Genetic and Evolutionary Analysis of Purple Leaf Sheath in Rice

Background Anthocyanin accumulates in many plant tissues or organs, in rice for example leading to red, purple red and purple phenotypes for protection from damage by biotic and abiotic stresses and for reproduction. Purple leaf, leaf sheath, stigma, pericarp, and apiculus are common in wild rice and landraces and occasionally found in modern cultivars. No gene directly conferring anthocyanin deposited in a purple leaf sheath has yet been isolated by using natural variants. An F2 population derived from ssp. japonica cv. Tainung 72 (TNG72) with purple leaf sheath (PSH) crossed with ssp. indica cv. Taichung Sen 17 (TCS17) with green leaf sheath (GSH) was utilized to isolate a gene conferring leaf sheath color. Results By positional cloning, 10-and 3-bp deletions in the R2R3 Myb domain of OsC1 were uncovered in GSH varieties TCS17 and Nipponbare, respectively. Allelic diversity, rather than gene expression levels of OsC1, might be responsible for anthocyanin accumulation. Parsimony-based analysis of genetic diversity in 50 accessions, including cultivars, landraces, and A-genome wild rice, suggests that independent mutation occurred in Asian, African, South American, and Australian species, while O. meridionalis had a divergent sequence. OsC1 was thought of as a domestication related gene, with up to 90 % reduction of genetic diversity in GSH; however, no values from three tests showed significant differences from neutral expectations, implying that OsC1 had not been subjected to recent selection. Haplotype network analysis revealed that species from different continents formed unique haplotypes with no gene flow. Two major groups of haplotypes corresponding to 10-bp deletion and other sequences were formed in Asian rice, including O. rufipogon, O. nivara and O. sativa. Introgressions of OsC1 between subspecies through natural and artificial hybridization were not rare. Because artificial and natural selection imposed admixture on rice germplasm in Taiwan, the genealogy of OsC1 might not be congruent with the current distribution of alleles through lineage diversification. Conclusion OsC1 is responsible for purple leaf sheath, and much new information about OsC1 is provided e.g., new alleles, non-domestication syndrome, and incongruence of genealogy with geographic distribution. Electronic supplementary material The online version of this article (doi:10.1186/s12284-016-0080-y) contains supplementary material, which is available to authorized users.

studied in maize, Petunia, Arabidopsis and other model plants (Dooner et al. 1991;Brenda 2001;Koes et al. 2005). In addition to the genes encoding enzymes participating in the anthocyanin synthesis pathway, several regulatory genes including members of the C1, Pl, B and R gene families in maize have been identified and their functions elucidated. C1 and Pl proteins containing Myb DNA binding domains regulate downstream genes of the flavonoid synthesis pathway; while B and R proteins containing a basic helix-loop-helix (bHLH) domain are transcriptional activators (Chandler et al. 1989). Based on sequence similarity, OsC1, OsB1 and OsB2, which are homologous to maize C1 and B, were isolated from rice (Reddy et al. 1998;Sakamoto et al. 2001). The N-terminal and bHLH domains of OsB1 and OsB2 take advantage of protein-protein interaction with OsC1 that have an R2R3 Myb domain, and these proteins regulate directly the downstream genes of the flavonoid synthesis pathway (Sakamoto et al. 2001;Koes et al. 2005).
Asian rice, Oryza sativa, was domesticated from wild species, O. rufipogon, an estimated 10,000 years ago. The domestication syndromes are considered to include aspects of grain color, grain size, yield, and other desirable agronomic traits. Domestication-related genes have been classified in terms of crop domestication, improvement and diversification (Kovach et al. 2007;Larson et al. 2014). Shattering genes, sh4 and qSH1, were deliberately modified to influence harvest efficiency as recently as the past 100 years, contributing directly to rice domestication (Zhang et al. 2009). Another key domesticationrelated gene, sd-1, resulting in semi-dwarf stature, was a key element of the 'Green Revolution' in the 1960s in Asia by virtue of dramatically increasing grain yield (Asano et al. 2007). The purple apiculus trait which is common in wild rice but rare in cultivars is controlled by a regulatory gene, OsC1. Allelic diversity of OsC1 revealed signatures of selection in cultivated Asian rice but not in indigenous improved rice varieties in North India (Saitoh et al. 2004;Choudhury et al. 2014). Nevertheless, some crop improvement traits are regional preferences, such as grain texture and flavor regulated by waxy and BADH2 which harbor allelic diversity in different landraces and cultivars (Olsen and Purugganan 2002;Kovach et al. 2009).
In rice, purple leaf sheath (PSH) as well as purple apiculus and stigma is common in wild species and landraces; however, green leaf sheath (GSH) is prevalent in modern cultivars. One or two major QTLs were suggested to confer leaf sheath color, and two QTLs mapped on chromosomes 1 and 6 could explain more than 50 % of phenotypic variation (Hadagal et al. 1980;Yue et al. 2006). A purple leaf sheath gene, PSH1 (t), was narrowed down to an interval of 23.5 kb on chromosome 1 encompassing 6 candidate genes after high resolution of linkage mapping. No gene directly conferring PSH has yet been isolated by using natural variants.
In this study, an F 2 segregating population of ssp. japonica cv. Tainung 72 (TNG72) with purple leaf sheath × ssp. indica cv. Taichung Sen 17 (TCS17) with green leaf sheath was utilized to isolate a gene conferring leaf sheath color by positional cloning. Four accessions with various levels of anthocyanin accumulation in the leaf sheath were used to investigate the relationship between gene expression and anthocyanin content. Analyses of haplotype and nucleotide diversity based on 50 rice accessions which included improved cultivars, landraces, and wild species were conducted to reveal if the gene has been responsive to artificial selection and the associated geographic distribution of its alleles.

