Aluminium Toxicity and Stress Resistance : Transgenic Approach

DOI : 10.17577/IJERTV2IS120563

Download Full-Text PDF Cite this Publication

Text Only Version

Aluminium Toxicity and Stress Resistance : Transgenic Approach

Aluminium Toxicity and Stress Resistance : Transgenic Approach

Nidhi Gupta and Ashwani Kumar1

Department of Biotechnology, C.C.S. University, Meerut-250004, India

1Former Head of the Department of Botany, University of Rajasthan, Jaipur 302004

Abstract

Aluminium toxicity and tolerance mechanisms differ strikingly with its chemical form, and the study of aluminium related processes is complicated by the complex chemistry of aluminium. Therefore the experimental results may differ with experimental conditions such as pH and coexisting ions, even when the same concentration of Al is used. Therefore, germplasmsthose are collected from acid soil areas shows best tolerance or sensitivity and thus suitable for entry scheme in Al- tolerance breeding. To identify tolerant somatic cell variants, genotypes with high aluminium tolerance as well as genetic engineering methods, in vitro techniqueshavebeen used.Stimulation of Al- tolerant genes and proteins due to Al exposure provides an impetus reason to the researchersfor molecular studies in plants. In this direction, the first approach was the expression of a Pseudomonas aeruginosa citrate synthase gene in tobacco. However, the molecular and genetic bases are still not

well understood. Aluminium resistance genes have yet to be cloned from any species, with the exception of ALMT1 from wheat.

Key words: Aluminium, Genetic engineering, Molecular studies, ALMT1.

  1. Aluminum, third most abundant metal, represents approximately 8% of the total mineral components in the earths crust (Verstraeten, et al., 2008). It has a ubiquitous presence in the human environment and thus, in acid soils, its toxicity shows the primary growth-limiting factor in plants (Foy, 1992). In poor Ca and Mg soils, it becomes more severe (Vitorello,

    et al., 2005). Aluminum, in its Al3+ cationic

    form, is very inimical to agriculture, as it becomes toxic in nature (pH below 5) which injures plant root cells and interfere nutrient and water uptake in crop plants(Samac andTesfaye, 2003), thus damaged root system and inhibits plant root growth(Barceló and Poschenrieder, 2002).

    Although Al toxicity has become one of the active area for research; however, physiological, molecular and genetic basis are still not wellunderstood.The cellular components and processes have been proposed to be most affectedby Al toxicity.Some of the most affected components are; cell nuclei, cell division and mitosis (Silva,et al., 2000), uptake of Caand other ions (Ryan,et al., 1993; Liu and Luan, 2001), composition, physical properties and structure of the plasma membrane (Zhang,et al., 1997; Ishikawa and Wagatsuma, 1998), oxidative stress (Yamamoto,et al., 2003) and cytoskeletal dynamics (Sivaguru,et al., 1999).

    A number of studies haveproposed thatAl3+induces the formation of ROSand oxidative stress which results in Al toxicity. This all helps in the synthesis of oxidative stress response proteins. Moreover, it

    enhances the enzymes activity (Catalase and SOD) and lipid peroxidation in Pisumsativum (Yamamoto, et al., 2001) Glycine max (Cakmak and Horst, 1991), and Nicotianatabacum (Ono, et al., 1995; Yamamoto, e al., 1997; Ikegawa, et al., 2000).It is also suggested that the oxidative stress brings to changes in the expression of various genes in Arabidopsis (Sugimoto and

    Sakamoto, 1997; Richards, et al., 1998), tobacco (Ezaki, et al., 2000) and wheat (Snowden and Gardner, 1993; Cruz-Ortega, et al., 1997; Hamel, et al., 1998). For example, Al induces the expression of genes that encode blue-copper proteins, glutathione S-transferase and peroxidases.

    Ezaki, et al. (2000) observed that due to over-expression of some induced proteins, there was an increase in Al tolerance and increased tolerance to oxidative stress in Arabidopsis. Study in yeast has also shown that rather than organic acid efflux, over- expression of genes is the reason for Al tolerance (MacDiarmid and Gardner, 1998).

