- Research article
- Open Access
Evolutionary history of the NAM-B1 gene in wild and domesticated tetraploid wheat
BMC Genetics volume 18, Article number: 118 (2017)
The NAM-B1 gene in wheat has for almost three decades been extensively studied and utilized in breeding programs because of its significant impact on grain protein and mineral content and pleiotropic effects on senescence rate and grain size. First detected in wild emmer wheat, the wild-type allele of the gene has been introgressed into durum and bread wheat. Later studies have, however, also found the presence of the wild-type allele in some domesticated subspecies. In this study we trace the evolutionary history of the NAM-B1 in tetraploid wheat species and evaluate it as a putative domestication gene.
Genotyping of wild and landrace tetraploid accessions showed presence of only null alleles in durum. Domesticated emmer wheats contained both null alleles and the wild-type allele while wild emmers, with one exception, only carried the wild-type allele. One of the null alleles consists of a deletion that covers several 100 kb. The other null-allele, a one-basepair frame-shift insertion, likely arose among wild emmer. This allele was the target of a selective sweep, extending over several 100 kb.
The NAM-B1 gene fulfils some criteria for being a domestication gene by encoding a trait of domestication relevance (seed size) and is here shown to have been under positive selection. The presence of both wild-type and null alleles in domesticated emmer does, however, suggest the gene to be a diversification gene in this species. Further studies of genotype-environment interactions are needed to find out under what conditions selection on different NAM-B1 alleles have been beneficial.
The domestication of tetraploid wheats began more than 10,000 years ago [1, 2]. The process originated in the Fertile Crescent, where stands of wild tetraploid emmer (Triticum turgidum subsp. dicoccoides) can still be found (reviewed in ). The circumstances surrounding the domestication of the tetraploid wheats, resulting in domesticated emmer (Triticum turgidum subsp. dicoccum) and durum wheat (Triticum turgidum subsp. durum), have long been debated. Some studies suggest a monophyletic origin of domesticated wheat [4, 5], possibly with gene flow between wild and domesticated populations , while others propose a polyphyletic origin [6, 7]. More recently it has been suggested that domesticated tetraploid wheats arose from a mixed set of wild emmer populations . The hexaploid wheats, including bread wheat Triticum aestivum subsp. aestivum, arose as a result of hybridization between free-threshing Triticum turgidum and the wild diploid Aegilops tauschii [9, 10]. There also appears to have been introgression of genetic material from wild tetraploid populations into hexaploid wheat, which could have happened either post-domestication or via the tetraploid progenitor [10,11,12].
Domestication of wheat affected several traits, most notably leading to the evolution of a non-brittle rachis (under control of two major genes: Br-A2 and Br-A3 ). Other traits in the domestication syndrome are free-threshing (influenced by the genes Q and Tg) [14, 15] and increased seed size . The latter is influenced by the gene Gpc-B1, also known as NAM-B1, which has consequently been suggested to be a domestication gene . In order to be considered a domestication gene three criteria should be fulfilled: it should underlie a trait associated with domestication, it should have experienced positive selection, and it should be at near or complete fixation for the causative allele behind the trait .
The function of NAM-B1 is well characterized as a NAC transcription factor . Three alleles have been described of which only the wild-type (henceforth WT) is functional. The other two, a one-basepair insertion frameshift mutation (henceforth +1 bp) and a deletion (henceforth del) of unknown size, are null alleles. The WT allele accelerates senescence and facilitates remobilization of nutrients from flag leaf into maturing grain [20,21,22,23,24]. This results in grain that has higher concentrations of protein and micronutrients [22, 25,26,27,28]. In contrast, the null alleles delay senescence, which can prolong the grain-filling period and thereby increase seed size . Whereas the WT allele has been found to increase protein and mineral content throughout environments, the effect on seed size is more dependent on genetic background and environment . Distelfeld, et al.  suggested that the seed size enhancing effects of the null alleles are more pronounced in cooler, wetter climates that allows a longer grain-filling period.
In a study by Uauy, et al.  the WT allele of NAM-B1 was found to be present in all investigated wild emmers and in most of the domesticated emmers, while it was absent in the bread or durum wheats. The +1 bp allele was found in all durum wheats and a few of the domesticated emmers and bread wheats, while most bread wheats appeared to carry the deletion. Based on this screening the authors concluded that the WT allele was lost during domestication of the progenitors of bread wheat and durum . Asplund, et al. , however, could show that the WT allele was present in four historical specimens of hexaploid landrace wheats. This suggested that the absence of the WT allele in modern wheat varieties was at least partly the result of more recent selection. The presence of the WT allele was later confirmed in extant hexaploid wheats where it was prominent among Fennoscandian landrace spring wheats . Based on their global distribution, the null alleles could, however, arguably be considered to be near fixation in bread wheat.
