Brown algae comprise many types of seaweeds in oceans and serve important functions in marine ecosystems1. Taxonomically, brown algae belong to the very large Class Phaeophyceae, in the division Heterokontophyta. They are eukaryotes, distinguished by having chloroplasts surrounded by four membranes2. This suggests that they arose from a symbiotic relationship between a basal eukaryote and another eukaryotic organism with chloroplasts. Here we examine a brown alga, Nemacystus decipiens. The phylogenetics of N. decipiens and a closely related species, Cladosiphon okamuranus, are a matter of some debate. According to Silberfeld et al.3, both N. decipiens and C. okamuranus are classified as members of the family Chordariaceae of the order Ectocarpales. On the other hand, Migita and Yotsuji4 and Yoshida et al.5 classified N. decipiens as a member of the family Spermatochnaceae of the order Chordariales, and C. okamuranus is as a member of the family Chordariaceae within the same order. In this report, we adopt the latter classification.

Brown algae provide food resources6. Major cultured seaweeds in Japan include Laminaria, Saccharina, Undaria, Cladosiphon, and Nemacystus. In Okinawa, C. okamuranus and N. decipiens represent major food products. N. decipiens (“ito-mozuku” in Japanese) and C. okamuranus (“Okinawa mozuku” in Japanese) are morphologically similar (Fig. 1A,C). Both have frond-like sporophytes, and the diameter of main axes is less than 1 mm in the former and 1~2 mm in the latter. Sporophytes are composed of cortexes in the outer layer and the medullas in the inner layer, the former of which contains assimilatory filaments. The two algae are distinguishable by a lumen-like space found only in C. okamuranus sporophytes (Fig. 1B,D). N. decipiens and C. okamuranus have been cultivated in Okinawa for more than 25 and 35 years, respectively (Supplementary Fig. S1A). Cultivation has established 19 strains of N. decipiens and 5 of C. okamuranus. It is reported that approximately 800 tons of N. decipiens were produced in fiscal year 2017, versus ~17,000 tons of C. okamuranus.

Figure 1
figure 1

Nemacystus decipiens (A, ito-mozuku) and Cladosiphon okamuranus (C, Okinawa mozuku) have fibrous sporophytes, less than 1 mm and 1~2 mm in diameter, respectively (B,D). Those sporophytes have cortexes that contain assimilatory filaments surrounding the medullas. Sporophytes of C. okamuranus have lumens. a, assimilatory filament; c, cortex; l, lumen; m, medulla; Scale bar, 10 cm (A,C) and 500 µm (B,D). The photograph of C. okamuranus sporophyte was provided by Mr. Kenji Iwai under a CC BY open access license.

In addition, brown algae produce carotenoids, including fucoxanthin, which is essential for photosynthesis. Brown algae also produce fucoidan7, one of the sulfated polysaccharides found in the cell-wall matrix of brown algae. It has anticoagulant, antithrombin, and antitumor activities8. Brown algae also known synthesize alginates9,10. Therefore, they are a source of important biomaterials in the fisheries industry.

Due to global environmental changes, including temperature increase, acidification, and pollution, brown algal aquaculture is facing critical conditions11. Continuous efforts to maintain and improve culture methods are required, and genomic information is essential for this. So far, the genomes of Ectocarpus siliculosus12 (Order Ectocarpales), Saccharina japonica13 (Order Laminariales), and Cladosiphon okamuranus14 (Order Chordariales) have been decoded. In a previous study, we decoded the ~130-Mbp genome of C. okamuranus, which is a good fucoidan producer (250 milligram per gram dry weight)7,15. We identified and characterized genes for enzymes involved in the sulfated fucan biosynthetic pathway14. l-fucokinase phosphatizes l-fucose to fucose-1-phosphate and GDP-fucose pyrophosphorylase catalyzes fucose-1-phosphate to GDP-fucose. We isolated mRNA indicating that in C. okamuranus, these two genes have fused, which may be advantageous for producing fucoidan. N. decipiens has also been recognized as a good source of fucoidan (250 milligram per gram dry weight)7,15. In this study, we decoded a draft genome of Nemacystus decipiens and compared it to other brown algal genomes.