    1. Conventional

      To improve nutrient use efficiency and to enhance crop productivity, a diverse set of approaches like molecular breeding, agronomyis required. Multiple aspects are required or have to be considered for the simultaneous crop improvement like crop performance, evaluated in a multidisciplinary approach as in biotic and abiotic stress, etc.(Parry and Hawkesford, 2012).

    2. Transgenic approaches for increasing Al resistance

      It is estimated that, by the year 2050, world population will beraised by two billion people. To fulfill their demands like food, bre, fodder and other animal feed, crop production will need to be increased by more than 50% and this can be done by increasing cropping intensity and yields, even in the challengingcultivating conditions like acids soil lands, unsuitable for farming.Acid soils are widely distributed in Asia, sub-Sarahan Africa and other regions where, there is heavy population.Thisproblem of acid soils is most severe in the humid tropics. In Colombia, for example, 70% of the agricultural land is acidic. Plant crops which shows high sensitivity to soil acidity (example; maize, soybean, cotton, etc.) are unable to grow well in the tropics (Fuente, et al., 1997 and Barinaga, 1997).

      As the land area cannot be increased and aerable land is limited, it is imperative to use acid soils for cultivation. Hence, transgenic crops are in great need for such areas.For enhancing Al tolerance, a wealth of studies can be sited in literature on the expression of genes in plants. For this, two different approaches have been taken: 1) Al-induced

      plant genes expression and 2) expression of genes to increase organic acid production. However, it is doubtful that alteration in the single gene expression will confer high levels of Al tolerance, due to the complex physiological effect of Al on plant cells. Some studies have revealed that combinations of transgenes can increase Al tolerance in plants (Ezaki,et al., 2001).

      Moreover, it may also be possible to identify microbial genes that confer Al tolerance in their host and enhance Al tolerance in plants. For example, two genes, on encoding for an Arabidopsis blue copper-binding protein and other a tobacco putative GDP- dissociation inhibitor, have shown Al tolerance to yeast (Ezaki,et al., 2000).

    1. Germplasm sources

      Germplasm of some species (e.g. in barley and alfalfa) are limited for Al tolerance. Whereas some of the Al-tolerant crop varieties show a large number andmost of them are obtained and developed from highly acidic soils lands of the world (Hede, et al., 2001; Stodart, et al., 2007; Caniato, et al., 2011). For example, out of 250 bread

      wheat landraces, originated from 21 countries, 25 accessions were found to be Al tolerant and were collected from highly acid soils area of Nepal. Adaptation,natural selection orhuman selection by early agriculturalists might be the reason for such associations (Stodart, et al., 2007; Caniato, et al., 2011). Therefore, it may be logical and appropriate strategy of collecting germplasms from acid soil areas for Al- tolerance species.

    2. Genes for Al tolerance

      To reduce Al stress, the identification of stress-regulated genes plays an important role (Abate, et al., 2013). Some of the Al stress regulated genes, for example, could play an important role against oxidative stress or in alleviating phosphate deficiency. It is to be noted that due to the precipitation with Al, nutrients deficiency, especially phosphate, takes place in plants(Houe and Diallo, 2008).As studied in many plant species like rye (Secalecereale), triticale (Triticale ssp.) and sicklesenna(Cassia tora), Al exposure induces Al-resistance related genes and proteins (Li,et al., 2000a, b; Ma,et al., 1997a).

      In some cases, when Al-sensitive cultivar and Al-tolerant cultivar werecrossed, it was observed that resistance against Al toxicity is due to a single, dominant locus while two loci are responsible for resistance, in some other cases (Garnin and Carver, 2003). Wheat, in its inheritance, is one of the most and longtime studied plants for Al- resistance, and genetic studies have shown that Al-tolerance in wheat plant is controlled by multi-genes (Takagi, 1983; Aniol, 1990; Carver and Ownby, 1995).For example,wheat genotype- Atlas 66was reported, having a complex genetic mechanism with several genes for Al resistance(Berzonsky, 1992).Alt2 orAltBHis one of the loci in wheat (Milla and Gustafson, 2001), mapped on the long arm of chromosome-4D.