Although many genes in various crops, including NAM-B1 , have been proposed to be domestication genes, only a few have been shown to have been targeted by selection . When exposed to selection not only the favored genetic variant increases in frequency, but also other, neutral, polymorphisms linked to it. The result is a genetic region with reduced genetic diversity [32, 33], a so-called selective sweep. It has been suggested that during domestication much, if not most, selection will act on already existing genetic variants that become beneficial when artificial selection is applied . The resulting soft sweeps, are expected to leave more subtle traces in the genome than selection acting on de novo mutations [18, 34] and classic tests for selective sweeps will have limited power to detect soft sweeps. Evidence of selection is, however, needed to be able to call a gene a domestication gene . In order to further investigate NAM-B1’s previously suggested status as a domestication gene [17, 35,36,37], we therefore set out to determine whether we could detect traces of selection in the NAM-B1 region of tetraploid wheat with the +1 bp allele, and whether the strength of selection acting on the gene could be estimated. In addition we sought to determine the size of the deletion allele.
Two different sets of plant materials were used (Additional file 1). The first set was used to determine the size of the deletion. It consisted of six hexaploid wheats with known NAM-B1 genotypes; ‘Anza’ (del), ‘Glenlea’ (del), ‘Little club’ (del), ‘Chinese spring’ (+1 bp), ‘Aurore’ (+1 bp) and PI 350731 (WT), with the nullisomic line N6BT6D used as a control to exclude amplification of homologous regions on chromosomes other than 6B.
The second set was used to investigate the presence of a selective sweep in the NAM-B1 region. In a first screen, 94 tetraploid landrace wheats were genotyped for the NAM-B1 gene. The materials primarily originated from the Mediterranean and Near East, and comprised of 18 wild emmers, 61 domesticated emmers and 15 durum wheats. From these, 40 wheats were chosen for the second set of plant materials, which also included six hexaploid wheats used in a previous study  and five outgroup accessions of Aegilops speltoides, Aegilops tauschii and Triticum monococcum. The tetraploid accessions were chosen so that, whenever possible, different genotypes were represented among the different subspecies: ten domesticated emmers with WT and ten with +1 bp allele, ten wild emmers with WT and one with +1 bp, and nine durum wheats all of which carried the +1 bp allele.
DNA was extracted from leaf tissue using either DNeasy Plant Mini Kit (Qiagen) or E-Z 96 Plant DNA kit (Omega bio-tek).
Primers (Additional file 2) targeting regions within and around NAM-B1 (Fig. 1) were used to determine whether each particular region was deleted or not in the first set of plant materials. Lack of amplification in ‘Anza’, ‘Glenlea’ and ‘Little club’ but with successful amplification in ‘Chinese spring’, ‘Aurore’ and PI 350731 was interpreted as that region being deleted.
The 94 tetraploid wheats were genotyped for NAM-B1 according to Asplund, et al. . The resulting PCR fragments were run on an ABI 3130xl Genetic Analyzer with MegaBACE ET400-R Size Standard. Accessions showing no amplification after multiple PCR attempts, but where amplification outside the deleted region verified DNA quality, were considered to carry the deletion.
The second set of plant materials was used to look for signs of a selective sweep. Nine fragments in NAM-B1 and the surrounding genomic region on chromosome 6B were amplified using PCR (Additional file 2). Four reference genes; MdhA, Mp7A, Gsp1B, and 11B , believed to be unlinked to NAM-B1, were included for comparison. PCR specificity to chromosome 6B was verified by failure to amplify DNA from the nullisomic line N6BT6D.
For PCR amplification in both sets each reaction contained 0.05 U/μl of DreamTaq DNA polymerase (Thermo Scientific), 1 x DreamTaq Buffer (Thermo Scientific), 0.2 mM of each dNTP (Thermo Scientific), 0.1 μM each of forward and reverse primer, respectively, and 1 μl of DNA template. PCR conditions were as given in Additional file 2. Unincorporated nucleotides and primers were removed from the PCR products using 0.014 U/μl Exonuclease I (Thermo Scientific) and 0.0071 U/μl FastAP Thermosensitive Alkaline Phosphatase (Thermo Scientific) incubated at 37 °C for 30 min followed by 5 min at 95 °C. Sequencing was performed by Eurofins MWG Operon, Germany, and Macrogen Europe, The Netherlands.
DNA sequence analysis
Geneious (6.0.5) was used to edit and align the DNA sequences and for constructing neighbor-joining trees (Tamura-Nei). DnaSP (ver 5.10.01)  was used to test for selection by calculating Tajima’s D  and Fu and Li’s D and F  statistics. Where outgroup data was not available Fu and Li’s D* and F* statistics were calculated instead. The strength of selection acting on NAM-B1 was estimated according to Olsen, et al. .
The deletion allele
Of the three known alleles at NAM-B1 one is a deletion. By PCR-amplifying targets in the region surrounding the gene (Fig. 1) in six hexaploid wheats with known NAM-B1 genotypes we found that the deletion covered a fragment located 25 kb away from NAM-B1 on the telomeric side of the gene (henceforth t_25kb) but not the t_75kb fragment. On the centromeric side of the gene the deletion covered a fragment located 174 kb away from NAM-B1 (henceforth c_174kb). We did, however, find amplification in one accession carrying the deletion (‘Anza’) at Xucw70_b located between BAC DQ871219.1, that contains NAM-B1, and the adjacent BAC EU835198 located less than 0.3 cM away from NAM-B1. The two other accessions with the deletion (‘Glenlea’ and ‘Little club’) did not show any amplification until c_Yr36 + 3, located within EU835198 but further away on the centromeric side, suggesting that the region contains multiple deletions. In conclusion, the deletion was found to cover a region of more than 200 kb, stretching from approximately 25 kb on the telomeric side and past a fragment located 174 kb into the centromeric side of NAM-B1.
