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没有证据表明番茄抗性基因产物Cf-9与番茄叶霉病菌无毒基因产物AVR9之间存在结合。

No evidence for binding between resistance gene product Cf-9 of tomato and avirulence gene product AVR9 of Cladosporium fulvum.

作者信息

Luderer R, Rivas S, Nürnberger T, Mattei B, Van den Hooven H W, Van der Hoorn R A, Romeis T, Wehrfritz J M, Blume B, Nennstiel D, Zuidema D, Vervoort J, De Lorenzo G, Jones J D, De Wit P J, Joosten M H

机构信息

Laboratory of Phytopathology, Wageningen University, The Netherlands.

出版信息

Mol Plant Microbe Interact. 2001 Jul;14(7):867-76. doi: 10.1094/MPMI.2001.14.7.867.

Abstract

The gene-for-gene model postulates that for every gene determining resistance in the host plant, there is a corresponding gene conditioning avirulence in the pathogen. On the basis of this relationship, products of resistance (R) genes and matching avirulence (Avr) genes are predicted to interact. Here, we report on binding studies between the R gene product Cf-9 of tomato and the Avr gene product AVR9 of the pathogenic fungus Cladosporium fulvum. Because a high-affinity binding site (HABS) for AVR9 is present in tomato lines, with or without the Cf-9 resistance gene, as well as in other solanaceous plants, the Cf-9 protein was produced in COS and insect cells in order to perform binding studies in the absence of the HABS. Binding studies with radio-labeled AVR9 were performed with Cf-9-producing COS and insect cells and with membrane preparations of such cells. Furthermore, the Cf-9 gene was introduced in tobacco, which is known to be able to produce a functional Cf-9 protein. Binding of AVR9 to Cf-9 protein produced in tobacco was studied employing surface plasmon resonance and surface-enhanced laser desorption and ionization. Specific binding between Cf-9 and AVR9 was not detected with any of the procedures. The implications of this observation are discussed.

摘要

基因对基因模型假定,对于宿主植物中决定抗性的每一个基因,病原体中都有一个相应的决定无毒力的基因。基于这种关系,预计抗性(R)基因和匹配的无毒力(Avr)基因的产物会相互作用。在此,我们报告了番茄R基因产物Cf-9与致病真菌番茄叶霉病菌的Avr基因产物AVR9之间的结合研究。由于无论有无Cf-9抗性基因,番茄品系以及其他茄科植物中都存在AVR9的高亲和力结合位点(HABS),因此在COS细胞和昆虫细胞中产生Cf-9蛋白,以便在没有HABS的情况下进行结合研究。用产生Cf-9的COS细胞和昆虫细胞以及这些细胞的膜制剂进行了用放射性标记的AVR9的结合研究。此外,将Cf-9基因导入已知能够产生功能性Cf-9蛋白的烟草中。采用表面等离子体共振和表面增强激光解吸电离技术研究了AVR9与烟草中产生的Cf-9蛋白的结合。用任何一种方法都未检测到Cf-9和AVR9之间的特异性结合。讨论了这一观察结果的意义。

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