Mutations in Arabidopsis yellow stripe-like1 and yellow stripe-like3 reveal their roles in metal ion homeostasis and loading of metal ions in seeds

Here, we describe two members of the Arabidopsis (Arabidopsis thaliana) Yellow Stripe-Like (YSL) family, AtYSL1 and AtYSL3. The YSL1 and YSL3 proteins are members of the oligopeptide transporter family and are predicted to be integral membrane proteins. YSL1 and YSL3 are similar to the maize (Zea mays) YS1 phytosiderophore transporter (ZmYS1) and the AtYSL2 iron (Fe)-nicotianamine transporter, and are predicted to transport metal-nicotianamine complexes into cells. YSL1 and YSL3 mRNAs are expressed in both root and shoot tissues, and both are regulated in response to the Fe status of the plant. Beta-glucuronidase reporter expression, driven by YSL1 and YSL3 promoters, reveals expression patterns of the genes in roots, leaves, and flowers. Expression was highest in senescing rosette leaves and cauline leaves. Whereas the single mutants ysl1 and ysl3 had no visible phenotypes, the ysl1ysl3 double mutant exhibited Fe deficiency symptoms, such as interveinal chlorosis. Leaf Fe concentrations are decreased in the double mutant, whereas manganese, zinc, and especially copper concentrations are elevated. In seeds of double-mutant plants, the concentrations of Fe, zinc, and copper are low. Mobilization of metals from leaves during senescence is impaired in the double mutant. In addition, the double mutant has reduced fertility due to defective anther and embryo development. The proposed physiological roles for YSL1 and YSL3 are in delivery of metal micronutrients to and from vascular tissues.     

A loss-of-function mutation in AtYSL1 reveals its role in iron and nicotianamine seed loading

The Arabidopsis Yellow Stripe 1-Like (YSL) proteins have been identified by homology with the maize (Zea mays) Yellow Stripe 1 (YS1) transporter which is responsible for iron-phytosiderophore (PS) uptake by roots in response to iron shortage. Although dicotyledonous plants do not synthesize PS, they do synthesize the PS precursor nicotianamine, a strong metal chelator essential for maintenance of iron homeostasis and copper translocation. Furthermore, ZmYS1 and the rice (Oryza sativa) protein OsYSL2 have metal-nicotianamine transport activities in heterologous expression systems. In this work, we have characterized the function of AtYSL1 in planta. Two insertional loss-of-function ysl1 mutants of Arabidopsis were found to exhibit increased nicotianamine accumulation in shoots. More importantly, seeds of both ysl1 knockouts contained less iron and nicotianamine than wild-type seeds, even when produced by plants grown in the presence of an excess of iron. This phenotype could be reverted by expressing the wild-type AtYSL1 gene in ysl1 plants. ysl1 seeds germinated slowly, but this defect was rescued by an iron supply. AtYSL1 was expressed in the xylem parenchyma of leaves, where it was upregulated in response to iron excess, as well as in pollen and in young silique parts. This pattern is consistent with long-distance circulation of iron and nicotianamine and their delivery to the seed. Taken together, our work provides strong physiological evidence that iron and nicotianamine levels in seeds rely in part on AtYSL1 function.     

Put the metal to the petal: metal uptake and transport throughout plants

Compared to other organisms, plants have expanded families of transporters that are involved in the uptake and efflux of metals. Fortunately, in many cases, the examination of double mutants has been sufficient to overcome the challenge of studying functionally redundant gene families. Plants that lack two heavy-metal-transporting P-type ATPase family members (HMA2 and HMA4) reveal a function for these transporters in Zn translocation from roots to shoots. Likewise, the phenotype of plants that lack two natural resistance associated macrophage protein (NRAMP) homologs (NRAMP3 and NRAMP4) implicate these metal uptake proteins in the mobilization of vacuolar Fe stores during seed germination. Most families of metal transporters are ubiquitous but the Yellow Stripe1-Like (YSL) family is plant specific and YSL family members have been implicated in the transport of metals that are complexed with a plant specific chelator called nicotianamine (NA).     

