The Legume SHR-SCR Module Predetermines Nodule Founder Cell Identity

豆科植物-根瘤菌共生固氮是可持续性农业氮肥的最重要来源。根瘤作为豆科植物共生固氮的一种特化植物侧生器官, 提供了根瘤菌生物固氮必需的微环境, 是根瘤菌的安身之本, 因此, 根瘤的正常发育是实现豆科植物-根瘤菌共生固氮的结构基础。根瘤器官的从头发生主要起始于根瘤菌诱导的根皮层细胞分裂。通常认为豆科植物的根皮层具备有别于非豆科植物根皮层的某种特异属性, 从而响应根瘤菌并与之建立固氮共生, 但长期以来该属性决定的分子机制一直不明确。近日, 中国科学院分子植物科学卓越创新中心王二涛团队以蒺藜苜蓿(Medicago truncatula)等豆科植物和拟南芥(Arabidopsis thaliana)等非豆科植物为研究对象, 发现豆科植物中保守的SHR-SCR干细胞模块决定了其皮层细胞分裂潜能从而赋予根瘤器官发生的命运。该研究揭示了豆科植物根瘤发育的全新机制, 提供了研究和理解植物-根瘤菌固氮共生进化的重要线索, 对提高豆科作物固氮效率和非豆科作物固氮工程具有重要意义。     

豆科植物共生结瘤的分子基础和调控研究进展

豆科植物与根瘤菌共生互作的结果导致了一个新的植物器官――根瘤的形成, 根瘤菌生活在根瘤中, 它们具有将氮气转化为能被植物同化的氨的能力。该文阐述了根瘤的形成过程和类型, 并主要以模式豆科植物蒺藜苜蓿(Medicago truncatula)和日本百脉根(Lotus japonicus)为例, 对近年来共生结瘤过程中宿主植物对根瘤菌结瘤因子的识别和信号传递、侵入线形成和固氮的分子基础, 以及宿主植物对根瘤形成的自主调控机制、环境中氮素营养对结瘤的影响研究进行了综述, 指出当前豆科植物与根瘤菌共生互作研究存在的问题, 并对今后的研究方向作了分析与展望。     

一氧化氮对豆科植物结瘤及固氮的影响机制

豆科植物-根瘤菌共生过程受双方基因复杂且精细的调控, 能够产生特异的根瘤结构并可将大气中的惰性氮气(N₂)转化为可被植物直接利用的氨态氮。结瘤与固氮受多种因素影响, 其中, 一氧化氮(NO)作为一种自由基反应性气体信号分子, 可参与调节植物的许多生长发育过程, 如植物的呼吸、光形态建成、种子萌发、组织和器官发育、衰老以及响应各种生物及非生物胁迫。在豆科植物中, NO不仅影响寄主与菌共生关系的建立, 还参与调控根瘤菌对氮气的固定并提高植株氮素营养利用效率。该文主要从豆科植物及共生菌内NO的产生、降解及其对结瘤、共生固氮的影响和对环境胁迫的响应, 阐述了NO调控豆科植物共生体系中根瘤形成和共生固氮过程的作用机制, 展望了NO信号分子在豆科植物共生固氮体系中的研究前景。     

豆科植物-根瘤菌共生固氮的免疫调控机制

在长期进化中,根瘤菌与豆科植物形成一种独特的互惠共生关系——共生固氮。根瘤菌-豆科植物共生互作与病原细菌激发植物病原反应极为相似,然而根瘤菌的入侵和定殖并没有激发宿主豆科植物过度的防御反应,植物也进化出特殊的共生信号转导和根瘤发育途径来"邀请"根瘤菌的入侵和定殖。此外,植物防御反应也很大程度上调控根瘤菌与豆科植物共生的宿主特异性。越来越多的研究表明,植物防御反应在调控根瘤菌匹配识别、入侵、定殖以及类菌体发育等方面起关键调控作用。从植物免疫反应角度综述了根瘤菌与豆科植物共生互作的最新进展,通过与病原菌-植物互作的病原反应对比,论述了根瘤中植物感知微生物相关分子模式(MAMP,Microbe-Associated Molecular Patterns)和效应蛋白引起的免疫反应的调控机制。     

豆科植物早期共生信号转导的研究进展

豆科植物与根瘤菌建立特异的共生关系,在寄主根部产生固氮根瘤。此过程包含了共生信号识别与传递、根瘤菌侵染、根瘤形成以及固氮功能实现等生物学事件。研究人员已经从2种豆科模式植物蒺藜苜蓿（Medicago truncatula）和百脉根（Lotus japonicus）的共生固氮体系中,筛选到许多与根瘤菌共生相关的突变体及其相对应的功能基因,建立起包含结瘤因子识别、共生信号传递和转录响应在内的早期共生信号途径。该文对豆科植物早期共生信号途径的新进展进行了综述。     

