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在拟南芥中,植物与病原体的不亲和互作会诱导脯氨酸积累和AtP5CS2基因激活。

Proline accumulation and AtP5CS2 gene activation are induced by plant-pathogen incompatible interactions in Arabidopsis.

作者信息

Fabro Georgina, Kovács Izabella, Pavet Valeria, Szabados László, Alvarez María E

机构信息

CIQUIBIC-CONICET, Departamento de Química Biológica, Facultad de Ciencias Químicas Universidad Nacional de Córdoba, 5000 Córdoba, Argentina.

出版信息

Mol Plant Microbe Interact. 2004 Apr;17(4):343-50. doi: 10.1094/MPMI.2004.17.4.343.

Abstract

Accumulation of free L-proline (Pro) is a typical stress response incited by osmotic injuries in plants and microorganisms. Although the protective role of Pro in osmotic stress is not well understood, it is thought to function as compatible osmolyte or as a scavenger of reactive oxygen species (ROS). Here we show that, in Arabidopsis thaliana, Pro biosynthesis can be activated by incompatible plant-pathogen interactions triggering a hypersensitive response (HR). Pro accumulates in leaf tissues treated with Pseudomonas syringae pv. tomato avirulent strains (avrRpt2 and avrRpm1) but remains unchanged in leaves infected with isogenic virulent bacteria. Incompatible interactions lead to transcriptional activation of AtP5CS2, but not AtP5CS1, encoding the rate limiting enzyme in Pro biosynthesis pyrroline-5-carboxylate synthase (P5CS). AtP5CS2:GUS and AtP5CS2:LUC transgenes were induced inside and around the HR lesions produced by avirulent Pseudomonas spp. in transgenic plants. Pro accumulation was faster and stronger when stimulated by avrRpm1 than by avrRpt2, and was compromised in the low-salicylic acid plants NahG and eds5 when signaled through the RPS2-dependent pathway. In addition, Pro content and AtP5CS2 expression were enhanced by ROS in wild-type plants, suggesting that ROS may function as an intermediate signal in AtP5CS2-mediated Pro accumulation.

摘要

游离L-脯氨酸(Pro)的积累是植物和微生物中由渗透损伤引发的典型应激反应。尽管Pro在渗透胁迫中的保护作用尚未完全明确,但人们认为它作为相容性渗透剂或活性氧(ROS)清除剂发挥作用。在此我们表明,在拟南芥中,Pro生物合成可由引发超敏反应(HR)的不亲和植物-病原体相互作用激活。Pro在经丁香假单胞菌番茄致病变种无毒菌株(avrRpt2和avrRpm1)处理的叶片组织中积累,但在感染同基因致病细菌的叶片中保持不变。不亲和相互作用导致AtP5CS2而非AtP5CS1转录激活,AtP5CS2编码Pro生物合成中的限速酶吡咯啉-5-羧酸合成酶(P5CS)。在转基因植物中,由无毒假单胞菌属产生的HR损伤内部及周围,AtP5CS2:GUS和AtP5CS2:LUC转基因被诱导。avrRpm1刺激时Pro的积累比avrRpt2更快更强,并且当通过RPS2依赖途径发出信号时,在低水杨酸植物NahG和eds5中Pro积累受损。此外,野生型植物中ROS增强了Pro含量和AtP5CS2表达,表明ROS可能作为AtP5CS2介导的Pro积累中的中间信号发挥作用。

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