Result
Accumulation of Anthocyanins in Tissues of TNG72 and TCS17 at Various Growth Stages TNG72 possessed purple coleoptile, leaf sheath, apiculus, and stigma, and the degrees of purple color varied at different growth stages (Fig. 1a-e). The leaf sheath of TNG72 was green at the 4-leaf stage but gradually turned purple until the active tillering stage, remaining purple until maturity. TNG72 accumulated various amounts of anthocyanin with different localization in rice tissues. However, TCS17 remained green for the entire life cycle, representing the most common phenotype of cultivated rice (Fig. 1a-e).
Both TNG72 and TCS17 possess green leaf blades for their entire life. The anthocyanin contents of TNG72 and TCS17 leaf blades did not differ significantly although TNG72 was somewhat higher at both seedling and tillering stages (Fig. 1f ) and may have already had anthocyanins at a level too low to be discerned visually. On the other hand, TNG72 had significantly higher (p < 0.05) anthocyanin content in leaf sheaths than TCS17. Leaf sheath anthocyanin contents were estimated as 0.06 μmol/g and 0.01 μmol/g at the 4-leaf seedling stage; and 1.16 μmol/g and 0.05 μmol/g at active tillering for TNG72 and TCS17, respectively (Fig. 1f ).

Isolation of the Gene Conferring the Leaf Sheath Color
The F 2 population of TNG72 ×TCS17 was used to identify the gene conferring leaf sheath color by positional cloning. A total of 632 F 2 progenies included 473 and 159 individuals exhibited PSH and GSH, respectively. The segregation ratio of 2.9:1 (PSH: GSH) followed single-gene Mendelian inheritance, indicating that GSH was recessive. A randomly selected 46 F 2 plants with green leaf sheath were genotyped with 117 polymorphic markers distributed over the 12 rice chromosomes, permitting the gene to be coarsely mapped between CH0639 and RM276 on the short arm of chromosome 6 ( Fig. 2). An additional 113 F 2 plants with GSH were genotyped with 3 more markers for fine mapping. The target interval was 162.04 kb, between CH0611 and RM253 encompassed by 3 BACs, OsJNBa00161019, OsJNBb0015B15, and P0529B09. By retrieving the Rice Genome Annotation Project database (RGAP, http:// rice.plantbiology.msu.edu), it was found that one of 25 candidate genes, Os06g10350, annotated as a MYB family transcription factor, was the most likely gene. Os06g10350 corresponded to Os06g0205100, annotated as transcription factor MYB6, O. sativa C1, a rice homolog of maize C1 in the Rice Annotation Project database (RAP, http://rapdb.dna.affrc.go.jp/). TNG72 with PSH possessed a full-length OsC1 DNA sequence encoding 272 amino acids. TCS17 with GSH had a 10-bp deletion in the R3 Myb domain, which was considered a core domain in exon 3 of OsC1. The 10-bp deletion resulted in a frame shift, translating only 207 amino acids and leading to a premature stop codon. In the reference genome sequence of Nipponbare on RGAP, a 3-bp deletion of part of the R3 Myb domain in exon 2 was noted, for which Nipponbare has GSH. The results revealed that an aberrant R3 Myb domain of anthocyanin regulatory C1 protein caused a deficit in anthocyanin synthesis in TCS17 and Nipponbare.

