Beyond osmolytes and transcription factors: drought tolerance in plants <Emphasis Type="Italic">via</Emphasis> protective proteins and aquaporins

Mechanisms of drought tolerance have been studied by numerous groups, and a broad range of molecules have been identified to play important roles. A noteworthy response of stressed plants is the accumulation of novel protective proteins, including heat-shock proteins (HSPs) and late embryogenesis abundant (LEA) proteins. Identification of gene regulatory networks of these protective proteins in plants will allow a wide application of biotechnology for enhancement of drought tolerance and adaptation. Similarly, aquaporins are involved in the regulation of water transport, particularly under abiotic stresses. The molecular and functional characterization of protective proteins and aquaporins has revealed the significance of their regulation in response to abiotic stresses. Herein, we highlight new findings regarding the action mechanisms of these proteins. Finally, this review also surveys the current advances in engineering drought tolerant plants, particularly the engineering of protective proteins (sHSPs and LEA) and aquaporins for imparting drought stress tolerance in plants.     

Plant Responses to Drought,Acclimation, and Stress Tolerance

At the whole plant level, the effect of stress is usually perceived as a decrease in photosynthesis and growth. That is why this review is focused mainly on the effect of drought on photosynthesis, its injury, and mechanisms of adaptation. The analysed literature shows that plants have evolved a number of adaptive mechanisms that allow the photochemical and biochemical systems to cope with negative changes in environment, including increased water deficit. In addition, the acquisition of tolerance to drought includes both phenotypic and genotypic changes. The approaches were made to identify those metabolic steps that are most sensitive to drought. Some studies also examined the mechanisms controlling gene expression and putative regulatory pathways.     

Physiological responses of the legume model Medicago truncatula cv. Jemalong to water deficit

In Medicago truncatula Gaertn. cv. Jemalong plants some mechanisms involved in drought resistance were analysed in response to a progressive water deficit imposed by suppression of soil irrigation. Withholding water supply until the soil had reached one-half of its maximum water content had no significant effect on leaf RWC, gas exchanges or chlorophyll fluorescence parameters. Under severe drought conditions, the plants resistance to water shortage involved mainly drought avoidance mechanisms through a decrease in stomatal conductance. The consequent decrease in the internal CO₂ concentration (C_i) should have limited the net CO₂ fixation (A). Since A decreased slightly more than C_i under severe water deficit, non-stomatal limitations of photosynthesis may have also occurred. Analysis of A/C_i curves showed reduced carboxylation efficiency due to limitations in RuBP regeneration and Rubisco activity, confirming the presence of non-stomatal limitations of photosynthesis. Drought tolerance mechanisms involving osmotic adjustment and an increase in cell membrane integrity were also present. Altogether, these mechanisms allowed M. truncatula cv. Jemalong plants to still maintain a quite elevated level of net CO₂ fixation rate under severe water deficit conditions. These results may contribute to identify useful physiological traits for breeding programs concerning drought adaptation in legumes.     

Proteins and Metabolites Regulated by Trinexapac-ethyl in Relation to Drought Tolerance in Kentucky Bluegrass

Plants have developed various mechanisms in adaptation to water deficit stress, including growth retardant to reduce water loss. Previous studies reported that plants treated with a growth inhibitor, trinexapac-ethyl (TE), had improved drought tolerance. The objective of this study was to determine alterations in proteins and metabolite accumulation associated with drought tolerance improvement in a perennial grass species, Kentucky bluegrass (Poa pratensis), induced by TE application. Plants were treated with TE [1.95 ml l⁻¹ (v:v); a.i. TE = 0.113%] through foliar spray for 14 days, and then subjected to drought stress by withholding irrigation for 15 days in growth chambers. TE-treated plants exhibited significantly higher relative water content and photosynthetic capacity and lower membrane leakage than nontreated plants under drought stress, suggesting TE-enhanced drought tolerance in Kentucky bluegrass. Physiological improvement in drought tolerance through TE application was associated with the increased accumulation of various proteins and metabolites, including ferritin, catalase, glutathione-S-transferase, Rubisco, heat shock protein 70, and chaperonin 81, as well as fatty acids (palmitic acid, α-linolenic acid, linoleic acid, and octadecanoic acid). Our results suggest that TE may regulate metabolic processes for antioxidant defense, protective protein synthesis, photorespiration, and fatty acid synthesis, and thereby contribute to better drought tolerance in Kentucky bluegrass.     