黄色条纹/黄色条纹样蛋白与植物中的铁转运功能

黄色条纹/黄色条纹样蛋白（yellow stripe/yellow stripe like,YS/YSL）在植物金属转运,尤其是在微量营养元素铁的分配和利用过程中发挥重要作用。近年来,植物的铁长距离运输机制已成为研究的热点之一。YS/YSL转运蛋白涉及铁的转移、运输、装载和卸载。鉴定并精确解析YS/YSL的功能对于阐明铁的长距离运输机制具有重要的意义。本文综述了YS/YSL的蛋白质性质、金属转运活性、底物特异性及其功能表达,以期为植物YS/YSL相关铁转运机制研究奠定基础,并为提高作物籽粒铁营养提供理论依据。     

TcYSL3, a member of the YSL gene family from the hyper-accumulator Thlaspi caerulescens, encodes a nicotianamine-Ni/Fe transporter

The two main features of plant hyper-accumulator species are the massive translocation of heavy metal ions to the aerial parts and their tolerance to such high metal concentrations. Recently, several lines of evidence have indicated a role for nicotianamine (NA) in metal homeostasis, through the chelation and transport of NA-metal complexes. The function of transport of NA-metal chelates, required for the loading and unloading of vessels, has been assigned to the Yellow Stripe 1 (YSL)-Like family of proteins. We have characterized three YSL genes in Thlaspi caerulescens in the context of hyper-accumulation. The three YSL genes are expressed at high rates compared with their Arabidopsis thaliana homologs but with distinct patterns. While TcYSL7 was highly expressed in the flowers, TcYSL5 was more highly expressed in the shoots, and the expression of TcYSL3 was equivalent in all the organs tested. In situ hybridizations have shown that TcYSL7 and TcYSL5 are expressed around the vasculature of the shoots and in the central cylinder in the roots. The exposure to heavy metals (Zn, Cd, Ni) does not affect the high and constitutive expression of the TcYSL genes. Finally, we have demonstrated by mutant yeast complementation and uptake measurements that TcYSL3 is an Fe/Ni-NA influx transporter. This work provides therefore molecular, histological and biochemical evidence supporting a role for YSL transporters in the overall scheme of NA and NA-metal, particularly NA-Ni, circulation in a metal hyper-accumulator plant.     

Yellow stripe1. Expanded roles for the maize iron-phytosiderophore transporter

Graminaceous monocots, including most of the world's staple grains (i.e. rice, corn, and wheat) use a chelation strategy (Strategy II) for primary acquisition of iron from the soil. Strategy II plants secrete phytosiderophores (PS), compounds of the mugineic acid family that form stable Fe(III) chelates in soil. Uptake of iron-PS chelates, which occurs through specific transporters at the root surface, thus represents the primary route of iron entry into Strategy II plants. The gene Yellow stripe1 (Ys1) encodes the Fe(III)-PS transporter of maize (Zea mays). Here the physiological functions performed by maize YS1 were further defined by examining the pattern of Ys1 mRNA and protein accumulation and by defining YS1 transport specificity in detail. YS1 is able to translocate iron that is bound either by PS or by the related compound, nicotianamine; thus, the role of YS1 may be to transport either of these complexes. Ys1 expression at both the mRNA and protein levels responds rapidly to changes in iron availability but is not strongly affected by limitation of copper or zinc. Our data provide no support for the idea that YS1 is a transporter of zinc-PS, based on YS1 biochemical activity and Ys1 mRNA expression patterns in response to zinc deficiency. YS1 is capable of transporting copper-PS, but expression data suggest that the copper-PS uptake has limited significance in primary uptake of copper.     

Brachypodium distachyon as a new model system for understanding iron homeostasis in grasses: phylogenetic and expression analysis of Yellow Stripe-Like (YSL) transporters

Background and Aims

Brachypodium distachyon is a temperate grass with a small stature, rapid life cycle and completely sequenced genome that has great promise as a model system to study grass-specific traits for crop improvement. Under iron (Fe)-deficient conditions, grasses synthesize and secrete Fe(III)-chelating agents called phytosiderophores (PS). In Zea mays, Yellow Stripe1 (ZmYS1) is the transporter responsible for the uptake of Fe(III)–PS complexes from the soil. Some members of the family of related proteins called Yellow Stripe-Like (YSL) have roles in internal Fe translocation of plants, while the function of other members remains uninvestigated. The aim of this study is to establish brachypodium as a model system to study Fe homeostasis in grasses, identify YSL proteins in brachypodium and maize, and analyse their expression profiles in brachypodium in response to Fe deficiency.

