Salix suchowensis is an early-flowering shrub willow that provides a desirable system for studies on the basic biology of woody plants. The current reference genome of S. suchowensis was assembled with 454 sequencing reads. Here, we report a chromosome-scale assembly of S. suchowensis generated by combining PacBio sequencing with Hi-C technologies. The obtained genome assemblies covered a total length of 356 Mb. The contig N50 of these assemblies was 263,908 bp, which was ~65-fold higher than that reported previously. The contiguity and completeness of the genome were significantly improved. By applying Hi-C data, 339.67 Mb (95.29%) of the assembled sequences were allocated to the 19 chromosomes of haploid willow. With the chromosome-scale assembly, we revealed a series of major chromosomal fissions and fusions that explain the genome divergence between the sister genera of Salix and Populus. The more complete and accurate willow reference genome obtained in this study provides a fundamental resource for studying many genetic and genomic characteristics of woody plants.
The Salicaceae family contains the sister genera of Salix (willows) and Populus (poplars), which are diecious catkin-bearing woody plants. Willows and poplars are distributed widely in many regions of the world. They exhibit high wood production and are commercially important in artificial plantations. Within the Salicaceae family, Populus trichocarpa was the first sequenced woody plant1, making it a widely adopted model system for various types of genetic studies on tree species. The P. trichocarpa v3.0 assembly is ~430 Mb, with a contig N50 and scaffold N50 of 205 kb and 8 Mb, respectively. A total of 41,335 protein-coding genes are predicted in the P. trichocarpa genome. In recent years, the genomes of P. euphratica Oliv2, P. pruinosa Schrenk3, P. alba var. pyramidalis4, P. alba5, P. tremula, and P. tremuloides6 have also been sequenced, assembled, and annotated. Moreover, the first draft genome assemblies of a P. deltoides (http://phytozome.jgi.doe.gov) and a P. tremula×alba hybrid (http://aspendb.uga.edu/s717) have been made publicly available online. Compared to poplars, whole-genome-sequencing studies on willow species have been lagging behind; only the genome sequences of S. purpurea7 and S. suchowensis8 have been reported. The genome of S. purpurea (http://phytozome.jgi.doe.gov) was assembled with Illumina sequencing reads, resulting in a genome assembly of 392 Mb. Within this assembly, 276 Mb (~70%) of sequences were anchored along different willow chromosomes aided by a genetic map7. For S. suchowensis, a genome assembly covering a total length of 303.8 Mb was obtained from Roche-454 sequencing reads. Anchored with a genetic map constructed for the sequenced individual, 229.2 Mb of sequence assemblies were positioned onto the 19 chromosomes of the S. suchowensis genome8.
Salicaceae species possess relatively small genomes. However, it is difficult to achieve high-quality genome assemblies for these species using short-read sequencing technologies due to the high heterozygosity and abundant repetitive sequences in their genomes. There is an active demand to improve the currently assembled S. suchowensis genome, which shows inaccuracy and low contiguity. In recent years, the single-molecule, real-time (SMRT) PacBio9 sequencing and chromosome conformation capture (Hi-C)10 techniques have been used to make significant advances in improving the assembly of plant genomes at the chromosomal level. Single-molecule sequencing can generate reads with an average length of >10 kb, which overcomes the restriction of the short reads generated from the Illumina sequencing platform. Additionally, Hi-C technology captures chromatin interactions within the nucleus, which can be used to infer the location of unanchored contigs and, thus, help to reconstruct haplotypes at the chromosomal level. Recently, several high-quality plant genomes have been obtained by using PacBio sequencing and Hi-C technologies11,12,13.
According to the taxonomy of Salicaceae, there are only ~29 species in genus Populus14. By contrast, over 300 species have been distinguished in genus Salix15. Poplars generally take the form of large trees, while willows exhibit different growth forms, including large trees, subtrees and small shrubs. Poplars and willows are not only important industrial fiber resources but are also widely used for landscaping. S. suchowensis is a small shrub that normally arrives at sexual maturity at one year of age. This species also possesses other characteristics that are favorable for basic genetic studies, such as ease of vegetative propagation and a predisposition to hybridization. Taken together, these characteristics make S. suchowensis an ideal model system for revealing the genetic mechanisms underlying the unique biological processes of woody plants. In this study, we aimed to obtain a highly contiguous, chromosome-scale genome assembly by combining PacBio sequencing and Hi-C technologies. The new assembly provides a much better reference genome for S. suchowensis, which will facilitate studies on Salicaceae species and serve as a valuable genomic resource for the woody plant research community.