Natural Variation in Leaf Sheath Colors
Purple leaf sheath is a common phenotype in wild rice. In this study, among the 7 wild rices utilized in the Oryza Map Alignment Project (OMAP), all except O. nivara (103813) exhibit PHS. One accession of O. rufipogon collected from Taiwan also has purple leaf sheath. Nevertheless, the majority of cultivated rice has GSH.
Among the 43 accessions of O. sativa selected to study genetic diversity of OsC1, 17 indica and 12 japonica accessions possess green leaf sheath, while 5 indica and 9 japonica accessions possess purple leaf sheath (Table 1). Because of the intention to study allelic variation of OsC1, more japonica landraces exhibiting various degrees of purple color on the leaf sheath were included.
Various degrees of purple color were obvious among different rice accessions. Fourteen accessions, including 2 cultivars and 3 landraces of indica rice, and 1 cultivar and 8 landraces of japonica rice, ranged from light to dark purple. According to the RHS (Royal Horticultural Society) Color Charts 5th Edition, the leaf sheath of 6, 3, 3, and 2 accessions showed tyran rose, pansy purple, red purple, and blackish purple, respectively (Fig. 3a). The estimated anthocyanin content of the GSH cultivar, Tainung 67 (TNG67), was 0.03 μmol/g. The anthocyanin contents of 14 PSH ranged from 1.04-42.77 μmol/g, for which Chuan4 with tyran rose had the least while Kun Shan Wu Siang Keng (KSWSK) with blackish purple had the most. The 14 accessions could be divided into 7 groups with significant differences (LSD, p ≤0.05), in which color degrees were in proportion to anthocyanin contents (Fig. 3a).
One japonica GSH accession, TNG67, and 3 japonica PSH accessions, TNG72, Shang Chi Tsao Tao (SCTT) and KSWSK, exhibiting different degrees of purple color in the leaf sheath were used to evaluate gene expression of OsC1. At the active tillering stage, the estimated anthocyanin contents of these four accessions were significantly different (Fig. 3a). The relative gene expression of 3 accessions with purple leaf sheath was 18-fold higher than TNG67, a highly significant difference (Fig. 3b). Nevertheless, there were no significant differences among the 3 PSH accessions by using LSD analysis.

Nucleotide Diversity and Haplotype Network of OsC1
Fifty accessions collected from 9 countries, mainly from Taiwan, were subjected to analysis of OsC1 nucleotide variation and its haplotype network (Table 1). These 50 accessions could be classified into 5 groups, with Groups I-IV sharing high similarity of DNA sequence while Group V including 6 A-genome wild rices exhibited more allelic diversity (Fig. 4). For Group I, all 14 accessions shared high sequence similarity with TNG72. The majority of Group I belonged to ssp. japonica except 1 indica cultivar, Tainung Sen 20. The leaf sheaths of three accessions were tyran rose or pansy purple. Nevertheless, 8 accessions had GSH although OsC1 function was predicted to be normal. Group II, consisting of 4 indica and 2 japonica accessions, shared the same sequence as SCTT. There were 5 SNPs that differentiated the group from the OsC1 sequence of TNG72, and one SNP located at position 1,192 bp in exon 3 conferred nonsynonymous substitution of valine to alanine.
All 6 accessions had PSH with colors of tyran rose, pansy purple, and red purple. Group III, including 5 accessions, had one SNP in common at position 918 bp on exon 3, resulting in nonsynonymous substitution from proline to glutamine.  5).
OsC1 in the 7 A-genome wild rices, as expected, exhibited rich nucleotide diversity, especially in O. meridonalis, as revealed by haplotype number (H), haplotype diversity (H d ), polymorphic sites (S), pairwise nucleotide difference (π T , π sil ), and Watterson's estimators of θ T and θ sil (Table 2). Nucleotide diversity of OsC1 in cultivated O. sativa was apparently reduced. In general, more genetic variation was detected in indica than japonica rice. Greater sequence polymorphism was noted in PSH than GSH accessions in both indica and japonica rice despite characterizing more GSH accessions. Up to 90 % reduction of genetic diversity in GSH was revealed by the average number of pairwise nucleotide differences per site based on the total number of polymorphic sites (π T ); however, less reduction in silent sites was indicated by π sil and θ sil (Table 2).
Tajima's D and Fu and Li's D & F were applied to test whether OsC1 deviated from the neutral expectation of heterozygosity, but no values were statistically significant, indicating no evidence of strong selection (Table 3).
The overall values were negative in O. sativa and the other A-genome species. Positive values, implying balancing selection, were noted in indica PSH accessions but not in japonica PSH accessions. Negative selection or purifying selection acting on OsC1 could not be ruled out in indica GSH accessions (0.01 ≤ p ≤ 0.05).  Asian rice could be divided two major subgroups, with Group A including two haplotypes (H1, H2) and Group B including 11 haplotypes (H3-H13) (Fig. 5). All accessions of Group A exhibited GSH, and haplotype H1 containing 15 indica accessions and 3 japonica landraces all had the same 10-bp deletion. One indica landrace, Cheng Ching Yu, has an additional single nucleotide substitution, resulting in another haplotype, H2 (Figs. 4 and 5). Group B contained 27 accessions, 11 GSH and 16 PSH with various degrees of purple. According to the haplotype network, 3 major clusters, B1-B3, could be resolved within Group B. The 12 accessions of Cluster B1 shared the same sequence with PSH TNG72 but 7 were phenotypically GSH. All 6 accessions of Cluster B2 (4 indica and 2 japonica landraces), expressed pansy purple and red leaf sheath, similar to SCTT. Cluster B3 had 2 GSH and 3 PSH accessions sharing high sequence similarity with KSWSK. Interestingly, O. rufipogon (Taiwan Type 1) and KSWSK were embodied in one haplotype, H7. The indica cultivar TNS20 and the japonica cultivar Nipponbare had their own additional mutations and were separated into two distinct haplotypes, H4 and H11, respectively. The two accessions of O. nivara formed different haplotypes, H12 and H13, and were split from Cluster B1 because of diverse nucleotide sequences in both upstream and genic regions (Figs. 4 and 5).

