|Home | About | Journals | Submit | Contact Us | Français|
Multiple genes and transcription factors are involved in the uptake and translocation of iron in plants from soil. The sequence information about iron uptake and translocation related genes is largely unknown in lentil (Lens culinaris Medik.). This study was designed to develop iron metabolism related molecular markers for Ferritin-1, BHLH-1 (Basic helix loop helix), or FER-like transcription factor protein and IRT-1 (Iron related transporter) genes using genome synteny with barrel medic (Medicago truncatula). The second objective of this study was to analyze differential gene expression under excess iron over time (2 h, 8 h, 24 h). Specific molecular markers were developed for iron metabolism related genes (Ferritin-1, BHLH-1, IRT-1) and validated in lentil. Gene specific markers for Ferritin-1 and IRT-1 were used for quantitative PCR (qPCR) studies based on their amplification efficiency. Significant differential expression of Ferritin-1 and IRT-1 was observed under excess iron conditions through qPCR based gene expression analysis. Regulation of iron uptake and translocation in lentil needs further characterization. Greater emphasis should be given to development of conditions simulating field conditions under external iron supply and considering adult plant physiology.
Iron (Fe) uptake in plants is a complex physiological process governed by homeostatic mechanisms in the plant. Homeostatic mechanisms involve absorption, translocation and redistribution of Fe within the plant system at a particular concentration (10-9–10-4 mol/l) (Römheld and Schaaf, 2004). Lower iron concentration leads to Fe-deficiency symptoms including chlorosis and necrosis in leaves and ultimately loss in biomass as well as grain yield. Higher concentrations of Fe within the plant system results in generation of free radical species which damage various cellular components by interacting with protein, lipid, carbohydrates and even with DNA. According to Welch and Graham (2004), there are four different barriers controlling homeostatic mechanisms of mineral uptake in plants; (A) the root-soil interphase known as the rhizosphere, (B) root-cell plasma membrane, (C) translocation to edible plant organs (grains/tubers), and (D) bioavailability of minerals.
Ferritin is an iron-carrying protein in plants and has a multimeric (24-mer) cage-like structure that carries up to 4500 atoms of Fe within its core (Crichton et al., 1978; Wade et al., 1993). The ferritin protein is highly conserved within the animal and plant kingdom (Ragland et al., 1990). Ferritin meets the metabolic need for iron when required by the metabolome as well as prevents any kind of oxidative stress (Harrison et al., 1998). Plant ferritin subunit sequences share between 39 and 49% similarity with mammalian ferritin sequences (Briat et al., 2009). This similarity increases when comparisons are made within the plant kingdom or among close plant families. Iron homeostasis is important due to the minute balance that exists between iron deficiency and toxicity and that affects plant physiology. Impaired plant physiology ultimately affects crop yield. Ferritin regulates iron homeostasis to prevent interaction of iron with other cellular components which may result in generation of free radicals during oxidative stress. In plants, ferritin consists of a single kind of subunit and ferritin bound Fe is highly bioavailable (Kalgaonkar and Lonnerdal, 2008).
Lentil (Lens culinaris Medik.) is a eudicot plant and uses strategy I where ferric iron is reduced at the rhizosphere and absorbed as ferrous iron by the root. Monocot plants use a different strategy to uptake iron from the soil (strategy II). The uptake of iron is mediated through phytosiderophores and the ferric iron enters the plant system through root in case of monocot plants (strategy II). In Arabidopsis thaliana, reduction of ferric Fe is accomplished by Fe reductase FRO2 (ferric reductase oxidase-2; Robinson et al., 1999). This was the first report of cloning and gene function elucidation of any major iron metabolism related gene in plants. Uptake of ferrous Fe into the root is carried out by the metal transporter IRT1 (iron-regulated transporter; Eide et al., 1996; Vert et al., 2002). The basic helix-loop-helix (BHLH) transcription factor family in plants is a ubiquitous regulator and is highly conserved, regulating different types of genes during transcription (Heim et al., 2003). The BHLH transcription factor or FIT (FER-like Fe deficiency-induced transcription factor) is reported to be responsible for high-level expression of FRO2 and IRT-1 (Colangelo and Guerinot, 2004; Jakoby et al., 2004; Yuan et al., 2005). It is pertinent to mention that iron uptake, translocation and storage is a complex pathway and multiple genes or gene families are involved. However, from crop breeding point of view breeders always need a high-throughput and less time consuming techniques to identify few potential genotypes in a large set of germplasms. These three genes were targeted in lentil with a long-term objective in mind to develop an assay to find lentil genotypes which better perform under excess iron supply. The results of this experiment would give an initial thrust to such objectivities in lentil where limited amount of sequence information is available till date.