Genome sequencing and assembly
In this study, we generated a total of 33.29 Gb PacBio sequencing reads from the SMRT sequencing platform, achieving ~87x coverage of the S. suchowensis genome (Suupplementary Table S1). First, the raw PacBio sequencing reads were self-corrected and assembled, which produced assembly groups containing 5346 contigs. Then, 902 redundant contigs (alternative contigs) were identified and removed through sequence alignment analysis. Finally, 3444 primary contigs were retained to reconstruct the haploid pseudomolecule for each chromosome. The obtained genome assembly contains 3444 contigs, covering a total length of 356.5 Mb, with a GC content of 34.94% and a contig N50 of 263.9 Kb (Supplementary Table S2). The 373 largest contigs cover >50% of the genome length, and 1926 large contigs represent ~90% of the genome.
In total, 40.48 Gb clean reads were obtained from Hi-C sequencing, covering over 98x of the S. suchowensis genome (Supplementary Table S3). We assessed the quality of the Hi-C data, in which 92.56% of Hi-C sequencing reads were mapped to the assembled contigs, 53.60% of which were unique mapped read pairs (Supplementary Table S3). Integrating 81.47% of the valid interaction pairs from the unique paired alignments, the PacBio sequencing assemblies were categorized and ordered to construct chromosome-scale scaffolds, resulting in a total of 1201 contigs, with a scaffold N50 of 16.8 Mb (Table 1 and Fig. 1). Then, the derived contigs were assembled into 19 pseudomolecules by means of agglomerative hierarchical clustering and the use of LACHESIS analysis tools. In total, 339.7 Mb of sequences were anchored along the 19 chromosomes in willow, representing 95.28% of the assembled contigs (Supplementary Table S4 and Fig. 2). Among the anchored contigs (2913), 2262 contigs (309.88 Mb) were oriented on the 19 pseudochromosomes. The longest and shortest pseudomolecules were chromosomes I and XII, with lengths of 34.97 Mb and 10.67 Mb, respectively.
We identified a total of 168.5 Mb of non-redundant repetitive elements (47.27% of the genome assembly), 28.27% of which were retrotransposons and 5.32% of which were DNA transposons (Supplementary Table S5), which was higher than the percentage in the previous assembly (125.6 Mb, 41.4%). Similar to S. suchowensis genome v1.0, long terminal retrotransposons (LTRs) were found to dominate (21.84%) the repetitive sequences. Among these sequences, Gypsy and Copia LTRs represented 10.86% and 10.53% of the total genome length, respectively, and accounted for 24 and 23% of the identified repetitive elements, (Fig. 1), whereas non-LTR elements spanned a physical length of 6.67 Mb and accounted for 1.87% of the genome length. In S. suchowensis genome v2.0, the class II elements (DNA transposons) represented 5.32% of the genome length. Further analysis revealed that the abundance of repetitive elements in the assembled chromosomes (1432/Mb) was much higher than that in the unanchored scaffolds (378/Mb). By contrast, the content of repetitive sequences was much higher in unanchored scaffolds than in the assembled chromosomes8. This comparison indicates that the negative effect of repetitive sequences on genome assembly can be effectively overwhelmed by long sequence reads.
Sequence annotation predicted 36,937 protein-coding genes in S. suchowensis genome v2.0 by combining the de novo, homology-based and transcriptome-based predictions (Supplementary Fig. S1). The average gene size was 3440 bp, with 5.6 exons per gene (Table 1). Among the predicted genes, 31,863 were anchored on the 19 chromosomes and covered a total length of 115.10 Mb, with a total exon length of 40.68 Mb (Fig. 1 and Supplementary Table S6). Based on high centromere-associated repeat abundance and a low gene content relative to the other regions of the chromosomes, the centromeres was predicted and positioned in each chromosome (Fig. 1), which revealed four acrocentric chromosomes (Chr_III, Chr_IX, Chr XIV, Chr_XVIII) and 15 submetacentric chromosomes in the genome of S. suchowensis. Among the predicted protein-coding genes, 30,260 (81.92%) were supported by transcriptome data from at least one of five tissues, including tender roots, young leaves, vegetative buds, nonlignified stems and bark (Supplementary Table S7). In total, 36,150 (97.87%) predicted genes showed functional annotations in at least one protein database (Supplementary Table S8). Conserved domain features were detected in 40.6% of the protein-coding genes. Additionally, we further annotated the noncoding RNAs and predicted 846 tranfer RNA (tRNA) genes, 261 ribosomal RNA (rRNA) genes, and 172 microRNA (miRNA) genes (Supplementary Table S9).