Enhancing drought tolerance in C(4) crops

Adaptation to abiotic stresses is a quantitative trait controlled by many different genes. Enhancing the tolerance of crop plants to abiotic stresses such as drought has therefore proved to be somewhat elusive in terms of plant breeding. While many C(4) species have significant agronomic importance, most of the research effort on improving drought tolerance has focused on maize. Ideally, drought tolerance has to be achieved without penalties in yield potential. Possibilities for success in this regard are highlighted by studies on maize hybrids performed over the last 70 years that have demonstrated that yield potential and enhanced stress tolerance are associated traits. However, while our understanding of the molecular mechanisms that enable plants to tolerate drought has increased considerably in recent years, there have been relatively few applications of DNA marker technologies in practical C(4) breeding programmes for improved stress tolerance. Moreover, until recently, targeted approaches to drought tolerance have concentrated largely on shoot parameters, particularly those associated with photosynthesis and stay green phenotypes, rather than on root traits such as soil moisture capture for transpiration, root architecture, and improvement of effective use of water. These root traits are now increasingly considered as important targets for yield improvement in C(4) plants under drought stress. Similarly, the molecular mechanisms underpinning heterosis have considerable potential for exploitation in enhancing drought stress tolerance. While current evidence points to the crucial importance of root traits in drought tolerance in C(4) plants, shoot traits may also be important in maintaining high yields during drought.     

Programmed proteome response for drought avoidance/tolerance in the root of a C(3) xerophyte (wild watermelon) under water deficits

Water availability is a critical determinant for the growth and ecological distribution of terrestrial plants. Although some xerophytes are unique regarding their highly developed root architecture and the successful adaptation to arid environments, virtually nothing is known about the molecular mechanisms underlying this adaptation. Here, we report physiological and molecular responses of wild watermelon (Citrullus lanatus sp.), which exhibits extraordinarily high drought resistance. At the early stage of drought stress, root development of wild watermelon was significantly enhanced compared with that of the irrigated plants, indicating the activation of a drought avoidance mechanism for absorbing water from deep soil layers. Consistent with this observation, comparative proteome analysis revealed that many proteins induced in the early stage of drought stress are involved in root morphogenesis and carbon/nitrogen metabolism, which may contribute to the drought avoidance via the enhancement of root growth. On the other hand, lignin synthesis-related proteins and molecular chaperones, which may function in the enhancement of physical desiccation tolerance and maintenance of protein integrity, respectively, were induced mostly at the later stage of drought stress. Our findings suggest that this xerophyte switches survival strategies from drought avoidance to drought tolerance during the progression of drought stress, by regulating its root proteome in a temporally programmed manner. This study provides new insights into the complex molecular networks within plant roots involved in the adaptation to adverse environments.     

木本植物应对干旱胁迫的响应机制：基于水力学性状视角

干旱最显著的影响表现在区域尺度的森林死亡事件中,可以在短时间内杀死数百万棵树木。鉴于未来极端干旱事件的频率和强度可能随温度的升高而增加,迫切需要明确树木对干旱胁迫的响应对策以及衰退死亡机理,揭示木本植物在干旱环境中存活和死亡的生理机制,了解树木在未来气候下的适应机制,提高预测树木对干旱反应的准确性。在常用植物功能性状的基础上,重点纳入与植物水分运输能力及耐旱性相关的水力学性状,系统总结了:1)植物木质部水分运输的物理机制;2)植物应对干旱胁迫的水力响应过程:3)干旱胁迫下木本植物水分利用对策;以及4)干旱胁迫下木本植物衰退/死亡机理。最后,提出3个尚待解决的主要问题:1)加强纳入水力性状阐明植物对干旱胁迫的响应和调节机制;2)加强从全株植物的角度考虑植物不同组织性状间的关系;3)深入探究树木干旱致死机理。     

