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Molecular characterization of TaSTOP1 homoeologues and their response to aluminium and proton (H+) toxicity in bread wheat (Triticum aestivumL.)

BMC Plant Biology volume 13, Article number: 134 (2013) Cite this article

Abstract

Background

Aluminium (Al) toxicity is considered to be one of the major constraints affecting crop productivity on acid soils. Being a trait governed by multiple genes, the identification and characterization of novel transcription factors (TFs) regulating the expression of entire response networks is a very promising approach. Therefore, the aim of the present study was to clone, localize, and characterize the TaSTOP1 gene, which belongs to the zinc finger family (Cys2His2 type) transcription factor, at molecular level in bread wheat.

Results

TaSTOP1 loci were cloned and localized on the long arm of homoeologous group 3 chromosomes [3AL (TaSTOP1-A), 3BL (TaSTOP1-B) and 3DL (TaSTOP1-D)] in bread wheat. TaSTOP1 showed four potential zinc finger domains and the homoeologue TaSTOP1-A exhibited transactivation activity in yeast. Expression profiling of TaSTOP1 transcripts identified the predominance of homoeologue TaSTOP1-A followed by TaSTOP1-D over TaSTOP1-B in root and only predominance of TaSTOP1-A in shoot tissues of two diverse bread wheat genotypes. Al and proton (H+) stress appeared to slightly modulate the transcript of TaSTOP1 homoeologues expression in both genotypes of bread wheat.

Conclusions

Physical localization of TaSTOP1 results indicated the presence of a single copy of TaSTOP1 on homoeologous group 3 chromosomes in bread wheat. The three homoeologues of TaSTOP1 have similar genomic structures, but showed biased transcript expression and different response to Al and proton (H+) toxicity. These results indicate that TaSTOP1 homoeologues may differentially contribute under Al or proton (H+) toxicity in bread wheat. Moreover, it seems that TaSTOP1-A transactivation potential is constitutive and may not depend on the presence/absence of Al at least in yeast. Finally, the localization of TaSTOP1 on long arm of homoeologous group 3 chromosomes and the previously reported major loci associated with Al resistance at chromosome 3BL, through QTL and genome wide association mapping studies suggests that TaSTOP1 could be a potential candidate gene for genomic assisted breeding for Al tolerance in bread wheat.

Background

Aluminium (Al) toxicity is one of the major concerns for crop productivity in acidic soil, accounting for more than 50% of the global arable land [1]. Al is one of the highly abundant elements in the earth crust and under low pH conditions (acidic soils), it is solubilised in the soil in a toxic ionic form that inhibits root elongation. The primary response of plants to Al toxicity is the rapid inhibition of root growth, particularly in the root apex by blocking the process of cell division along with cell elongation, and subsequently inefficient absorption of nutrients and water from soil, resulting in the reduction of plant growth and overall productivity [2].

Plant species differ in the level of Al resistance because they evolved different mechanisms to overcome the selective pressure of Al toxicity imposed under acid soils [3]. These mechanisms can be broadly divided into two categories: Al resistance and Al tolerance. The Al resistance mechanism is often based on the Al exclusion from the root apex or the external detoxification of Al in the rhizosphere through the release of organic acid anions (oxalate, citrate and malate) from the roots limiting Al uptake [4]. On the other hand, the tolerance mechanism may involve the entrance of Al through the roots and its relocation (in the vacuole) or internal detoxification through Al chelating with organic acids (citrate and oxalate) [5]. These mechanisms have been validated at the molecular level, particularly with the functional characterization of the major genes such as ALMT (Aluminium-Activated Malate Transporter) and MATE (Multidrug and Toxic compound Exudation) in bread wheat (Triticum aestivum L.) [6] and sorghum (Sorghum bicolor L. Moench) [7], respectively. In addition, genes encoding transporters have been identified through mutational analysis, especially ABC transporters type (ALS1 and ALS3) in Arabidopsis [8, 9] and bacterial-type ABC transporters (STAR1 and STAR2) in rice (Oryza sativa L.) [10]. Recently, a plasma membrane localized transporter Nrat1 (Nramp aluminum transporter 1) was also found to be associated with Al tolerance particularly to trivalent form of Al in rice [11]. These genes are essential for Al resistance, and seem to be a part of the pathway involved in the secondary level of protection through uptake and redistribution of Al to less sensitive tissues in plants, although their actual function in Al tolerance mechanism in plant is still unclear.

There is strong evidence supporting the important role of regulatory genes (transcriptional factors) in plant tolerance to abiotic stresses [12–15]. Recently, the zinc finger transcription factors, STOP1 (sensitive to proton rhizotoxicity) and ART1 (Al resistance transcription factor) have been identified in Al sensitive mutants of Arabidopsis and rice, respectively [16, 17]. Transcriptome analysis under Al stress revealed that 101 and 31 genes were down-regulated in the Arabidopsis stop1 [18] and rice art1 mutants [17], respectively. Interestingly, the major genes related to Al tolerance, particularly ALMT1 and MATE1 were regulated by these transcription factors [18, 19]. Recently, the contribution of ART1 locus to the variation for Al tolerance in rice has also been identified in QTL analysis [20]. The limited impact of single functional genes in plant stress tolerance has been associated with the polygenic nature of such traits. Thus, the identification and characterization of key regulatory genes that act as master regulators controlling entire response networks would be the most promising and sustainable approach to modify complex traits in plants as they coordinate the expression of many target genes [21].

Wheat is one of the most important natural allopolyploid species, as it is not only directly or indirectly contributing in the food supply for nearly half of the worlds’ population but also can serve as a model plant for other economically important polyploid crop species. It is considered as one of the sensitive crop to Al stress among cereals. Bread wheat, with hexaploid nature comprised from three genomes (AABBDD) are organized in seven homoeologous groups, each homoeologous group has individual gene in triplicate form (from each of A, B and D genomes). Consequently, it is of great interest to reveal how the expressions of homoeologues genes are regulated in hexaploid wheat because theoretically, all the three homoeologues of a gene are assumed to be uniformly expressed. In the previous decade, several studies have been conducted in order to identify the molecular markers (random DNA markers) linked to Al tolerance through QTL mapping and genome-wide association analyses [22–26]. So far only two candidate genes ALMT1 and MATE1 for Al tolerance in wheat have been identified and also mapped on chromosome 4DL using Chinese Spring deletion lines and 4BL through QTL mapping, respectively [22, 27, 28]. Recently, the three homoeologues of TaMATE1 have been cloned [29], although, no information is available on the expression of respective homoeologues of these candidate genes for Al tolerance in hexaploid wheat. Therefore, in order to improve Al tolerance in bread wheat, identification of three homoeologues of the candidate gene is a promising strategy that could be utilized to develop functional markers for genomic assisted breeding programme in wheat. Herein, we report on the identification, physical localization, and molecular characterization of a novel transcription factor TaSTOP1 homoeologues genes in bread wheat for Al and proton (H+) tolerance.

Results

Cloning and structure of TaSTOP1

In order to clone the STOP1 in wheat, primers from wheat EST showing highest similarity with Arabidopsis thaliana STOP1 were used to amplify the TaSTOP1 in bread wheat genotype Barbela 7/72/92. Further, 5’ and 3’ UTR ends of TaSTOP1 were amplified using RACE as described in material and methods. TaSTOP1 was amplified in six different bread wheat genotypes and its multiple alignments suggested the mixed amplification from distinct wheat genomes (A, B, and D). Moreover, the comparison of the TaSTOP1 cDNA sequence with genomic sequence revealed that TaSTOP1 gene does not contain introns.

