Rairdan Gregory J, Moffett Peter
Boyce Thompson Institute for Plant Research, Ithaca, New York 14853, USA.
Plant Cell. 2006 Aug;18(8):2082-93. doi: 10.1105/tpc.106.042747. Epub 2006 Jul 14.
Plant nucleotide binding and leucine-rich repeat (NB-LRR) proteins contain a region of homology known as the ARC domain located between the NB and LRR domains. Structural modeling suggests that the ARC region can be subdivided into ARC1 and ARC2 domains. We have used the potato (Solanum tuberosum) Rx protein, which confers resistance to Potato virus X (PVX), to investigate the function of the ARC region. We demonstrate that the ARC1 domain is required for binding of the Rx N terminus to the LRR domain. Domain-swap experiments with Rx and a homologous disease resistance gene, Gpa2, showed that PVX recognition localized to the C-terminal half of the LRR domain. However, inappropriate pairings of LRR and ARC2 domains resulted in autoactive molecules. Thus, the ARC2 domain is required to condition an autoinhibited state in the absence of elicitor as well as for the subsequent elicitor-induced activation. Our data suggest that the ARC region, through its interaction with the LRR, translates elicitor-induced modulations of the C terminus into a signal initiation event. Furthermore, we demonstrate that physical disruption of the LRR-ARC interaction is not required for signal initiation. We propose instead that this activity can lead to multiple rounds of elicitor recognition, providing a means of signal amplification.
植物核苷酸结合富含亮氨酸重复序列(NB-LRR)蛋白包含一个同源区域,称为ARC结构域,位于NB和LRR结构域之间。结构建模表明,ARC区域可细分为ARC1和ARC2结构域。我们利用赋予马铃薯X病毒(PVX)抗性的马铃薯(Solanum tuberosum)Rx蛋白来研究ARC区域的功能。我们证明,ARC1结构域是Rx N端与LRR结构域结合所必需的。用Rx和同源抗病基因Gpa2进行的结构域交换实验表明,PVX识别定位于LRR结构域的C端一半。然而,LRR和ARC2结构域的不适当配对导致了自激活分子。因此,ARC2结构域在没有激发子时需要调节自抑制状态,以及随后激发子诱导的激活。我们的数据表明,ARC区域通过与LRR的相互作用,将激发子诱导的C端调节转化为信号起始事件。此外,我们证明信号起始不需要LRR-ARC相互作用的物理破坏。相反,我们提出这种活性可以导致多轮激发子识别,提供一种信号放大的手段。