Methods

The YSL family of proteins in brachypodium and maize were identified based on sequence similarity to ZmYS1. Expression patterns of the brachypodium YSL genes (BdYSL genes) were determined by quantitative RT–PCR under Fe-deficient and Fe-sufficient conditions. The types of PS secreted, and secretion pattern of PS in brachypodium were analysed by high-performance liquid chromatography.

Key Results

Eighteen YSL family members in maize and 19 members in brachypodium were identified. Phylogenetic analysis revealed that some YSLs group into a grass-specific clade. The Fe status of the plant can regulate expression of brachypodium YSL genes in both shoots and roots. 3-Hydroxy-2′-deoxymugineic acid (HDMA) is the dominant type of PS secreted by brachypodium, and its secretion is diurnally regulated.

Conclusions

PS secretion by brachypodium parallels that of related crop species such as barley and wheat. A single grass species-specific YSL clade is present, and expression of the BdYSL members of this clade could not be detected in shoots or roots, suggesting grass-specific functions in reproductive tissues. Finally, the Fe-responsive expression profiles of several YSLs suggest roles in Fe homeostasis.     

Metal movement within the plant: contribution of nicotianamine and yellow stripe 1-like transporters

Background: Since the identification of the genes controlling the root acquisitionof iron (Fe), the control of inter- and intracellular distributionhas become an important challenge in understanding metal homeostasis.The identification of the yellow stripe-like (YSL) transporterfamily has paved the way to decipher the mechanisms of long-distancetransport of Fe. Scope: Once in the plant, Fe will systematically react with organicligands whose identity is poorly known so far. Among potentialligands, nicotianamine has been identified as an important moleculefor the circulation and delivery of metals since it participatesin the loading of copper (Cu) and nickel in xylem and preventsFe precipitation in leaves. Nicotianamine is a precursor ofphytosiderophores, which are high-affinity Fe ligands exclusivelysynthesized by Poaceae species and excreted by roots for thechelation and acquisition of Fe. Maize YS1 is the founding memberof a family of membrane transporters called YS1-like (YSL),which functions in root Fe–phytosiderophore uptake fromthe soil. Next to this well-known Fe acquisition role, mostof the other YSL family members are likely to function in plant-widedistribution of metals since (a) they are produced in vasculartissues throughout the plant and (b) they are found in non-Poaceaespecies that do not synthesize phytosiderophores. The hypothesizedactivity as Fe–nicotianamine transporters of several YSLmembers has been demonstrated experimentally by heterologousexpression in yeast or by electrophysiology in Xenopus oocytesbut, despite numerous attempts, proof of the arabidopsis YSLsubstrate specificity is still lacking. Reverse genetics, however,has revealed a role for AtYSL members in the remobilizationof Cu and zinc from senescing leaves, in the formation of pollenand in the Fe, zinc and Cu loading of seeds. Conclusions: Preliminary data on the YSL family of transporters clearly arguesin favour of its role in the long-distance transport of metalsthrough and between vascular tissues to eventually support gametogenesisand embryo development.     

ZmYS1 functions as a proton-coupled symporter for phytosiderophore- and nicotianamine-chelated metals