Genome sequencing and assembly

Details of sequencing and genome assembly are presented in Supplementary Table S1. The Illumina MiSeq platform (average library size, 700 base-pair (bp)) generated a total of 47.1 giga-base-pair (Gbp) of paired-end sequence data (average read length = 309 bp). The HiSeq 4000 platform generated a total of 33.0 Gbp of mate-pair sequences; 4.3 Gbp for 2 kb, 4.4 Gbp for 3 kb, 4.3 Gbp for 4 kb, 4.4 Gbp for 5 kb, 4.4 Gbp for 6 kb, 4.2 Gbp for 7 kb, 3.0 Gbp for 9 kb, 2.2 Gbp for 11 kb, and 1.9 Gbp for a 13 kb library (average read length 151 bp). A total of 80.1 Gbp of sequences data was obtained (Supplementary Table S1).

The genome size of N. decipiens was estimated by counting K-mer frequencies of raw reads (K-mer = 32). In Supplementary Fig. S2A, the peak appeared at around ~95. The calculated genome size was ~190 Mbp. A total read of 80.1 Gbp would correspond to approximately 420-fold sequencing coverage of the estimated genome.

Table 1 Comparison of draft genome assemblies of three brown algae, Nemacystus decipiens (Order Spermatochnaceae), Cladosiphon okamuranus (Order Chordariales), and Ectocarpus siliculosus (Order Ectocarpales).

Illumina paired-end reads were assembled de novo using Platanus. The assembled genome contained 411,597 contigs with an N50 size of 6,265 bp (Table 1). The longest contig was 135,338 bp, and approximately 47% of sequences were covered with contigs over 2 kb in length. Subsequent scaffolding of 411,597 Platanus output was performed with SSPACE, using Illumina mate-pair sequence information (Supplementary Table S1). Gaps inside the scaffolds were closed with GapCloser. Contaminating bacterial and microbial scaffolds identified using Maxbin and RNAmmer were deleted. Final assembly of the N. decipiens genome was 685 scaffolds with an N50 size of 1.863 Mbp. Total length of scaffolds reached 154 Mbp (Table 1).

CEGMA analysis indicated 93.6% sequences for partial yields and 84.3% sequences for complete yields (Table 1). For comparison, CEGMA partial and complete values for genome sequences of C. okamuranus and E. siliculosus are 88.3% and 87.5%, and 83.1% and 72.6% (Table 1), respectively. This suggests that the assembled genome of N. decipiens has the higher quality of the three brown algal genomes.

GC content

The GC content of the N. decipiens genome was calculated as ~56% (Supplementary Fig. S2B; Table 1), versus 54% for both C. okamuranus and E. siliculosus (Table 1).

RNA-seq, assembling, and mapping

Transcriptomic data are essential to analyze composition and expression of genes. RNA extracted from protonemas (Supplementary Fig. S1B) was sequenced using the HiSeq. 4000 platform (average library size was 260 nucleotides (nts), and read length 151 nts) (Supplementary Table S1). A total of 28.5 giga nts were generated. Transcripts assembled with the Velvet/Oases yielded 204,065 contigs (a total of 345 mega nts) with an N50 size of 3,313 nts. 152,212 (74.6%) assembled transcripts were aligned to the assembled genome (with default settings) with blat software. These data were used to produce gene models and annotations.

Gene modeling

Assembled RNA sequences and putative protein coding loci found with blastx were incorporated as AUGUSTUS “hints.” The number of gene models was 15,156 (Table 1). This is larger than the 12,999 predicted genes of C. okamuranus (on 541 scaffolds, version 2:, and fewer than the 17,418 predicted genes of E. siliculosus (version 2: The average length of N. decipiens genes was 7,902 bp and that of exons (coding sequences) was 2,710 bp.

The C. okamuranus and E. siliculosus genomes are intron-rich12,14; average numbers of introns per gene are 9.14 and 6.96, and average intron lengths are 530 bp and 740 bp, respectively (Table 1). This feature was more prominent in the N. decipiens genome. The average number of introns per gene was 10.24, and the average length of an intron was 588 bp (Table 1). Land plants and non-brown algae have lower average numbers of introns per gene; 5.43 in Arabidopsis thaliana, 4.39 in Oryza sativa ssp. japonica, 3.89 in Hordeum vulgare, 4.35 in Zea mays, 5.34 in Physcomitrella patens, 5.69 in Marchantia polymorpha, 6.63 in Klebsormidium nitens, 3.82 in Chara braunii and 8.07 in Chlamydomonas reinhardtii, respectively17. This feature of brown algal genes should be examined in future.

