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Sub-cellular markers highlight intracellular dynamics of membrane proteins in response to abiotic treatments in rice

机译:子细胞标记突出膜蛋白的细胞内动态响应稻中的非生物处理

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Background Cell biology approach using membrane protein markers tagged with fluorescent proteins highlights the dynamic behaviour of plant cell membranes, not only in the standard but also in changing environmental conditions. In the past, this strategy has been extensively developed in plant models such as Arabidopsis. Results Here, we generated a set of transgenic lines expressing membrane protein markers to extend this approach to rice, one of the most cultivated crop in the world and an emerging plant model. Lines expressing individually eight membrane protein markers including five aquaporins ( Os PIP1;1, Os PIP2;4, Os PIP2;5, Os TIP1;1, Os TIP2;2) and three endosomal trafficking proteins ( Os Rab5a, Os GAP1, Os SCAMP1) were obtained. Importantly, we challenged in roots the aquaporin-expressing transgenic lines upon salt and osmotic stress and uncovered a highly dynamic behaviour of cell membrane. Conclusion We have uncovered the relocalization and dynamics of plasma membrane aquaporins upon salt and osmotic stresses in rice. Importantly, our data support a model where relocalization of Os PIPs is concomitant with their high cycling dynamics.
机译:背景技术使用标记为荧光蛋白标记的膜蛋白标记的背景细胞生物学方法突出了植物细胞膜的动态行为,不仅在标准中,而且在不断变化的环境条件下。过去,这种策略在诸如拟南芥等植物模型中广泛开发。结果在此,我们产生了一组表达膜蛋白标记物的转基因系,以将这种方法延伸到米饭中,是世界上最耕种的作物之一和新兴植物模型。表达单独八个膜蛋白标记,包括五个水蛋白(OS pip1; 1,OS pip2; 4,OS pip2; 5,OS tip1,OS Tip2; 2)和三种内体贩运蛋白(OS Rab5a,OS Gap1,OS Scamp1 )获得了。重要的是,我们在盐和渗透胁迫下挑战在盐和渗透胁迫下表达水通道蛋白表达的转基因系,并发现细胞膜的高度动态行为。结论我们已经发现了水稻盐和渗透胁迫浆液和渗透胁迫下血浆膜水下蛋白的重新定位和动态。重要的是,我们的数据支持一个模型,其中OS PIPS的重定位伴随着它们的高循环动态。

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