A unified framework of plant adaptive strategies to drought: Crossing scales and disciplines

Plant adaptation to drought has been extensively studied at many scales from ecology to molecular biology across a large range of model species. However, the conceptual frameworks underpinning the definition of plant strategies, and the terminology used across the different disciplines and scales are not analogous. ‘Drought resistance’ for instance refers to plant responses as different as the maintenance of growth and productivity in crops, to the survival and recovery in perennial woody or grassland species. Therefore, this paper aims to propose a unified conceptual framework of plant adaptive strategies to drought based on a revised terminology in order to enhance comparative studies. Ecological strategies encapsulate plant adaptation to multidimensional variation in resource variability but cannot account for the dynamic and short‐term responses to fluctuations in water availability. Conversely, several plant physiological strategies have been identified along the mono‐dimensional gradient of water availability in a given environment. According to a revised terminology, dehydration escape, dehydration avoidance, dehydration tolerance, dormancy, and desiccation tolerance are clearly distinguishable. Their sequential expression is expressed as water deficit increases while cavitation tolerance is proposed here to be a major hydraulic strategy underpinning adaptive responses to drought of vascular plants. This continuum of physiological strategies can be interpreted in the context of the ecological trade‐off between water‐acquisition vs. water‐conservation, since growth maintenance is associated with fast water use under moderate drought while plant survival after growth cessation is associated with slow water use under severe drought. Consequently, the distinction between ‘drought resistance’ and ‘drought survival’, is emphasized as crucial to ensure a correct interpretation of plant strategies since ‘knowing when not to grow’ does not confer ‘drought resistance’ but may well enhance ‘drought survival’. This framework proposal should improve cross‐fertilization between disciplines to help tackle the increasing worldwide challenges that drought poses to plant adaptation.     

When is breeding for drought tolerance optimal if drought is random?

* Increasing climatic unpredictability associated with characteristics of some species makes plant drought-tolerance an important drought-adaptation strategy. Using norm-of-reaction functions, or empirically determined functions that enable us to predict the state of a trait given the state of an environmental variable, allows modelling of plant performance when water availability varies randomly. * A mathematical model is proposed to evaluate drought-tolerance and growth strategies given a set of environmental parameters: the frequency of rainy days, the soil water-storage capacity, plant water use and plant growth rates. This model compares the performance of genotypes that differ in drought tolerance expressed as the ability to grow in drier soils, and assumes a general trade-off function between drought tolerance and maximum plant growth rate. * It is worth selecting plants with a greater degree of drought tolerance, expressed by the ability to grow in drier soils whenever the frequency of rains is smaller than the rate of soil water depletion. Otherwise, maximizing growth rate at the expense of drought tolerance is the best strategy. The nature of the trade-off between drought tolerance and plant growth rate also constrains the selection for optimal drought-adapted genotypes. * Breeders will have to consider these aspects of plant-environment interactions before establishing selection programs for drought adaptation.     