Allelic Diversity of OsC1 Responsible for Variation in Leaf Sheath Colors
Plants accumulate anthocyanin in various tissues as an aid to survival and reproduction. In rice, anthocyanin is deposited in the root, leaf sheath, internode, leaf blade, lemma, palea, apiculus, stigma, and pericarp. Tissuespecific anthocyanin accumulation is common in numerous genotypes. Purple pigmented traits in different tissues do not always co-segregate (Sakamoto et al. 2001). However, purple leaf sheath, apiculus, and stigma cosegregated in the F 2 population of PSH TNG72 × GSH TCS17 (Fig. 1) and other populations (Fan et al. 2008;Gao et al. 2011). Anthocyanin accumulation in the apiculus had previously been related to OsC1 (Takahashi 1957;Saitoh et al. 2004) but in the leaf sheath was thought to be inherited by polygenes or a single gene ( Fig. 2; Fan et al. 2008;Wang et al. 2009;Gao et al. 2011).
OsC1, conferring leaf sheath color, was isolated from the F 2 population of TNG72 × TCS17 by positional cloning (Fig. 2), differing from PSH1 (t) but the same as a locus identified from the somaclonal line Z418 (Wang et al. 2009;Gao et al. 2011). The PSH allele was dominant to GSH in crosses between natural germplasm or mutant lines. PSH TNG72 had a full length OsC1 allele encoding 272 amino acids while GSH TCS17 had a 10bp deletion in the R3 Myb domain in exon 3, resulting in truncated translations of 207 amino acids. GSH cultivar Nipponbare had another mutated allele, a 3-bp deletion in the R3 Myb domain in exon 2 (Fig. 2). Among the 50 accessions analyzed herein, the 10-bp deletion was found in 17 indica landraces and improved cultivars 70  146 d#7  163  165  166  167  177 d#12  180  194 d#10  204  216  221 d#3  228  270  273  277  360 d#3  404  425  428  430  432  433 i#1  448  457  458  462  480 d#9  481  492  495  498 d#6  509 d#2  511  513 d#6  516  520  526  527  528  531  532  534  536  539  542 d#8  553  554  555  556  557  558  560  563  565  567  568  569  571 i#1  574  575  576  577  579  583  588 d #7  593  596 d#1  599  630 653 659   (  from Taiwan, China, and the Philippines, and 2 japonica landraces from Taiwan (Fig. 4). The 10-bp deletion was conserved in 17 indigenous varieties in Northeast India and only observed in indica varieties from Taiwan, China, India, and Indonesia (Saitoh et al. 2004;Choudhury et al. 2014). Ten GSH accessions without the 10-bp deletion of OsC1 had other mutated alleles or genes, leading to absence of anthocyanin pigmentation. Deletions of 3-bp in exon 2 and 2-bp in exon 3, both in the R3 Myb domain, were found in japonica rice from Japan and China, respectively (Figs. 2 and 4; Saitoh et al. 2004). Two GSH accessions, Midon and T65, had an amino acid substitution at position 918. However, three other accessions with the same substitution, Asamurasaki, KSWSK, and O. rufipogon, had blackish purple leaf sheath. Thus, mutations in genes other than OsC1 were suggested to also eliminate anthocyanin pigmentation, a hypothesis  Fig. 5 Haplotype network analysis for OsC1. A total of 17 haplotypes, H1-H17, were discerned, and each is represented by a rectangle. In Asian rice, two major groups, Group a and Group b, are classified. Group b can be subdivided into three clusters, B1, B2, and B3, indicated by ovals. Blue dots and triangles indicate indica and japonica accessions, respectively. Text color resembles the color of leaf sheath (green, purple). Box line color resembles the color of leaf sheath of majority of accessions, green, pansy purple, red purple, and blackish purple, respective, besides red resembles admixture of different colors. Black nodes represent inferred branch on which each single nucleotide polymorphism occurred that was supported by seven japonica accessions having the same OsC1 coding sequence as PSH TNG72 (Fig. 4). OsC1, containing an R2R3 Myb domain, is thought to function as a transcription factor, regulating other genes involved in anthocyanin synthesis and enhancing another transcription factor, bHLH, regulating anthocyanin structural gene DFR (Dooner et al. 1991;Ithal and Reddy 2004). Failure of anthocyanin synthesis could result from malfunction of OsC1 or any downstream proteins: for example, PSH1 (t) conferring purple leaf sheath was mapped on chromosome 1 (Wang et al. 2009). One of two activator genes, OsB1 and OsB2 encoding basic helix-loop-helix (bHLH) transcription factors, incorporated with maize C1 could induce anthocyanin synthesis in the aleurone layer; however, the lack of function of these two genes in T65 resulted in green leaf blade and leaf sheath (Sakamoto et al. 2001). One japonica GSH accession, TNG67 which is a descendant of T65, had significantly reduced expression of OsC1 despite having a full length amino acid encoding sequence (Fig. 3), suggesting feedback regulation of gene expression.