      Rye (Secalecereale) hasalso shown an excellent resistance to abiotic stresses including Al, when compared to its close relative wheat(Aniol and Gustafson, 1984). In fact, a greater number of Al tolerant loci are detected than in wheat (Aniol and Gustafson, 1984; Gallego and Benito, 1997; Hede, et al., 2001). Another member of the sametribe, Barley (Hordeumvulgare), has also shown Al-resistance locus, Alp, on the long arm of chromosome-4 (Minella and Sorrells, 1992). Sorghum (Sorghum bicolor

      L. Moench) exhibits a simple pattern of inheritance with a single locus (Magalhaes, 2002; Magalhaes, et al., 2003). BnALMT1 and BnALMT2, two genes from rape (Brassica napus),have shown Al tolerance and homology to ALMT1 from wheat(Panda, et al., 2009). Al resistance in rice was identified under the control of two genes, STAR1 and STAR2 (Huang, et al., 2009).

      Triticale is a hybrid, obtained by crossing wheat and rye synthetically, whose tolerance against Al toxicity is believed to be inherited from rye and is largely grown on acid soils in South America, Europe and Australia (Pfeiffer, 1993). It is believed that genes necessary for Al tolerance are carried on the short arm of chromosome 3R (Aniol and Gustafson, 1984). A Brazilian genetic study reveals that oat (Avena sativa) has only one or two dominant genes against Al with tolerance genotype carrying AlaAla (Ezaki, et al., 2000). Under Al stress, expression mechanism of two GST genes in Arabidopsis AtGST1 and AtGST11 was studied(Ezaki, et al., 2004).

      In the early eighties, Luis Herrera-Estrella was the first to develop transgenic plants. Heacquainted the citrate synthase (CSb) gene in rice and corn (Barinaga,

      1997).When transgenic CSb plants weregrown under extreme acidic conditionswith high aluminum concentration, lower root growth inhibition was found as compared to the untransformed plants. It might be because the citrate synthase produced by transgenic plants was preventing Al uptake (Prakash, 1997). Moreover, the Mexican scientists had introduced a bacterial CSb gene into tobacco and papaya and found these genetically engineered plants more tolerant to the insidious metal (Prakash, 1997).

      Thus, transgenic plants may help in using the soils for cultivationthat were once inhospitable because of toxicity(Barinaga, 1997). This technology of genetic engineering seems to have great potential in enhancing agricultural yield and productivity, specially, in developing countries where there is urgent requirement of more food and where toxic effects of aluminum are at their worst; thus helps in fighting with problems of the real world.

  2. Production ofa successful and productive transgenic plant depends on 1)characteristics of the gene expression cassettes, 2)DNA deliver method into the recipient cellsand 3)

    tissue culture and selection techniques used to regenerate fertile plants from the transformed cells (Repellin, et al., 2001). Systematic optimization of the above steps would help in the development of transformation protocols for plants. Certain criteria must be accomplished to demonstrate the transgenic nature of a plant(Potrykus, 1990) such as detailed information for phenotypic, genetic and molecularcharacterization of the primary transformant and its offspring. However, it is not mandatory that stable transmission and expression of the transgenic plant would always be achieved, but it is an essential factor for developing commercial cultivars.

More than 50% of the worlds aerable lands are acidic. Al, in its cationic form, Al3+, gets easily solubilized in this acidic soil, thus becomestoxic and represents plant growth inhibition asprimary factor in plants.