Development of gene specific markers and their utilization in understanding metabolic pathways are important genomic goals to achieve in any crop species for their effective utilization in genetic studies or molecular breeding applications per se. Availability of specific DNA markers for iron metabolism related genes in lentil are not available. The objectives of the study were to, (1) develop gene (Ferritin-1, BHLH-1, and IRT-1) specific molecular markers in lentil and (2) analyze their gene expression under excess iron over time.
‘CDC Redberry’ (Vandenberg et al., 2006) seedlings were raised in the laboratory and fresh tissue was collected for DNA and RNA extraction. Seeds were germinated on wet filter paper in an incubator maintained at 25°C. Seedlings were transferred to 50 mL tubes containing distilled water for hydroponic growth with 16:8 h light: dark cycle and at 25°C for eight days after germination. After complete development of the first true leaf (of growth), treatments were applied 18–21 days after germination and included: (1) iron deficient condition (control with distilled water), (2) excess iron condition (addition of 500 μM of Fe-EDTA, 150 mM of sodium citrate, and 75 μM FeSO4) (Lobréaux et al., 1995). Treatments were applied for 24 h and samples were collected 2, 8, and 24 h after treatment. Three biological replications were included for each treatment.
Full length coding sequences (CDS) for three ferritin genes (ferritin-1, ferritin-2, ferritin-3) for Medicago truncatula were acquired from the NCBI (National Center for Biological Information) nucleotide database on 15 April 2015. The complete coding sequence of Ferritin-2 mRNA (NCBI reference sequence: XM_003616637.1) of M. truncatula was downloaded in FASTA format and used to perform a nucleotide BLAST search against CDC Redberry 454 contig sequences in the Knowpulse database1. The contig sequence with the highest bit score and lowest e-value and, therefore, having the highest similarity with the query sequence (M. truncatula Ferritin-2) was identified. The contig sequence was downloaded from the Knowpulse database and Primer-BLAST2 was used to design primer pairs using default parameters (Table Table11). One primer pair (FerrClo5) used for the development of qPCR compatible primers for the Ferritin gene in lentil. In addition, one primer pair specific to a lentil BHLH (Basic Helix Loop Helix) transcription factor or FER-like transcription factor gene sequence (Sen Gupta et al., 2016) was synthesized. Primers were also designed for the iron-related transporter gene based on the IRT1 mRNA coding sequence (CDS) (LegumeIP database reference no. IMGA[Medtr8g105030.1] of M. truncatula for the amplification of lentil IRT-1 in the qPCR experiment. The amplicon of the ferritin gene as well as the BHLH transcription factor gene were beyond the range of optimum product size (>250 bp) for qPCR experiments and thus were gel purified using a gel purification kit (IBI, MIDSCI, St. Louis, MO, USA) (Vogelstein and Gillespie, 1979) following manufacturer’s instructions and sequenced using the Sanger sequencing method (Etonbiosciences Inc., San Diego, CA, USA). The gene sequences were aligned with the respective M. truncatula mRNA sequences (Ferritin-2 and BHLH transcription factor gene, respectively) and primers were designed for qPCR experiments based on the putative exonic sequences, their sequence identity, gap, and the desired product size using Primer3 software2. Based on these sequences one primer pair for Ferritin-1 and another primer pair for the BHLH-1 transcription factor were designed for qPCR. Primers for IRT-1 were directly used in qPCR and were within the qPCR compatible product size range (<100 bp amplicon size).
Total RNA was extracted from 100 mg of fresh leaves of individual treatments using the QIAGEN® RNeasy Mini Kit (QIAGEN, Valencia, CA, USA) according to manufacturer instructions. The quality of the RNA extracts were determined by the spectrophotometer Nano-Drop (ND-1000) (NanoDrop Technologies, Welmington, DE, USA). To check the integrity of the RNA, the samples were stained, separated and visualized by electrophoresis in a 1% agarose gel. Details about the quality of the RNA samples can be found in Supplementary Table S1. The first strand of cDNA was synthesized from 1 μg of total RNA in a 20 μL reaction using SuperScript III First Strand Synthesis Supermix RT-PCR Kit (Invitrogen, USA). The cDNAs were diluted to 2 ng μL-1.