O. nivara
Fourteen PSH accessions exhibited variation in intensity of purple coloring of the leaf sheath, classified as tyran rose, pansy purple, red purple, and blackish purple. The anthocyanin contents of these 14 PSH accessions differed significantly (Fig. 3). However, OsC1 gene expression among three accessions with diverse anthocyanin contents, TNG72, SCTT, and KSWSK, showed only slight and non-significant differences. These three accessions represented three different haplotypes, H3, H7, and H10, respectively (Fig. 5). Allelic variation of OsC1 accounted for anthocyanin accumulation and pigmentation in the leaf sheath, for which nonsynonymous mutations at the C-terminal domain were found herein.  The C terminus of R2R3 Myb transcription factors is an activation and repression domain (Dubos et al. 2010). Allelic variation of OsC1 and Purple leaf (Pl) coding regions also caused diverse intensities of purple apiculus pigmentation (Sakamoto et al. 2001;Saitoh et al. 2004). Allelic variation resulting in diversified phenotypes is very common, as exemplified by the great impact of different alleles of Wx and starch synthesis related genes on rice grain appearance, cooking and eating quality (Tian et al. 2009;Zhang et al. 2012;Wu et al. 2015). However, other genes participating in anthocyanin synthesis and environmental effects cannot be neglected (Sakamoto et al. 2001). Anthocyanin accumulation is frequently responsive to abiotic stresses, such as UVB radiation, temperature, and soil acidity (Reddy et al. 2004).
A cis-element related to light regulation (−10PEHVPSBD, Thum et al. 2001) was found in the promoter region of OsC1 in TNG72 by using the PLACE database (https:// sogo.dna.affrc.go.jp/, Higo et al 1999). We noted that the leaf sheath accumulated more anthocyanin when rice plants were grown in soil under natural light than in hypotonic solution in the growth chamber.

