Ian C. Dodd

Hormonal changes in relation to biomass partitioning and shoot growth impairment in salinized tomato (Solanum lycopersicum L.) plants

Following exposure to salinity, the root/shoot ratio is increased (an important adaptive response) due to the rapid inhibition of shoot growth (which limits plant productivity) while root growth is maintained. Both processes may be regulated by changes in plant hormone concentrations. Tomato plants (Solanum lycopersicum L. cv Moneymaker) were cultivated hydroponically for 3 weeks under high salinity (100 mM NaCl) and five major plant hormones (abscisic acid, ABA; the cytokinins zeatin, Z, and zeatin-riboside, ZR; the auxin indole-3-acetic acid, IAA; and the ethylene precursor 1-aminocyclopropane-1-carboxylic acid, ACC) were determined weekly in roots, xylem sap, and leaves. Salinity reduced shoot biomass by 50–60% and photosynthetic area by 20–25% both by decreasing leaf expansion and delaying leaf appearance, while root growth was less affected, thus increasing the root/shoot ratio. ABA and ACC concentrations strongly increased in roots, xylem sap, and leaves after 1 d (ABA) and 15 d (ACC) of salinization. By contrast, cytokinins and IAA were differentially affected in roots and shoots. Salinity dramatically decreased the Z+ZR content of the plant, and induced the conversion of ZR into Z, especially in the roots, which accounted for the relative increase of cytokinins in the roots compared to the leaf. IAA concentration was also strongly decreased in the leaves while it accumulated in the roots. Decreased cytokinin content and its transport from the root to the shoot were probably induced by the basipetal transport of auxin from the shoot to the root. The auxin/cytokinin ratio in the leaves and roots may explain both the salinity-induced decrease in shoot vigour (leaf growth and leaf number) and the shift in biomass allocation to the roots, in agreement with changes in the activity of the sink-related enzyme cell wall invertase.

Root-to-shoot signalling: Assessing the roles of ‘up’ in the up and down world of long-distance signalling in planta

An important mediator of shoot physiological processes can be the supply of signal molecules (other than water and nutrients) from the root system. Root-to-shoot signalling is often considered to be important in regulating shoot growth and water use when soil conditions change without any demonstrable change in shoot water or nutrient status. Changes in xylem sap composition are often thought to be synonymous with changes in root-to-shoot signalling, even though there is considerable re-cycling of compounds between xylem and phloem. Techniques used to collect xylem sap are reviewed. Elucidating the roles of putative root signal molecules in planta has usually taken priority over identifying the sources of signal molecules in xylem sap. The roles of several signal molecules are considered. This choice is selective, and the failure of known signals to account for observed physiological changes in some systems has lead to the conclusions that other novel signals can be important. The efficacy of a given signal molecule can depend on the shoot water and nutrient status, as demonstrated by variation in stomatal responses to abscisic acid. If such variation is widespread in crop species, this may have implications for the increasing intentional use of root-to-shoot signals to modify crop water use and shoot architecture. Research into root-to-shoot signalling may become increasingly reductionist, in trying to evaluate the contribution of root signals versus local processes to observed physiological changes. However, future challenges are to successfully integrate this basic research into improved crop production systems.

Rhizosphere bacteria containing 1‐aminocyclopropane‐1‐carboxylate deaminase increase yield of plants grown in drying soil via both local and systemic hormone signalling

Decreased soil water availability can stimulate production of the plant hormone ethylene and inhibit plant growth. Strategies aimed at decreasing stress ethylene evolution might attenuate its negative effects. An environmentally benign (nonchemical) method of modifying crop ethylene relations - soil inoculation with a natural root-associated bacterium Variovorax paradoxus 5C-2 (containing the enzyme 1-aminocyclopropane-1-carboxylate (ACC) deaminase that degrades the ethylene precursor ACC), was assessed with pea (Pisum sativum) plants grown in drying soil. Inoculation with V. paradoxus 5C-2, but not with a transposome mutant with massively decreased ACC deaminase activity, improved growth, yield and water-use efficiency of droughted peas. Systemic effects of V. paradoxus 5C-2 included an amplified soil drying-induced increase of xylem abscisic acid (ABA) concentration, but an attenuated soil drying-induced increase of xylem ACC concentration. A local bacterial effect was increased nodulation by symbiotic nitrogen-fixing bacteria, which prevented a drought-induced decrease in nodulation and seed nitrogen content. Successfully deploying a single bacterial gene in the rhizosphere increased yield and nutritive value of plants grown in drying soil, via both local and systemic hormone signalling. Such bacteria may provide an easily realized, economic means of sustaining crop yields and using irrigation water more efficiently in dryland agriculture.