Transposable elements and other repetitive components

We examined the proportion of transposable elements and repetitive elements in the assembled N. decipiens genome. DNA transposons and retrotransposons accounted for 0.2098% and 2.0143% of the N. decipiens genome, respectively (Supplementary Table S2). DNA transposons included EnSpm (0.0440% of assembled sequences), Helitron (0.0186%), hAT (0.0157%), and Polinton (0.0110%). Retrotransposons included LTR (long terminal repeat) retrotransposons such as Gypsy (0.8189%), Copia (0.4700%), and Bel_Pao (0.0681%), and the non-LTR retrotransposon CR1 (0.0016%). Percentages for LINE (long interspersed nuclear elements) are 0.0733% for Jockey, 0.0458% for Tx1 and 0.0072% for L1, and that for SINE (short interspersed nuclear elements) is 0.0024%. Repetitive sequences, including unclassified repeats comprised 8.8% of the N. decipiens genome (Supplementary Table S2). This is less than the two other brown algae, i.e.,11.2% for C. okamuranus and 22.7% for E. siliculosus, respectively (Table 1). An interesting question for future studies is how the variation in quality and quantity of repetitive sequences affects the composition of brown algal genomes.

Genome browser

A genome browser has been established at: Gene annotations from domain searches and Blast2GO18 are provided on the site.

Phylogenetic position of Nemacystus decipiens

Based on morphological and molecular criteria, N. decipiens was classified as belonging to the family Spermatochnaceae of the order Chordariales4,5. On the other hand, C. okamuranus has been classified into the family Chordariaceae of the same order. Another brown alga, E. siliculosus, belongs to the order Ectocarpales. To examine phylogenetic relationship of the three algae, we carried out molecular phylogenetic analysis based on a comparison of nucleotide sequences of 32 protein-coding genes in mitochondria genomes of 38 brown algae. As shown in Fig. 2 and Supplementary Fig. S3, N. decipiens and C. okamuranus form a clade corresponding to the order Chordariales while Scytosiphon lomentaria and three other species form a clade corresponding to the order Scytosiphonales, and E. siliculosus belongs to an independent clade of the order Ectocarpales (Fig. 2 and Supplementary Fig. S3). This indicates N. decipiens and C. okamuranus share a more recent common ancestor.

Figure 2
figure 2

Phylogenetic tree of 38 brown algae based on a comparison of 32 mitochondrial protein-coding gene sequences. Nemacystus decipiens forms a clade with Cladosiphon okamuranus, that may correspond to the order Chordariales. On the other hand, Ectocarpus siliculosus forms another clade in the order Ectocarpales. Full tree was shown in Fig. S3. Black dots represent 100% bootstraps. Scale bar, 0.1 substitutions/site.

Transcription factor genes

We searched for genes that encode transcription factors (TFs) in the N. decipiens genome using hmmer3 and the Pfam database (e-value cutoff <e−5), and compared them with those in the C. okamuranus14 and E. siliculosus16 genomes (Supplementary Table S3). The domains include HSF, Myb, bZIP, Zinc Finger, bHLH, CCAAT-binding, Homeobox, AP2-EREBP, Nin-like, TAF, E2F-DP, CBF/NF-Y/archaeal, and Sigma-70 r2/r3/r4 (Supplementary Table S3). It appears that the N. decipiens genome contains 299 transcription factor genes (Supplementary Table S3), versus 257 in the C. okamuranus genome (version 2) and 274 in the E. siliculosus genome (version 2), suggesting a small expansion of the TF family in N. decipiens. The most abundant TFs occurred in the Myb family, with 79, 74, and 70 genes detected in N. decipiens, C. okamuranus, and E. siliculosus genome, respectively. Others that were plentiful in the N. decipiens genome were CBF/NF-Y/archaeal (42), bZIP (36), Sigma-70 r2/r3/r4 (32), Zinc Finger C2H2-type (26), Zinc Finger CCCH-type (22), and HSF (22). The N. decipiens genome contains four genes with bHLH domains, three with homeobox domains, and ten with TAF domains, respectively.