In this study, we evaluated the genome assemblies of S. suchowensis v1.0 and S. suchowensis v2.0 (Supplementary Table S10). We sequenced seven randomly selected bacterial artificial chromosomes (BACs) of S. suchowensis genomic DNA. Sequence alignment showed that S. suchowensis genome v2.0 covered 99.2% of the BAC sequences, while S. suchowensis genome v1.0 covered 93.1% of the BAC sequences (Supplementary Table S11). The BAC sequence alignment also showed that v2.0 exhibited better continuity and higher precision than v1.0. We further evaluated the quality of the new assembly with ~30 Gb of Illumina paired-end reads. The mapping ratio for the Illumina reads was 78.11% for v1.0, which increased to 90.38% for v2.0 (Supplementary Table S12). To assess the gene coverage, a total of 85,962 unigenes derived from RNA-Seq data for S. suchowensis8 were mapped to the two versions of the genome assemblies. More than 99.4% of these unigenes could be mapped to v2.0 (Supplementary Table S13), while ~97.6% of them could be mapped to v1.0. The completeness of the predicted genes in v2.0 was also assessed by sequence alignment with 1440 conserved Embryophyta genes from Benchmarking Universal Single-copy Orthologs (BUSCO)16, and the results showed that coverage of these genes was 94.8% and 89.6% for v2.0 and v1.0, respectively (Supplementary Table S10).
A total of 30,265 genes in S. suchowensis v2.0 were divided into 21,107 gene clusters, among which 18,692 gene clusters (23,397 genes) were shared with S. suchowensis v1.0, and 20,086 gene clusters (28,127 genes) were shared with P. trichocarpa v3.0 (Supplementary Fig. S2). The comparison of the protein-coding genes in S. suchowensis genome v1.0 with those in S. suchowensis genome v2.0, revealed that 25,891 genes in v1.0 were highly homologous to 31,694 genes in v2.0, indicating that the annotated genes in the updated genome were more complete than those in the previous version and included more multicopy genes. Furthermore, 5243 version-specific genes in v2.0 were analyzed for their distribution on the 19 chromosomes and among the unclustered contigs. Among these genes, 1743 were distributed among unclustered contigs, and the rest were distributed on the assembled chromosomes (Supplementary Table S14). GO enrichment analysis showed that the functions of these version-specific genes mainly included the respiratory electron transport chain, NADH dehydrogenase activity, ATP synthesis-coupled electron transport, and oxidative binding (Supplementary Fig. S3). The better gene coverage of the updated genome will greatly facilitate functional genomics studies in the future.
Gene family analysis
We characterized some important gene families in S. suchowensis genome v2.0. R genes containing nucleotide-binding site (NBS) domains play a vital role in conferring resistance to plant disease. In P. trichocarpa, 402R genes containing an NBS domain were detected17, including 143 coiled-coil-NBS-LRR (CNL) genes, 93 TIR-NBS-LRR (TNL) genes, 115 NBS-LRR (NL) genes, and 51 NBS genes, whereas 346R genes containing an NBS domain were identified in S. suchowensis v2.0, including 132 CNL genes, 83 TNL genes, 123 NL genes, and eight NBS genes (Fig. 3), suggesting either faster shrinkage or slower gain of R genes containing an NBS domain in S. suchowensis than in P. trichocarpa, especially for the NBS genes (51 vs. 8). In P. trichocarpa, chromosome XIX contains >70R genes, most of which are clustered at the peritelomeric end of this chromosome18. In S. suchowensis v2.0, chromosome XIX contains 107R genes, most of which are also located at the peritelomeric end.