Among higher plants graminaceous species have the unique ability to efficiently acquire iron from alkaline soils with low iron solubility by secreting phytosiderophores, which are hexadentate metal chelators with high affinity for Fe(III). Iron(III)-phytosiderophores are subsequently taken up by roots via YS1 transporters, that belong to the OPT oligopeptide transporter family. Despite its physiological importance at alkaline pH, uptake of Fe-phytosiderophores into roots of wild-type maize plants was greater at acidic pH and sensitive to the proton uncoupler CCCP. To access the mechanism of Fe-phytosiderophore acquisition, ZmYS1 was expressed in an iron uptake-defective yeast mutant and in Xenopus oocytes, where ZmYS1-dependent Fe-phytosiderophore transport was stimulated at acidic pH and sensitive to CCCP. Electrophysiological analysis in oocytes demonstrated that Fephytosiderophore transport depends on proton cotransport and on the membrane potential, which allows ZmYS1-mediated transport even at alkaline pH. We further investigated substrate specificity and observed that ZmYS1 complemented the growth defect of the zinc uptake-defective yeast mutant zap1 and transported various phytosiderophore-bound metals into oocytes, including zinc, copper, nickel, and, at a lower rate, also manganese and cadmium. Unexpectedly, ZmYS1 also transported Ni(II), Fe(II), and Fe(III) complexes with nicotianamine, a structural analog of phytosiderophores, which has been shown to act as an intracellular metal chelator in all higher plants. Our results show that ZmYS1 encodes a proton-coupled broad-range metal-phytosiderophore transporter that additionally transports Fe- and Ni-nicotianamine. These biochemical properties indicate a novel role of YS1 transporters for heavy metal homeostasis in plants.     

The iron-chelate transporter OsYSL9 plays a role in iron distribution in developing rice grains

Key message

Rice OsYSL9 is a novel transporter for Fe(II)-nicotianamine and Fe(III)-deoxymugineic acid that is responsible for internal iron transport, especially from endosperm to embryo in developing seeds.

Abstract

Metal chelators are essential for safe and efficient metal translocation in plants. Graminaceous plants utilize specific ferric iron chelators, mugineic acid family phytosiderophores, to take up sparingly soluble iron from the soil. Yellow Stripe 1-Like (YSL) family transporters are responsible for transport of metal-phytosiderophores and structurally similar metal-nicotianamine complexes. Among the rice YSL family members (OsYSL) whose functions have not yet been clarified, OsYSL9 belongs to an uncharacterized subgroup containing highly conserved homologs in graminaceous species. In the present report, we showed that OsYSL9 localizes mainly to the plasma membrane and transports both iron(II)-nicotianamine and iron(III)-deoxymugineic acid into the cell. Expression of OsYSL9 was induced in the roots but repressed in the nonjuvenile leaves in response to iron deficiency. In iron-deficient roots, OsYSL9 was induced in the vascular cylinder but not in epidermal cells. Although OsYSL9-knockdown plants did not show a growth defect under iron-sufficient conditions, these plants were more sensitive to iron deficiency in the nonjuvenile stage compared with non-transgenic plants. At the grain-filling stage, OsYSL9 expression was strongly and transiently induced in the scutellum of the embryo and in endosperm cells surrounding the embryo. The iron concentration was decreased in embryos of OsYSL9-knockdown plants but was increased in residual parts of brown seeds. These results suggested that OsYSL9 is involved in iron translocation within plant parts and particularly iron translocation from endosperm to embryo in developing seeds.

     

Successful Reproduction Requires the Function of Arabidopsis YELLOW STRIPE-LIKE1 and YELLOW STRIPE-LIKE3 Metal-Nicotianamine Transporters in Both Vegetative and Reproductive Structures