Comparison of orthologous gene groups

The Nemacystus genome contains 15,156 gene models, which is comparable to the genomes of Cladosiphon (12,999) and Ectocarpus (17,418)14,16. A total of 9,179 orthologous gene groups were conserved among the three algae (Fig. 3). In addition, 455 orthologous groups were shared by N. decipiens and C. okamuranus, 549 by C. okamuranus and E. siliculosus, and 623 by N. decipiens and E. siliculosus. 2,878, 1,093, and 5,007 groups were found to be unique in genomes of N. decipiens, C. okamuranus, and E. siliculosus, respectively. 1,526 of the 2,878 unique groups in the N. decipiens genome could be GO-annotated (Supplementary Table S4). Among these, 55.8% were categorized as “molecular function” 37.5% as “biological process,” and 6.3% as “cellular component.” This indicates that many genes unique to N. decipiens may not be involved in cellular structure or composition, but in physiological processes such as alanine dehydrogenase and xanthine phosphoribosyl transferase activity. In fact, many of these genes encoded enzymes involved in polysaccharide biosynthetic processes (Supplementary Table S5). Furthermore, 617 of 1,352 non-GO-annotated gene groups were not found in the non-redundant protein sequence database at NCBI, and 200 of the 617 genes were annotated (Supplementary Table S6).

Figure 3
figure 3

Numbers of orthologous gene groups among the three brown algae, Nemacystus decipiens, Cladosiphon okamuranus, and Ectocarpus siliculosus.

Extracellular matrix genes

The extracellular matrix (ECM) is composed of collagens, elastin, and proteoglycans, elements of which are polysaccharides and glycoproteins19,20,21. It regulates morphogenesis, cell differentiations, evolution of multicellularity, and cell-to-cell communication, and responses to stimuli from the environment19,20,21. In order to examine brown algae-unique and Chordariales (N. decipiens and C. okamuranus)-unique ECM components, we searched genes for those possibly associated with the ECM in genomes of the three brown algae, a diatom (Thalassiosira pseudonana), an oocyte (Phytophthora infestans), a green alga (Chlamydomonas reinhardtii), and a land plant (Arabidopsis thaliana), as described in the Materials and Methods. 676, 649, 901, 644, 1,116, 699, and 1,116 genes were defined as putative ECM genes in N. decipiens, C. okamuranus, E. siliculosus, T. pseudonana, P. infestans, C. reinhardtii, and A. thaliana genomes, respectively (Supplementary Tables S7 and S8). These genes were annotated with the Pfam database and the number of annotated domains was counted. As a result, 140, 88, and 159 unique domains were found in N. decipiens, C. okamuranus, and E. siliculosus, respectively (Fig. 4). 26 domains were shared among the three brown algae, and additional 23 domains were conserved in the order Chordariales (Fig. 4). One GlcNAc gene (PF11397.6) that was also annotated as glycosyl transferase family 60 was found in each of the three genomes. On the other hand, three and two glycosyl transferase family 2 genes (PF13704.4) was found only in N. decipiens and C. okamuranus genomes, respectively (Supplementary Tables S8). Glycosyl transferase is necessary for polysaccharide biosynthesis22. Although function of the gene has not been analyzed yet, the results suggest that N. decipiens and C. okamuranus evolved recently from a common ancestor that had acquired the glycosyl transferase family 2 gene, and that the GlcNAc gene may play an important role in polysaccharide biosynthesis in the brown algae.

Figure 4
figure 4

Upset plot representing domains associated with extracellular matrix in seven organisms. The 40 most abundant domains in the extracellular matrix are shown. indicates Nemacystus decipiens; C.ok, Cladosiphon okamuranus;, Ectocarpus siliculosus;, Thalassiosira pseudonana;, Phytophthora infestans;, Arabidopsis thaliana; and, Chlamydomonas reinhardtii. A set of 26 and additional set of 23 domains were shared among the three brown algae and among Chordariales, respectively. On the other hand, 140, 88, and 159 domains were unique in the genomes of N. decipiens, C. okamuranus, and E. siliculosus, respectively. The 10 domains were common in the seven organisms.