Allele distribution in tetraploid wheats
We screened 94 accessions of wild and landrace tetraploid wheats for NAM-B1 alleles. All 18 wild emmer accessions carried the WT allele except PI 355459 that carried the +1 bp allele and PI 233288 which was found to be heterozygous and was hence excluded from further study. In contrast, all the 15 durum wheats had the +1 bp allele except TRI 14552, which carried the deletion. Among the domesticated emmer accessions 25 out of the 61 genotyped carried the deletion, 17 had the +1 bp allele and 19 carried the WT allele (Fig. 2). Neither of the NAM-B1 alleles appeared to be limited to specific geographic areas. The WT allele was frequently found in accessions from the Middle East, reflecting that this is the most common allele among the wild emmers that are native to this region.
Phylogenetic and diversity analyses in the region surrounding NAM-B1
Fragments across the NAM-B1 region were sequenced in the second sample set to investigate the presence of a selective sweep. Neighbor-joining trees showed that the sequences formed two clusters; one consisting of WT accessions and another with accessions carrying the +1 bp allele both within the gene as well as outside of it (Fig. 3a-c) from t_76kb to c_141kb. The WT accessions were fairly polymorphic and in NAM-B1 the less variable +1 bp accessions formed a subclade within a group of WT wild emmers. In c_7kb (Additional file 3) and t_76kb (Fig. 3a) the occasional WT accession clustered among the +1 bp accessions. In c_157kb (Fig. 3d) accessions no longer clustered according to allele type, in concordance with the four reference genes.
The nucleotide diversity of the sequences from sample set two was examined with sequences being grouped by NAM-B1 genotype as well as by domestication status and subspecies (Fig. 4, Additional file 4 a–b). In all but three fragments (NAM-B1, one linked and one reference fragment) nucleotide diversity (π) was higher in wild emmer than in the domesticated wheats combined (three fragments for θ; NAM-B1, one linked and one reference). Inclusion of the +1 bp wild emmer had little effect on the diversity measures. Nucleotide diversity (π) was higher in WT accessions than in +1 bp accessions in all fragments. When comparing only domesticated wheats the WT nucleotide diversity (π) was higher than +1 bp diversity in all but three fragments; two reference fragments and one linked to NAM-B1 (three fragments for θ; two linked and one reference).
Tests for selection
The sequences from sample set two were also analyzed to see if any of the fragments showed significantly higher frequencies of rare alleles than expected under neutral theory, indicative of a selective sweep. Such an excess of rare alleles would reveal itself as negative test statistics when tested with Tajima’s D or Fu and Li’s D and F. For the four reference fragments both wild emmers and domesticated tetraploid wheats primarily produced negative test statistics (Fig. 5a-c, Additional file 5a–c). Wild emmers likewise tended to produce negative test statistics also in the fragments surrounding the NAM-B1 at least on the telomeric side and when tested with Tajima’s D. For most fragments test statistics continued to be negative after the inclusion of the +1 bp wild emmer. Domesticated wheats, in contrast, had in general positive test statistics throughout the NAM-B1 region.
When separated according to genotype, both domesticated wheats with WT and those with +1 bp had negative Tajima’s D values (Fig. 5a; Additional file 5a) for three out of the four reference fragments. Fu and Li’s test statistics were positive for the WT accessions in the reference gene from which results were obtained, and negative in two of the fragments for the +1 bp accessions (Fig. 5b-c, Additional file 5b–c). For the fragments in the NAM-B1 region Tajima’s D values were in general negative for the +1 bp accessions and positive for the WT accessions. In NAM-B1 itself this was the case for all three test statistics, with significant positive values for WT accessions, but the pattern was less clear for Fu and Li’s D in the fragments surrounding NAM-B1. In conclusion, selection test statistics tended to be negative in all species and allele groups with the exception of domesticated WT accessions for fragments in the NAM-B1 region.
In wheat, the markers Xucw70 and Xucw73, flanking the NAM-B1 region, are located 0.9 cM apart, corresponding to a 100 kb segment in rice . Using these values as an approximate estimate of the recombination frequency in the region and 141 kb as an estimate of the width of the selective sweep we followed Olsen, et al.  and estimated the strength of selection acting on NAM-B1 to 0.13.
Genetic effects of tetraploid wheat domestication
Domestication is expected to cause a genome-wide bottleneck with a resultant loss of genetic diversity [31, 42]. Consequently, wild emmer is expected to contain higher levels of genetic diversity than domesticated wheats [43,44,45]. Overall, we found higher levels of diversity in wild emmer than in domesticated wheats, both for the reference genes and to a higher extent in the NAM-B1 region, supporting the presence of a domestication bottleneck. The levels of genetic diversity detected in the reference fragments, although moderate, were similar or higher to those previously reported from the same genes also in wild emmer . We thus conclude that our sample of wild emmer well describes the diversity currently available in genebank holdings.