Three primer pairs were used for gene expression analysis, Ferritin1 (developed using PCR based cloning and sequencing), BHLH1 (developed using PCR based cloning and sequencing) and IRT1 (primer designed based on M. truncatula IRT1 gene sequence). Expression levels of mRNA were evaluated in a SYBR Green dye using an Applied Biosystems 7500 Fast Real-Time PCR System (Applied Biosystems, USA). PCR amplifications were carried out in triplicate in 20 μL reactions containing Maxima SYBR Green mixer (Fermentas, USA), 250 nM of each primer and 4 ng of cDNA. On each plate, the reference genes (GADPH and Actin) and negative controls were included. Amplification conditions were 50°C for 2 min, 95°C for 10 min, 40 cycles at 95°C for 15 s, 60°C for 1 min. The calibration curves for each primer pair were plotted using five serial dilutions of the cDNA in water. To verify the specificity of amplification a dissociation curve analysis step was added to the qPCR amplification protocol. Amplification efficiency, slope and R2 value were determined for each primer pair. Amplification efficiencies were calculated as E = (10-1/slope–1) × 100.
Cycle threshold (CT) values were determined using SDS software (Applied Biosystems, USA). Gene expression data were analyzed using the CT values and amplification efficiency values using method 2-ΔΔCT (Livak and Schmittgen, 2001). Geometric means of reference genes were used to normalize the CT values of the individual samples. The program REST 2009—Relative Expression Software Tool (Pfaffl, 2001) was used to determine if the differences between the treatments were statistically significant (P < 0.05).
After performing BLASTn analysis using ferritin-2 mRNA sequence of Medicago truncatula in the KnowPulse database (University of Saskatchewan, Canada) one contig sequence was identified, LcRBContig00605, based on BIT score (700), sequence identity (91%), and e-value (0) (Table Table11). BLASTn results using other plant species resulted in identification of this contig sequence (LcRBContig00605) (data not shown). Optimum PCR conditions for the designed primers (FerrClo5) in an ABI 7500 thermocylcer were established: 94°C for 5 minutes, followed by 30 cycles of 94°C for 1 min, 60°C for 1 m, 72°C for 1 min followed by a final elongation step of 72°C for 5 min. The amplified DNA fragment was gel purified and sequenced using Sanger’s method to obtain a 390 bp sequence. Alignment of the partial genomic DNA sequence with the M. truncatula ferritin-2 mRNA sequence (NCBI reference sequence: XM_003616637.1) showed a 92 bp sequence overlap with no gap (Figure Figure11). This potential exonic sequence was used to design primers (Ferritin-1) using Primer-BLAST (Table Table22).
Primer pairs developed in a previous study (Sen Gupta et al., 2016) were used to amplify the BHLH-1 gene in CDC Redberry genomic DNA. Optimum PCR conditions for BHLH-1 primer pairs in an ABI 7500 thermocylcer were established: 94°C for 5 min, followed by 30 cycles of 94°C for 1 min, 60°C for 1 min, 72°C for 1 min followed by a final elongation step of 72°C for 5 min. The amplified fragment sequenced by Sanger’s sequencing method and A 490 bp sequence was obtained. This sequence was aligned with M. truncatula BHLH mRNA sequence (NCBI reference number XM_003606283.1) and based on the alignment (Figure Figure22) a 75 bp sequence with no gap (potential exonic sequence) was used to design qPCR compatible primers for BHLH-1 in lentil using Primer-BLAST.
Using a M. truncatula iron regulated transporter gene mRNA sequence [LegumeIP database reference no. IMGA(Medtr8g105030.1)] primer pairs (IRT1) were designed for the qPCR study.
Dissociation curve analysis of the three pairs of primers (Ferritin-1, BHLH-1, IRT-1) showed specific amplification (Figure Figure33). Amplification efficiency of the designed primer pairs and reference genes (GADPH, Actin) were found to be >90% with the exception of BHLH-1 primer pairs (Table Table33). Slope values ranged from –0.02 to –3.55 and R2 values ranged between 0.0034 and 0.9972.
Using the 2-ΔΔCT method (Livak and Schmittgen, 2001), changes in gene transcripts were calculated for the treated samples (under excess iron condition) compared to the control treatments (iron-deficient condition) (Table Table44). The changes in gene transcript levels for Ferritin-1 and IRT-1 genes were not significantly different for the shoot tissue (Table Table55). A 2.72-fold increase in Ferritin-1 gene transcripts was observed in root tissue after 2 h of iron treatment (P < 0.05) (Table Table55). Similarly, a 3.6-fold increase in IRT-1 gene transcripts was observed (P < 0.05) (Table Table55).
Iron uptake from the soil and translocation within the plant is a complex physiological process. It involves multiple genes and transcription factors. The magnitude of mRNA transcript synthesis under excess iron conditions for iron metabolism related genes (Ferritin-1, BHLH-1, IRT-1) in lentil was evaluated in this study. Two genes, Ferritin-1 and IRT-1, were quantitatively assayed for differential gene expression as they exhibited amplification efficiency of >90 percent (Udvardi et al., 2008).
