Here we analyse genetic variation, population structure and diversity among 3,010 diverse Asian cultivated rice (Oryza sativa L.) genomes from the 3,000 Rice Genomes Project. Our results are consistent with the five major groups previously recognized, but also suggest several unreported subpopulations that correlate with geographic location. We identified 29 million single nucleotide polymorphisms, 2.4 million small indels and over 90,000 structural variations that contribute to within- and between-population variation. Using pan-genome analyses, we identified more than 10,000 novel full-length protein-coding genes and a high number of presence–absence variations. The complex patterns of introgression observed in domestication genes are consistent with multiple independent rice domestication events. The public availability of data from the 3,000 Rice Genomes Project provides a resource for rice genomics research and breeding.
Asian cultivated rice is grown worldwide and comprises the staple food for half of the global population. It is envisaged that by the year 20351 feeding this growing population will necessitate that an additional 112 million metric tons of rice be produced on a smaller area of land, using less water and under more fluctuating climatic conditions, which will require that future rice cultivars be higher yielding and resilient to multiple abiotic and biotic stresses. The foundation of the continued improvement of rice cultivars is the rich genetic diversity within domesticated populations and wild relatives2,3,4. For over 2,000 years, two major types of O. sativa—O. sativa Xian group (here referred to as Xian/Indica (XI) and also known as , Hsien or Indica) and O. sativa Geng Group (here referred to as Geng/Japonica (GJ) and also known as , Keng or Japonica)—have historically been recognized5,6,7. Varied degrees of post-reproductive barriers exist between XI and GJ rice accessions8; this differentiation between XI and GJ rice types and the presence of different varietal groups are well-documented at isozyme and DNA levels6,9. Two other distinct groups have also been recognized using molecular markers10; one of these encompasses the Aus, Boro and Rayada ecotypes from Bangladesh and India (which we term the circum-Aus group (cA)) and the other comprises the famous Basmati and Sadri aromatic varieties (which we term the circum-Basmati group (cB)).
Approximately 780,000 rice accessions are available in gene banks worldwide11. To enable the more efficient use of these accessions in future rice improvement, the Chinese Academy of Agricultural Sciences, BGI-Shenzhen and International Rice Research Institute sequenced over 3,000 rice genomes (3K-RG) as part of the 3,000 Rice Genomes Project12.
Here we present analyses of genetic variation in the 3K-RG that focus on important aspects of O. sativa diversity, single nucleotide polymorphisms (SNPs) and structural variation (deletions, duplications, inversions and translocations). We also construct a species pan-genome consisting of ‘core’ genes that are present in all individuals and ‘distributed’ (variable, accessory or dispensable) genes that are absent in some individuals13,14. The gene presence–absence variations (PAVs) represent another component of species genetic diversity. Our analyses provide new perspectives on rice intra-species diversity and evolutionary history.
Genome mapping, size and SNP variation
Baseline genome sequencing, analyses, and accession information and metadata for the 3,024 rice genomes are summarized in Supplementary Data 1 and Supplementary Notes. Fourteen accessions were excluded from further analyses after quality control. The remaining 3,010 genomes had an average mapping coverage of 92% (74.6–98.7%) (Supplementary Data 2 Table 1), when aligned to the O. sativa cv. Nipponbare IRGSP 1.0 reference genome15 (hereafter referred to as ‘Nipponbare RefSeq’). The estimated size of the genome was 375.1 ± 20.9 Mb, with 42.5 ± 0.4% guanine–cytosine content and 35.6 ± 3.7% repetitive sequence content (Supplementary Data 3 Table 1).
We identified over 29 million SNPs—27 million of which are bi-allelic—and found high concordance (>96%) with previous reports (Supplementary Notes)16,17. Filtering reduced this to a ‘base SNP’ set of approximately 17 million SNPs, which captured >99.9% of all SNPs with minor allele frequencies (MAF) > 0.25% (Extended Data Fig. 1). Half (56%) of non-transposable element (NTE) genes and the majority (91%) of transposable element (TE)-related genes have high-effect SNPs (Supplementary Data 2 Tables 2–4). NTE genes contained about 1.44 million moderate-to-high effect, and about 1.5 million low-effect, SNPs, which gave a ratio of 0.95 for moderate-to-high:low SNPs. For small indels, insertions affected 28% of NTE- and 50% of TE-related genes: deletions affected 41% of NTE- and 70% of TE-related genes. A typical genome in a major varietal group contains approximately 2 million (XI and cA), 0.3–0.8 million (GJ; depending on the subpopulation) or about 1.2 million (cB) SNPs (Supplementary Data 2 Table 5). The SNPs of a typical genome were classified as 7.9% moderate-to-high effect and 5.1% low effect.
Population structure and diversity
The 3K-RG accessions were classified into nine subpopulations (Fig. 1 and Extended Data Fig. 2a–d), most of which could be connected to geographic origins (Supplementary Data 1). There were four XI clusters (XI-1A from East Asia, XI-1B of modern varieties of diverse origins, XI-2 from South Asia and XI-3 from Southeast Asia); three GJ clusters (primarily East Asian temperate (named GJ-tmp), Southeast Asian subtropical (named GJ-sbtrp) and Southeast Asian tropical (named GJ-trp)); and single groups for the mostly South Asian cA and cB accessions. Accessions with admixture components <0.65 within XI and GJ were classified as ‘XI-adm’ and ‘GJ-adm’, respectively, and accessions that fell between major groups were classified as admixed (Extended Data Fig. 2a).
Distinct allele frequency profiles for SNPs of MAF > 10% occurred for the nine subpopulations with deviations from the neutral model reflecting different adaptations and demographic events (Extended Data Fig. 3a). Larger numbers of ‘private’ alleles were found in cA and cB than in other subpopulations (Extended Data Fig. 2e). Comparatively, XI subpopulations have smaller numbers of private alleles, probably owing to ongoing gene flow from natural hybridization and breeding. Doubleton sharing patterns within and between subpopulations showed the same trend (Extended Data Fig. 2f).
Linkage disequilibrium decay rates for combined subpopulations were higher in XI than GJ, with little variation between the two GJ subpopulations, as previously reported7,16,18. However, for the nine subpopulations, linkage disequilibrium decay between XI subpopulations varied more markedly, with XI-2 and XI-3 exhibiting faster linkage disequilibrium decay than XI-1A and XI-1B (Extended Data Fig. 3b). Furthermore, linkage disequilibrium decay correlates strongly with nucleotide diversity (π) among the nine subpopulations (R2 = 0.93, P value = 2.5 × 10−5) (Extended Data Fig. 3c).
Nucleotide diversity computation identified many regions of low genetic diversity that contained small numbers of genes under selective constraints (Extended Data Fig. 3d). Sh419, which controls non-shattering, showed an accordant profile of diversity reduction across all subpopulations (Fig. 2a) that indicates much longer selection, when compared to qSH120. At the semi-dwarf gene sd121 locus, a narrow region of reduced diversity occurred in all major groups, which is a similar pattern to that observed for qSH1. However, higher diversity in the surrounding 100-kb regions occurred in the cA, cB and XI groups, whereas the GJ groups had extended regions of reduced diversity, which reflects the breeding history associated with the ‘green revolution’22. Different patterns of diversity reduction were observed at other important loci. The Wx23 locus that affects amylose content and stickiness on cooking, the Badh2.124 locus that affects aroma and their surrounding regions are highly diverse in the XI, cA and cB groups, which indicates complex histories for selection for different types of eating quality; by contrast, both loci and their surrounding regions show low diversity in GJ. The Rc25 locus has very low diversity in all variety groups, with variable diversity in the surrounding regions in XI, cA and cB.
We compared SNP variation among TE-related genes, NTE-related genes, 1,021 genes with validated functions curated in the OGRO/QTARO database26,27 and a subset of 78 domestication and agronomically relevant genes (Supplementary Data 4). Genetic diversity was reduced significantly (P value < 10−12) near OGRO-curated genes and was often more extreme across the 78-gene subset in each subpopulation (Fig. 2b) when compared with all genomic regions containing genes, which suggests there may have been selection for these genes.