The Selection and Genealogy of OsC1
Traits considered part of domestication syndromes are favored by artificial selection during domestication, and consequently distinguish cultivated plants from their wild progenitors. During domestication, genetic diversity of whole genomes can be dramatically reduced because of the 'genetic bottleneck' effect of selecting a few individuals as a founder population. The genetic diversities of genes contributing to domestication syndromes and improvement traits are often accompanied by artificial selection for production and culture, and the geographic distribution of alleles might be altered by human migration (Kovach et al., 2007;Kovach and McCouch 2008;Olsen and Wendel 2013). In rice, OsC1 conferring purple leaf sheath, apiculus, and stigma has been suggested as a domestication gene (Choudhury et al. 2014). Wild types are generally purple while cultivars tend to be green, although exceptions exist as noted above. The nucleotide diversity of OsC1 was higher in O. rufipogon than in O. sativa, and OsC1 of the haplotype of Asian cultivated accessions showed evidence of selection (Saitoh et al. 2004). In addition to perennial O. rufipogon and annual O. rufipogon (also called O. nivara), OsC1 sequences of 4 other wild species, O. glaberrima, O. barthii, O. glumaepatula, and O. meridionalis which had not been previously reported were subjected to allelic variation analysis. Sequence variation existed both in noncoding and coding regions. While these species had PSH, a few nonsynonymous amino acid substitutions were detected (Fig. 4). O. meridionalis (from Australia) had extremely divergent OsC1 DNA sequence, forming a distinct haplotype by itself, and all parameters regarding nucleotide divergence of OsC1 decreased when it was not included in analysis (Table 2). African cultivated species, O. glaberrima, its progenitor O. barthii, and South American species, O. glumaepatula, also had their own specific sequences and formed 2 different haplotypes (Figs. 4 and 5). On the other hand, OsC1 in Asian rice shared sequence similarity and formed 13 interconnected haplotypes. Allelic variation of OsC1 in Asian, African, South American, and Australian rice reflected independent mutation without gene flow because of their geographic distribution. Two accessions of O. nivara and one accession of O. rufipogon together with 24 accessions of O. sativa were in Group B. The genealogy of OsC1 in the collected Asian rice accessions herein and other studies showed no distinct correlation with geographic distribution. The 10-bp deletion conferring GSH was prevalent in indica landraces and improved cultivars and rare in japonica accessions from many countries (Saitoh et al. 2004;Choudhury et al. 2014). The accessions in haplotypes H3 and H10 were collected from several countries (Fig. 5). Gene flow due to human activities might be an important factor in the geographic distribution of OsC1 alleles. Purple leaf sheath, stigma, and apiculus are widespread in wild forms and often found in landraces, while green leaf sheath as well as colorless stigma and apiculus are common in modern cultivars. OsC1 nucleotide divergence was up to 90 % lower in GSH than PSH although twice as many GSH accessions were studied (Table 2). However, no values from three neutral tests, Tajima's D, Fu and Li's D & F, were significantly differently from neutral expectations, indicating that OsC1 had not been subjected to selection-a conclusion that is supported by findings regarding OsC1 in indigenous rice varieties in Northeast India (Choudhury et al. 2014). Genetic diversity was higher in indica than japonica accessions both in 14 PSH and 20 GSH accessions, revealed by parameters reflecting nucleotide segregation at total polymorphic sites and silent sites, π T , θ T , π sil , and θ sil (Table 2, Fig. 4). This phenomenon is congruent with evidence that genetic diversity is larger in subspecies indica than japonica (Garris et al. 2005).
Selection might not be a driving force for reducing genetic diversity in GSH. There is no significant evidence that OsC1 deviated from neutral expectations in indica PSH or japonica PSH and GSH accessions. Nevertheless, indica GSH accessions might be experiencing relaxed purifying selection, indicated by neutrality tests at significance levels of 0.10 < P < 0.05 (Table 3). Unlike other domestication syndromes directly related to productivity and other desirable traits that were selected for particular purposes over several thousand years, GSH might have been selected unintentionally.
