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表达荧光蛋白 DsRed 和 EGFP 以可视化羽扇豆枯萎病菌定殖的早期事件。

Expression of the fluorescent proteins DsRed and EGFP to visualize early events of colonization of the chickpea blight fungus Ascochyta rabiei.

机构信息

National Institute of Plant Genome Research, Aruna Asaf Ali Marg, New Delhi, India.

出版信息

Curr Genet. 2010 Aug;56(4):391-9. doi: 10.1007/s00294-010-0305-3. Epub 2010 May 12.

Abstract

Ascochyta blight caused by the ascomycete fungus Ascochyta rabiei, is a major biotic constraint of chickpea (Cicer arietinum L.), resulting in disastrous crop losses worldwide. To study early stages of development and pathogenic mechanisms of the fungus, two binary vectors for the constitutive expression of the red fluorescent protein (DsRed-Express) and the green fluorescent protein (EGFP1) were constructed. Furthermore, we have developed an improved and highly reproducible Agrobacterium tumefaciens-mediated transformation protocol for A. rabiei. Transformation events were confirmed through Southern hybridizations that suggest single-copy integration of reporter genes in majority of the transformants. High level expression of both DsRed and EGFP proteins was obtained both in spores and in mycelia as detected by fluorescence microscopy. Intense fluorescence was used as a highly efficient vital marker to visualize early developmental changes of the fungus. The formation of infection structures like appressoria and germ tubes were observed both in vitro and in planta. This work will be useful to develop methodologies for understanding the mechanisms of Ascochyta-chickpea interaction and functional genomics of A. rabiei towards the isolation of virulence genes.

摘要

由子囊菌真菌茄壳二孢菌(Ascochyta rabiei)引起的炭疽病是鹰嘴豆(Cicer arietinum L.)的主要生物限制因素,导致全球灾难性的作物损失。为了研究真菌的早期发育和致病机制,构建了两个用于组成型表达红色荧光蛋白(DsRed-Express)和绿色荧光蛋白(EGFP1)的二元载体。此外,我们还开发了一种改进的、高度可重复的根癌农杆菌介导的茄壳二孢菌转化方案。通过Southern 杂交证实了转化事件,表明报告基因在大多数转化体中均以单拷贝整合。通过荧光显微镜检测到,在孢子和菌丝中均获得了 DsRed 和 EGFP 蛋白的高水平表达。荧光强度高,可作为一种高效的活体标记物,用于可视化真菌的早期发育变化。在体外和体内均观察到了附着胞和芽管等侵染结构的形成。这项工作将有助于开发用于理解茄壳二孢菌与鹰嘴豆相互作用机制和茄壳二孢菌功能基因组学的方法,以分离毒力基因。

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