The coding region of TaSTOP1 (TaSTOP1-A) from genome A has 1533 bp length and is differentiated from genomes B (TaSTOP1-B) and D (TaSTOP1-D) by having a 6-bp deletion (1276–1281 positions). TaSTOP1-B and TaSTOP1-D are differentiated by several SNPs in the respective open reading frame (ORF) [Additional file 1]. TaSTOP1-D in bread wheat genotype Barbela 7/72/92 has a full-length cDNA of 1970 bp, containing a coding region of 1539 bp that encodes a polypeptide of 512 amino acids (Figure 1). TaSTOP1-D has a molecular weight of 55.8 kD, with a 5.64 isoelectric point (pI). InterProScan function domain analysis suggests that TaSTOP1 belongs to the Cys2His2 zinc finger family protein. Subcellular prediction analysis indicated that TaSTOP1 protein is localized in the nucleus.

Figure 1
figure 1

Nucleotide sequence of TaSTOP1-D from Barbela 7/72/92 and its deduced protein (amino acid sequences). The nucleotide sequence was presented over the deduced amino acid sequence. Note: translation stop codon was noted by-.

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Phylogenetic studies for STOP1 gene among plant species

Deduced amino acid sequence of TaSTOP1 consists of 510 (TaSTOP1-A) and 512 (TaSTOP1-B and TaSTOP1-D) amino acids in bread wheat and the phylogenetic relationship with other STOP-like proteins from 32 different plant species was studied based on their full length sequences. Phylogenetic analysis of STOP like proteins clearly formed two distinct clusters which implied that STOP2 (AT5G22890) was completely distinct from STOP1 (AT1G34370) in Arabidopsis. Furthermore, STOP1 and STOP2 protein from monocotyledons can be clearly distinguished from eudicots (Figure 2A). TaSTOP1 homoeologues from bread wheat showed high similarity with STOP1 from Barley (Hordeum vulgare) and Brachypodium distachium with identities of 92 and 87%, respectively. Noticeably, the phylogenetic relationship of TaSTOP1 homoeologoues particularly TaSTOP1-A and TaSTOP1-D from bread wheat (AABBDD) displayed the maximum similarity with STOP1 like proteins from Triticum urartu (AA) and Aegilops tauschii (DD), respectively (Figure 2A).

Figure 2
figure 2

Phylogenetic tree and multiple alignments of potential Zinc Fingers domain of STOP-like proteins. Phylogenetic tree based on amino acid sequences showing the relationship of TaSTOP1 with other plant STOP1 type proteins (A). The deduced amino acid sequences were aligned with CLUSTALW. Comparison of ZFs domain of TaSTOP1 (TaSTOP1-A, TaSTOP1-B, TaSTOP1-D) with its homologous from Brachypodium (B.distachyon), Barley (H.vulgare), rice (O.sativa), sorghum (S.bicolor), maize (Z.mays) foxmillet (S.italica), and Arabidopsis (A.thaliana1 &A.thaliana2) (B). Horizontal bars indicate ZFs domain and asterisks indicate conserved motif of Cys2His2 or Cys2His2-Cys.

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Sequence alignment of STOP1 protein from bread wheat with its homologous from cereals [Brachipodium, barley, rice, sorghum, maize (Zea mays) and foxmillet (Setaria italic)] and Arabidopsis, shows that TaSTOP1 encodes a putative Cys2His2 zinc finger protein containing four potential zinc finger domains. Three zinc finger domains (ZF1, ZF2, and ZF4) are predicted as the Cys2His2 type, whereas ZF3 is predicted as the Cys2His-Cys or the Cys2His2 type (Figure 2B). Furthermore, sequence alignment revealed that STOP-like proteins share highly conserved regions in the ZF domains. In addition, the STOP1 protein also showed greater sequence conservation in the C-terminus than in the N-terminus among family members. The 6-bp deletion in TaSTOP1-A resulted in a loss of two amino acids [Pro (P) and Gln (Q)] at position 426 without changing the reading frame [Additional file 2]. We also observed in Barbela 7/72/92, two SNPs at position 221 (A replaced by G) and 1186 (G replaced by A) which substituted an Asn (N) by a Ser (S) and Asp (D) by Asn (N) in TaSTOP1-B than in both TaSTOP1-A and TaSTOP1-D homoeologues, respectively [Additional file 1]. Multiple alignment of STOP1 protein revealed that the SNP at position 1186 is located in the zinc finger domain (ZF4) of TaSTOP1 homoeologues (Figure 2B).

TaSTOP1localization on distinct wheat genomes

For localization of TaSTOP1 on homoeologous chromosomes, locus specific primer pairs were designed [Additional file 3] and TaSTOP1 homoeologues were amplified in a series of nullitetrasomic lines of Chinese Spring wheat along with Chinese Spring as a positive control. On the basis of the presence or absence of PCR products visualized in agarose gels, we observed that TaSTOP1 genes are located on homoeologous chromosomes 3A, 3B and 3D, and named TaSTOP1-A, TaSTOP1-B and TaSTOP1-D, respectively (Figure 3A-C). Furthermore, ditelosomic lines of Chinese Spring for homoeologous group 3 chromosomes were also used to assign the TaSTOP1 on chromosomal arms and confirmed that TaSTOP1-A, TaSTOP1-B and TaSTOP1-D genes are located on the long arm of homoeologous chromosomes 3A, 3B and 3D, respectively (Figure 3D).

Figure 3
figure 3

TaSTOP1 mapping on homoeologous chromosomes and their arms in bread wheat. TaSTOP1 mapping on wheat chromosomes from genome A (A), B (B) and D (C) using nullitetrasomic lines. M: Molecular-weight marker (100bp ladder), 1 to 7: Chinese Spring as control, N3AT3B, N3AT3D, N3BT3A, N3BT3D, N3DT3A, N3DT3B. Arms mapping of TaSTOP1-A, TaSTOP1-B and TaSTOP1-D with ditelosomic lines of homoeologous group 3 (D). 1, 4 and 7: Chinese Spring as a control; 2: Dt3AS; 3: Dt3AL; 5: Dt3BS; 6: Dt3BL; 8: Dt3DS and 9: Dt3DL.

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In order to further validate these results, physical chromosomal localization of TaSTOP1 was performed using Tyramide Signal Amplification FISH (Tyr-FISH) technique in the root-tip metaphase chromosome spreads of bread wheat genotype Barbela 7/72/92. For this purpose, a probe was developed by PCR amplification of TaSTOP1 from genomic DNA of Barbela 7/72/92. FISH with the TaSTOP1 specific probe on metaphase chromosomes depicted hybridization signals of TaSTOP1 on both chromatids of the long arms of three chromosomes (Figure 4A) and simultaneous re-probing of chromosome preparations with GAA- (red) and pAs1 (green) identified homoeologous group 3 with positive signals on chromosomes 3AL, 3BL and 3DL (Figure 4B). Some background was also observed but it was distinguished from true hybridization signals because they usually appear as dots without any pattern and not in both chromatids of the same chromosome. Only those signals having the same size and appearance on the same position of both chromatids of one specific chromosome were analyzed as true-positive hybridization signals.

Figure 4
figure 4

Physical localization of TaSTOP1 on homoeologous chromosome in the root-tip spreads of bread wheat genotype Barbela 7/72/92 using TYR-FISH technique. (A) Detection of positive hybridization signals of TaSTOP1 on both chromatids of the long arms of three chromosomes (B) and identification of chromosomes after re-probing with GAA- (red) and pAs1 (green). Note: The GAA-satellite sequence identifies A and B genome chromosomes whereas the pAs1 identifies chromosomes from the D genome. Arrow indicates the position of TaSTOP1 on respective chromosome (Scale bar = 10 microm).

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TaSTOP1 transactivation activity

The nuclear localization of TaSTOP1 protein was predicted by WOLF-PSORT programme [30]. TaSTOP1 is a putative transcription factor of the Cys2His2-type Zinc fingers family. The three homoeologues of TaSTOP1 showed similar genomic structure in bread wheat [Additional file 2]. Therefore, we only proceed to evaluate the transactivation potential of TaSTOP1 located on genome A (TaSTOP1-A). To this aim, we performed a modified yeast one-hybrid assay [31] to evaluate the ability of the lexA-TaSTOP1-A fusion protein to activate the lexA-driven expression of the lacZ gene in a heterologous yeast system, the results of which are illustrated in Figure 5. It is shown that lexA-TaSTOP1-A has the potential to transactivate lacZ expression either in the presence or absence of Al, further corroborating its potential role as a transcription factor.