AtMYB61, an R2R3-MYB transcription factor controlling stomatal aperture in Arabidopsis thaliana

Stomata, dynamic pores found on the surfaces of plant leaves, control water loss from the plant and regulate the uptake of CO(2) for photosynthesis. Stomatal aperture is controlled by the two guard cells that surround the stomatal pore. When the two guard cells are fully turgid, the pore gapes open, whereas turgor loss results in stomatal closure. In order to set the most appropriate stomatal aperture for the prevailing environmental conditions, guard cells respond to multiple internal and external signals. Although much is known about guard-cell signaling pathways, rather little is known about how changes in gene expression are involved in the control of stomatal aperture. We show here that AtMYB61 (At1g09540), a gene encoding a member of the Arabidopsis thaliana R2R3-MYB family of transcription factors, is specifically expressed in guard cells in a manner consistent with involvement in the control of stomatal aperture. Gain-of-function and loss-of-function mutant analyses reveal that AtMYB61 expression is both sufficient and necessary to bring about reductions in stomatal aperture with consequent effects on gas exchange. Taken together, our data provide evidence that AtMYB61 encodes the first transcription factor implicated in the closure of stomata.

Hormonal changes during salinity-induced leaf senescence in tomato (Solanum lycopersicum L.)

Leaf senescence is one of the most limiting factors to plant productivity under salinity. Both the accumulation of specific toxic ions (e.g. Na+) and changes in leaf hormone relations are involved in the regulation of this process. Tomato plants (Solanum lycopersicum L. cv Moneymaker) were cultivated for 3 weeks under high salinity (100 mM NaCl) and leaf senescence-related parameters were studied during leaf development in relation to Na+ and K+ contents and changes in abscisic acid (ABA), cytokinins, the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC), and the auxin indole-3-acetic acid (IAA). Na+ accumulated to a similar extent in both leaves 4 and 5 (numbering from the base of the plant) and more quickly during the third week, while concurrently K+ contents sharply decreased. However, photosystem II efficiency, measured as the Fv/Fm ratio, decreased from the second week of salinization in leaf 4 but only at the end of the third week in the younger leaf 5. In the prematurely senescent leaf 4, ABA content increased linearly while IAA strongly decreased with salinization time. Although zeatin (Z) levels were scarcely affected by salinity, zeatin-riboside (ZR) and the total cytokinin content (Z+ZR) progressively decreased by 50% from the imposition of the stress. ACC was the only hormonal compound that increased in leaf tissue coincident with the onset of oxidative damage and the decline in chlorophyll fluorescence, and prior to massive Na+ accumulation. Indeed, (Z+ZR) and ACC contents and their ratio (Z+ZR/ACC) were the hormonal parameters best correlated with the onset and progression of leaf senescence. The influence of different hormonal changes on salt-induced leaf senescence is discussed.

Hormonal Interactions and Stomatal Responses

Both environmental and hormonal factors and their interactions affect stomatal behavior. Methodologies for identifying hormonal interactions affecting stomatal function are reviewed. Although there is abundant evidence that abscisic acid (ABA) closes stomata, evidence that the other classical plant hormones (auxins, cytokinins, ethylene, gibberellins) in isolation alter stomatal response often comes from exogenous applications to detached epidermes and leaves, rather than correlation of endogenous concentrations with stomatal conductance (gs). Evidence for hormonal interactions comes from isolated tissues with exogenous hormones supplied at nonphysiological concentrations, or from variation in stomatal response to xylem ABA concentration in planta. The roles of hormonal changes in causing stomatal closure following changes in soil environment are considered. Although soil drying induces multiple changes in xylem sap composition, analysis of stomatal responses suggests a dominant role for increased endogenous ABA concentrations and relatively little evidence of roles for other hormones. A similar picture emerges from studies of soil compaction. Although soil flooding decreases ABA export from the root system, there is some evidence that apoplastic ABA accumulation elicits stomatal closure. Stomatal closure following nitrogen deprivation does not appear to involve ABA and may provide a suitable experimental system to investigate roles for other hormones. The availability of mutant or transgenic lines with altered hormone homeostasis or sensitivity provides opportunities to screen for altered stomatal behavior in response to different environments, and may provide new evidence that hormonal interactions are important in the control of stomatal behavior.