Therefore,Al toxicity has become one of the active areas for researchglobally, to determine the mechanisms responsible for Al toxicity and tolerance.Presence of Al in plant root cells interfere a number of biological activities, thus altering cellular mechanisms. To cope up, traditional

agricultural strategies, like, selection and breeding processes, may help in developing Al tolerant plant cultivars. Conventional plant breeding, along with classical cytogenetic techniques, represented the main method of cereal crop improvement. However, designing appropriate screening method remains a challenging task for characterizing Al tolerant species. A number of studies have been done to achieve the goal of developing crop varieties better suited for cultivation with Al toxicity in acid soil.In this regard, biotechnological tools have played an enormous role in providing suitable protocols for finding the genes from unrelated sources that become available to be introduced asexually into plants.Recombinant DNA techniques helped in the collection of different genes from microbes, plants and animals, some of which may be useful for crop improvement. Nutritional quality of rice and dough functionality in wheat have been improved by the use of biotechnological tools. Genomics, proteomics and bioinformatics; other tools of biotechnology, would also help in collecting the required information for the improvement of current cereal.

Verstraeten, SV, Aimo, L&Oteiza, PI (2008) Aluminium and lead: molecular mechanisms of brain toxicity. Archives of Toxicology Springer, 82, 789-802.

Vitorello VA, Capaldi FRC &Stefanuto VA (2005) Recent advances in aluminum toxicity and resistance in higher plants. Brazilian Journal of Plant Physiology, 17, 129-143.

Samac,DA &Tesfaye, M (2003) Plant improvement for tolerance to aluminum in acid soils a review. Plant Cell, Tissue and Organ Culture, 75, 189207.

Barcelo´, J &Poschenrieder, C (2002) Fast root growth responses, root exudates, and internal detoxication as clues to the mechanisms of aluminium toxicity and resistance: a review. Environmental and Experimental Botany, 48, 7592.

Silva, IR, Smyth, TJ, Moxley, DF, Carter, TE, Allen, NS &Rufty, TW (2000) Aluminumaccumulation at nuclei of cells in the root tip.Fluorescence detection using lumogallion and confocallaser scanning

microscopy.Plant Physiology, 123, 543

552.

Ryan, PR, DiTomaso, JM &Kochian,LV(1993) Aluminium toxicity in roots: an investigation of spatial sensitivity and the role of the root cap. Journal of Experimental Botany, 44, 437446.

Liu, K & Luan, S(2001) Internal aluminum block of plant inward K+channels.Plant Cell,

13, 145365.

Zhang, G,Slaski, JJ,Archambault,DJ and Taylor, GJ (1997) Alteration of plasma membrane lipids in aluminum-resistant and aluminum-sensitive wheat genotypes in response to aluminum stress. PhysiologiaPlantarum. 99, 302-308.

Ishikawa, S &Wagatsuma, T (1998) Plasma Membrane Permeability of Root-Tip Cells Following Temporary Exposure to Al Ions Is a Rapid Measure of Al Tolerance among Plant Species. Plant Cell Physiology, 39, 516-525

Yamamoto, Y, Kobayashi, Y, Devi, SR, Rikiishi, S & Matsumoto, H (2003) Oxidative stress triggered by aluminum in plant roots.Plant Soil, 255, 239-243.

Sivagur, M,Baluka, F, Volkmann, D,Felle, HH &HorstWJ (1999) Impacts of aluminum on the cytoskeleton of the maize root apex. Short-term effects on the distal part of the

transition zone.Plant Physiology, 119, 1073-

82.

Yamamoto, Y, Kobayashi, Y & Matsumoto, H (2001) Lipid peroxidation is an early symptom triggered by aluminum, but not the primary cause of elongation inhibition in pea roots. Plant Physiology, 125, 199208.

Cakmak, I& Horst, JH (1991) Effects of aluminum on lipid peroxidation, superoxide dismutase, catalase, and peroxidase activities in root tips of soybean (Glycine max). PhysiologiaPlantarum, 83, 463- 468.

Ono, K, Yamamoto, Y, Hachiya, A& Matsumoto, H(1995) Synergistic inhibition of growth by aluminum and iron of tobacco(NicotianatabacumL.)cells in suspension culture.Plant Cell Physiology, 36, 115125.

Yamamoto, Y, Hachiya, A & Matsumoto, H (1997) Oxidative damage to membrane by a combination of aluminum and iron in suspension-cultured tobacco cells.Plant Cell Physiology, 38, 133339.

