Cadmium transport and tolerance in rice: perspectives for reducing grain cadmium accumulation

1Cadmium (Cd) is a toxic heavy metal and is also known as one of the major environmental pollutants. Moderate Cd contamination of arable soils can result in considerable Cd accumulation in edible parts of crops. Such levels of Cd in plants are not toxic to crops but can contribute to substantial Cd dietary intake by humans. In the case of "Itai-itai disease", Cd-polluted rice was the major source of Cd intake in the patients. This is the early case of chronic Cd toxicity in general populations without specific industrial exposure. Even in recent general populations in Japan, the internal Cd level is higher than those of other countries and this is largely because of daily consumption of Japanese rice which contains relatively high Cd. Cd concentrations of recent Japanese rice have been constantly higher compared to those of other countries, although the values are much lower than the limit established by the Codex Alimentarius Commission of FAO/WHO (0.4 mg/kg). In some areas in China and Thailand, production of highly Cd-polluted rice and renal disfunctions among populations were reported. In the United States, increased consumption of rice and other cereals contributes to the recent increase of the dietary Cd intake. Many reports suggest importance to consider chronic effects of Cd exposure through foods. In Japanese populations, the average dietary Cd intake (3.0 μg Cd/kg body weight/week) exceeds the tolerable weekly intake (2.5 μg Cd/kg body weight) set by the European Food Safety Authority (EFSA) and is about 50% of a provisional tolerable monthly intake (25 μg Cd/kg body weight/month) established by the Joint Food and Agriculture Organization/World Health Organization (FAO/WHO) Expert Committee on Food Additives and Contaminants (JECFA). suggested to consider the high Cd availability of rice for humans because of relatively low iron and zinc contents in rice-based foods. These suggest the importance of reducing grain Cd accumulation in rice and other cereals for better human health.

2Recently, as a model plant of cereals, physiological and molecular understanding of Cd transport in rice plants have been advanced. In this review, we describe current knowledge of rice Cd transporters and their (possible) roles in Cd accumulation. Several trials to generate "low-Cd-rice" based on these findings are also described.

3The average Cd concentration in Japanese soils is 0.2 - 0.3 mg/kg DW, which is somewhat higher than those of agricultural soils in China, Indonesia and the United States. In paddy soils largely affected by industrial activities like mining and smelter, the Cd concentrations are much higher than the average. In agricultural soils, atmospheric deposition is known as a major source of Cd input. In paddy fields, irrigation water is another Cd source which continuously loads Cd into soils.

4Rice absorbs Cd2+ in soils, and after several processes of transport Cd finally accumulates into grains. Cd is rapidly transported from roots to shoots by the xylem after absorption. Substantial Cd is detected in the xylem sap and shoot tissues 1 h after Cd treatment to roots, and this activity of root-to-shoot translocation by the xylem is the determinant for shoot Cd accumulation level. On the other hand, in the panicle neck, phloem is the major Cd transport route into grains. In phloem sap, Cd binds to an unknown 13 kDa protein and SH-compounds. The real-time live-imaging technique using a positron emitting radio isotopes called PETIS revealed the detailed behavior of Cd in rice after absorption. They demonstrated that Cd is rapidly translocated from roots to shoots through culms and Cd tends to be retained in nodes. And after 7 h of Cd treatment, Cd is preferentially deposited into panicles rather than into leaf blades. These suggest that nodes are the important tissue for redirecting Cd transport from roots probably by transferring Cd from xylem to phloem. In addition to Cd absorbed from roots, remobilization of Cd in leaf blades is also likely to contribute to grain Cd accumulation. They suggest that a substantial amount of Cd accumulated in leaf blades before heading is remobilized and transported into grains during the ripening stage.