Structural variations (SVs) were called for 3,010 accessions but we focused on 453 accessions with sequencing depths > 20× and mapping depths > 15×, because genome coverage stabilized when sequencing depths exceeded 20× (Extended Data Fig. 4a, b). We identified 93,683 SVs, including 582 SVs larger than 500 kb, with an average of 12,178 SVs per genome. The average sizes of the detected deletions, inversions and duplications are 5.3 ± 0.6 kb, 127.1 ± 19.4 kb and 105.1 ± 22.7 kb, respectively (Fig. 3a, Extended Data Fig. 4c and Supplementary Data 3 Table 2).
SVs showed very strong XI–GJ differentiation. On average, each XI accession differed from Nipponbare RefSeq by 14,754 SVs (8,990 translocations, 5,411 deletions, 188 inversions and 165 duplications), or 3.5× as many as in GJ accessions (Fig. 3a). On average, each cA or cB accession differed from Nipponbare RefSeq by 12,997 SVs and 7,892 SVs, respectively. The total SV sequence that differentiated two GJ accessions was about 22 Mb, whereas it reached 71 Mb between XI and GJ accessions (Fig. 3b). Notably, 1,940 SVs disrupted protein-coding genes within GJ, whereas >6,518 occurred between XI and GJ accessions (Fig. 3c). The SV phylogenetic tree (based on 453 accessions) is similar to the SNP tree, and clearly separates XI, GJ, cA and cB accessions (Fig. 3d). Moreover, the 41,957 major-group-unbalanced SVs that were distributed unevenly among XI, GJ, cA and cB accessions (Fig. 3e) accounted for 44.7% of all SVs and 41.0% of the 582 large SVs.
Pan-genome and population differentiation
The widespread SV and genome size variation (Supplementary Data 3 Tables 1 and 2) encouraged us to investigate the influence of PAVs on protein-coding genes across the 3K-RG. We first used a ‘map-to-pan’ strategy28 to build the species pan-genome (Extended Data Fig. 5a, b), by combining the Nipponbare RefSeq and non-redundant novel de novo assembled sequences; then, PAVs were determined by examining gene-body and coding sequence (CDS) coverage of mapped reads for each accession.
We identified a total 268-Mb non-redundant novel sequences of length >500 bp with <90% identity to Nipponbare RefSeq from assemblies of the 3,010 genomes, from which 12,465 novel full-length genes and several thousand novel genes with partial sequences were predicted. Nipponbare RefSeq genes and full-length novel genes could be merged into 23,876 gene families. The O. sativa core pan-genome was formed by 12,770 (53.5%) gene families present in all 453 high-coverage genomes, 2,056 (8.6%) without significant gene loss >1% (P value > 0.05) in all major groups formed candidate core gene families, and the remaining 9,050 (37.9%) comprised distributed gene families (Fig. 4a, b and Supplementary Data 3 Table 3). In silico simulation indicated these 9,050 gene families underestimate the distributed pan-genome (Fig. 4c). Hence, the O. sativa pan-genome consists of between 12,770 and approximately 14,826 (53.5% to about 62.1%) core gene families, and at least 9,050 (37.9%) distributed gene families: each accession contains between 63.4% and about 73.5% core gene families and at least 26.5% distributed gene families (Fig. 4b). The core gene families have more members (Fig. 4d) and represent essential gene families. Indeed, 5,476 (36.9%) core or candidate core gene families are enriched in essential functions for growth, development and reproduction (using Gene Ontology, GO), whereas only 862 (9.5%) of the distributed gene families could be annotated with GO terms, showing enrichment in regulation of immune and defence responses and ethylene metabolism (Extended Data Fig. 6a, b).
Pan-genome sequence coverage was evaluated using two new reference genomes29, IR 8 from the XI group and N 22 from the cA group (Supplementary Data 3 Table 4). We found 98.4% of the IR 8 and 98.6% of the N 22 genome sequences could be mapped to the pan-genome, whereas only 94.3% and 94.0% could be found in Nipponbare RefSeq. By comparing pan-genome data with high-quality XI reference genomes of Zhenshan 97 and Minghui 6330, approximately 25% of the novel genes were shorter owing to gene predictions from fragmented sequences (Extended Data Fig. 5c, d). Novel gene assemblies were validated by mapping raw reads of the 453 high-coverage genomes to the 12,465 novel genes; 11,792 genes (94.6%) had >95% CDS and >85% gene-body coverages were present in at least two rice lines. By comparison, 99.9% of Nipponbare RefSeq annotated genes were detected in the 453 high-coverage genomes (Extended Data Fig. 5e). Approximately 30% of the full-length novel genes were expressed with >1 read per kilobase per million reads in one or more of the 226 publicly available RNA sequencing datasets31 (Extended Data Fig. 5f, g). Further, benchmarking universal single-copy orthologues32 evaluation suggested little redundancy in predicted genes (Extended Data Fig. 5h).
Analyses of the PAVs of genes (or gene families) were able to distinguish the major varietal groups, and show that there is considerable variation among and within subpopulations (Extended Data Fig. 7a–d). On average, major group accessions differ by about 4,000 (approximately 10%) genes and about 2,000 (approximately 10%) gene families, whereas XI and GJ accessions differ by more than 6,144 (about 14.9%) genes and 2,878 (14.3%) gene families (Fig. 4e and Extended Data Fig. 7e). The GJ pan-genome has 23,167 gene families comprising 46,115 genes, which makes it 1.9% smaller than XI in terms of gene families and 2.5% smaller in terms of genes. However, all GJ accessions have 240 core gene families (1,594 genes) in common, four times as many as in XI (Extended Data Fig. 7f). In addition, 5,733 major-group-unbalanced gene families were more frequent in some populations but lower in others, including hundreds of XI- and GJ-predominant gene families (Fig. 4f). Moreover, we identified 4,270 XI and 1,384 GJ subpopulation-unbalanced gene families, showing variation between subpopulations within each major group (Extended Data Fig. 7g).
Evolution and domestication of rice
To gain insights into the evolutionary history of the rice pan-genome, gene and gene family ages were estimated by aligning protein sequences to the NR protein database (ftp://ftp.ncbi.nlm.nih.gov/blast/db/) partitioned into 13 taxonomic levels (Extended Data Fig. 8a, b). We observed that: (1) new genes and gene families evolved at alternating rates from phylostratum 1 (PS1) (approximately 3.6 billion years ago) to the emergence of the terminal PS13 clade containing O. sativa (about 1.5 million years ago); (2) there was an explosive emergence of new genes accompanying the appearance of Oryza at PS12; (3) core genes tended to be more ancient, and most novel genes or gene families were younger and shorter (Extended Data Fig. 8c, d), consistent with recent reports for other species33; (4) significantly (P value < 0.001) higher SNP variation occurred in distributed genes than in core genes (0.0325 versus 0.0142 SNPs per base) (Extended Data Fig. 8e); and (5) a significantly (P value < 0.001) higher proportion of core genes were under negative selection as compared with those in the Nipponbare RefSeq (Extended Data Fig. 8f).
Regarding O. sativa domestication, we constructed haplotype plots for nine important domestication genes—Rc25, Bh434, PROG135, OsC136, Sh419, Wx23, GS337, qSH120 and qSW538 (Fig. 5a–c and Extended Data Fig. 9). Although a large number of XI samples carry an allele found in GJ, many XI accessions carry alleles at each of these loci that are absent in GJ (Fig. 5d). In fact, about 70% of XI accessions do not carry GJ introgressions in at least four genes, and only one XI sample (out of 1,789) had introgressed GJ haplotypes at all nine genes. This observation supports a model of independent domestication of some of the XI pool, rather than the simpler GJ-to-XI introgression hypothesis2. Furthermore, the 14-bp deletion in Rc25 for domesticated white pericarp was found in several XI lines that carried non-introgressed haplotypes (Extended Data Fig. 9), which suggests independent selection in part of the XI gene pool before introgression of the GJ haplotype became widespread in XI.