Wood formation is a unique biological process that occurs in woody plants. In this study, we dedicated special efforts to the analysis of genes involved in wood formation. Wood mainly consists of cellulose, hemicellulose and lignin. We annotated 28 gene families involved in cell wall formation, which included 296 genes involved in cellulose and hemicellulose biosynthesis, including ten fucosyltransferase (FUT) genes, six xyloglucan xylosyltransferase (XXT) genes, five hydroxyproline-rich glycoprotease (RGP) genes, 275 glycoside hydrolase (GH) genes, and 75 genes involved in lignin biosynthesis in S. suchowensis v2.0 (Supplementary Table S15). Phylogenetic analysis showed that the numbers of FUT, XXT, and RGP orthologous genes are similar in S. suchowensis, P. trichocarpa, and Arabidopsis thaliana (Fig. 4), but the number of GH orthologous genes in Arabidopsis is significantly lower than that in Salicaceae (Supplementary Fig. S4), especially for the GH17, GH18, and GH31 subfamilies. We propose that these gene subfamilies might play a role in secondary cell wall formation, which is a process unique to woody plants. Lignin is an amorphous polymer related to cellulose that provides rigidity and, together with cellulose, forms the woody cell walls of plants. In S. suchowensis v2.0, the 75 genes involved in lignin biosynthesis were clustered in ten gene families (Supplementary Fig. S5). In general, willow contains more genes involved in lignin biosynthesis than Arabidopsis (75 vs. 34) and fewer genes involved in lignin biosynthesis than Populus (75 vs. 90). In detail, the genes coding p-coumarate-3-hydroxylase (C3H), trans-cinnamate 4-hydroxylase (C4H), caffeic acid O-methyltransferase (COMT), ferulate-5-hydroxylase (F5H), and hydroxycinnamoyl-CoA shikimate/quinate hydroxycinnamoyl transferase (HCT) occur in multiple copies in S. suchowensis and P. trichocarpa, whereas they occur in a single-copy in A. thaliana. In particular, COMT, a potential target enzyme for modifying the composition of lignin in plants, is a single-copy gene in A. thaliana, while there are nine and 13 copies of COMT in S. suchowensis and P. trichocarpa, respectively (Supplementary Table S15).
Willows are characterized by an unusually high content of salicylic acid in their secondary metabolites19. Salicylic acid is a phytohormone that regulates signal transduction pathways involved in the defense against biotic and abiotic stresses. Gene annotation showed that there were 827 genes involved in salicylic acid biosynthesis and metabolism in S. suchowensis genome v2.0. The KEGG pathway analysis indicated that these genes were enriched in plant immune signaling to induce systemic acquired resistance, such as plant hormone signal transduction, MAPK signaling pathway-plant, plant-pathogen interaction, and alpha-linolenic acid metabolism pathways (Supplementary Fig. S6). The number of genes related to salicylic acid biosynthesis and metabolism is much higher in Populus than in Arabidopsis (1397 vs. 125, respectively), suggesting that salicylic acid may be involved in signal transduction processes specific to trees, such as plant hormone signal transduction and wood formation.
Whole-genome duplication analysis
We detected 11,037 and 15,092 paralogous gene pairs within the genomes of S. suchowensis and P. trichocarpa, respectively. We also identified 12,710 single-copy orthologous gene pairs between these two lineages. We calculated the fourfold synonymous third-codon transversion (4DTV) value for each gene pair. Plotting the 4DTV values for the paralogous gene pairs revealed two peaks in both willow and poplar (Fig. 5a, b). The peak associated with salicoid duplication appeared at 4DTV values of 0.101 and 0.082 in S. suchowensis and P. trichocarpa, respectively. Plotting the 4DTV values for single-copy orthologous gene pairs revealed a peak at a 4DTV value of 0.04 that was associated with the divergence of these two lineages (Fig. 5c). The comparison of the peak positions showed that the divergence of poplar and willow occurred after salicoid duplication in each lineage. The conclusion was further confirmed by analyzing the number of synonymous substitutions per synonymous site (Ks) for each gene pair. Salicoid duplication occurred at Ks values of 0.365 in S. suchowensis and 0.283 in P. trichocarpa, and the divergence of these two lineages occurred at a Ks value of 0.158 (Fig. 5d–f). Notably, the peaks associated with salicoid duplication were found to not overlap in these two lineages. The same scenario was also observed in previous reports20. The analysis of nucleotide substitution rates revealed that this characteristic was caused by the molecular clock clicking more slowly in willow than in poplar8. The visualization of synteny blocks (Fig. 6) revealed high collinearity in S. suchowensis and P. trichocarpa for 17 chromosomes. As found in previous studies21,22,23, large interchromosomal rearrangements were detected between chromosome I and chromosome XVI, suggesting that major chromosomal fusions and fissions occurred after salicoid duplication, leading to the divergence of the two sister genera.