Figure 5
figure 5

LexA-TaSTOP1-A exhibits transactivation potential in yeast. EGY48 cells co-expressing the lexA-TaSTOP1-A and a report cassette bearing the lacZ gene driven by a promoter containing lexA binding sites were grown in selective medium in the presence or absence of Al. Qualitative overlay-assay performed on solid medium (A) and quantitative measurements of β-galactosidase activity normalized to the A600 of cells (B). Values are means (± SD) of six independent transformants. Asterisks denote significant differences as identified by paired t-tests (**: P < 0.001).

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Expression profile of three TaSTOP1homoeologues in bread wheat

To understand the homoeologue specific expression of TaSTOP1 in bread wheat, we measured the temporal expression of TaSTOP1-A, TaSTOP1-B and TaSTOP1-D by Real-time qPCR in the root and shoot tissues of two bread wheat genotypes [Barbela 7/72/92 (Al resistant) and Anahuac (Al sensitive)] grown under Al stress (74 μM Al). The 18S RNA expression was used as an internal control. We noticed a biased transcription of homoeologues of TaSTOP1 gene in the root and shoot tissue of these diverse bread wheat genotypes (Figure 6). The transcript levels of homoeologue TaSTOP1-A under control as well as Al treatment were significantly higher than those of TaSTOP1-B and TaSTOP1-D in root and shoot tissues of both genotypes (depending upon genotypes, fold differences in the transcript abundance were about 5–6 and 6–11 for homoeologue TaSTOP1-A versus TaSTOP1-B in root and shoot, respectively) whereas expression of homoeologue TaSTOP1-D was only two-fold higher than TaSTOP1-B in the root tissues of both genotypes (Figure 6A and B). A slight induction (within the two hours of Al exposure) followed by return to basal levels of the homoeologue TaSTOP1-A transcripts was observed in the root tissues of Barbela 7/72/92 (Al resistant) whereas in the Anahuac (Al sensitive) under Al stress it was observed a quite stable transcript expression (Figure 6A). The expression of TaSTOP1-B was also almost unaltered in the roots of both genotypes under Al stress. Similarly, TaSTOP1-D was also constitutively expressed under Al stress in the roots of both genotypes except a rapid (2 h) and significant repression in the Al sensitive genotype Anahuac (Figure 6A). Nevertheless, a quite stable transcript expression of TaSTOP1 homoeologues was observed in the shoot of both genotypes except homoeologue TaSTOP1-A (Figure 6B). Interestingly, and similarly to roots, the expression of TaSTOP1-A in the shoots of both genotypes was also slightly induced under Al stress, however, its up-regulation was noticed only after 6 h and return to its basal level (Figure 6B). It is worth noting that the transcript levels of TaSTOP1-B of Al tolerant genotype Barbela 7/72/92 are lower in the shoot tissues, compared to the sensitive genotype Anahuac (Figure 6B).

Figure 6
figure 6

Relative transcript level (fold change) of TaSTOP1 homoeologues genes under Al stress in the roots (A) as well as shoots (B) and under proton (H+) stress in roots (C) of two bread wheat genotypes Barbela 7/72/92 and Anahuac. Among three homoeologues, the lowest Δ Ct value of a TaSTOP1 homoeologue [TaSTOP1-B in shoots of Barbela 7/72/92 (0 h; as control) and in roots of Anahuac (pH 6.0; as control) for Al and pH stress assay, respectively] was used as calibrator. Values are means (± SD) of three independent replicates. Asterisks indicate significant difference between the control and treatment sample in the respective genome of a genotype (Student´s t test, * P < 0.01).

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Moreover, to evaluate the transcript expression of TaSTOP1 homoeologues under protons (H+) stress, we also performed the relative quantification of homoeologue specific expression of TaSTOP1 transcript in root tissues of both genotypes under different levels of pH (6.0, 5.0 and 4.0). A slight gradual decrease in the transcript levels of TaSTOP1-A homoeologue was observed in the roots of Barbela 7/72/92 under protons (H+) stress, but a quite stable expression was observed in genotype Anahuac (Figure 6C). Furthermore, considerable up-regulation of the homoeologue TaSTOP1-B and slight repression of the homoeologue TaSTOP1-D transcript level was also observed under low pH (pH 4.0) in the roots of genotype Anahuac and Barbela 7/72/92, respectively (Figure 6C).

Discussion

So far only ALMT1 and MATE genes have been described as responsible for most of the genotypic variation for Al tolerance and are considered as major genes for Al resistance in bread wheat [32]. These genes have been identified in wheat [6, 27] and also in the model plant Arabidopsis [19, 33] and major cereals such as barley [34], maize [35], sorghum [7] and rye [36, 37]. The mechanisms underlying Al-tolerance in plant species have yet to be fully elucidated, as it seems that Al targets multiple cellular sites such as cell walls, plasma membranes, and cellular processes, like signal transduction pathways and homeostasis mechanisms [2, 5, 38, 39]. Recent evidence suggests that regulatory genes (transcription factors) play a key role in Al detoxification at different cellular levels [16, 17].

In the present study, a novel transcription factor gene named TaSTOP1 was cloned from an Al tolerant genotype Barbela 7/72/92 (Figure 1) which was derived from Portuguese bread wheat landrace Barbela through single seed descent method [40]. TaSTOP1 belongs to a member of Cys2His2 zinc finger family proteins that contains four potential zinc finger domains and has highly conserved regions in the zinc finger (ZF) domains (Figure 2B). Like other C2H2-type zinc finger proteins it contains more than one zinc finger motif with highly conserved amino acid sequence for DNA binding [16, 41]. Phylogenetic analysis clearly differentiated the STOP1 like proteins from monocots in a group (Figure 2A) and also suggested that genome A and B are more distant from genome D [Additional file 2], as genome D was incorporated recently in comparison to the A and B genomes in bread wheat [42]. In addition, our phylogenetic analysis results also support previous findings at molecular level that the A and D genomes in bread wheat were derived from T. urartu and A. tauschii, respectively [Additional file 2] [42].

In past, the nullitetrasomic and ditelosomic lines of Chinese Spring wheat have been extensively used in classical and molecular genetic studies for the identification of loci associated with numerous traits including Al tolerance [25, 43]. Thus, gene mapping has practical implications in plant genetics and breeding, and the determination of its physical localization is even more precise as it enables us to confirm the exact position of a gene on a chromosome. PCR based mapping of TaSTOP1 using nullitetrasomic and ditellosomic lines of Chinese Spring wheat revealed that TaSTOP1 is located on the long arm of wheat homoeologous group 3 chromosomes (Figure 3).

In situ hybridization is not only the most direct method for physical localization of genes in chromosomes, but also it is a valuable tool for the identification of copy numbers of a gene in species having a highly complex genome such as the bread wheat. Due to its hexaploid nature, most genes can be found in triplicate with one copy on each genome [44–46]. Tyramide signal amplification FISH (Tyr-FISH) technique has been successfully used for the identification of low copy number DNA sequences in wheat [47]. However, for the successful localization of a gene using the FISH technique, the minimum length of the probe size seems to be crucial. Recently, RD50 gene has been localized in bread wheat with a probe size of 2 kb [47]. Physical localization of TaSTOP1 by Tyr-FISH technique not only confirmed the results obtained from PCR based mapping, but also indicated that TaSTOP1 could be a single copy gene localized on the long arm of homoeologous group 3 chromosomes (Figure 4). In bread wheat, physical localization of single copy gene Glu-1 and RD50 with FISH technique has been demonstrated on long and short arms of the homoeologous group 1 chromosomes, respectively [47, 48]. In the present work, we were able for the first time to localize a gene with a probe size smaller than 2.0 kb demonstrating that the FISH technique can be used to simultaneously anchor homoeologous chromosomes with 1.5 kb probes even in bread wheat.