When comparing the two domesticated tetraploid wheat species, emmer and durum, the former tended to have higher diversity. This is in agreement with previous studies where low nucleotide diversity have been reported in domesticated wheats, in particular durum wheat [4, 46]. In contrast, in a study of Mediterranean wheats, Oliveira, et al.  found higher SNP diversity in the order: durum > domesticated emmer > wild emmer wheat, but noted that this may have been the consequence of ascertainment bias as the markers used had been developed from a panel of durum and rivet wheat.
For some of the fragments in this study, our unascertained sequences from domesticated emmer showed higher diversity than wild emmer, corroborating the results of Oliveira, et al. . A reticulated origin of domesticated emmer wheats  or gene flow between wild and domesticated species [5, 11] could have contributed to increasing the nucleotide diversity in parts of the genome of domesticated wheat. It has been argued, however, that the effect of introgression from wild wheats may have been limited, in particular as it would have posed a risk to losing recessive domestication traits [8, 47].
Many tests for selection, such as the ones used here, are also sensitive to population expansion and subdivision. The negative (albeit rarely significant) test statistics detected for most of the four reference fragments suggest population expansion, both in wild and domesticated tetraploid wheats. Population expansion following the initial domestication bottleneck is expected in the domesticated wheats, as a consequence of spread of agriculture. The evolutionary explanation for the negative test statistics for wild emmer is less clear, but the results corroborate those of previous studies [4, 12].
Null alleles at NAM-B1
There are two known null alleles at the NAM-B1 locus, one of which is a deletion (del) . We report here, for the first time, the presence of the del allele among durum wheats, which suggests that both null alleles occur in both durum and emmer landrace wheat. The rarity of the del allele among durum wheats (a single accession – TRI 14552) could be the result of genetic drift during a bottleneck during the formation of the species, but neither our reference genes nor the results of other studies have consistently suggested a strong bottleneck during durum formation [12, 48]. Further genetic analysis of the del carrying accession would be needed to rule out recent gene flow from domesticated emmer.
We have found that the deletion allele stretches over a region of at least 200 kb. Our data also suggest that more deletions occur in the same genetic region. A large proportion of the region surrounding NAM-B1 consists of repetitive sequence, facilitating repeated loss of DNA . This plasticity of the plant genomes, resulting from both repetitive DNA introducing variation and motifs involved in illegitimate recombination together with the functional overlap among genes in polyploids, has been suggested to be of major importance for crop evolution [17, 50,51,52]. In the case of NAM-B1 it has given rise to one of the two null alleles.
Accessions with the +1 bp allele form a subclade to accessions with the WT allele (Fig. 3b). The subclade, however, falls under the wild emmers rather than WT accessions of the domesticated subspecies. This strongly suggests that the +1 bp mutation first arose in wild emmer rather than in the domesticated forms. This is further supported by the presence of the +1 bp allele in a wild emmer accession. This accession, PI 355459, has the spikelet morphology and smooth breakage scars consistent with it being a true wild emmer, although we cannot rule out that the presence of the +1 bp allele is the result of gene flow from domesticated tetraploids back into wild emmers.
A selective sweep at NAM-B1
Genetic diversity at linked sites is expected to share a common genetic history, with alleles at different loci being non-randomly associated, in so-called linkage disequilibrium . Recombination will act to break up such associations and gene trees at unlinked or loosely linked parts of the genome are typically independent of each other. Selective sweeps, such as those expected following selection on traits beneficial to domesticated plants, will act to increase the extent of linkage disequilibrium and the amount of linkage disequilibrium will depend both on the strength of the sweep and the time since the sweep occurred .
We found that accessions cluster according to NAM-B1 genotype up to at least 141 kb on the centromere side and beyond 76 kb on the telomere side of NAM-B1, indicative of a large sweep. A sweep affecting a region of similar size (250 kb) has been reported to surround the Waxy (Wx) gene, causing the absence of amylose in glutinous rice , a primarily self-pollinating species like wheat. In contrast, the sweep located just upstream of teosinte branched 1 (tb1) in maize, a cross-pollinating species, is much smaller at 65.6 kb [55,56,57]. In maize the sweep appears to have been targeting the regulatory region where domesticated maize carries a transposon insertion that alters the expression levels of tb1 [57, 58]. This affects several downstream targets of tb1  resulting in, among other things, altered branching pattern. In the case of Wx the strength of selection was estimated to be on the order of 4.24–4.59  while the inferred selection coefficient in maize was much weaker at no more than 0.08 [55, 56]. Our estimate of the strength of selection suggests that the +1 bp allele has been more strongly selected than tb1 but less strongly selected than Wx.
In addition to increasing the extent of linkage disequilibrium, selective sweeps reduce the genetic diversity in the targeted region and its surrounding region. Consistent with this we found that the accessions of domesticated wheats carrying the +1 bp allele had lower levels of nucleotide diversity both in NAM-B1 and in surrounding fragments than both wild emmers and domesticated tetraploid wheats carrying the WT allele (Fig. 4a). For the reference genes the diversity differences between the two allele-groups were typically smaller.