Dissociation curve analysis (Figure Figure33) which is the dsDNA melting curve analysis (Udvardi et al., 2008) added at the end of PCR run showed the specificity for single amplicon amplification and expected melting temperature for the individual primer pairs. All of the three primer pairs exhibited a typical single peak with expected melting temperatures (Figure Figure33). Gene expression quantification values (CT values) were normalized using geometric means of CT values of the two reference genes (GADPH, Actin) (Vandesompele et al., 2002). Actin and GADPH were used in studies in lentil, pea and common bean exhibiting stability of expression across tissues and plant parts (Saha and Vandemark, 2012, 2013, DeLaat et al., 2014). The objective behind the normalization of qPCR data was to remove the sampling error, which may arise due to RNA quantity and quality differences across samples.
In this study, we developed gene-specific molecular markers for three genes (Ferritin-1, BHLH-1, IRT-1) in lentil. Primers for Ferritin-1and IRT-1 were used in differential gene expression analysis. Partial genomic DNA sequences of Ferritin-1 and BHLH-1 were submitted to the NCBI database. These sequences are available to clone full length genomic sequences of each gene in lentil. The partial genomic DNA sequence BHLH-1 gene can be further analyzed and used to develop qPCR compatible primers for this gene. It can be hypothesized from the comparative genomic synteny of lentil with M. truncatula (Phan et al., 2007) that a ferritin gene family does exist in lentil and other ferritin genes in M. truncatula (ferritin-1 and ferritin-3) could be used to develop molecular markers for the respective ferritin genes in lentil. In addition, once the lentil whole genome sequence is released cloning and characterization of ferritin and other iron metabolism related genes will be easier.
In gene expression analysis under excess iron it was observed that only samples with 2 h excess iron treatments exhibited significant differential gene expression (Table Table55) for both genes (Ferritin-1 and IRT-1) in root tissues. The absence of such kinetics in gene expression change for samples that were given 8 or 24 h excess iron treatments across the tissues was observed. The possible reason could be the different iron homeostasis mechanisms in lentil compared to other plant species studied under similar conditions. Development of an assay to find out the reason behind such variation could first start with the standardization of external iron treatments in lentil. In common bean by applying identical excess iron concentration (Lobréaux et al., 1995) in leaf tissue similar kinetics of differential gene expression of ferritin genes (PvFer1, PvFer2, and PvFer1) were observed (DeLaat et al., 2014). Out of the three genotypes (IAC-Diplomata, Carioca, and BAT 477) used there had been significant genotypic differences of ferritin gene expression for two ferritin genes (PvFer1, PvFer2) (DeLaat et al., 2014). There were no significant differences among the treatments (control with distilled water, osmotic shock causing polyethylene glycol (PEG) treated, excess iron treated, PEG + excess iron treated) for any of the ferritin genes (DeLaat et al., 2014). The interaction between time and treatment was only significant for the PvFer2 and interaction between time and cultivar was significant for the PvFer3 ferritin gene (DeLaat et al., 2014). In most of the treatments ferritin genes were up regulated, however, there were treatments where PvFer1 and PvFer3 were down regulated (DeLaat et al., 2014) over time. The above-mentioned facts for common bean ferritin genes support the results we obtained in the case of Ferritin-1 and IRT-1 genes under identical conditions. Further, the gene expression levels for iron metabolism related genes were low in lentil as evident by the high CT values. Number of biological replications may be increased to improve power of the test. The difference between seedling and adult plant physiology should be taken into consideration in future experiments. In summary, gene specific markers were developed for three iron metabolism related genes (Ferritin-1, BHLH-1, IRT-1) in lentil using PCR based cloning and significant differential expression was observed for Ferritin-1 and IRT-1 genes at the transcriptional level.
Conceived and designed the experiments: KM, DSG, SK. Performed the experiments: DSG. Analyzed the data: DSG. Contributed reagents/materials/analysis tools: KM. Wrote the paper: DSG, KM, SK. All authors have read and approved the manuscript.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
DSG thanks Indian Council of Agricultural Research, New Delhi for awarding Netaji Subhas ICAR International Fellowship for Doctoral study.
Funding. This work was supported by the North Dakota State University and a doctoral fellowship was awarded to DSG from Indian Council of Agricultural Research.
The Supplementary Material for this article can be found online at: http://journal.frontiersin.org/article/10.3389/fpls.2017.00579/full#supplementary-material