5These physiological studies indicate four major transport processes for rice Cd accumulation: (1) root Cd uptake, (2) root-to-shoot translocation by xylem flow, (3) redirection at nodes and (4) remobilization from leaves (Figure 1). After the first report by, several studies conducted QTL analyses to identify the responsible transporter gene for these processes. QTL analysis is a very useful approach because there is a clear genotypic difference in Cd accumulation in shoots and grains among cultivars. Generally, Cd accumulation in shoots and grains are potentially higher in indica cultivars compared to japonica cultivars and moreover, some specific cultivars among indica rice accumulate much higher Cd in vegetative tissues and grains. Recently, several transporters have been identified as a Cd transporter in rice by forward and reverse genetics and their functions in these processes will be reviewed in the following sections and summarized in Figure 1.

6In plants and mammals, many of transporters for divalent transition metals have a Cd2+ uptake activity. In mammals, ZIP8 and ZIP14, two transporters belonging to the Zinc-regulated transporter (ZRT) -like, Iron-regulated transporter (IRT) -like protein (ZIP) family, transport Cd2+ as well as Mn2+, Fe2+ and Zn2+. In plants, it has been demonstrated much earlier than in mammals that AtIRT1, a ZIP family transporter for Fe2+, Zn2+ and Mn2+ also mediates Cd uptake in roots of Arabidopsis thaliana. AtIRT1 is the primary transporter for the strategy-1 iron (Fe2+) uptake system in A. thaliana. In rice, iron is mainly absorbed by the strategy-2 system in the form of Fe-phytosiderophore, but Fe2+ transporters have been also identified which may function in Fe2+ uptake by roots. OsIRT1 and OsIRT2 have an influx activity of Cd2+ as well as Fe2+ in yeasts, suggesting that OsIRTs play some role in root Cd uptake especially after release of pounded water during intermittent water management (Ishimaru et al. 2006; ). They suggested that under flooded paddy soils, OsIRTs might be induced by lower levels of available iron and after water release induced OsIRTs might contribute to uptake of Cd which was much available in aerobic conditions. When OsIRT1 was overexpressed, Cd accumulation in roots and shoots was increased under MS medium containing excess Cd, but this phenotype was not observed in the field condition. These suggest that OsIRT1 is potentially involved in root Cd uptake but its contribution is largely affected by the environmental (soil) conditions.

7Transporters of natural resistance-associated macrophage protein (Nramp) family are also known to mediate Cd transport. In mammals, DCT1/DMT1/Nramp2 functions in Cd2+ uptake as well as uptake of Zn, Mn, Fe, Co and Ni ions. In plants, at the same time, it has been demonstrated that AtNramp1, AtNramp3 and AtNramp4 mediate inward Cd transport in yeasts and overexpression of AtNramp3 resulted in increased sensitivity to Cd. In rice, there are seven Nramp genes. OsNramp1, an iron transporter, has been established as a Cd-influx transporter in the plasma-membrane. The cell-type specificity of OsNramp1 expression was not examined but the mRNA expression was much higher in roots than in shoots. OsNramp1-overexpressing rice plants accumulated less Cd in roots and much Cd in shoots compared to the wild-type plants when grown in media containing 1 μM or less Cd, suggesting that OsNramp1 is possibly involved in Cd transport into roots. Much interesting finding of their report is higher expression of OsNramp1 in indica cultivars. Comparing Sasanishiki (a japonica cultivar) and Habataki (a indica cultivar), the root-to-shoot Cd translocation ability is greater in Habataki. Following QTL analysis of a mapping population obtained by crossing the two cultivars, a major QTL for high Cd accumulation in shoots of Habataki was detected on the short arm of Chr. 7. Although the responsible gene has not been identified, this QTL contains OsNramp1. There was no difference in the amino acid sequences of OsNramp1 between Habataki and Sasanishiki, but the gene expression was higher in Habataki and other indica cultivars probably caused by several insertion and deletion in the promoter region. This higher expression of OsNramp1 in indica cultivars may partly explain higher Cd accumulation in shoots of indica rice independent from the effect of OsHMA3, another Cd transporter described in the next section.