Utility of the 3K-RG panel
We demonstrated the use of the 3K-RG genomes and SNPs for trait mapping analyses for the highly heritable traits of grain length, grain width and bacterial blight resistance (Supplementary Notes). Major peaks for grain length with significantly (P value < 10−10) associated markers are on chromosomes 1, 3, 5, 6 and 7, and minor peaks are on chromosomes 4, 9, 10 and 11 (Extended Data Fig. 10a). Major peaks for grain width are found on chromosomes 1 and 5, with minor peaks on chromosomes 3 and 9 (Extended Data Fig. 10b). Genome-wide association study (GWAS) peaks were concordant with known loci, including GS337, GW539, and qGL740 for grain length, and GW5 for grain width. For grain width, the chromosome 9 novel peak coincides with OsFD141, which codes for a bZIP transcription factor involved in flowering time and developmental plasticity (its pleiotropic regulatory function may therefore also affect grain width). Twelve peaks were detected for bacterial blight resistance to strain C5 of Xanthomonas oryzae, with the largest clustered around the resistance gene Xa2642 on chromosome 11 (Extended Data Fig. 10c). Moreover, correlation between gene PAVs and plant height detected the well-known green revolution gene (sd1) as the first-ranked candidate. sd1 is classified as a distributed gene—caused by an approximately 385-bp deletion—and is significantly (P value < 10−20) associated with greatly reduced plant height; it was absent most frequently in XI-1A and XI-1B varieties (Extended Data Fig. 11).
We characterized genetic variation in the 3,010 sequenced accessions of O. sativa and found a high level of genetic diversity in rice. Although the 3K-RG analysis is expected to identify nearly all polymorphisms with MAF > 1%, our simulations suggest that it includes <40% of rare bi-allelic SNPs (MAF < 1%) in the International Rice Gene bank at the International Rice Research Institute (Extended Data Fig. 1c). We also characterized structural variation, and found that the average number of SVs between pairs of XI genomes (>12,000) was similar to that between two high-quality reference XI genomes30. The vast majority were deletions and translocations distributed across the genome (Extended Data Fig. 4c). Medium-sized SVs (≥500 kb) were mostly inversions and duplications, and a large percentage of them (37.9%) occur differentially between XI and GJ. We speculate that large numbers of SVs may contribute to the varying degrees of hybrid sterility and hybrid breakdown between XI and GJ accessions43. We also report pan-genome analyses for O. sativa, and the high numbers of PAVs highlight another component of within-species diversity for rice.
Our analysis brings more resolution to the within-species diversity of O. sativa (Extended Data Fig. 8e). Larger pan-genomes occur in XI than GJ accessions, but GJ accessions have more core genes than XI (Supplementary Data 3 Table 3), a result that was expected given the greater diversity within XI than GJ. This may relate to differences in eco-geographical distribution: GJ accessions experience harsher high- altitude and/or high-latitude environments, versus the less harsh but more diverse environments experienced by XI rice. Understanding the major group/subpopulation-core, -unbalanced and -predominant gene functions is expected to shed light on environmental adaptation of rice variety groups over thousands of years.
Although the 3K-RG population structure analyses based on SNPs and SVs were consistent with the five major groups that were previously known, additional subpopulations in the XI and GJ groups were identified and were suggestive of nine subpopulations that are correlated with geographic origin. Large numbers of SNPs, genes and gene families, and SVs were found to be unique to or predominant in single subpopulations. Varying patterns of diversity reduction across different rice subpopulations were observed in and around about 1,000 well-characterized genes. A closer look at patterns of haplotype sharing at domestication genes suggests that not all ‘domestication’ alleles came to XI from GJ. Taken together, our results—combined with archaeological evidence of XI cultivation for >9,000 years in both India and China44,45—support multiple independent domestications of O. sativa.
Our 3K-RG analysis highlights the genetic diversity that exists in rice germplasm repositories, and the usefulness of establishing a digital gene bank in which all accessions can be sequenced and catalogued. For example, we estimate that sequencing the rest of the gene bank of the International Rice Research Institute may enable the identification of >27 million additional SNPs (Extended Data Fig. 1d). The next challenge will be to examine associations of the 3K-RG genetic variation with agriculturally relevant phenotypes measured under multiple field and laboratory environmental conditions; this will guide and accelerate rice breeding by identifying genetic variation that will be useful in breeding efforts and future sustainable agriculture.
No statistical methods were used to predetermine sample size. The experiments were not randomized and investigators were not blinded to allocation during experiments and outcome assessments.
Sequencing data of the 3,000 Rice Genome project
The selection and sequencing of rice accessions have previously been described12. The SNPs/indels and SVs in 3,010 accessions were identified by mapping against the Nipponbare RefSeq, and the pan-genome sequence was created by integrating the Nipponbare RefSeq and non-redundant novel sequences derived from 3,010 rice assemblies. SV comparison and gene PAV analyses focused on 453 rice accessions with sequencing depth >20× and mapping depth >15× (Extended Data Figs. 4a, 5b).
Detection of SNPs and indels
Reads were aligned to the Nipponbare RefSeq using BWA-MEM (release 0.7.10)47. The mapped reads were then sorted and duplicates were removed by Picard tools (release 1.119) (http://broadinstitute.github.io/picard/). The reads around indels were realigned by GATK RealignerTargetCreator and IndelRealigner package (release 3.2-2)48. The variants were called for each accession by the GATK UnifiedGenotyper (release 3.2-2)48 with ‘EMIT-ALL-SITES’ option. A joint genotyping step for comprehensive SNP union and filtering step was performed on the 3,010 emit-all-sites VCF files. A variant position is reported if at least one sample supports it with QUAL no less than 30. A total of 29,399,875 SNPs (27,024,796 are bi-allelic) and 2,467,043 indels (small insertions and deletions <40 bp) were identified from the analyses of the genomes of 3,010 accessions. Three subsets of the 3K-RG Nipponbare SNPs were defined using the following filtering criteria: (1) a base SNP set of ~17 million SNPs created from the ~27 million high-quality bi-allelic SNPs by removing SNPs in which heterozygosity exceeds Hardy–Weinberg expectation for a partially inbred species, with inbreeding coefficient estimated as 1−Hobs/Hexp, in which Hobs and Hexp are the observed and expected heterozygosity, respectively (detailed in Supplementary Notes); (2) a filtered SNP set of ~4.8 million SNPs created from the ~17-million-SNP base SNP set by removing SNPs with >20% missing calls and MAF < 1%; and (3) a core SNP set of SNPs derived from the filtered SNP set using a two-step linkage disequilibrium pruning procedure with PLINK49,50, in which SNPs were removed by linkage disequilibrium pruning with a window size of 10 kb, window step of one SNP and r2 threshold of 0.8, followed by another round of linkage disequilibrium pruning with a window size of 50 SNPs, window step of one SNP and r2 threshold of 0.8.
Determining the effects of SNPs
The effects of all bi-allelic SNPs (low, medium and high effects) on the genome were determined based on the pre-built release 7.0 annotation from the Rice Genome Annotation Project (http://rice.plantbiology.msu.edu/) using SnpEff51 release 4.1l, with parameters -v -noLog -canon rice7. Using sequence ontology terms, a low-effect SNP was classified as ‘synonymous_variant’, ‘splice_region_variant’, ‘initiator_codon_variant’, ‘5_prime_UTR_premature_start_codon_gain_variant’ or ‘stop_retained_variant’. A moderate-effect SNP was identified as a ‘missense_variant’ and a high-effect SNP as a ‘start_lost’, ‘stop_gained’, ‘stop_lost’, ‘splice_donor_variant’ or ‘splice_acceptor_variant’. For indel effects, only indels with lengths that were not multiples of three were counted and SNPs overlapped with protein-coding regions (CDSs of RGAP 715 genes) were considered as the most disruptive effects on genes. Results of the SNP and indel effect analysis are given in Supplementary Data 2 Tables 3, 4. We computed the SNP numbers (proportions) of rare SNPs and homozygous singletons for a ‘typical genome’ of a subpopulation as the median SNP number (proportion) of the SNPs in a given category among those genomes for that subpopulation (Supplementary Data 2 Table 5).
