Martin G B, Frary A, Wu T, Brommonschenkel S, Chunwongse J, Earle E D, Tanksley S D
Department of Agronomy, Purdue University, West Lafayette, Indiana 47907-1150.
Plant Cell. 1994 Nov;6(11):1543-52. doi: 10.1105/tpc.6.11.1543.
Leaves of tomato cultivars that contain the Pto bacterial resistance locus develop small necrotic lesions within 24 hr after exposure to fenthion, an organophosphorous insecticide. Recently, the Pto gene was isolated and shown to be a putative serine/threonine protein kinase. Pto is one member of a multigene family that is clustered within a 400-kb region on chromosome 5. Here, we report that another member of this gene family, termed Fen, is responsible for the sensitivity to fenthion. Fen was isolated by map-based cloning using closely linked DNA markers to identify a yeast artificial chromosome clone that spanned the Pto region. After transformation with the Fen gene under control of the cauliflower mosaic virus (CaMV) 35S promoter, tomato plants that are normally insensitive to fenthion rapidly developed extensive necrotic lesions upon exposure to fenthion. Two related insecticides, fensulfothion and fenitrothion, also elicited necrotic lesions specifically on Fen-transformed plants. Transgenic tomato plants harboring integrated copies of the Pto gene under control of the CaMV 35S promoter displayed sensitivity to fenthion but to a lesser extent than did wild-type fenthion-sensitive plants. The Fen protein shares 80% identity (87% similarity) with Pto but does not confer resistance to Pseudomonas syringae pv tomato. These results suggest that Pto and Fen participate in the same signal transduction pathway.
含有Pto细菌抗性基因座的番茄品种叶片在接触有机磷杀虫剂倍硫磷后24小时内会出现小的坏死斑。最近,Pto基因被分离出来,显示为一种假定的丝氨酸/苏氨酸蛋白激酶。Pto是一个多基因家族的成员之一,该家族聚集在5号染色体上一个400 kb的区域内。在此,我们报道这个基因家族的另一个成员,称为Fen,负责对倍硫磷的敏感性。通过基于图谱的克隆方法,利用紧密连锁的DNA标记分离出Fen基因,以鉴定跨越Pto区域的酵母人工染色体克隆。用花椰菜花叶病毒(CaMV)35S启动子控制下的Fen基因转化后,通常对倍硫磷不敏感的番茄植株在接触倍硫磷后迅速出现广泛的坏死斑。另外两种相关杀虫剂,丰索磷和杀螟硫磷,也仅在转Fen基因的植株上引发坏死斑。携带花椰菜花叶病毒35S启动子控制下的Pto基因整合拷贝的转基因番茄植株对倍硫磷表现出敏感性,但程度低于野生型对倍硫磷敏感的植株。Fen蛋白与Pto蛋白有80%的一致性(87%的相似性),但不赋予对番茄丁香假单胞菌的抗性。这些结果表明,Pto和Fen参与相同的信号转导途径。