8The ability of xylem-mediated Cd translocation into shoots is shown as a major determinant for shoot Cd accumulation in many plants including rice. In A. thaliana and A. halleri (a Cd/Zn hyperaccumulator), the key transporters for xylem Cd transport have been first identified. In A. thaliana, the P1B-type ATPase AtHMA2 and AtHMA4 regulate root-to-shoot translocation of Cd and Zn. In A. halleri, AhHMA4, a homolog of AtHMA4 plays a critical role in translocation of Cd and Zn into shoots. The enhanced promoter activity and increased gene copy number of AhHMA4 result in higher expression of AhHMA4 in root stele and contribute to hyperaccmulation and hypertolerance of Cd and Zn in A. halleri.

9Following the identification of the genes for xylem Cd transport in A. thaliana and A. halleri, OsHMA3 has been identified as a regulator for xylem Cd transport in rice by mediating vacuolar sequestration of Cd in root cells. Compared to AtHMA4 and AhHMA4, OsHMA3 has some unique features. All these HMAs mediate Cd efflux transport, but OsHMA3 reportedly does not transport other metals such as Zn, whereas AtHMA4 and AhHMA4 functions in both Zn and Cd transport. Subcellular localization also differs between OsHMA3 and others. OsHMA3 is suggested to be localized to the vacuolar membrane, but AtHMA4 and AhHMA4 are localized to the plasma-membrane. The major difference of OsHMA3 and Arabidopsis HMA4s is the physiological function in plants. In the Nipponbare background, RNAi-mediated knock-down of OsHMA3 increased root-to-shoot Cd translocation and the overexpression reduced shoot Cd accumulation. They suggests that in Nipponbare, OsHMA3 functions in vacuolar compartmentation of Cd in root cells and hence reduces the xylem loading of Cd and subsequent shoot Cd accumulation, whereas AtHMA4 and AhHMA4 facilitate loading of Cd into the xylem. This finding reveals the mechanism for limiting Cd translocation into shoots in japonica rice.

10At the same time, they found a single amino acid substitution in OsHMA3 from some indica cultivars (Anjana Dhan, Cho-ko-koku and Jarjan) which results in the loss-of-function. These cultivars show remarkably high Cd accumulation in shoots and grains even compared to other indica cultivars under the moderately Cd contaminated soil and the non-Cd-contamintation soil. Imaging analyses using PETIS demonstrated more rapid and greater Cd translocation from root-to-shoot in these Cd-high-accumulating cultivars. The loss-of-functional allele of OsHMA3 is responsible for exceedingly higher root-to-shoot Cd translocation in these cultivars, because the non-functional OsHMA3 may result in failure of Cd compartmentation into vacuoles in root cells. This allele has not been detected in several japonica cultivars and also other indica cultivars such as Habataki, suggesting that this OsHMA3 is not the casual gene for general difference in Cd accumulation between indica and japonica rice.

11There has been no report of transporters for phloem Cd transport in plants so far, although in rice, phloem mediates nearly 100% of the Cd deposition into grains. Xylem-to-phloem Cd transfer at nodes is suggested and phloem Cd transport through a panicle neck shows genotypic variation. These suggest the existence and involvement of transporters at nodes for phloem Cd transport into grains. Remobilization of Cd from leaf blades to grains also appears to be mediated by phloem transport.

12Recently, we have identified a transporter gene involved in phloem Cd transport. This rice gene, named OsLCT1, is the homolog of wheat Low-affinity Cation Transporter1, and encodes a Cd-efflux transporter on the plasma-membrane. OsLCT1 expression was higher in leaf blades and nodes during reproductive stages. Especially in node I, the uppermost node, OsLCT1 was mainly expressed in diffuse vascular bundles which connected to panicles. In the Nipponbare background, Cd levels in grains and phloem exudate from leaf blades were substantially reduced in RNAi plants compared to control plants, although Cd concentration in xylem sap did not differ. These results suggest that OsLCT1 in leaf blades functions in Cd remobilization by phloem, and in node I, OsLCT1 is likely to play a part in intervascular Cd transfer from enlarged large vascular bundles to diffuse vascular bundles, which connect to the panicle. This is the first identification of a transporter for phloem Cd transport in plants.