Subcellular prediction of TaSTOP1 protein in the nucleus is in agreement with data previously reported [18]. Zinc finger motifs are thought to recognize and bind to target DNA sequences, but they are not required for transcriptional activity [49, 50]. Our results clearly exhibited the transactivation potential of TaSTOP1-A at least in yeast (Figure 5). In present investigation, we observed highly similar genomic structure of TaSTOP1 genes [Additional files 1 and 2], therefore, it seems that TaSTOP1 transactivation function is constitutive and may not depend on the presence/absence of Al. The SNPs observed among TaSTOP1 homoeologues showed minor changes in respective amino acids of putative proteins which could alter the secondary structures by influencing the folding of these proteins (Additional file 1). Therefore, the three homoeologues of the same locus in bread wheat share high sequence similarity that could illustrate the flexibility of a polyploidy species in which due to the mutation in one homoeologue may be compensated for by the homoeologue [29].

Allopolyploidy plays an important role in plant evolution that arises with the merging of two or more genomes into single nucleus which may contribute either equally or disproportionately. However, recent molecular findings confirmed the asymmetric genomic expression pattern in natural and synthetic allopolyploid plant species, but the predominant transcript expression of one genome over the other genome(s) vary from gene to gene [51]. In hexaploid wheat, a uniform level of expression for all the three homoeologues has been reported for approximately 20% of the unigene loci [52], whereas 20-29% genes did not express at least one homoeoallele [52, 53]. Thus, the relative contribution of the three homoeologues of TaSTOP1 gene at transcript expression level was determined under Al and proton (H+) stresses in two bread wheat genotypes showing contrasting behaviour for Al toxicity. Transcript expression profiling of TaSTOP1 homoeologues in root and shoot tissues identified the predominance of TaSTOP1-A homoeologue followed by TaSTOP1-D over TaSTOP1-B in root and only predominance of TaSTOP1-A in shoot tissues of both genotypes under control and stress (Al and pH) conditions (Figure 6). Similarly, among the three homoeologues, the higher expression of one homoeologue of a MAD box transcription factor and Spa gene have also been observed in bread wheat [54, 55]. Although, the presence of cis elements within the 5' untranslated region of a gene is unusual, it is not aberrant or abnormal [56]. Surprisingly, sequence analysis of 5' UTR of TaSTOP1 genes differentiated the TaSTOP1-A homoeologue from TaSTOP1-B and TaSTOP1-D due to the presence of a pyrimidine-rich stretch and absence of light responsive element [Additional file 4]. In tomato, the deletion of the 5' UTR containing pyrimidine-rich stretch from the HMG2 promoter reduced the level of HMG2 gene expression by a factor of 10 [56]. Therefore, among the three homogeologues in bread wheat, the up- or down-regulation of the expression of specific homoeologue could be the result from either the dominancy of ancestral diploid donor parent or early polyploidization-cis-regulatory variation.

Interestingly, the time-dependent Al-responsive expression of TaSTOP1 homoeologues observed in the root tissues of two bread wheat showing contrasting phenotypes for Al toxicity suggests a putative role for TaSTOP1 in Al resistance (Figure 6A and B). Al responsive STOP1 expression has also been reported in Arabidopsis [16], alfalfa [57] and common bean [58]. Similarly to Arabidopsis, the transcript expression of homoeologues of TaSTOP1 in the roots of diverse bread wheat genotypes was also modulated in response to proton stress [16]. It is noticeable that genotype Barbela 7/72/92 is highly resistant to Al toxicity compared with Anahuac, but in the absence of Al under low pH we did not observe significant differences between these genotypes for root growth [Additional file 5]. It is worth noticing that the three homoeologues of TaSTOP1 have similar genomic structures, but showed a different transcript expression in response to Al and proton (H+) stress. These results may reveal that the homoeologues of TaSTOP1 are differentially contributing to Al or proton (H+) tolerance in bread wheat. Further work is in progress in order to definitely establish if these genes play a significant role in aluminium tolerance.

Conclusions

Bread wheat has wide genotypic variation for Al resistance [23, 40] and the role of several chromosomes such as chromosome arms 2DL, 3DL, 4BL, 4DL, 6AL, 7AS and chromosome 7D, in Al tolerance has been revealed in classical genetic studies through chromosome manipulation in wheat [43]. Furthermore, several QTL associated with Al tolerance in bread wheat have also been reported by many researchers [22, 24–26]. Contrarily to Arabidopsis and rice, due to the paucity of a priori candidate genes in wheat only two major QTL located on chromosome 4DL and 4BL have yet been elucidated at molecular level, showing the co-segregation with candidate genes TaALMT1 homoeologue (4DL) and TaMATE1 homoeologue (4BL), respectively [22, 27]. The classical studies using chromosomal manipulation as well as recent QTL mapping and genome-wide association analysis have also detected loci associated with Al resistance on homoeologous group 3 chromosomes (3A, 3B and 3D) in bread wheat [23–25, 43]. Recently, the role of a zinc finger transcription factor ART1 identified through mutational analysis in rice has also been shown in natural variation of Al tolerance in rice, earlier which was suggested that it was not involved in Al tolerance [20, 32].

In the present investigation, we cloned and characterized the novel candidate genes TaSTOP1 in bread wheat. The homoeologues of TaSTOP1 exhibited similar genomic structures, but showed biased transcript expression and different response to Al and proton (H+) toxicity. Furthermore, TaSTOP1-B homoeologue from Al tolerant genotypes Barbela 7/72/92 and Viloso Mole not only showed highest similarity but also contain the same SNP located in ZF4 domain than Al sensitive genotypes Anahuac, Chinese Spring and Saloio [Additional file 2] [40]. Finally, in order to correlate with Al tolerance, it would be very interesting either to functionally characterize or further verify the role of TaSTOP1 because gene(s) underlying the QTL on homoeologous group 3 chromosomes particularly 3BL has not been so far identified in this important cereal.

Methods

Plant material and growth condition

The seedlings of selected bread wheat genotypes Barbela 7/72/92, Anahuac, Chinese Spring, Ruivo, Viloso Mole and Saloio classified in relation to Al tolerance [40] were grown in hydroponic solution (0.4 mM CaCl2, 0.65 mM KNO3, 0.25 mM MgCl2.6H2O, 0.1 mM (NH4)2SO4 and 0.04 mM NH4NO3) and kept in controlled growth chamber under 14 h/26°C day and a 10 h/22°C night regime, with a light intensity of 150 μmol photons m-2s-1 and a relative humidity of 65%.

Al stress assay

Four days old seedlings of Al resistant bread wheat genotype Barbela 7/72/92 and Al susceptible genotype Anahuac growing in hydroponic solution with pH 4.0 were shifted in fresh nutritive solution having 74 μM Al whereas control seedling were raised in only fresh hydroponic solution. For root re-growth measurement, after 24 h, roots were immersed in 0.1% eriochrome cyanine R (Sigma, Germany) dye solution for 10 minutes and prior to measurement; seedlings were allowed to grow in fresh nutritive solution for 48 h. For visual detection of Al accumulation in roots, hematoxylin assay was performed [59] and root samples were observed under microscope.

DNA and RNA extraction

Total genomic DNA was isolated from young leaf samples using the DNeasy Plant Mini Kit (Qiagen, Germany) and total RNA was extracted using Trizol method followed by purification using PureLink™ RNA Mini Kit (Ambion, Invitrogen, USA). The first-strand cDNA was synthesized in a final volume of 20 μl reaction containing: 1 μg RNA, 2 μl 10× RT buffer, 0.8 μl of 25× dNTP mix (100 mM), 2 μl of 10× RT random primers and 1 μl of Multiscribe reverse transcriptase (Applied Biosystems, USA).