Prospects for utilising plant-adaptive mechanisms to improve wheat and other crops in drought- and salinity-prone environments

Breeding for adaptation to abiotic stress is extremely challenging due to the complexity of the target environments as well as that of the stress‐adaptive mechanisms adopted by plants. While many traits have been reported in the literature, these must be considered with respect to the type of environment for which a cultivar is targeted. In theory, stress‐adaptive traits can be divided into groups whose genes and/or physiological effects are likely to be relatively independent such that when parents with contrasting traits are crossed, adaptive genes will be pyramided. Currently the following groups of candidate traits are being considered for drought adaptation in wheat: traits relating to: (i) pre‐anthesis growth, (ii) water extraction, (iii) water use efficiency, (iv) photo‐protection. A number of mechanisms relating to root function have potential to ameliorate drought stress. Hydraulic redistribution (HR) of water by roots of dryland shrubs enables even relatively small amounts of rainwater to be moved down into the soil profile actively by the root system before it evaporates from the soil surface. Another example is the symbiotic relationship of plants with mycorrhizal fungi that produce a glycoprotein that has a positive effect on soil structure and moisture characteristics. From an agronomic point of view, crop water use efficiency can be increased by exploiting the stress‐adaptive mechanism whereby leaves reduce transpiration rate in response to a chemical root signal in response to drying soil. While there is limited genetic diversity for adaptation to salinity in wheat, tolerance has been found in the ancestral genomes of polyploid wheat and their relatives associated with sodium exclusion into the xylem. Wide crossing techniques such as production of synthetic hexaploids are being exploited to tap into this source of genetic diversity. Looking further into the future, progress is being made into understanding the regulatory mechanisms that are expressed under abiotic stress to maintain cellular homeostasis, as well as in the ability to genetically transform crop plants with genes from alien species.     

Role of AP2/EREBP transcription factors in gene regulation during abiotic stress.

Crop plants are exposed to many types of abiotic stress during their life cycle. Water deficit derived from drought, low temperature or high salt concentration in the soil, is one of the most common environmental stresses that affects growth and development of plants through alterations in metabolism and gene expression. Adaptation to these conditions may involve passive tolerance or active homeostatic mechanisms for maintaining water balance. Active responses occur at different levels in the plant and may represent a concomitant protection against other types of stress such as pathogen attack. Many morphological and physiological adaptations to water stress are under the control of the plant hormone abscisic acid and involve specific activation of target genes that in one way or another protect cells against water deficit or participate in the regulation of the drought response. Here, we discuss recent advances in our understanding of drought adaptation mediated by specific changes in gene expression and the role of AP2/EREBP nuclear factors in these processes.     

Interaction between PGPR and PGR for water conservation and plant growth attributes under drought condition

Drought is one of the key restraints to agricultural productivity worldwide and is expected to increase further. Drought stress accompanied by reduction in precipitation pose major challenges to future food safety. Strategies should be develop to enhance drought tolerance in crops like chickpea and wheat, in order to enhance their growth and yield. Drought tolerance strategies are costly and time consuming however, recent studies specify that plant growth promoting rhizobacteria (PGPR) and plant growth regulators (PGRs) can help plants to withstand under harsh environmental condition and enable plants to cope with drought stress. PGPR can act as biofertilizer and bioenhancer for different legumes and non-legumes. The use of PGPR and symbiotic microorganisms, may be valuable in developing strategies to assist water conservation in plants. The use of PGPR has been confirmed to be an ecologically sound way of enhancing crop yields by facilitating plant growth through direct or indirect mechanism. The mechanisms of PGPR for water conservation include secretion of exopolysaccharides, biofilm formation, alternation in phytohormone content, improvement in sugar concentration, enhancing availability of micro- and macronutrients and changes in plant functional traits. Similarly, plant growth regulators (PGRs) are specially noticed in actively growing tissues under stress conditions and have been associated in the control of cell division, embryogenesis, root formation, fruit development and ripening, and reactions to biotic and abiotic stresses and upholding water conservation status in plants. Previous studies also suggest that plant metabolites interact with plant physiology under stress condition and impart drought tolerance. Metabolites like, sugars, amino acids, organic acid and polyols play a key role in drought tolerance of crop plants grown under stress condition. It is concluded from the present study that PGRs in combination with PGPR consortium can be an effective formulation to promote plant growth and maintenance of plant turgidity under drought stress. This review is a compilation of the effect of drought stress on crop plants and described interactions between PGPR/PGRs and plant development, knowledge of water conservation and stress release strategies of PGPR and PGRs and the role of plant metabolites in drought tolerance of crop plants. This review also bridges the gaps that summarizes the mechanism of action of PGPR for drought tolerance of crop plants and sustainability of agriculture and applicability of these beneficial rhizobacteria in different agro-ecosystems under drought stress.     