13In addition to the transporters involved in long-distance Cd transport processes described above, rice genes related to excess Cd stress have been reported. These genes might function in subcellular Cd transport such as exclusion of Cd from cytoplasm to apoplast and compartmentation into vacuoles as well as damage repairing processes that appear to be a mechanism underlying plant Cd tolerance. In this section, recent findings of rice genes possibly functioning in Cd homeostasis are reviewed. Although understanding of Cd tolerance may not directly contribute to advance establishment of "low-Cd-rice", the genes related to Cd tolerance may be potentially applied to manipulate rice Cd accumulation by regulating such as subcellular Cd transport.

14Several ATP-binding cassette (ABC) proteins are suggested to mediate vacuolar compartmentation of Cd-glutathione and/or phytochelatin (PC) conjugates in baker's yeasts, fission yeasts, the worm Caenorhabditis elegans and A. thaliana. A member of ABC proteins of human and A. thaliana functions in Cd extrusion from the cytoplasm. We have recently reported that rice OsPDR5/ABCG43 is likely to encode an ABC-type protein for cellular Cd tolerance. The transcript of ABCG43 was remarkably induced in rice roots by Cd treatments, suggesting a possible involvement of ABCG43 in Cd tolerance in rice, although detailed mechanisms should be further investigated. A rice transporter for a Cd-PC conjugate would be also further identified, as demonstrated in A. thaliana.

15There are reports of rice genes for new mechanisms of Cd tolerance. A novel rice gene Low cadmium (LCD) is involved in Cd accumulation and tolerance. Knock-out of LCD resulted in reduced Cd accumulation and increased growth under excess Cd. But LCD-GFP was localized to the cytoplasm and nucleus, suggesting that LCD is not a membrane-transporter. LCD is not homologous to any other genes, and the authors concluded that LCD is a novel protein related to Cd homeostasis. reported that a novel cysteine-rich peptides encoded by OsCDT1 is possibly involved in rice Cd tolerance. Overexpression of OsCDT1 in A. thaliana increased the growth of plants under Cd exposure.

16These reports indicate that novel mechanisms mediated by unknown molecules functions in Cd tolerance in plants and also indicate that rice is a potential genetic material for mining new genes related to Cd stress and/or accumulation. We have screened mutant populations and various genotypes and found several Cd-sensitive lines (Figure 2a) and one Cd-tolerant line (Figure 2b). Because there exist few examples of Cd-tolerant lines, analyses of these lines would contribute to advance understanding of Cd toxicity and tolerance in organisms.

17Considering substantial contribution of Cd in rice grains to higher Cd intake in Asian people, reducing Cd pollution of paddy fields and rice grain Cd accumulation are major issues to the field of agricultural science. Not only in the case of "Itai-itai disease" in Japan, but in some areas in China and Thailand, there are reports of Cd contamination of paddy soils and rice grains and renal disfunction in the populations. In Japan, the Ministry of Agriculture, Forestry, and Fisheries of Japan encourages rice growers to keep paddy fields flooded before and after heading to reduce Cd uptake by rice in Cd-contaminated areas. This is based on the fact that under the flooded condition, the soil is under a reductive condition and a large part of Cd in the soil forms CdS with low solubility. On the other hand, once the field is drained, the soil becomes an oxidative condition and CdS in the soil is changed to Cd2+ which is much available to plants. This flooding water management before and after heading drastically reduces grain Cd concentrations, but on contrary, this treatment increases arsenic concentration in grains. Moreover, it seems difficult to uniform the flooding condition through entire paddy fields during the treatment, which may partially fail in reducing Cd availability in soils. Soil removal, replacement and soil inversion are possible other options and these have been conducted in some highly Cd-polluted paddy areas in Japan. This method is a quick solution for the contamination, but is cost-ineffective and requires a large amount of alternative soils. These features make it unpractical to apply this method to a much larger areas of paddies with moderate Cd contamination. Alternatively, several approaches to clean-up moderately Cd-polluted paddy soils have been suggested. Phytoextraction using the high-Cd-accumulating cultivar such as Cho-ko-koku and chemical washing of soils using ferric chloride are possible methods in terms of efficiency, cost and environmental effects.