The Asian cultivated species, O. sativa, evolved from Asian wild rice progenitors O. nivara (annual) and O. rufipogon (perennial). O. sativa was domesticated from divergent wild populations about 10,000 years ago and diversified into two major subspecies, indica and japonica, subsequently being subjected to a long period of natural and artificial diversifying selection (Gross and Zhao 2014). Indica and japonica subspecies are distinguishable in morphology and physiology, already recognized as Hsien (long grain) and Keng (short grain) in the Han dynasty, China, over 2,000 years ago (Oka 1988;Callaway 2014). Numerous genes related to differentiation between these two subspecies experienced mutation and diversifying selection, e.g., Phr1 responsible for phenol reaction; and GS3, qSW5 and GS5 responsible for grain shape (Yu et al. 2008;Lu et al. 2013). The 10bp deletion conferring GSH was prevalent in indica landraces and improved cultivars and rare in japonica, but not in its progenitor species. The OsC1 allele with 10-bp deletion was suggested to have originated and been an early target of domestication in subspecies indica (Figs. 4 and 5;Saitoh et al. 2004;Choudhury et al. 2014). In addition, 3-bp and 2-bp deletions in exon 2 and exon 3 of the R3 Myb domain were found in japonica rice from Japan and China, respectively. These two alleles were independent from the gene lineage of indica, which suggested mutation after subspecies divergence (Figs. 2 and 4;Saitoh et al. 2004).
Although reproductive barriers such as hybrid sterility and hybrid breakdown impede gene flow between cultivated rice and its wild progenitors, numerous interspecific crosses and successful introgressive hybridizations have been performed to unravel useful alleles and genes of wild species. Gene flow confounded with selection has been revealed at the genome level (Zhao et al. 2010;He et al. 2011;Yang et al. 2011) and in domesticationrelated genes including Wx, GS3, SD1, and qSH1 (Yamanaka et al. 2004;Konishi et al. 2006;Takano-Kai et al. 2009;Asano et al. 2011).
The genealogy of OsC1 suggests some gene flow events. O. rufipogon (Taiwan type 1) had an OsC1 sequence identical to that of Taiwan landrace KSWSK. One SNP aligned to japonica Asamursaki and Taichung 65 and indica Midon, accessions that were clustered in Group III and haplotype B3 (Fig. 4 and 5). Two O. nivara accessions also shared similar sequences to most japonica accessions and were classified as haplotype B1. Thus, OsC1 in three Asian wild accessions closely resembled that of japonica but not indica, a finding which might support the hypothesis that japonica and indica were domesticated independently from O. rufipogon (Yang et al. 2011;Wei et al. 2014). Gene flow between subspecies was not rare, as revealed by genealogy of OsC1 in 23 indica and 20 japonica accessions. In haplotype H1, three japonica landraces from Taiwan also possessed the 10-bp deletion specific to indica; in haplotype H10, one japonica landrace (Shang Chi Tsao Tao) and three indica accessions (Taiwan landrace Jinya-149, India landrace G124 and improved line IR1535) had the same allele (Figs. 4 and 5).
The genealogy of OsC1 might not be in agreement with rice phylogeography because of human behavior. In Taiwan, O. rufipogon and O. nivara were once found in several swamp sites (Chang 1976) but, unfortunately, all habitats were destroyed several decades ago. Archaeological evidence shows that tropical japonica or indica had been cultivated over 5,000 years by ancient indigenous peoples in Taiwan (Hsieh et al. 2011). In the early 17th century, numerous Chinese migrated and carried many landraces (mostly indica) from coastal regions of Fujian and Guangdong Provinces of China to Taiwan. By the early 20th century, 1,197 indica accessions were identified officially in Taiwan, and 1,256 japonica accessions were introduced from Japan (Iso 1964). More than 1,000 of these accessions were deposited in The T.T. Chang Genetic Resources Center at the International Rice Research Institute (IRRI), the Philippines. Taiwanese rice germplasm was thus an admixture of indigenous wild species, landraces, and introduced germplasm from China and Japan; and was subsequently spread over Southeast Asia via the germplasm deposited in IRRI. As a result, introgression of OsC1 may have occurred by hybridization between subspecies and both artificial and natural selection, clouding the true genealogy of OsC1.