Population structure and SNP diversity
Multi-dimensional scaling analysis was performed using the ‘cmdscale’ function in R, using the IBS distance matrix of the 3K-RG genomes computed with PLINK49,50 on the filtered SNP set. The same distance matrix was used to construct a phylogenetic tree by the unweighted neighbour-joining method, implemented in the R package phangorn52. The population structure of the 3K-RG dataset was analysed using ADMIXTURE software46 on the core SNP set (version 0.4, http://snp-seek.irri.org/download.zul). First, ADMIXTURE was run on 30 random 100,000-SNP subsets of the core SNP set with k (the number of groups) ranging from 5 to 18, and k = 9 was chosen because it was the minimal value of k to separate all previously known groups (cA, cB, XI, GJ-trp, GJ-tmp and part of GJ-sbtrp). With k = 9, ADMIXTURE was then run again on the whole core SNP set nine times with varying random seeds; the Q-matrices were aligned using CLUMPP software53 and clustered on the basis of similarity. Then, the matrices belonging to the largest cluster were averaged to produce the final matrix of admixture proportions. Finally, the group membership for each sample was defined by applying the threshold of ≥ 0.65 to this matrix. Samples with admixture components <0.65 were classified as follows. If the sum of components for subpopulations within the major groups XI and GJ was ≥ 0.65, the samples were classified as XI-adm or GJ-adm, respectively, and the remaining samples were deemed ‘fully’ admixed (admix). Branches of the phylogenetic tree were coloured according to the k = 9 admixture classification (Fig. 1).
We computed linkage disequilibrium decay in each subpopulation as follows. The value of r2 was computed for each pair of SNPs of frequency ≥ 10% in the respective subpopulations that are separated by at most 300 kb using PLINK. The distances were binned into 1-kb bins (separately for each chromosome) and the median value of r2 in each bin was taken. The medians for each chromosome were then averaged to produce a final r2 estimate for the bin. We computed nucleotide diversity (π) for non-overlapping 10-kb and 100-kb windows along the Nipponbare RefSeq by adopting an approach similar to VariScan54 for genome-wide DNA polymorphism analyses and implemented as a custom R script.
Detection of genomic SVs and population differentiation
Genomic-SV detection for each of the 3,010 rice accessions was performed using a customized version of novoBreak55 (https://sourceforge.net/projects/novobreak/?source=navbar) against the Nipponbare RefSeq. SVs inferred by no less than 3 reads were further filtered with the following conditions: (1) more than four supporting split reads or (2) no fewer than three discordant read pairs. We detected deletions, inversions and duplications with sizes between 100 bp and 1 Mb, and translocations. Here, translocations were SVs with ‘inter-chromosomal breakpoints’. All SVs that passed the filter criteria in the 3K-RG accessions were pooled together. Two adjacent SVs were identified as the same SV if their start and end positions varied no more than 1 kb, and the overlapping region was more than 50% of the total size. The presence–absence matrix of SVs in each accession was built based on this pooled SV dataset. To obtain reliable SV comparison analysis results, we focused only on the 453 high-depth accessions (Extended Data Fig. 4a). Major-group-unbalanced SVs were determined by two-sided Fisher’s exact test followed by Benjamini–Hochberg adjustment (false discovery rate (FDR) < 0.05), similar to the detection of major-group-unbalanced genes.
De novo assembly
A variation of SOAPdenovo256 (version r240) with customized k-mers was used to assemble the rice genomes. A k-mer value was initially set for each accession according to a linear model ‘K=2*int (0.38*(sequencing depth) +10)+1’, which was trained from 50 randomly selected rice accessions. The best k-mer value was decided by checking the N50 of the SOAPdenovo results. The command line for SOAPdenovo was ‘SOAPdenovo-63mer (or SOAPdenovo-127mer) all -s configure_file (average insertion length set as 460 in the configure file) -K k-mer -R -F’ with iteration over different k-mers until N50 of the assembly with that k-mer is higher than those with ‘k-mer +2’ and ‘k-mer −2’. On average, we needed to run SOAPdenovo ~3.94 times for each rice accession. The quality of the genome assembly was evaluated for these contigs using QUAST version 2.357.
Sequencing and de novo assembly of IR 8 and N 22 reference genomes
High molecular weight DNA was extracted from young leaves adopting the protocol58 with minor modifications. The PacBio library was prepared following the 20-kb protocol (see ‘User-Bulletin-Guidelines-for-Preparing-20-kb-SMRTbell-Templates document.pdf’, available from https://www.pacb.com/support/documentation/?fwp_documentation_search="PN%20100-286-700-04") and was sequenced on an RSII sequencer with movie collection time of 6 h. The raw data of N 22 and IR 8 were assembled with FALCON59 and Canu60, respectively. Contigs were polished twice with PacBio raw reads using Quiver (https://github.com/PacificBiosciences/GenomicConsensus) and the IR 8 assembly was further polished with 66× WGS 2× 150-bp Illumina data using Pilon61. Polished contigs were assigned to pseudomolecules using Genome Puzzle Master62. Assembly statistics can be found in Supplementary Data 3 Table 4. IR 8 and N 22 were applied to evaluate the completeness and redundancy of the pan-genome.
SOAPdenovo assembly for each accession was assessed by QUAST57 with Nipponbare RefSeq as the reference. From QUAST output, unaligned contigs longer than 500 bp were retrieved and merged. CD-HIT version 4.6.163 was used to remove redundant sequences at a cutoff of 90% identity with the command ‘-c 0.9 -T 16 -M 50000’. For remaining sequences, all-versus-all alignments with BLASTN were carried out to ensure that these sequences had no redundancy. Next, various contaminants including Archaea, bacteria, viruses, fungi and metazoans were removed. The non-redundant sequences were aligned to the NT database (downloaded from NCBI, 26 July 2014) with BLASTN with parameters ‘-evalue 1e-5 -best_hit_overhang 0.25 -perc_identity 0.5 -max_target_seqs 10’. Contigs of which the best alignments (considering E-values and identities) were not from Viridiplantae were considered as contaminants and were filtered out. The remaining contigs formed the non-redundant novel sequences. The rice species pan-genome was then generated by combining the Nipponbare RefSeq and non-redundant novel sequences.
Annotation of the pan-genome
The gene–transcript annotation of the Nipponbare RefSeq was downloaded from the Rice Annotation Project64, and if a protein-coding gene contained multiple transcripts only the transcript with the longest open reading frame was selected as the representative for the gene. Protein-coding genes on novel sequences were predicted using MAKER65, a gene prediction tool combining ab initio predictions, expression evidence and protein homologies. In detail, repeats were first masked (soft mask for low-complexity repeats) with RepeatMasker (www.repeatmasker.org) and RepeatRunner66. Two ab initio predictors, SNAP67 and AUGUSTUS68, were called by MAKER65 to predict gene models with their default parameters for rice. All rice expressed sequence tags (ESTs) were downloaded from GenBank (15 December 2014) and were aligned to the novel sequences with BLASTN. All rice proteins were downloaded from NCBI (15 December 2014) and were aligned to the novel sequences with BLASTX. To obtain more informative alignments, Exonerate69 was used to realign each sequence identified by BLAST around splice sites. EVidenceModeller70 was used to combine and refine the ab initio predictions with RNA and protein evidence. Incomplete gene models were removed before the consequent analysis.
Adjustment of predicted genes
We aligned the predicted transcripts against Nipponbare RefSeq to remove potential redundancy. Redundant genes were removed when the genes were clustered into gene families. However, when attempting to identify the number of novel genes, the redundant ones were removed first. We clustered all genes at a global identity of 95%, and removed novel genes that were not representative of the group.