Several members of the Yellow Stripe-Like (YSL) family of proteins are transporters of metals that are bound to the metal chelator nicotianamine or the related set of mugineic acid family chelators known as phytosiderophores. Here, we examine the physiological functions of three closely related Arabidopsis (Arabidopsis thaliana) YSL family members, AtYSL1, AtYSL2, and AtYSL3, to elucidate their role(s) in the allocation of metals into various organs of Arabidopsis. We show that AtYSL3 and AtYSL1 are localized to the plasma membrane and function as iron transporters in yeast functional complementation assays. By using inflorescence grafting, we show that AtYSL1 and AtYSL3 have dual roles in reproduction: their activity in the leaves is required for normal fertility and normal seed development, while activity in the inflorescences themselves is required for proper loading of metals into the seeds. We further demonstrate that the AtYSL1 and AtYSL2 proteins, when expressed from the AtYSL3 promoter, can only partially rescue the phenotypes of a ysl1ysl3 double mutant, suggesting that although these three YSL transporters are closely related and have similar patterns of expression, they have distinct activities in planta. In particular, neither AtYSL1 nor AtYSL2 is able to functionally complement the reproductive defects exhibited by ysl1ysl3 double mutant plants.The transition metals iron (Fe), copper (Cu), and zinc (Zn) are among the most important and most problematic of all the micronutrients used by plants. The importance of these metals stems from their roles as essential cofactors for cellular redox reactions involved in photosynthesis, respiration, and many other reactions. The problematic nature of these metals stems from the same distinct chemical properties that make them so valuable to living systems. These metals, particularly Cu and Fe, are highly reactive and, if overaccumulated, can cause cellular redox damage. Fe presents an additional problem for plants, because it is also only sparingly soluble in aqueous solution and thus is typically not “bioavailable” in soil (Guerinot and Yi, 1994). As a response to these key properties, plants have evolved multifaceted systems to control metal uptake by the root, translocation through the plant body, storage within tissues, and remobilization during reproduction and times of nutrient stress.The nonproteinogenic amino acid nicotianamine (NA) is a strong complexor of various transition metals, particularly Fe(II) (Anderegg and Ripperger, 1989) and Fe(III) (von Wiren et al., 1999), as well as Cu(II), Ni(II), Co(II), Mn(II), and Zn(II) (Anderegg and Ripperger, 1989). NA is present in shoots and roots at concentrations ranging between 20 and 500 nm g⁻¹ fresh weight (Stephan et al., 1990) and is present in both xylem (approximately 20 μm [Pich and Scholz, 1996]) and phloem (approximately 130 μm [Schmidke and Stephan, 1995]), suggesting that it is a major complexor of metals throughout the plant. Much of what we know about NA function in plants comes from studies of a mutant of tomato (Solanum lycopersicum) called chloronerva, in which the single gene encoding NA synthase is disrupted (Herbik et al., 1999; Higuchi et al., 1999; Ling et al., 1999). The chloronerva phenotype is complex. Plants exhibit interveinal chlorosis in young leaves and constitutively activate their root Fe uptake systems, indicating that they have inadequate Fe. However, mature leaves of chloronerva mutants contain excess Fe, implying that the Fe that is present is not being properly localized in the absence of NA. These chloronerva plants also have severe defects in translocation of Cu in the xylem, indicating a clear role for NA in Cu transport. The plants are sterile, indicating that NA is important during plant reproduction. Complementing these classical studies on chloronerva, Takahashi et al. (2003) have developed tobacco (Nicotiana tabacum) plants that heterologously express a barley (Hordeum vulgare) gene encoding the enzyme NA aminotransferase, which converts NA into a nonfunctional intermediate. Recently, the phenotype of quadruple NA synthase mutants was described in Arabidopsis (Arabidopsis thaliana; Klatte et al., 2009). In both studies, the plants exhibited many of the defects caused by the chloronerva mutation, including chlorosis and an array of reproductive abnormalities.Several members of the well-conserved Yellow Stripe-Like (YSL) family of proteins function as metal-NA transporters (DiDonato et al., 2004; Koike et al., 2004; Roberts et al., 2004; Schaaf et al., 2004; Murata et al., 2006; Gendre et al., 2007). The founding member of the YSL family, maize (Zea mays) Yellow Stripe1 (ZmYS1), is the primary means by which roots of grasses take up Fe from the soil. The grasses, a group that includes most of the world’s staple grains (e.g. rice [Oryza sativa], wheat [Triticum aestivum], and maize), use a chelation strategy for primary Fe uptake. In response to Fe starvation, grasses secrete