豆科植物早期共生信号转导的研究进展北大核心CSCD

豆科植物与根瘤菌建立特异的共生关系,在寄主根部产生固氮根瘤。此过程包含了共生信号识别与传递、根瘤菌侵染、根瘤形成以及固氮功能实现等生物学事件。研究人员已经从2种豆科模式植物蒺藜苜蓿(Medicago truncatula)和百脉根(Lotus japonicus)的共生固氮体系中,筛选到许多与根瘤菌共生相关的突变体及其相对应的功能基因,建立起包含结瘤因子识别、共生信号传递和转录响应在内的早期共生信号途径。该文对豆科植物早期共生信号途径的新进展进行了综述。     

关于根瘤菌类菌体有无细胞壁的探讨

根瘤菌与豆科植物共生产生固氮的特殊结构——根瘤,固氮的根瘤中既含根瘤菌又含类菌体。在共生的条件下,根瘤菌诱导根瘤的发育,自我繁殖,合成固氮酶并转化为类菌体。以前认为只有类菌体才能固氮,后经Child和     

根瘤内生细菌

在研究根瘤菌与豆科植物共生关系的过程中,人们发现根瘤中同时定居着许多与根瘤菌不同的内生菌,这些非共生细菌生活在根瘤中,但不引起植物产生明显的病害,为根瘤内生细菌.根瘤内生细菌不仅将植物作为其栖息场所,而且对宿主植物有促生、防病、内生联合固氮等广泛的生物学作用.     

硝酸盐调控豆科植物与根瘤菌共生固氮的机制研究

氮是植物生长发育所需的大量营养元素之一。硝态氮不仅可以被植物直接吸收利用,还可以作为重要的信号分子调控植物对氮素的响应、吸收、代谢相关基因的表达,从而影响植物的生长和发育。豆科植物可以通过与根瘤菌共生互作来获得生长所需的氮,但共生固氮是一个耗费植物能量的过程。当土壤中存在高浓度的氮素时,氮作为信号分子会影响共生固氮基因的功能从而抑制共生固氮过程。目前的研究表明,硝酸盐通过局部和系统的调控方式抑制共生固氮过程;结瘤自主调控(Autoregulation of nodulation,AON)和NLPs(NIN-like proteins)转录因子在硝酸盐抑制豆科植物根瘤形成中有着重要的作用。本文结合最近的研究进展,重点讨论NLPs转录因子和AON途径在硝酸盐抑制共生固氮过程的作用。     

豆科植物根瘤内生细菌的发现及其研究进展

近年来研究报道显示,某些豆科植物与根瘤菌在形成固氮共生体的同时,其根瘤内还存在多种其他类群的内生细菌,该现象在根瘤菌研究领域越来越引起关注和重视。本文综述了根瘤内生土壤杆菌、非共生根瘤菌、其它细菌的发现、种类及其对共生关系和植物生长的影响等研究进展,同时对该研究方向提出一些初步观点和认识,旨在增加人们对根瘤微生态的了解,拓展根瘤菌研究与应用的视野。     

Down-regulation of SymRK correlates with a deficiency in vascular bundle development in Phaseolus vulgaris nodules

The symbiotic interaction of legumes and rhizobia results in the formation of nitrogen-fixing nodules. Nodulation depends on the finely coordinated expression of a battery of genes involved in the infection and the organogenesis processes. After Nod factor perception, symbiosis receptor kinase (SymRK) receptor triggers a signal transduction cascade essential for nodulation leading to cortical cell divisions, infection thread (IT) formation and final release of rhizobia to the intracellular space, forming the symbiosome. Herein, the participation of SymRK receptor during the nodule organogenesis in Phaseolus vulgaris is addressed. Our findings indicate that besides its expression in the nodule epidermis, in IT, and in uninfected cells of the infection zone, PvSymRK immunolocalizes in the root and nodule vascular system. On the other hand, knockdown expression of PvSymRK led to the formation of scarce and defective nodules, which presented alterations in both IT/symbiosome formation and vascular system.     

Never too many? How legumes control nodule numbers

Restricted availability of nitrogen compounds in soils is often a major limiting factor for plant growth and productivity. Legumes circumvent this problem by establishing a symbiosis with soil-borne bacteria, called rhizobia that fix nitrogen for the plant. Nitrogen fixation and nutrient exchange take place in specialized root organs, the nodules, which are formed by a coordinated and controlled process that combines bacterial infection and organ formation. Because nodule formation and nitrogen fixation are energy-consuming processes, legumes develop the minimal number of nodules required to ensure optimal growth. To this end, several mechanisms have evolved that adapt nodule formation and nitrogen fixation to the plant's needs and environmental conditions, such as nitrate availability in the soil. In this review, we give an updated view on the mechanisms that control nodulation.     