Evaluation of pan-genome redundancy
We ran BUSCO (benchmarking universal single-copy orthologues) v.2.032 on CX140 (a Nipponbare accession) assembly, Nipponbare RefSeq, CX368 (an N 22 accession) assembly, N 22 high-quality reference genome and the pan-genome sequences. Augustus-3.2.368 and hmmer-3.1b71 were used for gene prediction in BUSCO. BUSCO was run with genome mode with embryophyta_odb9 as a reference.
All protein sequences of pan-genome were extracted and aligned to the GO sequence database (http://geneontology.org/ on 4 April 2015) with BLASTP. Only alignments with E-values < 1 × 10−5 and identity > 0.3 were used. GO terms for each gene were estimated to be the same as those of its best-hit protein. In total, 20,842 (43.3%) genes could be annotated. For a gene family, its GO terms are the non-redundant set of the GO terms of the genes within this gene family. Overall, 6,338 (26.5%) gene families could be annotated. Enrichment of GO terms was carried out using the GOstats72 package in R with all gene families as the background.
Validation of the non-Nipponbare RefSeq genes
We verified the novel genes by multiple approaches. First, for each gene, we examined the number of accessions that possessed it. We mapped the sequencing reads to the pan-genome sequences. Genes with CDS coverage over 0.95 and gene-body coverage over 0.85 were considered to be present. Second, we verified the novel genes with 226 RNA sequencing experiments from 17 projects30. RNA sequencing reads were first trimmed with Trimmomatic version 0.3273 with parameters ‘ILLUMINACLIP:2:30:10 LEADING:20 TRAILING:20 SLIDINGWINDOW:4:20 MINLEN:36’ and then aligned to the pan-genome sequences with a split-aligner HISAT2 version 2.0.1-beta74 using default parameters. The coverage of each gene was calculated with ‘BEDtools coverage’ in BEDtools suite version 2.17.075.
Gene family annotation
The genes were clustered to gene families with OrthoMCL version 2.0.976. All genes were extracted and translated into protein sequences and the protein sequences were compared by using all-by-all BLASTP (E-value = 1 × 10−5). OrthoMCL was applied to process the BLASTP output and cluster genes to gene families. Similarity of protein families was set to be 0.5 as suggested by a previous publication76.
Determination of gene presence or absence
We proposed a ‘map-to-pan’ strategy to determine gene presence or absence28. For the 453 accessions with high sequencing depth, although only about 60%–70% of their genomes can be de novo assembled (contig ≥ 500 bp), more than 98% of their genomes can be covered by short read mapping. This enabled the use of coverage of genes to determine their presence or absence. In practice, genes with CDS coverage over 0.95 and gene-body coverage over 0.85 were considered present. If one member of a gene family is present in a given rice accession, the gene family is considered as present.
Determination of core and distributed genes or gene families
A core gene (or gene family) is a gene (or gene family) present in all rice accessions, and we further defined candidate core genes (or gene families) as those with loss rates not significantly larger than 0.01 in all major groups. We first examined whether a gene (or a gene family) is distributed (loss rate > 0.01) in each type of O. sativa (XI, GJ, cA and cB). Binomial tests (with a null hypothesis of loss rate < 0.01) were carried out for each gene in each type. A P value below 0.05 meant that this gene (or a gene family) was lost in a significant proportion of rice accessions and is a distributed gene (or gene family) of these subpopulations. If a gene (or a gene family) was not determined to be distributed in all types (and it was not core), it was considered to be a candidate core gene (or gene family) of O. sativa. Other genes (or gene families) were considered to be distributed.
Determination of major-group-unbalanced, subpopulation-unbalanced and random genes or gene families
Distributed genes (or gene families) were divided further into major-group-unbalanced, subpopulation-unbalanced and random genes (or gene families). Major-group-unbalanced genes (or gene families) are defined as genes (or gene families) that are unequally distributed among XI, GJ, cA and cB groups. A two-sided Fisher’s exact test was used to determine whether the distribution of each gene (or gene family) is uniform. The P values of all genes were calculated with the ‘Fisher.test’ function in R and were then adjusted with the Benjamini–Hochberg FDR method. Genes (or gene families) with FDR < 0.05 were considered as major-group-unbalanced.
Subpopulation-unbalanced genes (or gene families) are defined as genes (or gene families) that are unequally distributed among subpopulations; thus, they can be divided into XI-subpopulation-unbalanced genes (or gene families) and GJ-subpopulation-unbalanced genes (or gene families). XI-subpopulation-unbalanced genes (or gene families) are defined as genes (or gene families) that are unequally distributed among XI-1A, XI-1B, XI-2 and XI-3 subpopulations. GJ-subpopulation-unbalanced genes (or gene families) can be defined similarly. The same statistical methods for the major groups were applied to determine the distribution balance for subpopulations. We defined genes (or gene families) that are neither major-group-unbalanced nor subpopulation-unbalanced to be ‘random’ genes.
Gene and gene-family age
Gene ages were inferred with previously described methods77. The NR protein database was downloaded from NCBI (28 March 2015) and all protein sequences were grouped according to 13 taxonomic levels (PS1: Cellular organisms; PS2: Eukaryota; PS3: Viridiplantae; PS4: Streptophyta, Streptophytina; PS5: Embryophyta; PS6: Tracheophyta, Euphyllophyta; PS7: Spermatophyta; PS8: Magnoliophyta, Mesangiospermae; PS9: Liliopsida, Petrosaviidae, Commelinids, Poales; PS10: Poaceae; PS11: BOP clade; PS12: Oryzoideae, Oryzeae, Oryza; and PS13: O. sativa) based on NCBI taxonomy. Thirteen BLASTP databases were built for protein sequences from PS1 to PS13. All genes on pan-genome sequences were first translated into proteins, and were aligned to the 13 databases using BLASTP with E-values < 1 × 10−5 and identity > 0.3. The age of a gene was considered as the taxonomic level of the oldest aligned protein. Genes that failed to align to all databases were assigned gene ages of PS13 (O. sativa). Some PS13 genes were reassigned as PS12 genes if they could be covered by 446 wild rice genomes2 with both gene-body coverage > 0.95 and CDS coverage > 0.95. The age of a gene family was considered as the age of the oldest gene within the gene family.
To test whether an XI sample had a non-introgression haplotype at a locus, we defined a D-value for a sample x as D(x) = d(x,XI) − d(x,GJ), in which d(x,XI) is the mean distance from sample x to a XI sample at the given locus.
With no gene flow from GJ to XI and vice versa, the D-value is negative for XI and positive for GJ. On the other hand, if an XI sample shares a haplotype with a GJ sample, the D-value will be positive and close to the D-values of GJ samples. For an XI sample, we rejected the hypothesis of GJ introgression if its D-value was negative and less than the lower bound of the 99% confidence interval for the D-value of GJ samples, which was computed on the subset of GJ consisting of samples with a positive D-value, to exclude the effect of potential XI-to-GJ introgression.
Further information on experimental design is available in the Nature Research Reporting Summary linked to this paper.
Code for studying pan-genome and gene and gene family PAVs are now integrated and published as the EUPAN toolkit28. Tailored novoBreak-germline is available at https://sourceforge.net/projects/novobreak/?source=navbar. Code for nucleotide diversity and SNP merging is available at https://github.com/dchebotarov/3k-SNP-paper. All other code is available from the corresponding authors upon request.
The BAM alignment file and variant calls in VCF format for each accession of the 3K-RG against Nipponbare RefSeq are freely downloadable from Amazon Public Data at https://aws.amazon.com/public-data-sets/3000-rice-genome/ and the Department of Science and Technology Advanced Science and Technology Institute of the Philippines (DOST-ASTI) IRODS site, as described on the 3K-RG project site (http://iric.irri.org/resources/3000-genomes-project). The SV and PAV data of 3K-RG are available in the figshare database78 (https://doi.org/10.6084/m9.figshare.c.3876022.v1).