Gene structure and cloning of full-length cDNA

The Arabidopsis thaliana AtSTOP1 (AT1G34370) protein sequence was retrieved from TAIR database (http://www.arabidopsis.org) and was used as the query sequence to search the GenBank wheat expressed sequence tag (EST) database. The homologous sequence of STOP1 in wheat was obtained via tblastn in NCBI (http://www.ncbi.nlm.nih.gov). Homologous wheat EST clones showing highest similarity with Arabidopsis STOP1 were retrieved. TaSTOP1 (wheat EST) specific primers were designed to perform the sequential analysis in bread wheat genotype Barbela 7/72/92 [Additional file 3]. Total RNA from the seedlings of Barbela 7/72/92 and Anahuac was employed to obtain the full-length cDNA of TaSTOP1 including 5’ UTR and 3’ UTR using Rapid Amplification of cDNA Ends (RACE) (SMARTer™ RACE cDNA Amplification Kit, clontech, USA). The genomic sequence of TaSTOP1 was obtained in six different bread wheat genotypes, namely Barbela 7/72/92, Anahuac, Ruivo, Viloso Mole, Saloio and Chinese Spring [Additional file 6].

Molecular analysis and construction of phylogenetic tree

The Pfam (http://www.sanger.ac.uk/Software/Pfam/search,shtml) software was used to identify potential domains and WOLF-PSORT (http://www.psort.org) was used to predict the intracellular localization of the TaSTOP1 protein. Fifty two STOP1 like protein sequences were collected from 32 different plant species including TaSTOP1 homoeologues from bread wheat genotype Barbela 7/72/92 using the Basic Local Alignment Search Tool (BLAST) programme from NCBI (http://blast.ncbi.nlm.nih.gov/Blast.cgi) [Additional file 7]. Phylogenetic tree was constructed by MEGA4 software using neighbor-joining method [60].

Mapping of TaSTOP1gene in wheat genome

All the nullitetrasomic and ditelosomic lines of Chinese Spring wheat except for the homoeologous group 2, 4 and 6 chromosomes used in present investigation were available in our lab, whereas remaining stocks were kindly provide by Prof. Adam J. Lukaszewski at Department of Botany and Plant Sciences, University of California, USA. On the basis of TaSTOP1 alignment, different pairs of specific primers for each TaSTOP1 homoeologue were designed [Additional file 3]. TaSTOP1 homoeologues (TaSTOP1-A, TaSTOP1-B and TaSTOP1-D) were amplified in the nullitetrasomic (N3AT3B, N3AT3D, N3BT3A, N3BT3D, N3DT3A and N3DT3B) and ditelosomic [Dt 3AL and 3AS (long and short arm), Dt 3BL and 3BS, Dt 3DL and 3DS] lines of Chinese Spring wheat. TaSTOP1 homoeologues were assigned to the chromosomal arms based on the presence/absence of the PCR amplification products.

Physical localization of TaSTOP1 was performed by in situ hybridization. Probe was prepared by PCR amplification of the 1.5 kb genomic region of TaSTOP1 from Barbela 7/72/92. Chromosome spreads from the root tips of Barbela 7/72/92 seedlings at mitotic metaphase, probe labelling and hybridization mixture were carried as described by Prieto et al. [61]. Probe labelling was confirmed by dot-blot and detection of hybridization signals was carried out using the Tyramide Signal Amplification Kit (TSAâ„¢, PerkinElmer Life and Analytical Sciences, Inc., Waltham, MA, USA). To identify wheat chromosomes with positive signals, samples were re-hybridized using simultaneously the pAS1 repetitive sequence and GAA-satellite sequence as probes [62, 63]. The GAA-satellite sequence identifies all the A and B wheat chromosomes [62] whereas the pAs1 identifies chromosomes from the D genome [63]. Individual slides were observed under a Nikon Eclipse 80i microscope (Nikon Instruments Europe BV, UK). Images were captured with a Nikon CCD camera using the appropriate Nikon 3.0 software and processed with Photoshop 4.0 software (Adobe Systems Inc., San Jose, California, USA).

Transactivation assay

TaSTOP1 was amplified by PCR from Barbela 7/72/92 using oligonucleotide primers containing restriction site for Kpn I [Additional file 3]. The Kpn I digested TaSTOP1 fragment was cloned in frame with the lexA gene in the plasmid YCp91 [31]. Transformation of the ligated products was performed in the Escherichia coli strain XL1-Blue recA1 endA1 gyrA96 thi-hsdR17 supE44 relA1 lac [F’proAB lacIqZDM15 Tn10 (Tetr)] (Stratagene, USA) and the positive clones were sequenced. The recombinant plasmid YCp91-TaSTOP1-A was transformed in the yeast strain EGY48, which harbours the plasmid pSH18.84 encoding the lacZ gene under the control of a promoter containing LexA – responsive cis elements. Transformants were grown in selective media and β-galactosidase measurements were performed as previously described [64, 65].

Analysis of TaSTOP1expression level

For Al assay, seedlings of two bread wheat genotypes Barbela 7/72/92 and Anahuac showing contrasting response to Al toxicity, were raised in hydroponic nutrient solution with pH 4.0 during four days and further, were shifted to fresh nutrient solution with (74 μM Al in the form of AlCl3·6H2O; stress treatment) or without Al (control treatment). Both root and shoot tissues were collected separately after treatment at specific time points (0, 2, 6, 12 and 24 h) from control and Al stress imposed seedlings. For pH assay, four days old seedlings of both genotypes grown in hydroponic nutritive solution with pH 6.0 were transferred in fresh nutritive solutions having different levels of pH (pH 6.0, pH 5.0 and pH 4.0). Root samples of both genotypes from each treatment were collected after 0 h and 6 h exposure to different levels of pH.

Three biological replicates of each sample were prepared and duplicate quantitative assays were performed for each cDNA sample. TaSTOP1 homoeologues gene expression pattern was determined using the SYBR Premix Ex Taq (Takara, Japan) and the ABI 7500 Real-Time FAST PCR System (Applied Biosystems, USA). The 2-ΔΔC T method [66] was used to quantify the relative expression levels of TaSTOP1 homoeologues in comparison to 18SRNA endogenous control.

Accession numbers

Sequence data from this article can be found in the GenBank database under the following accession numbers: Barbela 7/72/92 (TaSTOP1-A: GenBank number KF034793; TaSTOP1-B: GenBank number KF034794; TaSTOP1-D: GenBank number KF034795), Anahuac (TaSTOP1-A: GenBank number KF034796; TaSTOP1-B: GenBank number KF034797; TaSTOP1-D: GenBank number KF034798), Viloso Mole (TaSTOP1-A: GenBank number KF034801; TaSTOP1-B: GenBank number KF034802; TaSTOP1-D: GenBank number KF034803), Saloio (TaSTOP1-A: GenBank number KF034804; TaSTOP1-B: GenBank number KF034805; TaSTOP1-D: GenBank number KF034806), Chinese Spring (TaSTOP1-A: GenBank number KF034799; TaSTOP1-B: GenBank number KF034800) and Ruivo (TaSTOP1-D: GenBank number KF034807).

Abbreviations

ALMT:

Aluminium-activated malate transporter

MATE:

Multidrug and toxic compound exudation

ALS:

Al-sensitive

STAR:

Sensitive to Al rhizotoxicity

Nrat1:

Nramp aluminum transporter 1

STOP:

sensitive to proton rhizotoxicity

ART:

Al resistance transcription factor

QTL:

Quantitative trait loci/locus

SNP:

Single nucleotide polymorphism

ORF:

Open reading frame

ZF:

Zinc finger domains

FISH:

Fluorescent in situ hybridization.