Conclusion
We used positional cloning to isolate a PSH gene, revealing independent 10-and 3-bp deletions in the R2R3 Myb domain of OsC1 that occurred in different lineages. Allelic diversity resulted in different OsC1 protein function rather than gene expression levels, accounting for various degrees of anthocyanin accumulation and associated intensities of purple color. Allelic variation of OsC1 among wild species, landraces, and cultivars revealed greatly reduced genetic variation in GSH phenotypes, but there was little evidence that OsC1 had experienced recent selection, suggesting that it may have been enriched in cultivated forms by chance. Introgressions of OsC1 between subspecies indica and japonica were frequent through natural and artificial hybridization. Because of admixture of rice germplasm by artificial and natural selection in Taiwan, the genealogy of OsC1 might not be accurately reflected by the current distribution of alleles through lineage diversification.

Plant Materials
Tainung 72 (TNG72), registered by Taiwan Agriculture Research Institute in 1987, is known as an aromatic elite cultivar. Taichung Sen 17 (TCS17), registered by Taichung District Agricultural Research and Extension Station in 1984, is one of two leading indica varieties in Taiwan. An F 2 population of 624 individuals from a cross between these genotypes was planted in a paddy field at the Chiayi Agricultural Experiment Station (CAES), Taiwan, on January 21, 2008. The ratio of purple to green leaf sheath in the F 2 population was 2.92: 1 (465:159), indicating single gene inheritance with green sheath being recessive. The 159 F 2 individuals possessing GSH, which were predicted to be recessive homozygotes, were subjected to linkage analysis.
A panel of 50 accessions obtained from the National Plant Genetic Resources Center (NPGRC), Taiwan and The Oryza Map Alignment Project (OMAP) were used to reveal DNA sequence diversity of the gene conferring leaf sheath color. As detailed in Table 1 Regarding leaf sheath color, 20 and 30 accessions exhibited purple and green, respectively.

Measurement of Anthocyanin Contents
Total anthocyanin contents of leaf sheath and leaf blade harvested at four-leaf seedling and active tillering stages were quantified as described by Padmavati et al. (1997). Briefly, 0.5 g of fresh tissue was homogenized with extraction buffer and 1 % HCl/Methanol (V/V), for 24 h at 4°C with occasional shaking. The supernatant was saved after centrifugation at 10,000 rpm for 15 min at 4°C and absorbance at 530 nm measured using a spectrophotometer (Metertech SP8001, Taiwan). The relative contents of anthocyanin were estimated from A 530 using an mM extinction coefficient of 31.6 (Padmavati et al. 1997).

Genetic and Physical Mapping of the Gene Conferring Purple Sheath
For linkage analysis, 159 GSH F 2 progeny, predicted to be recessive homozygotes, were genotyped with 121 polymorphic markers, including 67 SSR and 54 indel markers distributed over the 12 rice chromosomes. SSR primer sequences were retrieved from Gramene (http:// www.gramene.org). The 54 indel markers were newly designed based on sequence divergence between Nipponbare (japonica) and 93-11 (indica) (Additional file 1: Table S1). DNA extraction and genotype assays of PCRbased markers was as described (Hsu et al. 2014). The linkage map was constructed with a LOD threshold of 3.5 by using MapMaker Exp 3.0 (Lander et al. 1987). The physical map of the target interval containing candidate genes was retrieved from the Rice Genome Annotation Project (RGAP, http://rice.plantbiology.msu.edu).

Gene Expression of OsC1
Four accessions displaying various degrees of PSH were subjected to quantitative real-time PCR (qPCR) to investigate the relationship of OsC1 gene expression with anthocyanin contents. These four accessions were japonica rice, Tainung 67 (TNG67, green), Tainung 72 (TNG72, light purple), Shang Chi Tsao Tao (SCTT, purple), and Kun Shan Wu Siang Keng (KSWSK, dark purple). Total RNA was extracted by using TRIZOL (Invitrogen, USA), and contaminating DNA was removed by using a TURBO DNA-free kit (Ambion, USA), according to manufacturer's protocols. Primers of OsC1 cDNA for qPCR were designed based on the gene sequence of GenBank accession number Y15219, and were forward primer: 5′-CAACgAg CTggTTTgAggCggT-3′ and reverse primer: 5′-TgAgA gACCACCTgTTgCCgAg-3′. Quantitation of gene expression and calculation of relative gene expression were as described (Hsu et al. 2014).
Genetic divergence of the OsC1 gene region was estimated with π (average nucleotide diversity per site, Nei and Li 1979) and θ w (number of segregating sites, Watterson 1975) according to DnaSP version 5.10.1 (Librado and Rozas 2009). Two neutrality tests, 1) Tajima's D and 2) Fu and Li's D* & F*, were conducted to investigate whether there was any deviation from neutrality by using DnaSP version 5.10.1. Tajima's D estimates the difference between the mean pairwise differences (π) and Watterson's estimator (θ w ) (Tajima 1989). Fu and Li's D* & F* test reveals the discrepancy between the number of polymorphic sites in external and internal groups (Fu and Li 1993). A haplotype network, based on the probability of parsimony and calculated for pairwise differences until it exceeds 0.95, was constructed using TCS1.21 (Templeton et al. 1992).

Additional file
Additional file 1: Table S1. Newly designed markers used in coarse mapping. (DOCX 17 kb)