内生真菌对植物抗旱性的影响

内生真菌广泛地存在于植物体内,它们在植物体内的生活不会对植物引起任何感病症状,而且内生真菌侵染对植物生长、生物和非生物胁迫抗性很好的促进作用,理解内生真菌在提高植物干旱胁迫耐受性方面的作用和机理对其在缓解植物干旱胁迫中的应用有重要意义。这篇综述介绍了植物内生真菌的多样性、对植物抗旱性的影响及其作用机理等方面的研究进展。内生真菌对植物抗旱性提高的机理包括:干旱耐受、干旱回避和干旱恢复。文中还对以后的研究进行了展望。     

植物应对干旱胁迫的阶段性策略

干旱是影响植物生存、生长和分布的最重要的非生物胁迫之一,全球暖干化将加剧干旱胁迫.植物对干旱胁迫的响应和适应机制一直是
学术研究的热点领域.本文综述了植物应对干旱胁迫的生长和生理响应,在已有的研究结果基础上,提出了植物应对干旱胁迫的阶段性响应策略.从干旱开始到干旱致死,植物经历了干旱开始-轻度干旱-中度干旱-严重干旱-极端干旱5个阶段,分别对应着应激响应-主动适应-被动适应3种响应方式和适应机制.不同阶段中植物抗旱机制的核心任务不同.最后提出了研究植物阶段性响应策略需要解决的关键科学问题及研究方向.     

植物水通道蛋白的干旱应答机制研究进展

干旱胁迫是严重影响全球作物生产的非生物胁迫之一,研究植物耐旱机制已成为一个重要领域。水通道蛋白是一类特异、高效转运水及其它小分子底物的膜通道蛋白,在植物中具有丰富的亚型,参与调节植物的水分吸收和运输。近10年来,水通道蛋白在植物不同生理过程中的作用,一直受到研究人员的关注,特别是在非生物胁迫方面,而研究表明水通道蛋白在干旱胁迫下对植物的耐旱性起着至关重要的作用,能维持细胞水分稳态和调控环境胁迫快速响应。水通道蛋白在植物耐旱过程中的调控机制及功能较复杂,而关于其应答机制和不同亚型功能性研究的报道甚少。该文综述了植物水通道蛋白的分类、结构、表达调控和活性调节,分别从植物水通道蛋白响应干旱表达调控机制、水通道蛋白基因表达的时空特异性、水通道蛋白基因的表达与蛋白丰度,水通道蛋白基因的耐旱转化四个方面阐明干旱胁迫下植物水通道蛋白的表达,重点阐述其参与植物干旱胁迫应答的作用机制,并提出水通道蛋白研究的主要方向。     

两个油菜种对水分胁迫的适应方式

本文报道了2个油菜种对水分胁迫的适应方式。研究表明:芥菜型油菜对水分胁迫的适应性强于甘蓝型。其主要原因是由于形态方面的抗旱性,包括发育良好的根系,较厚的蜡质关闭了气孔。同时芥菜型油菜能将其余部分的水分调用到生长区而免遭旱害。甘蓝型油菜叶水势下降快,在相同水势下其相对电导值低于芥菜型。同时还观察了2个种在干旱条件下叶绿体与其基粒的变化。总之,芥菜型具典型的高水势耐旱特性,而甘蓝型具低水势耐旱特性。     