References

  1. von Uexküll HR, Mutert E: Global extent, development and economic impact of acid soils. Plant-Soil Interactions at Low pH: Principles and Management. Edited by: Date RA, Grundon NJ, Raymet GE, Probert ME. 1995, Dordrecht, The Neth: Kluwer Academic, 5-19.

    Chapter  Google Scholar 

  2. Kochian LV, Hoekenga OA, Piñeros MA: How do crop plants tolerate acid soils? Mechanisms of aluminum tolerance and phosphorous efficiency. Annu Rev Plant Biol. 2004, 55: 459-493. 10.1146/annurev.arplant.55.031903.141655.

    Article  PubMed  CAS  Google Scholar 

  3. Simões CC, Melo JO, Magalhaes JV, Guimarães CT: Genetic and molecular mechanisms of aluminum tolerance in plants. Genet Mol Res. 2012, 11 (3): 1949-1957. 10.4238/2012.July.19.14.

    Article  PubMed  Google Scholar 

  4. Ryan PR, Delhaize E, Jones DL: Function and mechanism of organic anion exudation from plant roots. Annu Rev Plant Physiol Plant Mol Biol. 2001, 52: 527-560. 10.1146/annurev.arplant.52.1.527.

    Article  PubMed  CAS  Google Scholar 

  5. Ma JF: Syndrome of aluminum toxicity and diversity of aluminum resistance in higher plants. Int Rev Cytol. 2007, 264: 225-252.

    Article  PubMed  CAS  Google Scholar 

  6. Sasaki T, Yamamoto Y, Ezaki B, Katsuhara M, Ahn SJ, Ryan PR, Delhaize E, Matsumoto H: A wheat gene encoding an aluminum-activated malate transporter. Plant J. 2004, 37: 645-653. 10.1111/j.1365-313X.2003.01991.x.

    Article  PubMed  CAS  Google Scholar 

  7. Magalhães JV, Liu J, Guimarães CT, Lana UG, Alves VM, Wang YH, Schaffert RE, Hoekenga OA, Pineros MA, Shaff JE, Klein PE, Carneiro NP, Coelho CM, Trick HN, Kochian LV: A gene in the multidrug and toxic compound extrusion (MATE) family confers aluminum tolerance in sorghum. Nat Genet. 2007, 39: 1156-1161. 10.1038/ng2074.

    Article  PubMed  Google Scholar 

  8. Larsen PB, Geisler MJB, Jones CA, Williams KM, Cancel JD: ALS3 encodes a phloem-localized ABC transporter-like protein that is required for aluminum tolerance in Arabidopsis. Plant J. 2005, 41: 353-363.

    Article  PubMed  CAS  Google Scholar 

  9. Larsen PB, Cancel J, Rounds M, Ochoa V: Arabidopsis ALS1 encodes a root tip and stele localized half type ABC transporter required for root growth in an aluminum toxic environment. Planta. 2007, 225: 1447-1458. 10.1007/s00425-006-0452-4.

    Article  PubMed  CAS  Google Scholar 

  10. Huang CF, Yamaji N, Mitani N, Yano M, Nagamura Y, Ma JF: A bacterial-type ABC transporter is involved in aluminum tolerance in rice. Plant Cell. 2009, 21: 655-667. 10.1105/tpc.108.064543.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  11. Xia J, Yamaji N, Kasai T, Ma JF: Plasma membrane-localized transporter for aluminum in rice. Proc Natl Acad Sci USA. 2010, 107: 18381-18385. 10.1073/pnas.1004949107.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  12. Stockinger EJ, Gilmour SJ, Thomashow MF: Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA. 1997, 94: 1035-1040. 10.1073/pnas.94.3.1035.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  13. Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K: Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression, respectively, in Arabidopsis. Plant Cell. 1998, 10: 1391-1406.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  14. Haake V, Cook D, Riechmann JL, Pineda O, Thomas MF, Zhang JZ: Transcription factor CBF4 is a regulator of drought adaptation in Arabidopsis. Plant Physiol. 2002, 130: 639-648. 10.1104/pp.006478.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  15. Yamaguchi-Shinozaki K, Shinozaki K: Transcriptional Regulatory Networks in Cellular Responses and Tolerance to Dehydration and Cold Stresses. Annu Rev Plant Biol. 2006, 57: 781-803. 10.1146/annurev.arplant.57.032905.105444.

    Article  PubMed  CAS  Google Scholar 

  16. Iuchi S, Koyama H, Iuchi A, Kobayashi A, Kitabayashi S, Kobayashi Y, Ikka T, Hirayama T, Shinozaki K, Kobayashi M: Zinc finger protein STOP1 is critical for proton tolerance in Arabidopsis and coregulates a key gene in aluminum tolerance. Proc Natl Acad Sci USA. 2007, 104: 9900-9905. 10.1073/pnas.0700117104.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Yamaji N, Huang CF, Nagao S, Yano M, Sato Y, Nagamura Y, Ma JF: A zinc finger transcription factor ART1 regulates multiple genes implicated in aluminum tolerance in rice. Plant Cell. 2009, 21: 3339-3349. 10.1105/tpc.109.070771.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  18. Sawaki Y, Iuchi S, Kobayashi Y, Ikka T, Sakurai N, Fujita M, Shinozaki K, Shibata D, Kobayashi M, Koyama H: STOP1 regulates multiple genes that protect Arabidopsis from proton and aluminum toxicities. Plant Physiol. 2009, 150: 281-294. 10.1104/pp.108.134700.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  19. Liu JP, Magalhaes JV, Shaff J, Kochian LV: Aluminum activated citrate and malate transporters from the MATE and ALMT families function independently to confer Arabidopsis aluminum tolerance. Plant J. 2009, 57: 389-399. 10.1111/j.1365-313X.2008.03696.x.

    Article  PubMed  CAS  Google Scholar 

  20. Famoso AN, Zhao K, Clark RT, Tung C-W, Wright MH, Bustamante C, Kochian LV, McCouch SR: Genetic Architecture of Aluminum Tolerance in Rice (Oryza sativa) Determined through Genome-Wide Association Analysis and QTL Mapping. PLoS Genet. 2011, 7 (8): e1002221-10.1371/journal.pgen.1002221. doi:10.1371/journal.pgen.1002221

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  21. Century K, Reuber TL, Ratcliffe OJ: Regulating the regulators: The future prospects for transcription-factor-based agricultural biotechnology products. Plant Physiol. 2008, 147: 20-29. 10.1104/pp.108.117887.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  22. Raman H, Zhang KR, Cakir M, Appels R, Garvin DF, Maron LG, Kochian LV, Moroni JS, Raman R, Imtiaz M, Drake-Brockman F, Waters I, Martin P, Sasaki T, Yamamoto Y, Matsumoto H, Hebb DM, Delhaize E, Ryan PR: Molecular characterization and mapping of ALMT1, the aluminium-tolerance gene of bread wheat (Triticum aestivum L.). Genome. 2005, 48: 781-791. 10.1139/g05-054.

    Article  PubMed  CAS  Google Scholar 

  23. Raman H, Stodart B, Ryan PR, Delhaize E, Emebiri L, Raman R, Coombes N, Milgate A: Genome-wide association analyses of common wheat (Triticum aestivum L.) germplasm identifies multiple loci for aluminium resistance. Genome. 2010, 53 (11): 957-966. 10.1139/G10-058.

    Article  PubMed  CAS  Google Scholar 

  24. Zhou LL, Bai GH, Ma HX, Carver BF: Quantitative trait loci for aluminum resistance in wheat. Mol Breed. 2007, 19 (2): 153-161. 10.1007/s11032-006-9054-x.

    Article  CAS  Google Scholar 

  25. Cai S, Bai GH, Zhang D: Quantitative trait loci for aluminum resistance in Chinese wheat landrace FSW. Theor Appl Genet. 2008, 117 (1): 49-56. 10.1007/s00122-008-0751-1.