Microbial amelioration of crop salinity stress

The use of soil and irrigation water with a high content of soluble salts is a major limiting factor for crop productivity in the semi-arid areas of the world. While important physiological insights about the mechanisms of salt tolerance in plants have been gained, the transfer of such knowledge into crop improvement has been limited. The identification and exploitation of soil microorganisms (especially rhizosphere bacteria and mycorrhizal fungi) that interact with plants by alleviating stress opens new alternatives for a pyramiding strategy against salinity, as well as new approaches to discover new mechanisms involved in stress tolerance. Although these mechanisms are not always well understood, beneficial physiological effects include improved nutrient and water uptake, growth promotion, and alteration of plant hormonal status and metabolism. This review aims to evaluate the beneficial effects of soil biota on the plant response to saline stress, with special reference to phytohormonal signalling mechanisms that interact with key physiological processes to improve plant tolerance to the osmotic and toxic components of salinity. Improved plant nutrition is a quite general beneficial effect and may contribute to the maintenance of homeostasis of toxic ions under saline stress. Furthermore, alteration of crop hormonal status to decrease evolution of the growth-retarding and senescence-inducing hormone ethylene (or its precursor 1-aminocyclopropane-1-carboxylic acid), or to maintain source-sink relations, photosynthesis, and biomass production and allocation (by altering indole-3-acetic acid and cytokinin biosynthesis) seem to be promising target processes for soil biota-improved crop salt tolerance.

Root-synthesized cytokinins improve shoot growth and fruit yield in salinized tomato (Solanum lycopersicum L.) plants

Salinity limits crop productivity, in part by decreasing shoot concentrations of the growth-promoting and senescence-delaying hormones cytokinins. Since constitutive cytokinin overproduction may have pleiotropic effects on plant development, two approaches assessed whether specific root-localized transgenic IPT (a key enzyme for cytokinin biosynthesis) gene expression could substantially improve tomato plant growth and yield under salinity: transient root IPT induction (HSP70::IPT) and grafting wild-type (WT) shoots onto a constitutive IPT-expressing rootstock (WT/35S::IPT). Transient root IPT induction increased root, xylem sap, and leaf bioactive cytokinin concentrations 2- to 3-fold without shoot IPT gene expression. Although IPT induction reduced root biomass (by 15%) in control (non-salinized) plants, in salinized plants (100 mM NaCl for 22 d), increased cytokinin concentrations delayed stomatal closure and leaf senescence and almost doubled shoot growth (compared with WT plants), with concomitant increases in the essential nutrient K+ (20%) and decreases in the toxic ion Na+ (by 30%) and abscisic acid (by 20–40%) concentrations in transpiring mature leaves. Similarly, WT/35S::IPT plants (scion/rootstock) grown with 75 mM NaCl for 90 d had higher fruit trans-zeatin concentrations (1.5- to 2-fold) and yielded 30% more than WT/non-transformed plants. Enhancing root cytokinin synthesis modified both shoot hormonal and ionic status, thus ameliorating salinity-induced decreases in growth and yield.