In spite of the high level of linkage disequilibrium and the low genetic diversity indicative of a selective sweep at NAM-B1, neutrality tests mostly failed to detect the sweep. This was in many cases due to the lack of genetic diversity, itself an expected outcome of a selective sweep (e.g. ), among the +1 bp accessions. Where genetic diversity was present among the +1 bp accessions neutrality tests often produced the negative test statistics indicative of a selective sweep (Fig. 5; Additional file 5) although the tests were rarely significant. The lack of significance is surprising, given not only the expected selective history of the gene. The population expansion suggested for domesticated tetraploid wheats by the reference fragments and, for emmer, by previous studies  should have pushed also the fragments in the NAM-B1 region towards more negative test statistics.
Evolutionary history of the NAM-B1 region
It has been suggested that three criteria should be met in order for a gene to be called a domestication gene . The first criterion is that its function should be characterized and it should code for a trait of interest during domestication. Wheat carrying null alleles of NAM-B1 has been shown to have slower senescence rate, resulting in an increased grain weight [21, 23, 26] and based on this we consider NAM-B1 to fulfill the first criterion. Secondly there should be evidence of positive selection at the locus . From the location of the +1 bp accessions in the gene tree for NAM-B1 (Fig. 3b) we can deduce that the +1 bp allele likely arose in wild emmer, i.e. before domestication. The lack of genetic diversity in NAM-B1 among accessions carrying the +1 bp allele suggests that the insertion did not happen long before domestication and argues against a soft sweep at NAM-B1. The extensive linkage disequilibrium around NAM-B1 and the reduced genetic diversity strongly suggests a hard selective sweep on the +1 bp allele even as the region does not test significantly for selection. We therefore consider the selection criterion to also be fulfilled for NAM-B1.
The final criterion posits that causative alleles should be at or near fixation in all lineages from a single domestication event . In this and previous studies  NAM-B1 has been shown to be fixed for the null alleles in durum. Bread wheat, could be argued to be nearly fixed for the null alleles with the WT allele only persisting in Fennoscandian spring wheat . It can thus be argued that in terms of durum and bread wheat NAM-B1 is a bona fide domestication gene as has been suggested [17, 35,36,37]. In contrast, for domesticated emmer the WT allele was present in close to a third of the genotyped accessions, refuting the status of NAM-B1 as a domestication gene in the evolutionary lineage that gave rise to domesticated emmer. Durum is generally believed to have developed from emmer [4, 10, 12]. Under such a scenario it is not clear whether NAM-B1 can be called a domestication gene for tetraploid wheats. In comparison, the above-mentioned tb1 can be classified as a domestication gene since the alleles differ between wild and domesticated maize [57, 58]. In contrast, both wild-type and null-alleles of Wx occurs in domesticated rice, suggesting that Wx is instead a diversification gene . Our finding of both functional and null alleles in domesticated emmer wheat suggests that NAM-B1 should be considered a diversification gene for tetraploid wheats. Selection on NAM-B1 null alleles would have begun already in domesticated emmer, but intensified with the development of durum where the null alleles finally became fixed.
The strongly contrasting fates of the null alleles in bread wheat and durum compared to emmer raise the question of why the WT allele is still present in emmer. Although NAM-B1 null alleles increase grain weight, the effect on overall yield is not necessarily clear . This may be due to other factors effecting yield that under some conditions compensate for the reduced grain size in WT wheat . Distelfeld, et al.  proposed that a delayed senescence would only be beneficial in a mild humid climate where a prolonged grain-filling would be possible and result in larger grain. In a dry environment, prolonged grain-filling would instead be restricted by limited water availability and the yield effects of delayed senescence would be small or negative. Carter, et al.  did notice earlier senescence among wheat with the WT allele grown under greenhouse conditions, but not in plants grown in the field in an area with high mid-season growing temperatures.
It is possible that the selection of genes affecting senescence rate and grain size differ depending on climate. That this may be the case for NAM-B1 is supported by the fact that in bread wheat the WT allele occurs only in Fennoscandian spring wheats, where the benefits of a fast maturation seem to have outweighed the yield effects of the null alleles . The case is much less straightforward when it comes to the domesticated emmers in this study. The effects of genotype - environment interactions on seed size and yield have not yet been tested in emmer wheat. However, we note that accessions carrying the WT allele originated from Spain in the west to Iran in the east and from Ethiopia in the south to Belarus in the north, while accessions with null alleles originated from a similar area (Additional file 1). Environmental selection pressures acting similarly over this vast area to preserve the WT allele seem unlikely.
An alternative explanation could be gene flow between wild and domesticated emmer. Many of the emmers carrying the WT allele originated from areas where wild emmers grow (Iran: N = 5, Turkey: N = 3, Additional file 1) . Gene flow is supported by the clustering of WT emmers among the wild emmers in the NAM-B1 gene tree (Fig. 3b). Gene flow between wild emmer and domesticated emmer from central Europe or Africa, however, seems less likely. Durum wheat has been shown to have limited geographic structure in the Mediterranean area , and a dynamic history of wheat farming has been suggested . If this is the case for emmer, long distance seed trade could have spread WT emmer far from areas where gene flow from wild emmer can occur. Limited selection for seed size may have allowed genetic drift to preserve the WT allele in some populations.