Furthermore, we examined the extent of sequence divergence by estimating the number of nonsynonymous substitutions per nonsynonymous site (Ka)/Ks for paralogous genes arising from salicoid duplication in both S. suchowensis and P. trichocarpa (Fig. 7). The average Ka/Ks value was 0.286 for S. suchowensis and 0.311 for P. trichocarpa, suggesting that salicoid duplicated genes are subject to stronger purifying selection in S. suchowensis than in P. trichocarpa (Supplementary Table S16). At the chromosome level, the average Ka/Ks values for the salicoid duplicated genes ranged from 0.30 to 0.34 for the chromosomes of P. trichocarpa, whereas the corresponding values ranged from 0.27 to 0.3 in S. suchowensis (Supplementary Table S16). Thus, stronger purifying selection was observed for each chromosome in S. suchowensis than in P. trichocarpa, which would lead to the faster loss of duplicated genes in willow than in poplar and ultimately result in a smaller gene content in S. suchowensis than in P. trichocarpa20.
We proposed an improved chromosome-scale assembly of the S. suchowensis genome using PacBio long reads and Hi-C technology. The emergence of PacBio sequencing has led to a significant increase in contig N50 sizes compared to previous short-read assemblies. The first assembly of the S. suchowensis genome based on Sanger sequencing presents limitations due to its fragmentation and low continuity (Table 1). By combining single-molecule sequencing and Hi-C technology, S. suchowensis genome v2.0 spanning 356.5 Mb was obtained, and the contig and scaffold N50s are 264 Kb and 16.8 Mb, respectively, indicating high contiguity of the assembly. Despite the high heterozygosity of the S. suchowensis genome, we used Hi-C technology to accurately assign the final assembled contigs to the chromosomal positions and constructed 19 chromosomes of the S. suchowensis genome, accounting for 95.29% of the assembly. We accurately compared the quality of S. suchowensis genome v2.0 with that of the previous short-read assembly from a variety of aspects, verifying that our updated assembly achieved higher contiguity and quality in its extensive coverage of the genome and higher mapping ratios of the genomic reads, RNA-Seq short reads and conserved genes, suggesting that our assembly is a good alternative resource for diploid willow.
Compared with poplar genomes, willow genomes are generally smaller and contain fewer protein-coding genes. Using k-mer analysis, it was estimated that the genome size of S. suchowensis was ~425 Mb8, while that of S. purpurea was ~450 Mb7, both of which are slightly smaller than the estimated 485 Mb P. trichocarpa genome1. The assembled genome size of S. purpurea v1.0 is ~392 Mb, with 37,865 putative protein-coding genes7, while the sizes of the recently released S. purpurea genome v5.1 and v3.1 are ~329 Mb and ~313 Mb, with predicted coding genes of 35,125 and 34,464, respectively. The published genome size of S. suchowensis v1.0 is ~304 Mb, with only 24,931 putative protein-coding genes on 19 chromosomes24. Using PacBio sequencing long reads, the size of our improved genome assembly for S. suchowensis was 356.5 Mb, and 36,937 putative protein-encoding genes were predicted in the whole genome. With the obvious improvement in the contiguity of S. suchowensis genome v2.0, a greater number of genes were annotated than in the previous assembly. However, only 31,863 anchored and oriented genes were found on 19 chromosomes of the S. suchowensis genome, and the average Ka/Ks ratios of salicoid duplicated gene pairs on each chromosome in S. suchowensis were smaller than those in P. trichocarpa, suggesting that willow might be subjected to stronger purifying selection, which is consistent with previous studies indicating that willows have evolved faster than poplars, resulting in a reduced number of predicted genes and an overall smaller genome size8,20.