Genes associated with fucoidan biosynthesis

Fucoidans are a family of sulfated homo- and hetero-polysaccharides of brown algae that contain l-fucose residues. The family comprises a broad spectrum of polysaccharides, from compounds with high uronic acid content and low fucose and sulfate content to almost pure α-l-fucan with fucose as the dominant monosaccharide. Genes encoding key enzymes for polysaccharide metabolism in brown algae were first predicted from the E. siliculosus genome10. Six enzymes are involved in this pathway (Fig. 5). GDP (guanosine diphosphate)-mannose and l-fucose are original sources of GDP-fucose, which are transformed to sulfated fucan via fucan (Fig. 5).

Figure 5
figure 5

Identification of genes for enzymes in the biosynthetic pathway of sulfated fucan in three brown algae. Gene numbers in each genome are also shown. Nemacystus decipiens. C.ok: Cladosiphon okamuranus. Ectocarpus siliculosus.

With a Blast search, our previous analyses indicated that genes encoding these key enzymes are conserved between C. okamuranus and E. siliculosus, although those for downstream enzymes are likely expanded independently in each lineage (Fig. 5)14. Specifically, the C. okamuranus and E. siliculosus genomes each contain two genes for GDP-mannose 4,6-dehydratase, and one gene for GDP-l-fucose synthase (Fig. 5). Both genomes hold one gene for l-fucokinase (FK) and one gene for GDP-fucose pyrophosphorylase. We found that the N. decipiens genome contained the same number of genes for the four enzymes (Fig. 5). The number of fucosyltransferases and sulfotransferases is variable among the three brown algae (Fig. 5). The N. decipiens, C. okamuranus, and E. siliculosus genomes contain four, five, and four genes for fucosyltransferase, and ten, nine, and six genes for sulfotransferase, respectively (Fig. 5; details of this information are in Supplementary Tables S9).

Our previous study of the C. okamuranus genome found a possible fusion of the genes for l-fucokinase and GDP-fucose pyrophosphorylase (FK-GFPP)14, which was not found in the E. siliculosus genome (Figs 5 and 6). The present study confirmed that the genes are also fused in the N. decipiens genome (Fig. 6). There were no stop codons in the sequence of the transcript. The protein predicted by mRNA contained both the FK and GFPP domains (Supplementary Fig. S5). This suggests that the fused gene produces a bifunctional enzyme and that two enzyme-mediated processes are replaced by a single process. Although the function of the fused gene should be confirmed in the future, N. decipiens and C. okamuranus may have developed a more efficient means of producing sulfated fucans, compared to E. siliculosus.

Figure 6
figure 6

A diagrammatic representation of a syntenic region in genomes of three brown algae, Ectocarpus siliculosus (, Cladosiphon okamuranus (C.ok) and Nemacystus decipiens ( This region contains seven genes that encode Ankyrin repeat-containing protein, GDP-fucose pyrophosphorylase (GFPP), l-fucokinase (FK), ST-domain-containing protein, alpha/beta hydrolase, RNA-binding ASCH domain protein, and tyrosinase. In the E. siliculosus genome, all seven genes exist independently. However, in the C. okamuranus and N. decipiens genomes, the gene for l-fucokinase (FK) and the gene for GDP-fucose pyrophosphorylase (GFPP) are fused. In addition, in the N. decipiens genome, genes for ST-domain-containing protein and alpha/beta hydrolase are fused. These fusions are supported by corresponding mRNAs (Supplementary Figs S5 and S6), although the fused mRNA for the latter needs further examination. Insertion of a gene for topoisomerase DNA-binding C4 Zinc Finger protein was discovered in in the N. decipiens genome. Transcriptional direction is shown by the arrowhead. Numbers under genes indicate gene ID numbers.

The genomic region that contains FK-GFPP genes shows synteny among the three brown algae (Fig. 6). The FK-GFPP genes are inserted adjacent to an ankyrin repeat-containing gene at the 5′ flanking site and an ST-domain-containing gene, the alpha/beta hydrolase gene, the RNA-binding ASCH domain gene, and the tyrosinase gene on the 3′ flanking site. We found another possible fusion in the N. decipiens genome involving an ST-domain-containing gene with the alpha/beta hydrolase gene (Fig. 6 and Supplementary Fig. S5). Fusion seems probable because there were no stop codons in the sequences of the transcript and because RT-PCR analysis, in which two primers were designed to produce a ~2-kb single transcript resulted in a transcript of corresponding size (Supplementary Fig. S6). The ST-domain-containing gene was a component of 10 sulfotransferases. Although the function of the alpha/beta hydrolase has not been analyzed yet, this may be another means of facilitating sulfated fucan biosynthesis.