Epidermal and cortical roles of NFP and DMI3 in coordinating early steps of nodulation in Medicago truncatula

Legumes have evolved the capacity to form a root nodule symbiosis with soil bacteria called rhizobia. The establishment of this symbiosis involves specific developmental events occurring both in the root epidermis (notably bacterial entry) and at a distance in the underlying root cortical cells (notably cell divisions leading to nodule organogenesis). The processes of bacterial entry and nodule organogenesis are tightly linked and both depend on rhizobial production of lipo-chitooligosaccharide molecules called Nod factors. However, how these events are coordinated remains poorly understood. Here, we have addressed the roles of two key symbiotic genes of Medicago truncatula, the lysin motif (LysM) domain-receptor like kinase gene NFP and the calcium- and calmodulin-dependent protein kinase gene DMI3, in the control of both nodule organogenesis and bacterial entry. By complementing mutant plants with corresponding genes expressed either in the epidermis or in the cortex, we have shown that epidermal DMI3, but not NFP, is sufficient for infection thread formation in root hairs. Epidermal NFP is sufficient to induce cortical cell divisions leading to nodule primordia formation, whereas DMI3 is required in both cell layers for these processes. Our results therefore suggest that a signal, produced in the epidermis under the control of NFP and DMI3, is responsible for activating DMI3 in the cortex to trigger nodule organogenesis. We integrate these data to propose a new model for epidermal/cortical crosstalk during early steps of nodulation.     

Regulation of legume nodulation by acidic growth conditions

Legumes represent some of the most important crop species worldwide. They are able to form novel root organs known as nodules, within which biological nitrogen fixation is facilitated through a symbiotic interaction with soil-dwelling bacteria called rhizobia. This provides legumes with a distinct advantage over other plant species, as nitrogen is a key factor for growth and development. Nodule formation is tightly regulated by the plant and can be inhibited by a number of external factors, such as soil pH. This is of significant agricultural and economic importance as much of global legume crops are grown on low pH soils. Despite this, the precise mechanism by which low pH conditions inhibits nodule development remains poorly characterized.     

Symbiosis specificity in the legume: rhizobial mutualism

Legume plants are able to engage in root nodule symbiosis with nitrogen-fixing soil bacteria, collectively called rhizobia. This mutualistic association is highly specific, such that each rhizobial species/strain interacts with only a specific group of legumes, and vice versa. Symbiosis specificity can occur at multiple phases of the interaction, ranging from initial bacterial attachment and infection to late nodule development associated with nitrogen fixation. Genetic control of symbiosis specificity is complex, involving fine-tuned signal communication between the symbiotic partners. Here we review our current understanding of the mechanisms used by the host and bacteria to choose their symbiotic partners, with a special focus on the role that the host immunity plays in controlling the specificity of the legume - rhizobial symbiosis.     

Are common symbiosis genes required for endophytic rice-rhizobial interactions?

Legume plants are able to establish root nodule symbioses with nitrogen-fixing bacteria, called rhizobia. Recent studies revealed that the root nodule symbiosis has co-opted the signaling pathway that mediates the ancestral mycorrhizal symbiosis that occurs in most land plants. Despite being unable to induce nodulation, rhizobia have been shown to be able to infect and colonize the roots of non-legumes such as rice. One fascinating question is whether establishment of such associations requires the common symbiosis (Sym) genes that are essential for infection of plant cells by mycorrhizal fungi and rhizobia in legumes. Here, we demonstrated that the common Sym genes are not required for endophytic colonization of rice roots by nitrogen-fixing rhizobia.     

Partner choice in Medicago Truncatula–Sinorhizobium symbiosis

In nitrogen-fixing symbiosis, plant sanctions against ineffective bacteria have been demonstrated in previous studies performed on soybean and yellow bush lupin, both developing determinate nodules with Bradyrhizobium sp. strains. In this study, we focused on the widely studied symbiotic association Medicago truncatula–Sinorhizobium meliloti, which forms indeterminate nodules. Using two strains isolated from the same soil and displaying different nitrogen fixation phenotypes on the same fixed plant line, we analysed the existence of both partner choice and plant sanctions by performing split-root experiments. By measuring different parameters such as the nodule number, the nodule biomass per nodule and the number of viable rhizobia per nodule, we showed that M. truncatula is able to select rhizobia based on recognition signals, both before and after the nitrogen fixation step. However, no sanction mechanism, described as a decrease in rhizobia fitness inside the nodules, was detected. Consequently, even if partner choice seems to be widespread among legumes, sanction of non-effective rhizobia might not be universal.