phytosiderophores (PS): derivatives of the mugineic acid family that are structurally similar to NA and that form stable Fe(III) chelates in soil (Tagaki et al., 1984). This accomplishes solubilization of the otherwise nearly insoluble soil Fe. The YS1 protein, located at the root surface, then moves the Fe(III)-PS complexes from the rhizosphere into root cells (Romheld and Marchner, 1986; Curie et al., 2001; Roberts et al., 2004)Arabidopsis has eight YSL genes. Three of these (AtYSL1, At4g24120; AtYSL2, At5g24380; and AtYSL3, At5g53550) are expressed strongly in the xylem parenchyma of leaves and are down-regulated during Fe deficiency (DiDonato et al., 2004; Waters et al., 2006). We have previously shown that double mutant plants with lesions in both AtYSL1 and AtYSL3 display strong interveinal chlorosis. We have hypothesized that the function of these YSL transporters in vegetative tissues is to take up Fe that arrives in leaves via the xylem (Waters et al., 2006). All of the defects displayed by ysl1ysl3 double mutants can be alleviated if excess Fe is applied to the soil, demonstrating that these growth defects are caused primarily by a lack of Fe. Intriguingly, although Fe deficiency appears to be the basis of the double mutant phenotype, the concentrations of several metals are specifically altered in the double mutants (Waters et al., 2006). AtYSL1 single mutant plants have subtle phenotypes, the most striking of which is a decrease in both NA and Fe in seeds (Le Jean et al., 2005). Interestingly, leaves of these mutants contain excess NA, while Fe levels are normal. These observations are consistent with the more obvious and extensive phenotypes exhibited by the ysl1ysl3 double mutant and highlight the idea that AtYSL proteins affect the homeostasis of both Fe and NA.In addition to the vegetative defects mentioned above, the ysl1ysl3 double mutant has multiple defects in reproduction. Double mutant flowers produce few functional pollen grains and thus exhibit greatly reduced fertility. Many of the seeds that these plants do manage to produce are small and contain embryos arrested at various immature stages, which often fail to germinate. These fertility defects can be reversed by application of Fe-ethylenediamine-N,N′-bis(2-hydroxyphenylacetic acid) solution to the soil, again demonstrating that these growth defects are caused by a lack of Fe (Waters et al., 2006). Expression of YSL1 and YSL3 is very limited in flowers and developing siliques; furthermore, the patterns of expression of YSL1 and YSL3 are distinct and largely nonoverlapping in these structures. However, expression of AtYSL1 and AtYSL3 increases markedly during leaf senescence, a period in which many minerals are remobilized from leaves, presumably for delivery into developing seeds (Himelblau and Amasino, 2001). This model is in good agreement with the accepted model for nutrient loading into seeds proposed originally by Hocking and Pate (1977, 1978), which suggests that metals mobilized from vegetative structures account for 20% to 30% of the content in seeds. Direct measurements of metals in senescing and younger leaves demonstrated that double mutants failed to mobilize Zn and Cu from leaves. Seeds produced by the double mutant plants contained reduced levels of Zn and Cu, the same metals that failed to be mobilized out of the leaves (Waters et al., 2006). This led us to propose a model in which the activity of AtYSL1 and AtYSL3 in leaves was required for correct localization of metals into the seeds. However, seeds also had low Fe levels, even though Fe appeared to be mobilized normally from leaves of the double mutants.Here, we further investigate the role(s) of AtYSL1 and AtYSL3 in the allocation of metals into various organs of Arabidopsis. AtYSL1 and AtYSL3 are localized to the plasma membrane, and each is capable of suppressing the growth defect of yeast lacking normal Fe uptake, indicating that the most likely biochemical function for these proteins is in uptake of Fe(II)-NA complexes. We have used inflorescence grafting to determine the relative roles of AtYSL1 and AtYSL3 in leaves and inflorescences during seed development. These proteins are found to have dual roles: activity in the leaves is required for normal inflorescence development, while activity in the inflorescences themselves is required for proper loading of metals into the seeds. We have further examined the effect of overexpressing AtYSL3, which resulted in a small increase in Cu in shoots, and have demonstrated that the AtYSL1 protein, when expressed from the AtYSL3 promoter, can only partially rescue the phenotypes of the ysl1ysl3 double mutant, indicating that these proteins have distinct biochemical activities. A third AtYSL from the same subgroup of the YSL family, AtYSL2, also only partially complements the phenotypes of ysl1ysl3 double mutants, suggesting that although these three YSL transporters are closely related, they have distinct activities in planta.     