The following web tools are available for the mining, analysis and visualization of the 3K-RG dataset: SNP-Seek, http://snp-seek.irri.org; RMBreeding databases, http://www.rmbreeding.cn/index.php; rice cloud of genetic data public projects, http://www.ricecloud.org/; IRRI Galaxy, http://galaxy.irri.org/; and the 3,000 rice pan-genome browser79, http://cgm.sjtu.edu.cn/3kricedb/.
The 3K-RG sequencing data used for our analyses can be obtained via project accession PRJEB6180 from NCBI (https://www.ncbi.nlm.nih.gov/sra/?term=PRJEB6180), accession ERP005654 from DDBJ (https://www.ddbj.nig.ac.jp/index-e.html) and from the GigaScience Database (https://doi.org/10.5524/200001).
Seck, P. A., Diagne, A., Mohanty, S. & Wopereis, M. C. Crops that feed the world 7: rice. Food Secur. 4, 7–24 (2012).
Huang, X. et al. A map of rice genome variation reveals the origin of cultivated rice. Nature 490, 497–501 (2012).
Li, L. F., Li, Y. L., Jia, Y., Caicedo, A. L. & Olsen, K. M. Signatures of adaptation in the weedy rice genome. Nat. Genet. 49, 811–814 (2017).
Wang, H., Vieira, F. G., Crawford, J. E., Chu, C. & Nielsen, R. Asian wild rice is a hybrid swarm with extensive gene flow and feralization from domesticated rice. Genome Res. 27, 1029–1038 (2017).
Ting, Y. Origination of the rice cultivation in China. J. College of Agric. Sun Yat-Sen University 7, 11–24 (1949).
Glaszmann, J.-C. Isozymes and classification of Asian rice varieties. Theor. Appl. Genet. 74, 21–30 (1987).
Garris, A. J., Tai, T. H., Coburn, J., Kresovich, S. & McCouch, S. Genetic structure and diversity in Oryza sativa L. Genetics 169, 1631–1638 (2005).
Chang, T.-T. The origin, evolution, cultivation, dissemination, and diversification of Asian and African rices. Euphytica 25, 425–441 (1976).
Han, B. & Xue, Y. Genome-wide intraspecific DNA-sequence variations in rice. Curr. Opin. Plant Biol. 6, 134–138 (2003).
Agrama, H. A., Yan, W., Jia, M., Fjellstrom, R. & McClung, A. M. Genetic structure associated with diversity and geographic distribution in the USDA rice world collection. Nat. Sci. 2, 247–291 (2010).
Allender, C. The Second Report on the State of the World’s Plant Genetic Resources for Food and Agriculture. Rome: Food and Agriculture Organization of the United Nations (2010), 370 pp., ISBN 978–92–5-106534–1. Exp. Agric. 47, (574–574 (2011).
The 3,000 rice genomes project. The 3,000 rice genomes project. Gigascience 3, 7 (2014).
Golicz, A. A. et al. The pangenome of an agronomically important crop plant Brassica oleracea. Nat. Commun. 7, 13390 (2016).
Vernikos, G., Medini, D., Riley, D. R. & Tettelin, H. Ten years of pan-genome analyses. Curr. Opin. Microbiol. 23, 148–154 (2015).
Kawahara, Y. et al. Improvement of the Oryza sativa Nipponbare reference genome using next generation sequence and optical map data. Rice (N. Y.) 6, 4 (2013).
Xu, X. et al. Resequencing 50 accessions of cultivated and wild rice yields markers for identifying agronomically important genes. Nat. Biotechnol. 30, 105–111 (2012).
Alexandrov, N. et al. SNP-Seek database of SNPs derived from 3000 rice genomes. Nucleic Acids Res. 43, D1023–D1027 (2015).
McCouch, S. R. et al. Open access resources for genome-wide association mapping in rice. Nat. Commun. 7, 10532 (2016).
Li, C., Zhou, A. & Sang, T. Rice domestication by reducing shattering. Science 311, 1936–1939 (2006).
Konishi, S. et al. An SNP caused loss of seed shattering during rice domestication. Science 312, 1392–1396 (2006).
Sasaki, A. et al. Green revolution: a mutant gibberellin-synthesis gene in rice. Nature 416, 701–702 (2002).
Chandler, R. F. Jr. in Physiological Aspects of Crop Yield (ed. Dinauer, R.C.) (Crop Science Society of America, Madison, 1969).
Wang, Z. Y. et al. The amylose content in rice endosperm is related to the post-transcriptional regulation of the waxy gene. Plant J. 7, 613–622 (1995).
Chen, S. et al. Badh2, encoding betaine aldehyde dehydrogenase, inhibits the biosynthesis of 2-acetyl-1-pyrroline, a major component in rice fragrance. Plant Cell 20, 1850–1861 (2008).
Sweeney, M. T., Thomson, M. J., Pfeil, B. E. & McCouch, S. Caught red-handed: Rc encodes a basic helix-loop-helix protein conditioning red pericarp in rice. Plant Cell 18, 283–294 (2006).
Yamamoto, E., Yonemaru, J., Yamamoto, T. & Yano, M. OGRO: The overview of functionally characterized genes in rice online database. Rice (N. Y.) 5, 26 (2012).
Yonemaru, J.-I. et al. Q-TARO: QTL annotation rice online database. Rice (N. Y.) 3, 194–203 (2010).
Hu, Z. et al. EUPAN enables pan-genome studies of a large number of eukaryotic genomes. Bioinformatics 33, 2408–2409 (2017).
Stein, J. C. et al. Genomes of 13 domesticated and wild rice relatives highlight genetic conservation, turnover and innovation across the genus Oryza. Nat. Genet. 50, 285–296 (2018).
Zhang, J. et al. Extensive sequence divergence between the reference genomes of two elite indica rice varieties Zhenshan 97 and Minghui 63. Proc. Natl Acad. Sci. USA 113, E5163–E5171 (2016).
The IC4R Project Consortium. Information commons for rice (IC4R). Nucleic Acids Res. 44, D1172–D1180 (2015).
Simão, F. A., Waterhouse, R. M., Ioannidis, P., Kriventseva, E. V. & Zdobnov, E. M. BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics 31, 3210–3212 (2015).
Wilson, B. A., Foy, S. G., Neme, R. & Masel, J. Young genes are highly disordered as predicted by the preadaptation hypothesis of de novo gene birth. Nat. Ecol. Evol. 1, 0146 (2017).
Zhu, B. F. et al. Genetic control of a transition from black to straw-white seed hull in rice domestication. Plant Physiol. 155, 1301–1311 (2011).
Tan, L. et al. Control of a key transition from prostrate to erect growth in rice domestication. Nat. Genet. 40, 1360–1364 (2008).
Saitoh, K., Onishi, K., Mikami, I., Thidar, K. & Sano, Y. Allelic diversification at the C (OsC1) locus of wild and cultivated rice: nucleotide changes associated with phenotypes. Genetics 168, 997–1007 (2004).
Fan, C. et al. GS3, a major QTL for grain length and weight and minor QTL for grain width and thickness in rice, encodes a putative transmembrane protein. Theor. Appl. Genet. 112, 1164–1171 (2006).
Shomura, A. et al. Deletion in a gene associated with grain size increased yields during rice domestication. Nat. Genet. 40, 1023–1028 (2008).
Weng, J. et al. Isolation and initial characterization of GW5, a major QTL associated with rice grain width and weight. Cell Res. 18, 1199–1209 (2008).
Wang, Y. et al. Copy number variation at the GL7 locus contributes to grain size diversity in rice. Nat. Genet. 47, 944–948 (2015).
Taoka, K. et al. 14-3-3 proteins act as intracellular receptors for rice Hd3a florigen. Nature 476, 332–335 (2011).
Sun, X. et al. Xa26, a gene conferring resistance to Xanthomonas oryzae pv. oryzae in rice, encodes an LRR receptor kinase-like protein. Plant J. 37, 517–527 (2004).
Shen, R. et al. Genomic structural variation-mediated allelic suppression causes hybrid male sterility in rice. Nat. Commun. 8, 1310 (2017).