岩溶木本植物对干旱的生理生态适应

受全球气候变暖和季风气候影响,西南岩溶区年降水量及其在季节间的分配发生明显变化,无雨期频率和持续时间增加,且基岩风化严重,基质储水能力差,致使岩溶木本植物面临的季节性和地质性干旱加剧。该文通过参考相关文献分析结构性状和生理调节探讨岩溶木本植物如何适应地质性和季节性干旱。结果表明岩溶木本植物应对干旱的策略与其他干旱、半干旱区的植物大体一致,主要有抗旱和避旱两种策略:抗旱性植物一般具有比叶面积小、叶肉多汁、储水组织发达、细胞液浓度高等适应干旱的特征,可通过增加木材密度、增强木质部导管的抗栓塞性和提高水分利用效率以适应干旱; 避旱植物则可通过小而密的气孔和叶脉、发达的表皮毛、栅栏组织和维管束鞘等结构特征减少水分丧失,并可通过落叶、深根吸收深层水源和脱落酸(ABA)介导提早关闭气孔以适应干旱。虽然关于岩溶植物形态结构和生理调节对干旱适应机制的研究取得了一定进展,但仍然存在一些亟待解决的问题,例如:深入研究岩溶地区基岩水分状况及其对植物的贡献; 加强岩溶木本植物根系结构和生物量分配、树木构型及根际微生物与木本植物干旱适应的协同关系研究; 同时探索如何将岩溶植物生态适应研究成果应用于生产实践中,科学指导石漠化治理与生态修复。     

二氧化硫增强拟南芥植株对干旱的适应性

以模式植物拟南芥为材料,研究SO_2对植物干旱适应性的影响。采用分光光度法检测植物干旱生理指标的变化,并用半定量RT-PCR技术分析了拟南芥热激基因和干旱响应基因的转录水平。研究发现:4周龄拟南芥植株暴露于30mg/m3的SO_2后,6—72h间叶面气孔开度显著低于对照并逐渐减小,在暴露48h和72h时,热激转录因子HsfA2和热激基因Hsp17.7、Hsp17.6B、Hsp17.6C转录上调,干旱响应基因DREB2A、DREB2B和RD29A表达增强;在SO_2熏气72h后进行干旱胁迫,干旱期间SO_2预暴露植株的叶片相对含水量高于非熏气干旱处理组,植株萎蔫程度比后者明显减轻,且SO_2预暴露植株的地上组织中可溶性糖和脯氨酸含量升高,超氧化物歧化酶活性提高,丙二醛含量降低。结果表明:SO_2能降低气孔开度、提高抗氧化能力、上调热激基因和干旱响应基因转录,并能促进干旱期间植物细胞内渗透调节物质的合成和积累,促使抗氧化酶活性提高,从而降低干旱胁迫对植株造成的氧化损伤,增强拟南芥对干旱的适应性。植物通过基因转录应答、酶活性改变、渗透调节物质积累等,在适应环境高浓度SO_2的同时,提高了对干旱的适应性。     

拟南芥干旱相关突变体的远红外筛选及基因克隆

干旱胁迫是影响植物生长发育的主要限制因素之一。到目前为止, 许多研究都仅关注于植物对干旱反应的信号转导网络, 而对其中一些很重要的中间成分却知之甚少。保卫细胞定位于植物叶片的表皮中, 控制二氧化碳的吸收以及水分的散失, 已经成为一种高度特化的细胞体系, 可用来研究植物早期干旱信号转导机制。控制气孔的开度在提高植物的抗旱性方面具有重要意义。通过使用远红外热成像仪检测植物叶片表面温度的微小差异, 我们成功地筛选并获得了拟南芥(Arabidopsis thaliana)干旱敏感突变体doi1。在干旱胁迫条件下, 该突变体表现为叶面温度低于野生型, 且失水率比野生型高。利用TAIL-PCR技术成功克隆到该突变体基因NCED3, 并利用RT-PCR方法验证了TAIL-PCR结果的可靠性。