Development and Characterization of SSR Markers in Proso Millet Based on Switchgrass Genomics ()
1. Introduction
Proso millet (Panicum miliaceum L.) is reported to have been domesticated about 10,000 years ago in central and Eastern Asia and made its way from China to the Black Sea region of Europe by 5000 BC [1]. German-Russian immigrants introduced proso millet to North America in 1875 [2]. Proso millet is known as common millet, millet, and hog millet in the United States of America (USA); broomcorn millet in China; common millet in Japan, Korea, and other Pacific Asian countries; “hersey” millet in Germany; and French white in France [3]. It is currently grown in Asia, Australia, North America, Europe, and Africa [3-5].
Proso millet is the most suitable rotational crop in majority of dryland wheat producing areas in semi-arid High Plains of the USA [6]. It is grown mostly in Colorado, Nebraska, and South Dakota and to a lesser extent in North Dakota, Montana, Wyoming, Kansas, Oklahoma, Texas, Minnesota, Wisconsin, Iowa, Michigan, North Carolina, Georgia, and Florida [7]. Proso millet is highly diversified, has excellent nutritional properties and could become an important crop for food diversification [8]. It is used primarily for human consumption in Asia. In the USA, it is grown primarily for birdseed and livestock [8,9].
A very limited number of DNA markers are reported in proso millet. A few RAPD and AFLP markers were reported in proso millet for genetic diversity analysis [10-12]. Among all PCR-based markers, microsatellites or simple sequence repeat (SSR) markers are the most informative and useful because they are co-dominant, multi-allelic, highly reproducible, abundant and are evenly distributed in the plant genome [13,14]. Hu et al. (2009) [15] identified 46 SSRs markers from rice, wheat, oat and barley for genetic diversity analysis in proso millet. Cho et al. (2010) [16] developed 25 SSR markers from proso millet BAC library. To date only about 100 SSR markers are available, which is inadequate for proso millet genetic and breeding research. But unfortunately, developing SSR markers is expensive and a time-consuming task for any crop [17,18]. Comparative genomics has great potential to speed up development of genomic tools in minor crops such as proso millet using genome resources of other major crops such as rice, maize, sorghum and foxtail millet [19]. SSR markers developed in related species were successfully used in sorghum, and bermudagrass [20,21].
Switchgrass, where enormous genomic resource is available, is taxonomically the closest species to proso millet [22]. A detailed genome map consisting of more than 2000 SSR markers is available in switchgrass [23- 25]. Therefore, switchgrass genomic data are the most suitable for developing DNA markers for proso millet in a rapid and inexpensive way. The objectives of this report were to 1) test and characterize switchgrass SSR markers for using in proso millet, and 2) elucidate repeat-motifs in proso millet based on the new SSR marker analysis.
2. Materials and Methods
2.1. Plant Materials and SSR Markers
A set of 8 proso millet genotypes were used for testing efficacy of the switchgrass SSR markers. Plants were grown in 4-inch pots filled with Sunshine Mix 2 Basic Professional Growing Mix (Westco, Morill, NE, USA) in a greenhouse at the University of Nebraska, Panhandle Research and Extension Center, Scottsbluff. Leaf tissues of 21-day-old plants were used for DNA extraction.
A total of 548 SSR markers (540 genomic & 8 EST) of switchgrass were used [23,25] These SSR markers are evenly distributed throughout the switchgrass genome. Primers of these SSR markers were synthesized from MWG Biotech (Huntsville, AL) based on sequence reported by Wang et al. 2011 [25]. These 548 SSR markers were tested on 8 proso millet genotypes (Earlybird, Huntsman, Panhandle, Horizon, Plateau, PI436625, PI436626 and PI 463473) to determine potential polymorphic markers. Polymorphic SSR motif repeats were analyzed based on the data published by Wang et al. 2011 [25] and Okada et al. 2010 [24].