Arabidopsis SUMO E3 ligase SIZ1 is involved in excess copper tolerance

The reversible conjugation of the small ubiquitin-like modifier (SUMO) to protein substrates occurs as a posttranslational regulatory process in eukaryotic organisms. In Arabidopsis (Arabidopsis thaliana), several stress-responsive SUMO conjugations are mediated mainly by the SUMO E3 ligase SIZ1. In this study, we observed a phenotype of hypersensitivity to excess copper in the siz1-2 and siz1-3 mutants. Excess copper can stimulate the accumulation of SUMO1 conjugates in wild-type plants but not in the siz1 mutant. Copper accumulated to a higher level in the aerial parts of soil-grown plants in the siz1 mutant than in the wild type. A dramatic difference in copper distribution was also observed between siz1 and wild-type Arabidopsis treated with excess copper. As a result, the shoot-to-root ratio of copper concentration in siz1 is nearly twice as high as that in the wild type. We have found that copper-induced Sumoylation is involved in the gene regulation of metal transporters YELLOW STRIPE-LIKE 1 (YSL1) and YSL3, as the siz1 mutant is unable to down-regulate the expression of YSL1 and YSL3 under excess copper stress. The hypersensitivity to excess copper and anomalous distribution of copper observed in the siz1 mutant are greatly diminished in the siz1ysl3 double mutant and slightly in the siz1ysl1 double mutant. These data suggest that SIZ1-mediated sumoylation is involved specifically in copper homeostasis and tolerance in planta.     

Investigation of ascorbate-mediated iron release from ferric phytosiderophores in the presence of nicotianamine

Phytosiderophores (PS) are strong iron chelators, produced by graminaceous plants under iron deficiency. The ability of released PS to chelate iron(III), and subsequent uptake of this chelate into roots by YS1-type transport proteins, are well-known. The mechanism of iron release from the stable chelate inside the plant cell, however, is unclear. One possibility involves the reduction of ferric PS in the presence of an iron(II) chelator via ternary complex formation. Here, the conversion of ferric PS species by ascorbate in the presence of the intracellular ligand nicotianamine (NA) has been investigated at cytosolic pH (pH 7.3), leading to the formation of a ferrous NA chelate. This reaction takes place when supplying Fe(III) as a chelate with 2'-deoxymugineic acid (DMA), mugineic acid (MA), and 3-epi-hydroxymugineic acid (epi-HMA), with the reaction rate decreasing in this order. The progress of the conversion of ferric DMA to ferrous NA was monitored in real-time by high resolution mass spectrometry (FTICR-MS), and the results are complemented by electrochemical measurements (cyclic voltammetry), which allows detecting reactive intermediates and their change with time at high sensitivity. Hence, the combined results of electrochemistry and mass spectrometry indicate an ascorbate-mediated mechanism for the iron release from ferric PS, which highlights the role of ascorbate as a simple, but effective plant reductant.     

The role of trace metals in photosynthetic electron transport in O2-evolving organisms

Iron is the quantitatively most important trace metal involved in thylakoid reactions of all oxygenic organisms since linear (= non-cyclic) electron flow from H₂O to NADP⁺ involves PS II (2–3 Fe), cytochrome b₆-f (5 Fe), PS I (12 Fe), and ferredoxin (2 Fe); (replaceable by metal-free flavodoxin in certain cyanobacteria and algae under iron deficiency). Cytochrome c₆ (1 Fe) is the only redox catalyst linking the cytochrome b₆-f complex to PS I in most algae; in many cyanobacteria and Chlorophyta cytochrome c₆ and the copper-containing plastocyanin are alternatives, with the availability of iron and copper regulating their relative expression, while higher plants only have plastocyanin. Iron, copper and zinc occur in enzymes that remove active oxygen species and that are in part bound to the thylakoid membrane. These enzymes are ascorbate peroxidase (Fe) and iron-(cyanobacteria, and most al gae) and copper-zinc- (some algae; higher plants) superoxide dismutase. Iron-containing NAD(P)H-PQ oxidoreductase in thylakoids of cyanobacteria and many eukaryotes may be involved in cyclic electron transport around PS I and in chlororespiration. Manganese is second to iron in its quantitative role in the thylakoids, with four Mn (and 1 Ca) per PS II involved in O₂ evolution. The roles of the transition metals in redox catalysts can in broad terms be related to their redox chemistry and to their availability to organisms at the time when the pathways evolved. The quantitative roles of these trace metals varies genotypically (e.g. the greater need for iron in thylakoid reactions of cyanobacteria and rhodophytes than in other O₂-evolvers as a result of their lower PS II:PS I ratio) and phenotypically (e.g. as a result of variations in PS II:PS I ratio with the spectral quality of incident radiation).     