In this study we have shed light on the evolutionary history of NAM-B1. We have shown that the deletion allele covers several 100 kb and that the +1 bp likely arose among wild emmer. The +1 bp allele was then the target of a selective sweep, also extending over several 100 kb, and possibly stronger than the selection acting on the tb1 locus in maize. Both null alleles occur in domesticated emmer and durum and in the latter the null allele seems to be fixed. The frequent occurrences of the WT allele among domesticated emmer, however, raises questions as to whether the NAM-B1 gene is a bona fide tetraploid wheat domestication gene. Instead we propose it to be a diversification gene in this species.
- +1 bp:
Polymerase Chain Reaction
Single Nucleotide Polymorphism
- tb1 :
teosinte brached 1
- Wx :
Nesbitt M. When and where did domesticated cereals first occur in southwest Asia? In: RTJ C, Bottema S, editors. The Dawn of Farming in the Near East, vol. 6. Berlin: Ex oriente; 2002. p. 113–32.
Willcox G, Buxo R, Herveux L. Late Pleistocene and early Holocene climate and the beginnings of cultivation in northern Syria. The Holocene. 2009;19(1):151–8.
Özkan H, Willcox G, Graner A, Salamini F, Kilian B. Geographic distribution and domestication of wild emmer wheat (Triticum Dicoccoides). Genet Resour Crop Evol. 2010;58(1):11–53.
Haudry A, Cenci A, Ravel C, Bataillon T, Brunel D, Poncet C, Hochu I, Poirier S, Santoni S, Glemin S, et al. Grinding up wheat: a massive loss of nucleotide diversity since domestication. Mol Biol Evol. 2007;24(7):1506–17.
Luo MC, Yang ZL, You FM, Kawahara T, Waines JG, Dvorak J. The structure of wild and domesticated emmer wheat populations, gene flow between them, and the site of emmer domestication. Theor Appl Genet. 2007;114(6):947–59.
Thanh PT, Vladutu CI, Kianian SF, Thanh PT, Ishii T, Nitta M, Nasuda S, Mori N. Molecular genetic analysis of domestication traits in emmer wheat. I: map construction and QTL analysis using an F2Pupulation. Biotechnology & Biotechnological Equipment. 2014;27(2):3627–37.
Feldman M, Kislev ME. Domestication of emmer wheat and evolution of free-threshing tetraploid wheat. Israel Journal of Plant Sciences. 2007;55(3–4):207–21.
Civan P, Ivanicova Z, Brown TA. Reticulated origin of domesticated emmer wheat supports a dynamic model for the emergence of agriculture in the fertile crescent. PLoS One. 2013;8(11):e81955.
Huang S, Sirikhachornkit A, Su X, 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 U S A. 2002;99(12):8133–8.
Dvorak J, Deal KR, Luo MC, You FM, von Borstel K, Dehghani H. The origin of spelt and free-threshing Hexaploid wheat. J Hered. 2012;103(3):426–41.
Dvorak J, Akhunov ED, Akhunov AR, Deal KR, Luo MC. Molecular characterization of a diagnostic DNA marker for domesticated tetraploid wheat provides evidence for gene flow from wild tetraploid wheat to hexaploid wheat. Mol Biol Evol. 2006;23(7):1386–96.
Oliveira HR, Hagenblad J, Leino MW, Leigh FJ, Lister DL, Pena-Chocarro L, Jones MK. Wheat in the Mediterranean revisited - tetraploid wheat landraces assessed with elite bread wheat single nucleotide polymorphism markers. BMC Genet. 2014;15(1):54.
Nalam VJ, Vales MI, Watson CJ, Kianian SF, Riera-Lizarazu O. Map-based analysis of genes affecting the brittle rachis character in tetraploid wheat (Triticum Turgidum L.). Theor Appl Genet. 2006;112(2):373–81.
Simons KJ, Fellers JP, Trick HN, Zhang Z, Tai YS, Gill BS, Faris JD. Molecular characterization of the major wheat domestication gene Q. Genetics. 2006;172(1):547–55.
Faris JD, Zhang Z, Chao S. Map-based analysis of the tenacious glume gene Tg-B1 of wild emmer and its role in wheat domestication. Gene. 2014;542(2):198–208.
Gegas VC, Nazari A, Griffiths S, Simmonds J, Fish L, Orford S, Sayers L, Doonan JH, Snape JW. A genetic framework for grain size and shape variation in wheat. Plant Cell. 2010;22(4):1046–56.
Dubcovsky J, Dvorak J. Genome plasticity a key factor in the success of polyploid wheat under domestication. Science. 2007;316(5833):1862–6.
Meyer RS, Purugganan MD. Evolution of crop species: genetics of domestication and diversification. Nat Rev Genet. 2013;14(12):840–52.
Uauy C, Distelfeld A, Fahima T, Blechl A, Dubcovsky J. A NAC gene regulating senescence improves grain protein, zinc, and iron content in wheat. Science. 2006;314(5803):1298–301.
Kade M, Barneix AJ, Olmos S, Dubcovsky J. Nitrogen uptake and remobilization in tetraploid ÔLangdonÕ durum wheat and a recombinant substitution line with the high grain protein gene Gpc-B1. Plant Breed. 2005;124:343–9.