2.2. DNA Extraction and SSR Marker Analysis
Genomic DNA was isolated by micro prep CTAB DNA isolation method using about 100 mg leaf tissues [26]. DNA quality and quantity were checked on a 0.8% agarose gel using 0.5XTBE buffer and visualized under UV transillumination. Concentration of DNA in each sample was determined comparing intensity of bands of Lambda/ HindIII DNA markers. PCR consisted of 10 ulreaction volume containing 1× reaction buffer, 1 U Taq polymerase, 200 uMdNTPs, 2 mM MgCl2, 5 pmoles primers, 20 ng DNA. PCR cycle was: initial denaturation of 5 min at 94˚C; followed by 39 cycles of 45 s at 94˚C, 50 s at 55˚C, and 45 s at 72˚C and a final 10 min extension at 72˚C. PCR was done using BioRad S1000 Thermal cycler. PCR amplified products were separated in a 2% agarose gel using 0.5XTBE buffer and visualized under UV transillumination after staining with ethidium bromide @0.5 ug/ml. Markers (>50 bp) were scored manually using gel image and band size was determined considering 25 bp size difference between the bands. A SSR marker was considered polymorphic if two DNA bands of different sizes were observed at least in two genotypes. DNA bands of different sizes were considered different alleles and DNA bands of same size were considered as the same allele. Resolving power (Rp) of each SSR marker was calculated by following formula Rp = ∑ Ib and Ib = 1 − [2 × (0.5 − p)] where Ib is the allele informativeness and p is the proportion of accessions sharing the I allele [27]. The NCBI nucleotide database was searched for homology analysis with nucleotide sequences in other crops using primers sequences of the polymorphic SSR markers.
3. Results and Discussion
3.1. Switchgrass SSRs in Proso Millet
Of the 548 switchgrass SSR markers screened, 339 (62%) amplified and 209 markers (38%) did not amplify in proso millet. Of the 339 amplified markers, 254 (46%) were polymorphic. Many of these 254 markers were found to be highly polymorphic among the set of 8 proso millet genotypes as represented by one such SSR marker PVCA 21-22 (Figure 1). The high polymorphic nature of these markers was observed also from their high resolving power of each SSR marker, which ranged from 0.25 - 14.75 with an average 2.71 (Figure 2). A smallest resolving power of 0.25 was shown by six markers (PVCA 1431-32, PVCA 299-300, PVCA 985-86, PVCA 151-52, PVCA 415-16 and NFSG-246) while the highest resolving power of 14.75 was observed for PVCA 1387-88. As reported by Prevost and Wilkinson (1999) [27], higher resolving power is directly linked to the informativeness of the marker. Based on our data it seems that our SSR markers have moderate resolving power which can be useful to select the efficient marker set for future studies. The names of the 254 polymorphic SSR markers and their characteristics (allele sizes and Resolving power (Rp) values) are given in Table 1. We consider that the 339 SSR markers covered most of the proso millet genome since these markers were selected from most of the chromosomal regions of switchgrass. Lack of amplification of the proso millet genome by 38% of 548 switchgrass SSR markers could be due to insertion and/ or deletion present in SSR motifs, or point mutations and/or deletions in flanking repeats [28].
Approximately 98% of the polymorphic markers were genomic SSR markers and only 2% were EST SSR markers. This is similar to other reports in proso millet and in switchgrass [16,25]. High percentages of transferability of switchgrass markers into proso millet supports the utilization of cross species SSR markers as a useful resource for developing markers in minor crops where very limited or no work has been done at the molecular level. Similar results were obtained in other crops such as sorghum, bermudagrass, napiergrass, finger millet and other grasses [20,21,29,30]. Such high level of transferability is probably because many genomic regions are
Figure 1. Polymorphic profile of switch grass SSR marker PVCA 21-22 in 8 proso genotypes (M = 50 bp NEB DNA Ladder, NC = Negative control).
Figure 2. Resolving power values of 254 polymorphic SSR markers in proso millet.
conserved and syntenic between switchgrass and proso millet, which suggests amplification of either orthologous or paralogus genes [31].
Most of the polymorphic markers (181 out of 254) produced 2, 3 or 4 alleles and 73 markers have produced 1, 5, 6, 7 or 8 alleles. Total numbers of alleles amplified by each SSR marker on the set of 8 lines ranged from 1 to16. Highest alleles (16) were amplified by marker PVCA 1221-22. High frequency of SSR markers with 2 alleles also indicates diploid nature of proso millet genome. These indicate that proso millet genome is not 100% tetraploid but rather partially tetraploid and partially diploid although proso millet was reported as allotetraploid [32]. Amplification of multiple loci by a few SSR markers might be due to the multiple primer binding sites throughout the genome or within a single locus, which may be due to gene duplication or duplicated genomic regions [17]. This is in agreement with previous reports on proso millet, potato, and zoyagrass species [15, 27,33].