Liu, L., Lee, G.-A., Jiang, L. & Zhang, J. Evidence for the early beginning (c. 9000 cal. BP) of rice domestication in China: a response. Holocene 17, 1059–1068 (2007).
Fuller, D. Q., Allaby, R. G. & Stevens, C. Domestication as innovation: the entanglement of techniques, technology and chance in the domestication of cereal crops. World Archaeol. 42, 13–28 (2010).
Alexander, D. H., Novembre, J. & Lange, K. Fast model-based estimation of ancestry in unrelated individuals. Genome Res. 19, 1655–1664 (2009).
Li, H. & Durbin, R. Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics 25, 1754–1760 (2009).
McKenna, A. et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20, 1297–1303 (2010).
Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559–575 (2007).
Chang, C. C. et al. Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience 4, 7 (2015).
Cingolani, P. et al. A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3. Fly (Austin) 6, 80–92 (2012).
Schliep, K. P. phangorn: phylogenetic analysis in R. Bioinformatics 27, 592–593 (2011).
Jakobsson, M. & Rosenberg, N. A. CLUMPP: a cluster matching and permutation program for dealing with label switching and multimodality in analysis of population structure. Bioinformatics 23, 1801–1806 (2007).
Hutter, S., Vilella, A. J. & Rozas, J. Genome-wide DNA polymorphism analyses using VariScan. BMC Bioinformatics 7, 409 (2006).
Chong, Z. et al. novoBreak: local assembly for breakpoint detection in cancer genomes. Nat. Methods 14, 65–67 (2017).
Luo, R. et al. SOAPdenovo2: an empirically improved memory-efficient short-read de novo assembler. Gigascience 1, 18 (2012).
Gurevich, A., Saveliev, V., Vyahhi, N. & Tesler, G. QUAST: quality assessment tool for genome assemblies. Bioinformatics 29, 1072–1075 (2013).
Doyle, J. J. A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem. Bull. 19, 11–15 (1987).
Chin, C.-S. et al. Phased diploid genome assembly with single-molecule real-time sequencing. Nat. Methods 13, 1050–1054 (2016).
Koren, S. et al. Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation. Genome Res. 27, 722–736 (2017).
Walker, B. J. et al. Pilon: an integrated tool for comprehensive microbial variant detection and genome assembly improvement. PLoS ONE 9, e112963 (2014).
Zhang, J. et al. Genome puzzle master (GPM): an integrated pipeline for building and editing pseudomolecules from fragmented sequences. Bioinformatics 32, 3058–3064 (2016).
Fu, L., Niu, B., Zhu, Z., Wu, S. & Li, W. CD-HIT: accelerated for clustering the next-generation sequencing data. Bioinformatics 28, 3150–3152 (2012).
Ohyanagi, H. et al. The Rice Annotation Project Database (RAP-DB): hub for Oryza sativa ssp. japonica genome information. Nucleic Acids Res. 34, D741–D744 (2006).
Holt, C. & Yandell, M. MAKER2: an annotation pipeline and genome-database management tool for second-generation genome projects. BMC Bioinformatics 12, 491 (2011).
Smith, C. D. et al. Improved repeat identification and masking in Dipterans. Gene 389, 1–9 (2007).
Korf, I. Gene finding in novel genomes. BMC Bioinformatics 5, 59 (2004).
Stanke, M., Steinkamp, R., Waack, S. & Morgenstern, B. AUGUSTUS: a web server for gene finding in eukaryotes. Nucleic Acids Res. 32, W309–W312 (2004).
Slater, G. S. C. & Birney, E. Automated generation of heuristics for biological sequence comparison. BMC Bioinformatics 6, 31 (2005).
Haas, B. J. et al. Automated eukaryotic gene structure annotation using EVidenceModeler and the program to assemble spliced alignments. Genome Biol. 9, R7 (2008).
Finn, R. D. et al. HMMER web server: 2015 update. Nucleic Acids Res. 43, W30–W38 (2015).
Falcon, S. & Gentleman, R. Using GOstats to test gene lists for GO term association. Bioinformatics 23, 257–258 (2007).
Bolger, A. M., Lohse, M. & Usadel, B. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30, 2114–2120 (2014).
Kim, D., Langmead, B. & Salzberg, S. L. HISAT: a fast spliced aligner with low memory requirements. Nat. Methods 12, 357–360 (2015).
Quinlan, A. R. & Hall, I. M. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26, 841–842 (2010).
Li, L., Stoeckert, C. J., Jr & Roos, D. S. OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res. 13, 2178–2189 (2003).
Zhang, Y. E., Vibranovski, M. D., Landback, P., Marais, G. A. & Long, M. Chromosomal redistribution of male-biased genes in mammalian evolution with two bursts of gene gain on the X chromosome. PLoS Biol. 8, e1000494 (2010).
Hu, Z. et al. Novel sequences, structural variations and gene presence variations of Asian cultivated rice. Sci. Data https://doi.org/10.1038/sdata.2018.79 (2018).
Sun, C. et al. RPAN: rice pan-genome browser for ~3,000 rice genomes. Nucleic Acids Res. 45, 597–605 (2017).
This work was supported by the 863 Program (2014AA10A601) and National Key R&D Program (2016YFD0100904) from the Chinese Ministry of Science & Technology, Bill & Melinda Gates Foundation Project (OPP1130530), the Agricultural Science and Technology Innovation Program Cooperation and Innovation Mission (CAAS-ZDXT201800), CAAS Innovative Team Award, International S&T Cooperation Program of China (2012DFB32280), Shenzhen Peacock Plan, National Key Technology Support Program (2015BAD01B02), Fundamental Research Funds for Central Non-Profit of CAAS (Y2017CG21) and National Natural Science Foundation of China (31501291, 61472246 and 61272250). IRRI was supported by the CGIAR Research Program CRP 3.3 (Global Rice Science Partnership). We thank the High-Performance Computing Centers at Shanghai Jiao Tong University, Agricultural Genomics Institute of CAAS and State Key Laboratory of Agricultural Genomics, BGI-Shenzhen (2011DQ782025). We thank M. Roa of the Philippine Genome Center Core Facilities for Bioinformatics, Department of Science and Technology-Advanced Science and Technology Institute of the Philippines, CyVerse, and XSEDE for computing and bioinformatics support; Z. Chong from University of Alabama for help in running novoBreak; the AXA Chair Research Fund and the Bud Antle Endowed Chair for the sequence analysis of IR 8 and N 22 genomes; and Amazon Public Data for free hosting of the 3K-RG analyses results.
Nature thanks M. Bevan, H. Tang and the other anonymous reviewer(s) for their contribution to the peer review of this work.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
Extended Data Fig. 1 SNP filtering, discovery rate, and projected discovery upon further sequencing.
a, Proportion of heterozygous calls versus allele frequency. Each dot represents a SNP from a random sample of 100,000 SNPs. Blue curve shows theoretical Hardy–Weinberg equilibrium. The points have opacity of 5%, such that regions with higher point densities are highlighted. The bulk of SNPs lie on the Hardy–Weinberg equilibrium curve scaled by a factor of about 0.05, which implies a Wright’s inbreeding coefficient of F = 0.95. b, The same plot with colour representing the outcome of filtering. The SNPs that are marked ‘keep’ (black) form the base SNP set. c, The estimated proportion of gene bank SNPs captured by 3K-RG samples, per frequency. The 3,010 samples capture more than 99.99% of gene-bank SNPs of frequency greater than 0.25%. d, Projected new SNP discovery rate based on simulations. For a given number of samples (x axis), the graph shows estimated mean number of new SNPs discovered in the last sample.
Extended Data Fig. 2 Population structure and subpopulation differentiation.
a, ADMIXTURE analyses for k = 5 to k = 15. b–d, Multidimensional scaling plots for all (n = 3,010) (b), XI (n = 1,786) (c) and GJ (n = 849) (d) accessions. e, Private and specific SNPs in each subpopulation. Private alleles are defined as being present in at least 4 accessions in a subpopulation and not found in other subpopulations; population-specific alleles are common in the subpopulation (≥20%) but of low frequency (<2%) in others. f, Doubleton sharing—that is, SNPs shared by two accessions—within and between subpopulations, with values normalized by the sample sizes.
