO)和盐)而上调,这与生物中的Sl; INT7有关非生物胁迫信号转导反应。为了获得对Sl:IN77的可能功能的更多了解,生成了其中SI; INT7在C末端与绿色荧光蛋白(GFP)融合的构建体。随后,通过微粒轰击在烟草叶和洋葱皮中瞬时表达含35S :: S1; INT7 :: GFP的构建体。随后,对被轰击的烟草和洋葱组织进行共聚焦激光显微镜检查发现,与单独使用对照GFP构建体观察到的整个细胞位置相比,主要在质膜中观察到了GFP-S1; INT7的表达。根据我们目前对C2H4介导的果实成熟控制以及与其他胁迫信号通路的串扰程度的了解,讨论了这些结果。 (C)2008 Elsevier Ireland Ltd.保留所有权利。

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