The 254 polymorphic SSR markers amplified a total of 984 alleles (amplified DNA markers) among the set of 8 proso millet genotypes. Sizes of alleles by the switchgrass SSRs in proso millet ranged from 50 bp to 1300 bp with varied number of bands of each size. Amplified DNA bands in ranges of 50 - 200 bp, 200 - 400 bp, 400 - 600 bp, 600 - 800 bp, 800 - 1000 bp, >1000 bp were 377 (38%), 325 (33%), 138 (14%), 98(10%), 23 (2%) and 23(2%), respectively. When SSR marker sizes in proso millet were compared with expected switchgrass sizes, only 9 markers (PVCA1535-36PVCA1565-66, PVCA1731-32, PVCA1209-10, PVCA1705-06, PVCA1869-70, PVCA2623-24, PVCA281-82, PVCA301-302) showed exact matches with that of switchgrass and majority of marker sizes were different in proso millet. This high level of differences indicates significant genome reorganization in proso millet after speciation during evolution which was reported in wheat [34].
3.2. SSRs and Possible Association with Abiotic Stresses
We found that eight SSR markers are part of the mRNA, UniGenes or genomic sequences in other crops (Table 2). The SSR marker PVCA1017-1018 has 100% sequence similarity with the mRNA sequence involved in glutathione metabolism in sorghum. Another SSR marker PVCA723-724 is located on the rice BAC clone from where Sub-1 gene was cloned. Glutathione metabolism in sorghum and Sub-1 gene in rice were reported to be associated with drought and flood tolerance, respectively [35,36]. It is likely that, these genes are still present in the proso millet genome and are showing different mechanism for drought tolerance. This evolutionary conservation for these genes provides a valuable source for further marker development for abiotic stresses in proso millet.
3.3. Repetitive DNA in Proso Millet
Repeat motifs of the 254 polymorphic SSR primers in proso millet were analyzed to elucidate the type of repetitive DNA in proso millet. Of the total 254 polymorphic markers 221 (87%) were di-nucleotide repeats and the remaining 33 (13%) were triand other composite repeats (Table 3). Of all these repeat-motifs, 196 were perfect (77%) and 58 were compound (23%) repeats. Of the 221 di-nucleotide motifs, the most abundant repeatmotif was AG/GA (47%) followed by AC/CA (22%) repeat motif in proso millet. Together the AG/GA and AC/CA repeat motif contributed 69% of all the polymorphic markers in proso millet. The third most abundant di-nucleotide repeats in proso millet were GT/TG and CT/TC repeats, which together was 11%. All the remaining di-nucleotide repeats accounted for 7% of all the repeats.
A high level of di-nucleotide repeats in polymorphic SSRs in proso millet matches with other reports where (CA/GT) n and (CT/AG)n were predominant repeat motifs and were found in the euchromatin and hetrochromatin regions, respectively [37]. The AG/GA repeats were shown to be related to drought tolerance in rice [38]. Therefore, it may not be surprising that AG/GA repeats are the pre-dominant repeat motifs in proso millet since proso millet is known to have good tolerance to low soil moisture condition. This result is similar to the report presented by Cho et al. and 42% AC/CA repeats. However, it is opposed to AT/TA and CT/GA repeats as predominant repeats in other plants [39,40].
Table 2. Eight switchgrass SSR markers, which are polymorphic in proso millet and their possible functional association in other crops based on sequence similarities available in NCBI data base.
Table 3. 254 polymorphic SSR markers and their type and repeat-motifs, and its relative frequency in proso millet.
4. Conclusion
To the best of our knowledge, this is the first report of such a large set (339) of SSR markers for proso millet using cross species genomic resources. This will help to advance proso millet genomic research and will ultimately lead to genetic improvement of this crop.
Acknowledgements
This research was funded by the Nebraska Wheat Board and Cross Road Coop and Friends of Proso Millet Research Fund. Partial funding for D.K. Santra was from Hatch project (NEB-43-105) and the graduate research assistancefor S.G. Rajput was from the Agronomy and Horticulture Department of the University of Nebraska-Lincoln.
NOTES