Extended Data Fig. 3 Genetic diversity within subpopulations.
a, MAF histogram. b, Genome-wide linkage disequilibrium. c, Nucleotide diversity versus linkage disequilibrium. d, Diversity scans (π) for all chromosomes for major groups (XI, GJ, cA and cB) using 100-kb windows in which centromeric regions are highlighted in grey.
Extended Data Fig. 4 Selection of high-depth accessions and summary of SVs.
a, Number of accessions with sequencing depths ≥ 20× and mapping depth ≥ 15×. b, Mapping coverage of the 3,010 rice genomes to the Nipponbare RefSeq as a function of sequence depth. c, Circular presentation of different types of structural variation detected in 453 high-coverage rice genomes when compared against the Nipponbare RefSeq. Chr, outermost circle represents 12 rice chromosomes with marks in Mb; Repeat, red heat map represents repeat content in 500-kb windows; DEL, green/blue colour with inner/outer bars represents the average frequencies of deletions detected in XI and GJ; DUP, green/blue colour with inner/outer bars represents the average frequencies of duplications detected in XI and GJ; INV, green/blue colour with inner/outer bars represents the average frequencies of inversions detected in XI and GJ; TRA, grey colour represents translocations across each genome with an average frequency > 0.3 in either XI or GJ.
Extended Data Fig. 5 Map-to-pan strategy for rice pan-genome analyses.
a, Map-to-pan pipeline for pan-genome analyses: (1) pan-genome sequences were derived by combining Nipponbare RefSeq and de novo assembled non-redundant novel sequences; (2) gene annotations were derived by combining Nipponbare RefSeq annotations and evidence-based gene predictions on novel sequences; (3) reads from each sample were mapped to pan-genome sequences; and (4) gene presence or absence was determined by coverage of mapped reads. Raw data for this pipeline is shown in grey boxes and the main output is shown in blue. P/A: presence/absence. b, Proportions of assembled genomes as a function of the sequencing depth (based on the Nipponbare RefSeq). c, d, Gene-length differences between the novel pan-genome genes and genes derived from the genome of Minghui 63 (MH63) (c) or Zhenshan 97 (ZS97) (d). Generally, the distribution should be symmetric: a ratio of > 0 means the novel gene is longer and a ratio < 0 means the novel gene is shorter. The dashed red lines show the symmetric distributions of the >0 part and the blue regions show the gene proportion with shorter lengths. e–g, Genomic (e) and transcriptomic (f, g) validation of novel genes. e, Validation based on genomic sequencing data, in which numbers of the Nipponbare RefSeq and non-Nipponbare RefSeq genes identified (>95% CDS coverage and >85% gene-body coverage) are shown against the numbers of supporting rice accessions in the 453 rice lines; f, g, Validation based on the mapping rates of the publicly available RNA sequencing data of rice, including gene expression (f) and coverage of the coding sequence (g). h, BUSCO evaluation for 1,440 highly conserved genes; CX140, the assembly of Illumina sequencing data of Nipponbare accessions; Ref-Nip, Nipponbare RefSeq. CX368, the assembly of Illumina sequencing data of accession N 22; Ref-N22, assembly of N 22 PacBio sequencing data.
Extended Data Fig. 6 Representative enriched biological processes of core and distributed gene families.
a, b, Representative enriched biological processes of core (a) and distributed gene families (b) are shown, with all terms sorted by their enriched P values (red bars). One-sided hypergeometric test built in the GOstats R package was used to calculate the P value of each GO term. The numbers of gene families involved in each GO term are shown in blue.
Extended Data Fig. 7 Characterization of gene or gene family presence or absence variations.
a, b, Phylogenetic trees of the 453 rice accessions constructed on the basis of the presence or absence of the distributed genes (a) and gene families (b); both of which classified the 453 accessions into two major groups (XI and GJ), with each being further divided into several subpopulations that are tagged with different colours representing their classifications based on the SNP. c, d, Gene (c) or gene family (d) numbers per accession in different subpopulations; gene or gene family numbers were significantly different among XI subpopulations (Kruskal–Wallis tests, P value = 9.8 × 10−8 (gene) or 1.0 × 10−6 (gene family)). Box plots show the median, box edges represent the first and third quartiles and the whiskers extend to 1.5× interquartile range. e, The average number of genes that are different between two accessions in which all combinations of the 453 accessions were considered, and the proportions were calculated as the number of such differentiating genes adjusted by the gene numbers held in common by the two genome types. f, Venn diagram of the numbers of the core + candidate core gene families among the major groups of O. sativa. g, Cluster analysis of 4,270 XI-subpopulation-unbalanced gene families and 1,384 GJ-subpopulation-unbalanced gene families.
Extended Data Fig. 8 Evolution of the pan-genome of O.sativa.
a, b, The numbers of gene families (a) and genes (b) that emerged at different evolutionary times, from PS1 (single-cell organisms) to PS13 (O. sativa). c, The age distribution of the core and distributed gene families. d, Coding sequence length distribution for Nipponbare RefSeq genes with different ages. e, f, SNP variation of the core and distributed genes against the Nipponbare RefSeq. e, The density of SNPs in the coding region of core and distributed genes in the 3,010 rice lines; SNP density in core genes is lower than that in candidate core genes (two-sided Wilcoxon test) and SNP density in candidate core genes is lower than that in distributed genes (two-sided Wilcoxon test). Box plots show the median, box edges represent the first and third quartiles, and the whiskers extend to 1.5× interquartile range. f, Ka/Ks of the core and distributed genes. After removing genes with no synonymous SNPs, there are 3,144 core, 455 candidate core and 800 distributed genes with Ka/Ks > 1 and 10,005 core, 1,727 candidate core and 3,957 distributed genes with Ka/Ks < 1. Two sided χ-square tests were used to determine the difference of the proportions. **P < 0.01, ***P < 0.001.
Extended Data Fig. 9 Haplotypes around the red pericarp (Rc) gene.
Rows correspond to samples and columns correspond to SNPs. The colour of the rectangle denotes the number of non-Nipponbare alleles in a genotype. a, Haplotypes of 3,010 samples in a region ±25 kb around Rc show the presence of many distinctly non-GJ haplotypes that carry either the wild-type or domesticated allele at the causative deletion site. b, Zoomed-in view of a subset of 90 samples and 53 SNPs within the Rc gene and 15-kb downstream highlights the wide dispersal of non-GJ domesticated haplotypes.
Extended Data Fig. 10 Genome-wide association for grain length, grain width and bacterial blight isolate C5.
a–c, GWAS for grain length (GRLT, n = 2,012) (a), grain width (GRWD, n = 2,012) (b) and bacterial blight isolate C5 (BBL C5, n = 381) (c). GWAS was performed using filtered and linkage disequilibrium-pruned SNPs for historical trait data on source accessions for grain length and grain width (223,743 SNPs) and for newly acquired lesion length data for bacterial blight isolate C5 (148,999 SNPs). Manhattan plots for linkage disequilibrium-pruned datasets are shown to the left and quartile–quartile plots for expected versus observed −log(P) values to the right. Major peaks are annotated for known gene loci.
Extended Data Fig. 11 sd1 gene and its correlation with plant height.
a, The plot shows the correlation of the gene presence or absence variation with plant height (n = 323). The P values were calculated with Spearman’s correlation. b, Examples show that semi-dwarfism results from an approximately 385-bp deletion in the sd1 locus. c, Distribution of the presence or absence of the sd1 gene in the 453 rice accessions. d, sd1 frequencies in rice subpopulations.
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Wang, W., Mauleon, R., Hu, Z. et al. Genomic variation in 3,010 diverse accessions of Asian cultivated rice. Nature 557, 43–49 (2018). https://doi.org/10.1038/s41586-018-0063-9
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