Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA/CSIC), Campus de Montegancedo UPM, Pozuelo de Alarcón (Madrid), Spain; Departamento de Biotecnología-Biología Vegetal, Escuela Técnica Superior de Ingeniería Agronómica, Alimentaría y de Biosistemas, UPM, Madrid, Spain.
Centro de Biotecnología y Genómica de Plantas, Universidad Politécnica de Madrid (UPM) - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA/CSIC), Campus de Montegancedo UPM, Pozuelo de Alarcón (Madrid), Spain; Departamento de Biotecnología-Biología Vegetal, Escuela Técnica Superior de Ingeniería Agronómica, Alimentaría y de Biosistemas, UPM, Madrid, Spain.
Mol Plant. 2024 May 6;17(5):699-724. doi: 10.1016/j.molp.2024.04.003. Epub 2024 Apr 9.
Beyond their function as structural barriers, plant cell walls are essential elements for the adaptation of plants to environmental conditions. Cell walls are dynamic structures whose composition and integrity can be altered in response to environmental challenges and developmental cues. These wall changes are perceived by plant sensors/receptors to trigger adaptative responses during development and upon stress perception. Plant cell wall damage caused by pathogen infection, wounding, or other stresses leads to the release of wall molecules, such as carbohydrates (glycans), that function as damage-associated molecular patterns (DAMPs). DAMPs are perceived by the extracellular ectodomains (ECDs) of pattern recognition receptors (PRRs) to activate pattern-triggered immunity (PTI) and disease resistance. Similarly, glycans released from the walls and extracellular layers of microorganisms interacting with plants are recognized as microbe-associated molecular patterns (MAMPs) by specific ECD-PRRs triggering PTI responses. The number of oligosaccharides DAMPs/MAMPs identified that are perceived by plants has increased in recent years. However, the structural mechanisms underlying glycan recognition by plant PRRs remain limited. Currently, this knowledge is mainly focused on receptors of the LysM-PRR family, which are involved in the perception of various molecules, such as chitooligosaccharides from fungi and lipo-chitooligosaccharides (i.e., Nod/MYC factors from bacteria and mycorrhiza, respectively) that trigger differential physiological responses. Nevertheless, additional families of plant PRRs have recently been implicated in oligosaccharide/polysaccharide recognition. These include receptor kinases (RKs) with leucine-rich repeat and Malectin domains in their ECDs (LRR-MAL RKs), Catharanthus roseus RECEPTOR-LIKE KINASE 1-LIKE group (CrRLK1L) with Malectin-like domains in their ECDs, as well as wall-associated kinases, lectin-RKs, and LRR-extensins. The characterization of structural basis of glycans recognition by these new plant receptors will shed light on their similarities with those of mammalians involved in glycan perception. The gained knowledge holds the potential to facilitate the development of sustainable, glycan-based crop protection solutions.
除了作为结构屏障的功能外,植物细胞壁还是植物适应环境条件的重要元素。细胞壁是动态结构,其组成和完整性可以响应环境挑战和发育线索而改变。这些细胞壁变化被植物传感器/受体感知,以在发育过程中以及在感知压力时触发适应性反应。由病原体感染、创伤或其他应激引起的植物细胞壁损伤会导致细胞壁分子(如碳水化合物(聚糖))的释放,这些分子作为损伤相关分子模式(DAMPs)发挥作用。DAMPs 被模式识别受体(PRRs)的细胞外结构域(ECDs)感知,以激活模式触发的免疫(PTI)和抗病性。同样,与植物相互作用的微生物细胞壁和细胞外层释放的聚糖被特定的 ECD-PRR 识别为微生物相关分子模式(MAMPs),触发 PTI 反应。近年来,被植物识别的 DAMP/MAMP 寡聚糖数量有所增加。然而,植物 PRRs 识别聚糖的结构机制仍然有限。目前,这方面的知识主要集中在 LysM-PRR 家族的受体上,该受体参与了对各种分子的感知,如真菌来源的壳寡糖和脂寡糖(即细菌和菌根的 Nod/MYC 因子),分别触发不同的生理反应。然而,最近其他植物 PRR 家族也被牵连到寡聚糖/多糖的识别中。这些包括其 ECD 中具有亮氨酸丰富重复和 Malectin 结构域的受体激酶(RKs)(LRR-MAL RKs)、其 ECD 中具有 Malectin 样结构域的长春花受体样激酶 1 样组(CrRLK1L),以及壁相关激酶、凝集素-RKs 和 LRR-伸展蛋白。这些新的植物受体识别聚糖的结构基础的表征将揭示它们与参与聚糖感知的哺乳动物受体的相似性。获得的知识有可能促进基于聚糖的可持续作物保护解决方案的发展。