Ikegawa, H, Yamamoto, Y& Matsumoto, H (2000) Responses to aluminum of suspension-cultured tobacco cells in a

simple calcium solution.Soil Science and Plant Nutrition, 46, 503-514.

Sugimoto, M & Sakamoto, W(1997) Putative phospholipid hydroperoxide glutathione peroxidase gene from Arabidopsis thaliana induced by oxidative stress. Genes and Genetic System, 72, 311 316.

Richards, KD, Schott, EJ, Sharma, YK, Davies, KR & Gardner, RC(1998) Aluminum induces oxidative stress genes in Arabidopsis thaliana. Plant Physiology, 116, 409418.

Ezaki, B, Gardner, RC, Ezaki, Y & Matsumoto, H (2000) Expression of aluminum-induced genes in transgenic Arabidopsis plants can ameliorate aluminum stress and/or oxidative stress. Plant Physiology, 122, 657665.

Snowden, KC& Gardner, RC(1993)Five genes induced by aluminum in wheat (Triticumaestivum) roots. Plant Physiology, 103, 855861.

Cruz-Ortega, R, Cushman, JC &Ownby, JD(1997) cDNA clones encoding 1,3-b- glucanase and a mbrim-like cytoskeletal protein are induced by Al toxicity in wheat roots. Plant Physiology, 114, 1453 60.

Hamel, F, Breton, C &Houde, M (1998) Isolation and characterization of wheat aluminum-regulated genes: possible involvement of aluminum as a pathogenesis response elicitor. Planta, 205, 531538.

MacDiarmid, CW & Gardner, RC (1998) Overexpression of the Saccharomyces cerevisiae magnesium transport system confers resistance to aluminum ion. The Journal of Biological Chemistry, 273, 1727-

32.

Parry, MAJP &Hawkesford, MJ (2012) An integrated approach to crop genetic improvement. Journal of Integrative Plant Biology, 54, 250259.

de la Fuente, J, Ramirez-Rodriguez, V, Cabrera-Ponce, J& Herrera-Estrella, L (1997) Aluminum tolerance in transgenic plants by alteration of citrate synthesis.Science, 276, 1566-68.

Barinaga, M(1997) Making plants aluminum tolerant. Science, 276, 1497.

Ezaki, B, Katsuhara, M, Kawamura, M & Matsumoto, H (2001) Different mechanisms of four aluminum (Al)-resistant transgenes for Al toxicity in Arabidopsis. Plant Physiology,127, 918-927.

Hede, A, Skovmand, B& Lopez-Cesati, J (2001) Acid soils and aluminum toxicity.In Application of physiology in wheat breeding.Ed.M Reynolds. pp. 172182. CIMMYT, Mexico, D.F.

Stodart, BJ, Raman, H, Coombes, N & Mackay, M (2007) Evaluating landraces of bread wheat (Triticumaestivum L.) for tolerance to aluminium under low pH conditions. Genetic Resources and Crop Evolution, 54, 759-766.

Caniato, FF, Guimaraes, CT, Hamblin, M, Billot, C, Rami, J-F, Hufnagel, B, Kochian, LV, Liu, J, Garcia, AAF, Hash, CT, Ramu, P, Mitchell, S, Kresovich, S, Oliveira, AC, de Avellar, G, Borem, A, Glaszmann, J-C, Schaffert, RE &Magalhaes, JV (2011). The Relationship between Population Structure and Aluminum Tolerance in Cultivated Sorghum.PLoS ONE, 6, e20830.

Abate, E,Hussien, S, Laing, M&Mengistu, F (2013) Aluminium toxicity tolerance in cereals: Mechanisms, genetic control and breeding methods, A review. African Journal of Agricultural Research, 8, 711-

722.

Houde, M& Diallo, AO (2008) Identification of genes and pathways associated with aluminum stress and tolerance using transcriptome profiling of wheat near-isogenic lines. BMC Genomics, 9, 400.