As described above, the present decoding of a draft genome of the “ito-mozuku” alga, Nemacystus decipiens, identified 15,156 protein-coding genes, approximately 78% of which were substantiated by corresponding mRNAs. CEGMA analysis showed that the N. decipiens genome assembly is of higher quality than those of the two other brown algae. To facilitate understanding of brown algal biology, we compared features of the three genomes. First, molecular phylogeny using 32 mitochondrial genes showed that N. decipiens and C. okamuranus share a more recent common ancestor. Although taxonomic classification of these brown algae should include morphological and life cycle data, the results appear to support the order Chordariales, including N. decipiens and C. okamuranus. An intimate relationship between N. decipiens and C. okamuranus can also be deduced from their morphology.

Our present analysis of genes for components of extracellular matrix (ECM) showed that 26 and 23 types of domain-containing genes are common in genomes of the brown algae and Chordariales, respectively. In contrast 16 domains were shared by Stramenopiles, and majority of domains was species specific (Fig. 4, Supplementary Fig S4, Supplementary Tables S7 and S8). This result was consistent with a previous report21, suggesting independent evolution of ECM-associated genes of the brown algae. The GlcNAc that is also annotated as glycosyl transferase family 60 was shared among N. decipiens, C. okamuranus, and E. siliculosus, whereas the glycosyl transferase family 2 gene was unique to N. decipiens and C. okamuranus (Supplementary Table S8). These results suggest that each organism has unique ECMs, whereas the glycosyl transferase family 60 gene is one of the key genes for polysaccharide biosynthesis in brown algae, and the glycosyl transferase family 2 was acquired and abundant in the Chordariales lineage.

A search for genes of enzymes involved in sulfated fucan biosynthesis identified all genes in this pathway. Our previous study demonstrated the fusion of genes for l-fucokinase (FK) and GDP-fucose pyrophosphorylase (GFPP), in the genome of C. okamuranus, but not E. siliculosus14. This suggests that “Okinawa mozuku” may have developed a more efficient way to synthesize sulfated fucans. The present study confirmed the presence of a fused gene of FK-GFPP in the N. decipiens genome as well. This fusion was supported by the corresponding mRNA. In addition, we found that the ST-domain-containing gene and the alpha/beta hydrolase gene are fused to each other in N. decipiens (Fig. 6). This fusion is evidenced by the lack of a stop codon between the sequences and by the results of RT-PCR analysis in which two primers designed to produce a ~2-kb transcript resulted in a single transcript of corresponding size (Supplementary Fig. S6). The ST-domain-containing gene was a sulfotransferase. Therefore, this draft genome of Nemacystus decipiens may provide a platform for future studies of sulfated fucan biosynthesis.

Cultivation of “ito-mozuku” in the Onna Fisheries Cooperative has a long history, commencing with the isolation of the “Ito5” strain in 1993 (Supplementary Fig. S1). We decoded the genome of the “Onna-1” strain, established in 2006. The Onna Fisheries Cooperative now maintains more than ten strains with different sporophyte morphology and responses to environmental changes. Due to world-wide environmental changes, including oceanic temperature rise, acidification, and pollution, brown algal culture is now facing critical conditions11. Continuous efforts toward maintenance and improvement are urgent. Genomic information about the “Onna-1” strain provides a reference for characterization of other strains with different features, and may facilitate subsequent improvement of “ito-mozuku” aquaculture to resist various environmental changes.

Materials and Methods

Biological materials

Nemacystus decipiens, “ito-mozuku” in Japanese, employed strains established and maintained by the Onna Fisheries Cooperative. The first, “Ito5,” was isolated from a wild population in 1993 (Supplementary Fig. S1A). The “Onna-1” strain was selected in 2006 and has been steadily maintained. This strain was used in the present study. It is cultivated at 22.5 °C with a 12-h light-dark cycle in sea water containing 0.5% KW21 (Daiichi Seimo Co. Ltd., Kumamoto, Japan).