    Article  PubMed  CAS  Google Scholar 

  26. Navakode S, Weidner A, Lohwasser U, Röder MS, Börner A: Molecular mapping of quantitative trait loci (QTLs) controlling aluminium tolerance in bread wheat. Euphytica. 2009, 166 (2): 283-290. 10.1007/s10681-008-9845-8.

    Article  CAS  Google Scholar 

  27. Ryan PR, Raman H, Gupta S, Horst WJ, Delhaize E: A second mechanism for aluminum resistance in wheat relies on the constitutive efflux of citrate from roots. Plant Physiol. 2009, 149: 340-351. 10.1104/pp.108.129155.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  28. Delhaize E, Ma JF, Ryan PR: Transcriptional regulation of aluminium tolerance genes. Trends Plant Sci. 2012, 17 (6): 341-348. 10.1016/j.tplants.2012.02.008.

    Article  PubMed  CAS  Google Scholar 

  29. Tovkach A, Ryan PR, Richardson AE, Lewis DC, Rathjen TM, Ramesh S, Tyerman SD, Delhaize E: Transposon-mediated alteration of TaMATE1B expression in wheat confers constitutive citrate efflux from root apices. Plant Physiol. 2013, 161 (2): 880-892. 10.1104/pp.112.207142.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  30. Horton P, Park KJ, Obayashi T, Fujita N, Harada H, Adams-Collier CJ, Nakai K: WoLF PSORT: protein localization predictor. Nucleic Acids Res. 2007, 35 (2): W585-W587.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Menezes RA, Amaral C, Delaunay A, Toledano M, Rodrigues-Pousada C: Yap8p activation in Saccharomyces cerevisiae under arsenic conditions. FEBS Lett. 2004, 566 (1): 141-146.

    Article  PubMed  CAS  Google Scholar 

  32. Ryan PR, Tyerman SD, Sasaki T, Furuichi T, Yamamoto Y, Zhang WH, Delhaize E: The identification of aluminium-resistance genes provides opportunities for enhancing crop production on acid soils. J Exp Bot. 2011, 62 (1): 9-20. 10.1093/jxb/erq272.

    Article  PubMed  CAS  Google Scholar 

  33. Hoekenga OA, Maron LG, Pineros MA, Cancado GMA, Shaff J, Kobayashi Y, Ryan PR, Dong B, Delhaize E, Sasaki T, Matsumoto H, Yamamoto Y, Koyama H, Kochian LV: AtALMT1, which encodes a malate transporter, is identified as one of several genes critical for aluminum tolerance in Arabidopsis. Proc Natl Acad Sci USA. 2006, 103: 9738-9743. 10.1073/pnas.0602868103.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  34. Furukawa J, Yamaji N, Wang H, Mitani N, Murata Y, Sato K, Katsuhara M, Takeda K, Ma JF: An aluminum-activated citrate transporter in barley. Plant Cell Physiol. 2007, 48: 1081-1091. 10.1093/pcp/pcm091.

    Article  PubMed  CAS  Google Scholar 

  35. Maron LG, Pineros MA, Guimarães CT, Magalhaes JV, Pleiman JK, Mao C, Shaff J, Belicuas SN, Kochian LV: Two functionally distinct members of the MATE (multi-drug and toxic compound extrusion) family of transporters potentially underlie two major aluminum tolerance QTLs in maize. Plant J. 2010, 61: 728-740. 10.1111/j.1365-313X.2009.04103.x.

    Article  PubMed  CAS  Google Scholar 

  36. Collins NC, Shirley NJ, Saeed M, Pallotta M, Gustafson JP: An ALMT1 gene cluster controlling aluminum tolerance at the Alt4 locus of rye (Secale cereale L.). Genetics. 2008, 179: 669-692. 10.1534/genetics.107.083451.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  37. Yokosho K, Yamaji N, Ma JF: Isolation and characterization of two MATE genes in rye. Func Plant Biol. 2010, 37: 296-303. 10.1071/FP09265.

    Article  CAS  Google Scholar 

  38. Barceló J, Poschenrieder C: Fast root growth responses, root exudates, and internal detoxification as clues to the mechanisms of aluminium toxicity and resistance: A review. Environ Exp Bot. 2002, 48: 75-92. 10.1016/S0098-8472(02)00013-8.

    Article  Google Scholar 

  39. Poschenrieder C, Gunse B, Corrales I, Barceló J: A glance into aluminum toxicity and resistance in plants. Sci Total Environ. 2008, 400: 356-368. 10.1016/j.scitotenv.2008.06.003.

    Article  PubMed  CAS  Google Scholar 

  40. Martins-Lopes P, Maçãs B, Guedes-Pinto H: Portuguese bread wheat germplasm evaluation for aluminium tolerance. Cereal Res Commun. 2009, 37 (2): 179-188. 10.1556/CRC.37.2009.2.4.

    Article  CAS  Google Scholar 

  41. Wolfe SA, Nekludova L, Pabo CO: DNA recognition by Cys(2)His(2) zinc finger proteins. Annu Rev Biophys Biomol Struct. 2000, 29: 183-212. 10.1146/annurev.biophys.29.1.183.

    Article  PubMed  CAS  Google Scholar 

  42. Huang S, Sirikhachornkit A, Su XJ, Faris J, Gill B, Haselkorn R, Gornicki P: Genes encoding plastid acetyl-CoA carboxylase and 3-phosphoglycerate kinase of the Triticum/Aegilops complex and the evolutionary history of polyploid wheat. Proc Natl Acad Sci USA. 2002, 99 (12): 8133-8138. 10.1073/pnas.072223799.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  43. Aniol A, Gustafson JP: Chromosome location of genes controlling aluminum tolerance in wheat, rye, and triticale. Can J Genet Cytol. 1984, 26: 701-705.

    Article  Google Scholar 

  44. Clarke BC, Phongkham T, Gianibelli MC, Beasley H, Bekes F: The characterisation and mapping of a family of LMW-gliadin genes: Effects on dough properties and bread volume. Theor Appl Genet. 2003, 106: 629-635.

    PubMed  CAS  Google Scholar 

  45. Danyluk J, Kane NA, Breton G, Limin AE, Fowler DB, Sarhan F: TaVRT-1, a putative transcription factor associated with vegetative to reproductive transition in cereals. Plant Physiol. 2003, 132: 1849-1860. 10.1104/pp.103.023523.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  46. Watanabe N, Koval SF: Mapping of chlorina mutant genes on the long arm of homologous group 7 chromosomes in common wheat with partial deletion lines. Euphytica. 2003, 129: 259-265. 10.1023/A:1022276724354.

    Article  CAS  Google Scholar 

  47. Pérez R, de Bustos A, Jouve N, Cuadrado A: Localization of Rad50, a single-copy gene, on group 5 chromosomes of wheat, using a FISH protocol employing Tyramide for Signal Amplification (Tyr-FISH). Cytogenet Genome Res. 2009, 125: 321-328. 10.1159/000235938.

    Article  PubMed  Google Scholar 

  48. Cabrera A, Martin A, Barro F: In-situ comparative mapping (ISCM) of Glu-1 loci in Triticum and Hordeum. Chromosome Res. 2002, 10: 49-54. 10.1023/A:1014270227360.

    Article  PubMed  CAS  Google Scholar 

  49. Sakamoto H, Maruyama K, Sakuma Y, Meshi T, Iwabuchi M, Shinozaki K, Yamaguchi-Shinozaki K: Arabidopsis Cys2/His2-type zinc-finger proteins function as transcription repressors under drought, cold, and high-salinity stress conditions. Plant Physiol. 2004, 136: 2734-2746. 10.1104/pp.104.046599.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  50. Lin R, Ding L, Casola C, Ripoll DR, Feschotte C, Wang H: Transposase-derived transcription factors regulate light signalling in Arabidopsis. Science. 2007, 318: 1302-1305. 10.1126/science.1146281.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  51. Feldman M, Levy AA, Fahima T, Korol A: Genomic asymmetry in allopolyploid plants: wheat as a model. J Exp Bot. 2012, 63 (14): 5045-5059. 10.1093/jxb/ers192.