Li, X, Ma, J &Matsumoto, H (2000a) Pattern of aluminium induced secretion of organic acids differ between rye and wheat. Plant Physiology, 123, 1537-44.

Li, XF, Ma, JF, Hiradate, S & Matsumoto, H (2000b) Mucilage strongly binds aluminium but does not prevent roots from aluminium injury in Zea mays.Plant Physiology, 108,152-160.

Ma, J, Zheng, S& Matsumoto, H (1997a) Specific secretion of citric acid induced by Al stress in Cassia tora L. Plant Cell Physiology. 38, 101925.

Garvin, D & Carver, BF (2003) Role of the genotype in tolerance to acidity and aluminium toxicity. In: Rengel Z (ed) Handbook of soil acidity, Marcel Dekker, New York.

Takagi, H, Namai, H & Murakami, K (1983) Exploration of aluminum tolerant genes in wheat.InS Sakamoto, ed, Proceedings 6th International Wheat Genetics Symposium. Kyoto, Japan.

Aniol, A (1990) Genetics of tolerance to aluminium in wheat (TriticumaestivumL.Thell) Plant Soil,123, 223-227.

Carver, BF &Ownby, JD (1995) Acid soil tolerance in wheat. Advances in Agronomy, 54, 117-173.

Berzonsky, WA (1992)The genomic inheritance of aluminum tolerance in Atlas 66 wheat. Genome, 35, 689693.

Milla, MAR& Gustafson, JP (2001) Genetic and physical characterization of chromosome 4DL in wheat.Genome, 44, 883892.

Aniol, A &Gustafson, JP (1984) Chromosome location of genes controlling aluminium tolerance in wheat, rye and triticale. Canadian Journal of Genetics and Cytology, 26, 701705.

Gallego, F & Benito, C (1997) Genetic control of aluminium tolerance in rye (Secalecereale L.).Theoretical and Applied Genetics, 95, 393399.

Minella, E &Sorrells, M (1992) Aluminum Tolerance in Barley Genetic Relationships among Genotypes of Diverse Origin.Crop Science, 32, 593598.

Magalhaes, J (2002) Molecular genetics and physiological investigations of aluminum tolerance in sorghum (Sorghum bicolor L. Moench).PhD thesis, Cornell University, US.

Magalhaes, J, Garvin, D, Sorrels, M, Klein, P, Schaffert, R, Wang, Y, Li, L&Kochian, L (2003) Comparative Mapping of AltSB, a Novel Aluminum Tolerance Gene in Sorghum bicolor (L.) Moench, Reveals Inter-Tribe Synteny among Al Tolerance Genes in the Poaceae. Genetics, 167, 53-63.

Panda, SK,Baluska, F & Matsumoto, H (2009) Aluminum stress signaling in plants.PlantSignaling & Behavior, 4, 592-

97.

Huang, CF, Yamaji, N, Mitani, N, Yano, M, Nagamura, Y & Ma, JF (2009)A bacterial- type ABC transporter is involved in aluminum tolerance in rice. Plant Cell, 21, 655667.

Pfeiffer, WH (1993) Estimation of triticale area in countries growing 1,000 hectares or more in 1986. 11, 199192.

Ezaki,B, Suzuki, M, Motoda, H, Kawamura, M, Nakashima, S& Matsumoto, H (2004) Mechanism of Gene Expression of Arabidopsis Glutathione S-

Transferase,AtGST1, and AtGST11 in

Response to Aluminum Stress.Plant Physiology, 134, 167282.

Prakash, CS (1997) Crops engineered to tolerate Aluminium Toxicity.Center for Plant Biotechnology Research, Tuskegee University.

Repellin, A, BÃ¥ga1, M,Jauhar, PP&Chibbar, RN (2001)Genetic enrichment of cereal crops via alien gene transfer: New challenges. Plant Cell, Tissue and Organ Culture,64,159183.

Potrykus, I (1990) Gene transfer to cereals: an assessment. Biotechnology, 8, 535542.

Leave a Reply