Rhizosphere manipulations to maximize ‘crop per drop’ during deficit irrigation

Although much of global agriculture is rain-fed, production is frequently (and sometimes catastrophically) constrained by rainfall. Supplementary irrigation can stabilize yield from year-to-year and conventionally has aimed to meet full crop evapotranspiration (ET), since the relationship between ET and crop yield is near-linear at suboptimal water supply (Fereres and Soriano, 2007). Changes in climate (rainfall patterns) and/or resource management (irrigation quotas) will mean that future crops, either unintentionally or deliberately, will receive deficit irrigation (DI, less water than crop ET), necessarily drying the soil, limiting leaf expansion and gas exchange and, consequently, yield. Although decreased cellular turgor can limit leaf growth and gas exchange, under many circumstances plant roots can sense drying soil, and transmit chemical signals to the shoots to regulate their physiology (Davies and Zhang, 1991; Dodd et al., 1996). Much work has aimed to substantiate this ‘chemical signalling hypothesis’ by determining the production and distribution of various signals (e.g. the plant hormones ABA, cytokinins, ethylene), their role in regulating plant responses to soil drying (e.g. using mutants and/or transgenics altered in signal synthesis or sensitivity), and the importance of the root system as a signal source (e.g. using reciprocal grafts of wild-type plants and such mutants and/or transgenics; Dodd, 2005; Hartung and Wilkinson, 2009). This research area is largely ‘ABA-centric’, in part, due to its undoubted importance in regulating plant water use (Hartung and Wilkinson, 2009) and relative ease of measurement (Dodd et al., 1996). Other signals have been relatively ignored, even though mild soil drying can significantly change both plant cytokinin (Kudoyarova et al., 2007) and ethylene (Sobeih et al., 2004) status. High-throughput, multianalyte physico-chemical techniques to quantify plant hormones in multiple plant organs (especially reproductive structures that directly influence crop yield) following rhizospheric stress (Albacete et al., 2008) need to be applied to real plants growing in the field under realistic soil drying scenarios. Such information will provide a sound physiological basis to underpin efforts aimed at manipulating long-distance hormonal signalling in planta. Several genetic manipulations have altered plant hormone signalling in crop plants, although the role of the root system (and its contribution to long-distance signalling) has not specifically been elucidated. A maize ACC synthase mutant with decreased leaf ethylene synthesis showed delayed leaf senescence and greater photosynthesis under drought compared to wild-type plants (Young et al., 2004). Brassica napus plants with genetically enhanced stomatal sensitivity to ABA showed increased seed yield under drought (Y Wang et al., 2005). Tomato plants with constitutive ABA overproduction showed increased leaf and whole plant water use efficiency (Thompson et al., 2007), but their delayed leaf area development (hence soil coverage to minimize evaporation) may diminish the expected gains in crop-level water use efficiency. Notwithstanding any physiological limitations of such technologies, socioeconomic factors may mitigate against their widespread adoption, such as consumer acceptance of GM crops and the significant biotechnological effort (and associated cost) required to make such genetic manipulations available in all crops/varieties. For these reasons, there remains a need for management options to minimize the yield penalties of deficit-irrigated crops. This article emphasises progress in understanding how rhizosphere manipulations, specifically partial rootzone drying and the introduction of plant growth-promoting rhizobacteria, alter plant root-to-shoot signalling to regulate leaf expansion and gas exchange and hence yield.

Rootstock-mediated changes in xylem ionic and hormonal status are correlated with delayed leaf senescence, and increased leaf area and crop productivity in salinized tomato

Tomato crop productivity under salinity can be improved by grafting cultivars onto salt-tolerant wild relatives, thus mediating the supply of root-derived ionic and hormonal factors that regulate leaf area and senescence. A tomato cultivar was grafted onto rootstocks from a population of recombinant inbred lines (RILs) derived from a Solanum lycopersicum x Solanum cheesmaniae cross and cultivated under moderate salinity (75 mM NaCl). Concentrations of Na(+), K(+) and several phytohormones [abscisic acid (ABA); the cytokinins (CKs) zeatin, Z; zeatin riboside, ZR; and the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC)] were analysed in leaf xylem sap in graft combinations of contrasting vigour. Scion leaf area correlated with photosystem II (PSII) efficiency (F(v)/F(m)) and determined fruit productivity. Xylem K(+) (but not Na(+)), K(+)/Na(+), the active CK Z, the ratio with its storage form Z/ZR and especially the ratio between CKs and ACC (Z/ACC and Z + ZR/ACC) were positively loaded into the first principal component (PC) determining both leaf growth and PSII efficiency. In contrast, the ratio ACC/ABA was negatively correlated with leaf biomass. Although the underlying physiological mechanisms by which rootstocks mediate leaf area or chlorophyll fluorescence (and thus influence tomato salt tolerance) seem complex, a putative potassium-CK interaction involved in regulating both processes merits further attention.