18In combination to these soil remediation methods, establishment of "low-Cd-rice" based on genetic and molecular findings is expected as a promising approach to reduce human Cd intake. Regulation of Cd transporters by the transgenic technique has been used successfully to reduce Cd accumulation in rice plants. Overexpression of a functional allele of OsHMA3 in Nipponbare background resulted in drastic reduction of grain Cd concentration under a soil with relatively high Cd concentration (1.5 mg/kg). These OsHMA3 overexpressing rice reported in their manuscript did not show any reduction in zinc and iron contents in grains, although the growth of the plants was not reported. This phenotype is noteworthy because zinc and iron are important minerals for human. However, Cd accumulation of these OsHMA3 overexpressing rice under moderate or slight Cd contamination often observed in fields should be examined further.

19Knock-down of OsLCT1 also reduced grain Cd by 50% under the soil containing 0.2 mg Cd/kg. This soil Cd concentration is comparable to the average of Cd levels in Japanese soils, suggesting the significant potential of OsLCT1 alleles in establishing a rice cultivar which accumulates less Cd in grain under soils with slight Cd contamination. Importantly, the growth and mineral contents in grains were not negatively affected in these OsLCT1-knockdown plants.

20These studies are good examples of the molecular approach based on physiological observations. Xylem loading and phloem transport are both shown as important transport processes determining grain Cd accumulation and the regulation of the responsible genes for the respective process enables reducing grain Cd levels without affecting quantity and quality of products. But one of the further issues for marketing "low-Cd-rice" in Japan is to establish "low-Cd-rice" by a non-transgenic approach. In Japan, the present consumers largely prefer non-transgenic agricultural products rather than those of genetically modified plants. Screening non-functional allele of OsLCT1 from chemically or radiation mutagenized populations with a background of major cultivars such as Koshihikari and establishing "low-Cd Koshihikari" is a possible practical approach. Another possible strategy is a marker-assisted breeding. For example, identification of a QTL for low-Cd-accumulation from a low-Cd-accumulating cultivar will enable to establish "low-Cd Koshihikari" by introducing the low-Cd QTL into Koshihikari by a marker-assisted breeding.

21Manipulation of transporter genes expression also enables to generate high-Cd-accumulating rice. Overexpression of OsNramp1 and OsIRT1 increased shoot Cd accumulation in rice plants. Knock-down of OsHMA3 also increased root-to-shoot Cd translocation. These high-Cd-accumulating plants will be applied to remove Cd from Cd-polluted paddy soils (phytoextraction). introduced a non-functional allele of OsHMA3 from a high-Cd-accumulating cultivar Jarjan into Koshihikari by marker-assisted selection. These plants with a Jarjan allele of OsHMA3 showed a good Cd-removing ability from soils in a background of Koshihikari. They demonstrated that marker-assisted selection enabled to generate a high-Cd-accumulating rice with resistance to shattering and lodging and with larger biomass. These plants will increase the efficiency of phytoextraction operation in the field compared to using the high-Cd-accumulating rice such as Cho-ko-koku and Jarjan.

22Within the last few years, understanding of Cd transport and identification of the responsible genes in rice have been largely advanced. But it is possible that unknown transporters or other molecules are involved in rice Cd transport and tolerance. Moreover, mining of useful alleles is essential to establish non-transgenic low/high-Cd-accumulating rice. The progress of understanding and application in rice regarding Cd transport may be extended to other cereals.

23The authors declare that they have no competing interests.

24SU and TF wrote the manuscript. Both authors have read and approved the final manuscript.