    Article  PubMed  CAS  Google Scholar 

  52. Mochida K, Yamazaki Y, Ogihara Y: Discrimination of homoeologous gene expression in hexaploid wheat by SNP analysis of contigs grouped from a large number of expressed sequence tags. Mol Genet Genomics. 2004, 270: 371-377. 10.1007/s00438-003-0939-7.

    Article  Google Scholar 

  53. Bottley A, Xia GM, Koebner RMD: Homoeologous gene silencing in hexaploid wheat. Plant J. 2006, 47: 897-906. 10.1111/j.1365-313X.2006.02841.x.

    Article  PubMed  CAS  Google Scholar 

  54. Shitsukawa N, Tahira C, Kassai K, Hirabayashi C, Shimizu T, Takumi S, Mochida K, Kawaura K, Ogihara Y, Murai K: Genetic and epigenetic alteration among three homoeologous genes of a class E MADS box gene in hexaploid wheat. Plant Cell. 2007, 19: 1723-1737. 10.1105/tpc.107.051813.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  55. Ravel C, Martre P, Romeuf I, Dardevet M, El-Malki R, Bordes J, Duchateau N, Brunel D, Balfourier F, Charmet G: Nucleotide polymorphism in the wheat transcriptional activator Spa influences its pattern of expression and has pleiotropic effects on grain protein composition, dough visco elasticity, and grain hardness. Plant Physiol. 2009, 151: 2133-2144. 10.1104/pp.109.146076.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  56. Daraselia ND, Tarchevskaya S, Narita JO: The promoter for tomato 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene 2 has unusual regulatory elements that direct high-leve1 expression. Plant Physiol. 1996, 112: 727-733. 10.1104/pp.112.2.727.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  57. Chen Q, Zhang XD, Wang SS, Wang QF, Wang GQ, Nian HJ, Li KZ, Yu YX, Chen LM: Transcriptional and physiological changes of alfalfa in response to aluminium stress. J Agric Sci. 2011, 149: 737-751. 10.1017/S0021859611000256.

    Article  CAS  Google Scholar 

  58. Eticha D, Zahn M, Bremer M, Yang ZB, Rangel A, Rao IM, Horst W: Transcriptomic analysis reveals differential gene expression in response to aluminium in common bean (Phaseolus vulgaris) genotypes. Ann Bot. 2010, 105: 1119-1128. 10.1093/aob/mcq049.

    Article  PubMed  CAS  PubMed Central  Google Scholar 

  59. Polle E, Konzak CF, Kittrick JA: Visual detection of aluminium tolerance levels in wheat by hematoxylin staining of seedlings roots. Crop Sci. 1978, 18: 823-827. 10.2135/cropsci1978.0011183X001800050035x.

    Article  CAS  Google Scholar 

  60. Tamura K, Dudley J, Nei M, Kumar S: MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24: 1596-1599. 10.1093/molbev/msm092.

    Article  PubMed  CAS  Google Scholar 

  61. Prieto P, Ramirez MC, Ballesteros J, Cabrera A: Identification of intergenomic translocations involving wheat, Hordeum vulgare and Hordeum chilense chromosomes by FISH. Hereditas. 2001, 135: 171-174.

    Article  PubMed  CAS  Google Scholar 

  62. Pedersen C, Rasmussen SK, Linde-Laursen I: Genome and chromosome identification in cultivated barley and related species of the Triticeae (Poaceae) by in situ hybridization with the GAA-satellite sequence. Genome. 1996, 39: 93-104. 10.1139/g96-013.

    Article  PubMed  CAS  Google Scholar 

  63. Rayburn AL, Gill BS: Isolation of a D-genome specific repeated DNA sequence from Aegilops squarrosa. Plant Mol Biol Rep. 1986, 4: 102-109. 10.1007/BF02732107.

    Article  CAS  Google Scholar 

  64. Miller JH: Experiments in Molecular Genetics: Assay of β-Galactosidase. 1972, NY: CSH Laboratory Press, Cold Spring Harbor, 352-355.

    Google Scholar 

  65. Azevedo D, Nascimento L, Labarre J, Toledano MB, Rodrigues-Pousada C: The S. cerevisiae Yap1 and Yap2 transcription factors share a common cadmium-sensing domain. FEBS Lett. 2007, 581 (2): 187-195. 10.1016/j.febslet.2006.11.083.

    Article  PubMed  CAS  Google Scholar 

  66. Livak KJ, Schmittgen TD: Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT. Method. 2001, 25 (4): 402-408. 10.1006/meth.2001.1262.

    Article  CAS  Google Scholar 

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Acknowledgements

We thank Fundação para a Ciência e Tecnologia (FCT) of Portugal for providing grants to ALGO (SFRH/BD/45556/2008) and RAM (SFRH/BPD/26506/2006) and PML (PEst-OE/EQB/LA0023/2011). We thank Dr. Renato Rodrigues-Pousada (L’Aquila University, Italy) and anonymous reviewers for valuable comments on manuscript.

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  1. Centro de Genómica e Biotecnologia, Instituto de Biotecnologia e Bioengenharia (CGB/IBB), Universidade de Trás-os-Montes e Alto Douro (UTAD), 1013, Vila Real, 5001-801, Portugal

    Ana Luísa Garcia-Oliveira, Henrique Guedes-Pinto & Paula Martins-Lopes

  2. Departamento de Genética, Facultad de Biología, Universidad Complutense de Madrid (UCM), Madrid, 28040, Spain

    Ana Luísa Garcia-Oliveira & César Benito

  3. Departamento de Mejora Genética Vegetal, Instituto de Agricultura Sostenible (IAS, CSIC), 4084, Alameda del Obispo s/n., Córdoba, 14080, Spain

    Pilar Prieto

  4. Instituto de Tecnologia Química e Biológica (ITQB), Universidade Nova de Lisboa, Oeiras, Portugal

    Ana Luísa Garcia-Oliveira, Regina de Andrade Menezes & Claudina Rodrigues-Pousada

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The authors declared that they have no competing interests.

Authors’ contributions

ALGO performed most of the experiments and drafted the manuscript; PP helped in in-situ hybridization assay; RAM helped in transactivation assay and CB guided for cloning, chromosomal localization and figure preparation, CRP, HGP and PML coordinated the experiments and helped in finalizing the manuscript. Finally, all authors read and approved the final manuscript.

Electronic supplementary material

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Additional file 1: Multiple alignments of the homoeologues of TaSTOP1 in bread wheat genotype Barbela 7/72/92.(PNG 555 KB)

12870_2013_1347_MOESM2_ESM.doc

Additional file 2: Phylogenetic tree and multiple alignments of TaSTOP1 homoeologues in different species of wheat including some bread wheat genotypes.(DOC 114 KB)

Additional file 3: Detail of primers used in present investigation.(RTF 84 KB)

Additional file 4: Alignment of homoeologues of TaSTOP1 5UTR region.(RTF 41 KB)

Additional file 5: Physiological characterization of Barbela 7/72/92 and Anahuac roots under Al stress.(DOC 2 MB)

Additional file 6: Nucleotide and protein sequence of TaSTOP1 in different bread wheat genotypes.(RTF 100 KB)

Additional file 7: Detail of STOP like proteins in different plant species used for phylogenetic analysis.(RTF 307 KB)

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Garcia-Oliveira, A.L., Benito, C., Prieto, P. et al. Molecular characterization of TaSTOP1 homoeologues and their response to aluminium and proton (H+) toxicity in bread wheat (Triticum aestivumL.). BMC Plant Biol 13, 134 (2013). https://doi.org/10.1186/1471-2229-13-134

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  • DOI: https://doi.org/10.1186/1471-2229-13-134

Keywords

BMC Plant Biology

ISSN: 1471-2229

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