Uauy C, Brevis JC, Dubcovsky J. The high grain protein content gene Gpc-B1 accelerates senescence and has pleiotropic effects on protein content in wheat. J Exp Bot. 2006;57(11):2785–94.
Distelfeld A, Cakmak I, Peleg Z, Ozturk L, Yazici AM, Budak H, Saranga Y, Fahima T. Multiple QTL-effects of wheat Gpc-B1 locus on grain protein and micronutrient concentrations. Physiol Plant. 2007;129(3):635–43.
Asplund L, Bergkvist G, Leino MW, Westerbergh A, Weih M. Swedish spring wheat varieties with the rare high grain protein allele of NAM-B1 differ in leaf senescence and grain mineral content. PLoS One. 2013;8(3):e59704.
Pearce S, Tabbita F, Cantu D, Buffalo V, Avni R, Vazquez-Gross H, Zhao R, Conley CJ, Distelfeld A, Dubcovksy J. Regulation of Zn and Fe transporters by the GPC1 gene during early wheat monocarpic senescence. BMC Plant Biol. 2014;14:368.
Olmos S, Distelfeld A, Chicaiza O, Schlatter AR, Fahima T, Echenique V, Dubcovsky J. Precise mapping of a locus affecting grain protein content in durum wheat. Theor Appl Genet. 2003;107(7):1243–51.
Brevis JC, Dubcovsky J. Effects of the chromosome region including the locus on wheat grain and protein yield. Crop Sci. 2010;50(1):93.
Brevis JC, Morris CF, Manthey F, Dubcovsky J. Effect of the grain protein content locus Gpc-B1 on bread and pasta quality. J Cereal Sci. 2010;51(3):357–65.
Waters BM, Uauy C, Dubcovsky J, Grusak MA. Wheat (Triticum aestivum) NAM proteins regulate the translocation of iron, zinc, and nitrogen compounds from vegetative tissues to grain. J Exp Bot. 2009;60(15):4263–74.
Asplund L, Hagenblad J, Leino MW. Re-evaluating the history of the wheat domestication gene NAM-B1 using historical plant material. J Archaeol Sci. 2010;37(9):2303–7.
Hagenblad J, Asplund L, Balfourier F, Ravel C, Leino MW. Strong presence of the high grain protein content allele of NAM-B1 in Fennoscandian wheat. Theor Appl Genet. 2012;125(8):1677–86.
Olsen KM, Wendel JF. A bountiful harvest: genomic insights into crop domestication phenotypes. Annu Rev Plant Biol. 2013;64:47–70.
Wang RL, Stec A, Hey J, Lukens L, Doebley J. The limits of selection during maize domestication. Nature. 1999;398(6724):236–9.
Olsen KM, Caicedo AL, Polato N, McClung A, McCouch S, Purugganan MD. Selection under domestication: evidence for a sweep in the rice waxy genomic region. Genetics. 2006;173(2):975–83.
Innan H, Kim Y. Pattern of polymorphism after strong artificial selection in a domestication event. Proc Natl Acad Sci U S A. 2004;101(29):10667–72.
X-G H, B-H W, Liu D-C, Wei Y-M, Gao S-B, Zheng Y-L. Variation and their relationship of NAM-G1 gene and grain protein content in Triticum Timopheevii Zhuk. J Plant Physiol. 2013;170(3):330–7.
Hu X-G, Wu B-H, Yan Z-H, Dai S-F, Zhang L-Q, Liu D-C, Zheng Y-L. Characteristics and polymorphism of NAM gene from Aegilops section sitopsis species. African Journal of Agricultural Reseearch. 2012;7(37):5252–8.
Hebelstrup KH. Differences in nutritional quality between wild and domesticated forms of barley and emmer wheat. Plant Sci. 2017;256:1–4.
Librado P, Rozas J. DnaSP v5: a software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25(11):1451–2.
Tajima F. Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. Genetics. 1989;123(3):585–95.
YX F, Li WH. Statistical tests of neutrality of mutations. Genetics. 1993;133(3):693–709.
Distelfeld A, Uauy C, Olmos S, Schlatter A, Dubcovsky J, Fahima T. Microcolinearity between the grain protein content QTL region in wheat chromosome arm 6BS and rice chromosome 2. Funct Integr Genomics. 2004;4:59–66.
Wright SI, Bi IV, Schroeder SG, Yamasaki M, Doebley JF, McMullen MD, Gaut BS. The effects of artificial selection on the maize genome. Science. 2005;308(5726):1310–4.
Tanksley SD, McCouch SR. Seed banks and molecular maps: unlocking genetic potential from the wild. Science. 1997;277(5329):1063–6.
Doebley JF, Gaut BS, Smith BD. The molecular genetics of crop domestication. Cell. 2006;127(7):1309–21.
Leigh FJ, Mackay I, Oliveira HR, Gosman NE, Horsnell RA, Jones H, White J, Powell W, Brown TA. Using diversity of the chloroplast genome to examine evolutionary history of wheat species. Genet Resour Crop Evol. 2013;60(6):1831–42.