In summary, the development of genomic assembly technologies makes it possible to produce chromosome-level scaffolds in a rapid and cost-effective way. The updated S. suchowensis genome v2.0 includes a high-quality chromosomal-level assembly and many important genes, offering novel insights into genome evolution, functional innovation and key regulatory pathways in Salix and providing excellent genetic resources for comparative genome studies among Salicaceae species.
Materials and methods
The same material of female cultivated shrub willow used for the first assembly was selected from the germplasm resources of S. suchowensis preserved at Nanjing Forestry University. Fresh young leaves were collected and immediately frozen in liquid nitrogen for genomic DNA isolation and library construction. According to the recommendations of Pacific Biosciences, genomic DNA was fragmented to a target size of ~20 kb to construct the PacBio genome sequencing library. All the DNA libraries were sequenced using the PacBio platform (Pacific Biosciences, CA, USA) with P6-C4 sequencing chemistry. The genomic DNA was sheared to construct short insertion paired-end (PE) libraries following the manufacturer’s instructions (Illumina, CA, USA). All libraries were sequenced at 2×100 bp on the Illumina HiSeq X ten platform. All sequencing procedures were performed by the BioMarker Technologies Company (Beijing, China).
The PacBio SMRT-Analysis package (https://www.pacb.com) was used for the quality control of the raw polymerase reads; sequencing adaptors were removed, and low-quality short reads were filtered. Owing to the high error rate of the raw PacBio long reads, we first used the error correction module embedded in Canu25 to correct these errors. Then, the high-quality PacBio clean reads were de novo assembled by using Canu with default parameters, which produced assembly agglomerations containing 5346 contigs for the preliminary assembly. Owing to the high heterozygosity of the S. suchowensis genome, the clean PacBio subreads were aligned back to the assembled contigs by using BLASR26, and the contigs were further corrected with Quiver from the SMRT-Analysis package. The Illumina short reads obtained from the S. suchowensis genome were aligned onto the optimized contigs using BWA-MEM27, and parsing was performed with SAMtools28. As a result, 3444 primary contigs were retained to reconstruct the haploid pseudomolecule for each chromosome.
Chromosome-scale assembly with Hi-C data
Hi-C libraries were constructed from fresh leaf tissue of S. suchowensis, which is the same line that we sequenced for genome assembly. The Hi-C libraries were sequenced on the Illumina HiSeq X ten platform (Illumina, CA, USA) at the BioMarker Technologies Company (Beijing, China). Owing to the limitation of the short reads involved in the Hi-C procedure, we used HiC-Pro29 to process these Hi-C sequencing data, including the mapping of the Hi-C sequencing reads to the assembled contigs with the BWA-aln aligning algorithm without any mismatches30 and with the detection of valid contacts. The preassembled contigs split into segments of 50 kb on average, combined with uniquely matched Hi-C data, were clustered, ordered and directed onto the pseudochromosomes with LACHESIS software31. To improve the chromosome-scale assembly quality, manual adjustment of orientation errors with obvious discrete chromatin interaction patterns was performed. The final chromosome assemblies were divided into 100 kb bins with equal lengths, and the interaction signals generated by the valid mapped read pairs between each bin were visualized in a heat map.
We used a combination of de novo prediction and homology-based searches to annotate transposable elements in the genome. To construct a de novo repeat library, the specific transposable elements in our assembly were first screened using LTR FINDER32, RepeatScout33 and PILER-DF34, and these repetitive sequences were then classified into families with PASTEClassifier35. Finally, RepeatMasker36 was applied to perform a homology-based repeat search using both the de novo repeat library and the known Repbase37 transposable elements database.
The repeat-masked genome assembly was used for annotating gene models through a combination of ab initio prediction, homology-based prediction and RNA-Seq-assisted prediction methods. Five different ab initio gene prediction programs were used to identify gene models. In the homology-based prediction, protein sequences from Arabidopsis thaliana, Oryza sativa, Populus trichocarpa, and Eucalyptus grandis downloaded from Phytozome (https://phytozome.jgi.doe.gov) were aligned to the assembly with TBLASTN38, and then GeMoMa39 was used to construct exact gene models from all initially aligned coding sequences. Additionally, RNA-Seq data from five different tissues of S. suchowensis, including the roots, stems, leaves, buds and bark, were mapped to the genome assembly using HISAT and Stringtie40. TransDecoder (http://transdecoder.github.io) and GeneMarkS-T41 were used to identify transcripts from the mapping results. Finally, all gene models predicted from the above three approaches were integrated by using EvidenceModeler (EVM) v1.1.142 to generate consensus gene sets and were filtered with PASA43 to detect spliced gene structures and generate non-redundant gene models.