Loading and bioavailability of iron in cereal grains

Cereal plants take up iron from the soil via a phytosiderophore-mediated chelation system. Following root absorption, iron is transported through the xylem and phloem of the plant with the help of a variety of efflux and influx transporters belonging to the Zrt Irt-like protein (ZIP) and yellow stripe-like (YSL) protein families. Iron-regulated transporter1, a member of the ZIP family, mobilises ferrous [Fe(II)] ions, while several YSL family members such as YSL2, YSL15 and YSL18 can transport both ferric [Fe(II)] and ferrous [F`III)] ions into developing grains via chelation with mugineic acid or its derivatives. The iron is accumulated largely in the outer aleurone layer and embryo of the grains, which are removed during milling, leaving behind consumable endosperm that contains a very low amount of iron. This review highlights the uptake, transport and loading mechanisms for iron in cereal grains and provides an overview of strategies adopted for developing highly iron-enriched grains.     

Ectopic expression of nicotianamine synthase genes results in improved iron accumulation and increased nickel tolerance in transgenic tobacco

Heavy metals are essential for basic cellular processes but toxic in higher concentrations. This requires the precise control of their intracellular concentrations, a process known as homeostasis. The metal-chelating, non-proteinogenous amino acid nicotianamine (NA) is a key component of plant metal assimilation and homeostasis. Its precise function is still unknown. Therefore, this article aims to contribute new information on the in vivo function of NA and to evaluate its potential use for plant nutrition and crop fortification. For this purpose, a nicotianamine synthase gene of Arabidopsis thaliana was ectopically expressed in transgenic tobacco plants. The presence of extra copies of the nicotianamine synthase gene co-segregated with up to 10-fold elevated levels of NA in comparison with wild type. The increased NA level led to: (a) a significantly increased iron level in leaves of adult plants; (b) the accumulation of zinc and manganese, but not copper; (c) an improvement of the iron use efficiency in adult plants grown under iron limitation; and (d) an enhanced tolerance against up to 1 m m nickel. Taken together, the data predict that NA may be a useful tool for improved plant nutrition on adverse soils and possibly for enhanced nutritional value of leaf and seed crops.     

Isolation and characterization of a barley yellow stripe-like gene, HvYSL5

Yellow stripe-like (YSL) family transporters, belonging to a novel subfamily of oligopeptide transporter (OPT), has been proposed to be involved in metal uptake and long-distance transport, but only a few of them have been functionally characterized so far. In the present study, we isolated an uncharacterized member of the YSL family, HvYSL5, in barley based on expressed sequence tag (EST) information. HvYSL5 shared 50% identity with HvYS1, a transporter for the ferric-mugineic acid complex, at the amino acid level. Promoter analysis showed that the HvYSL5 upstream sequence contains both iron deficiency response element 1 and 2 (IDE1 and 2). HvYSL5 was expressed in the roots and the expression was greatly induced by Fe deficiency, but not by deficiency of other metals including Zn, Cu and Mn. Spatial investigation showed that much higher expression of HvYSL5 was found in the mature zones of the roots, but not in the root tips. Furthermore, the expression showed a diurnal rhythm, being the highest in the morning, but with no expression in the afternoon. HvYSL5 was localized in all root cells, and subcellular localization analysis showed that HvYSL5 is likely to be localized in the vesicles. Knockdown of HvYSL5 did not result in any detectable phenotype changes. Although the exact role of HvYSL5 remains to be examined, our results suggest that it is involved in the transient storage of Fe or phytosiderophores.