Laido G, Mangini G, Taranto F, Gadaleta A, Blanco A, Cattivelli L, Marone D, Mastrangelo AM, Papa R, De Vita P. Genetic diversity and population structure of tetraploid wheats (Triticum Turgidum L.) estimated by SSR, DArT and pedigree data. PLoS One. 2013;8(6):e67280.
Heun M, Abbo S, Lev-Yadun S, Gopher A. Posidonia oceanica cadmium induces changes in DNA A critical review of the protracted domestication model for Near-Eastern founder crops: linear regression, long-distance gene ow, archaeological, and archaeobotanical evidence. J Exp Bot. 2012;63(12):4333–41.
Oliveira HR, Campana MG, Jones H, Hunt HV, Leigh F, Redhouse DI, Lister DL, Jones MK. Tetraploid wheat landraces in the mediterranean basin: taxonomy, evolution and genetic diversity. PLoS One. 2012;7(5):e37063.
Chantret N, Salse J, Sabot F, Rahman S, Bellec A, Laubin B, Dubois I, Dossat C, Sourdille P, Joudrier P, et al. Molecular basis of evolutionary events that shaped the hardness locus in diploid and polyploid wheat species (Triticum and Aegilops). Plant Cell. 2005;17(4):1033–45.
Kidwell MG, Lisch D. Transposable elements as sources of variation in animals and plants. Proc Natl Acad Sci U S A. 1997;94(15):7704–11.
Parisod C, Alix K, Just J, Petit M, Sarilar V, Mhiri C, Ainouche M, Chalhoub B, Grandbastien MA. Impact of transposable elements on the organization and function of allopolyploid genomes. The New phytologist. 2010;186(1):37–45.
Renny-Byfield S, Wendel JF. Doubling down on genomes: polyploidy and crop plants. Am J Bot. 2014;101(10):1711–25.
Slatkin M. Linkage disequilibrium--understanding the evolutionary past and mapping the medical future. Nat Rev Genet. 2008;9(6):477–85.
Nielsen R. Molecular signatures of natural selection. Annu Rev Genet. 2005;39:197–218.
Wang SJ, Magoulas C, Hickey D. Concerted evolution within a trypsin gene cluster in drosophila. Mol Biol Evol. 1999;16(9):1117–24.
Clark RM, Linton E, Messing J, Doebley JF. Pattern of diversity in the genomic region near the maize domestication gene tb1. Proc Natl Acad Sci U S A. 2004;101(3):700–7.
Studer A, Zhao Q, Ross-Ibarra J, Doebley J. Identification of a functional transposon insertion in the maize domestication gene tb1. Nat Genet. 2011;43(11):1160–3.
Clark RM, Wagler TN, Quijada P, Doebley J. A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture. Nat Genet. 2006;38(5):594–7.
Studer AJ, Wang H, Doebley JF. Selection during maize domestication targeted a gene network controlling plant and inflorescence architecture. Genetics. 2017;207(2):755–65.
Chapman MA, Burke JM. Evidence of selection on fatty acid biosynthetic genes during the evolution of cultivated sunflower. Theor Appl Genet. 2012;125(5):897–907.
Tabbita F, Lewis S, Vouilloz JP, Ortega MA, Kade M, Abbate PE, Barneix AJ, Gill K. Effects of the Gpc-B1 locus on high grain protein content introgressed into Argentinean wheat germplasm. Plant Breed. 2013;132(1):48–52.
Carter AH, Santra DK, Kidwell KK. Assessment of the effects of the Gpc-B1 allele on senescence rate, grain protein concentration and mineral content in hard red spring wheat (Triticum aestivum L.) from the Pacific northwest region of the USA. Plant Breed. 2012;131(1):62–8.
The authors are grateful to the genebanks NPGS, INIA, IPK and NordGen for kindly providing seeds from the accessions used in this study.
This work was funded by the Lagersberg foundation, Erik Philip Sörensen foundation and Carl Tryggers foundation.
Availability of data and materials
Sequences are available in GenBank under the accession numbers MG587126 - MG587711.
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List of wheat accessions and their sites of origin. (XLSX 14 kb)
List of PCR amplified fragments. Primer sequences and PCR conditions. (XLSX 10 kb)
Neighbor-joining trees of wheat sequences in fragments surrounding NAM-B1 and reference genes. (A) Reference gene 11B. (B) Reference gene Gsp1B. (C) Reference gene MdhA. (D) Reference gene Mp7A. (E) Fragment t_10kb. (F) Fragment c_7kb. (G) Fragment c_174kb. (H) Fragment c_Yr36 + 3. (I) Fragment c_Yr36 + 52. (PDF 410 kb)
Nucleotide diversity and Theta W Tables. A) Nucleotide diversity (π). B) Theta W. (XLSX 11 kb)
Neutrality tests. Tables over the resulting test values from the neutrality tests. (A) Tajima’s D. (B) Fu and Li’s D and D*. (C) Fu and Li’s F and F*. (XLSX 14 kb)
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Lundström, M., Leino, M.W. & Hagenblad, J. Evolutionary history of the NAM-B1 gene in wild and domesticated tetraploid wheat. BMC Genet 18, 118 (2017). https://doi.org/10.1186/s12863-017-0566-7
- Selective sweep
- Grain protein content (GPC)
- Domestication gene