Functional annotations of the predicted genes were further assigned with BLAST44 according to the best match of the alignments against the non-redundant plant protein database and non-redundant nucleotide and protein sequences from the NCBI45. The Gene Ontology (GO) terms for each gene were obtained from the GO database46. The protein motifs and domains were predicted by using InterProScan47 to search against various domain databases. The tRNA genes were searched by using tRNAscan-SE48 software with the eukaryote parameters. Additionally, microRNA and rRNA genes were identified by using INFERNAL49 to search the miRBase50 and Pfam51 databases, respectively.
Assessment of genome assembly and annotation
The S. suchowensis BAC sequences were aligned to the updated S. suchowensis genome using the MUMmer52 program. We mapped DNA sequencing data (>50×) from the Illumina HiSeq X ten platform against the first assembly and the updated assembly using BWA-MEM software27 and then compared the mapping status of the two genomes with SAMtools28. The transcriptomic short reads derived from different tissues of S. suchowensis (including the roots, stems, leaves, buds, and bark) from the previously published genome8 were aligned to both genome assemblies with STAR53. BUSCO16 was used to evaluate the completeness of the assembled genome. Orthofinder54 was used to classify the orthologs between S. suchowensis v2.0 and P. trichocarpa v3.0. We used BLASTP44 to identify the common genes between S. suchowensis v2.0 and S. suchowensis v1.0. GO enrichment analysis was carried out with the clusterProfiler55 R package.
Gene family analysis
We used two software programs, BLASTP44 and HMMER56, to search for homologous proteins harboring the conserved domains of related gene families in S. suchowensis genome v2.0 with an expected value (e-value) threshold of <1e-10. The predicted protein sequences were further confirmed using both the NCBI conserved domain database (CDD)45 tool and the Simple Modular Architecture Research Tool (SMART)57 to analyze the conserved domains. The final deduced full-length amino acid sequences were aligned by using the ClustalW program with default parameters58. The phylogenetic tree was constructed using MEGA X via the neighbor-joining (NJ) method with 1000 bootstrap iterations59 and visualized using the Interactive Tree of Life (iTOL) web tool (http://itol.embl.de)60.
We performed a pathway enrichment analysis at the KEGG pathway database (http://www.genome.jp/kegg) to identify enriched metabolic or signal transduction pathways associated with salicylic acid. The classification of biological terms and the analysis of the enrichment of the salicylic acid biosynthesis and metabolism clusters in the KEGG pathways were completed with the clusterProfiler R package55.
We identified the collinearity within the assembled S. suchowensis v2.0 chromosomes, as well as that between the S. suchowensis v2.0 and P. trichocarpa v3.0 chromosomes. By running a BLASTP44 alignment for each genome pair, we searched for putative paralogous and orthologous genes within and between genomes. Fourfold degenerate sites were located, and the 4DTV values were calculated using in-house Perl scripts. The 4DTV range associated with salicoid duplication was determined by plotting the distribution frequency histogram of 4DTV values. For each salicoid duplicated gene pair, Ka and Ks values and Ka/Ks ratios were calculated using the Nei-Gojobori algorithm implemented in KaKs_Calculator 2.061. The boxplot of Ka/Ks values was generated with R software (version 3.6.1; www.r-project.org). The synteny blocks were identified and visualized by using the MCSCAN toolkit implemented in Python [https://github.com/tanghaibao/jcvi/wiki/MCscan-(Python-version)]. The image of the entire S. suchowensis genome was produced using Circos62.
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The work is supported by the National Key Research and Development Plan of China (2016YFD0600101). It was also supported by the PAPD (Priority Academic Program Development) program at Nanjing Forestry University.
Conflict of interest
The authors declare that they have no conflict of interest.
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Wei, S., Yang, Y. & Yin, T. The chromosome-scale assembly of the willow genome provides insight into Salicaceae genome evolution. Hortic Res 7, 45 (2020). https://doi.org/10.1038/s41438-020-0268-6