The life cycle of N. decipiens includes both haploid (n) and diploid (2n) generations (Supplementary Fig. S1B)4. The 2n protonemas mature into sporophytes, and are harvested for market. Because the strain has been maintained as protonemas without contamination from other eukaryotes, it is easy to extract genomic DNA14, with protonemas as the dominant material.

Frozen sections

Frozen sporophytes were embedded in Tissue-Tek O.C.T. compound (Sakura Finetek USA, Inc., Torrance, USA) and sectioned at 20 µm with Cryo-microtome CM3050S (Leica Microsystems GmbH, Wetzlar, Germany). Semi-thin sections were observed with an Axio Imager Z1 (Carl Zeiss, Oberkochen, Germany).

DNA extraction, genome sequencing, and assembly

For DNA extraction, 2n protonemas of N. decipiens were frozen in liquid nitrogen and crushed to powder with a frozen-cell crusher, Cryo-Press (Microtec Co., Ltd, Chiba, Japan). Genomic DNA was extracted from the powder using a DNA-Suisui-VS extraction kit (Rizo Co., Ltd, Ibaraki, Japan). Illumina MiSeq and HiSeq 4000 platforms were used for sequencing23. Libraries were prepared with slight protocol modifications provided by the manufacturer. Fragmented genomic DNA was further purified using Blue Pippin (Sage Science, Beverly, MA, USA). A paired-end library consisting of 700-bp clones was prepared for the MiSeq using a TruSeq DNA PCR-Free LT Sample Prep Kit (Illumina, San Diego, CA, USA), and 2-, 3-, 4-, 5-, 6-, 7-, 9-, 11-, and 13-kbp mate-pair libraries were prepared for the HiSeq 4000 using a Nextera Mate Pair Sample Prep Kit (Illumina) (Supplementary Table S1). The BioProject ID was PRJDB7493.

K-mer counting and estimation of genome size were done with JELLYFISH 2.2.0 software24,25 and GenomeScope26. Adapter sequences were trimmed from all reads using Trimmomatic-0.3027. High-quality paired-end reads (quality >20) were assembled de novo using Platanus 1.2.428 to create contigs. Subsequent scaffolding of the Platanus output was performed using SSPACE 3.029, based on Illumina mate-pair information. Gaps inside scaffolds were closed using GapCloser 1.1230. Assembled sequences were aligned with blastn (1e−50) to another sequence. Sequences that aligned by more than 50% were removed as errors arising from diploid sequences. CEGMA 2.5 software31 was used to evaluate genome assembly. Sequences likely originated from bacteria and other microbiota were removed from the assembled genome with Maxbin version 2.232 and RNAmmer 1.233.

Paired-end genomic DNA reads that were not used in the N. decipiens genome were collected with kneaddata v0.6.1 ( Those reads were assembled with novoPlasty (version2.7.2)34 for the chloroplast and mitochondrial genomes of N. decipiens.

Transcriptome analyses

RNA was isolated from 2n protonemas (Supplementary Fig. S1B). Total RNA was extracted according to manufacturer instructions, using DNase and RNeasy Plant mini kits (QIAGEN, Hilden, Germany). Transcriptome libraries were prepared using a TruSeq Stranded mRNA Library Prep kit (Illumina). RNA was sequenced as per manufacturer instructions for the Illumina HiSeq 4000. Only sequences of high quality (quality >20) were assembled, using Velvet 1.2.1035 and Oases 0.2.0836.

Gene model prediction

A set of gene model predictions (Nemacystus decipiens Gene Model ver. 1) was generated with AUGUSTUS 3.2.137, which was trained on 9,793 transcriptome contigs recommended by PASA 2.2.038. Gene models were produced by running AUGUSTUS on a repeat-masked genome, along with RepeatModeler-1.1.8 (, and refined with PASA.

Transposable elements and repetitive sequences

Repetitive sequences were detected as described previously39. Tandem repeats were detected and classified using RepeatModeler. A de novo repeat library was generated with RepeatScout (version 1.0.5)40. Transposons and SINE in the scaffold were identified using RepeatMasker (ver. 4.0.7, with the Repbase (version 21.01)41.

Gene annotation and identification

In order to identify putative N. decipiens orthologous genes, reciprocal BLAST analysis was performed. This was carried out using mutual best hits of genes of C. okamuranus, E. siliculosus, and non-redundant protein sequences database from NCBI against N. decipiens gene models (BLASTP) or their assembly (TBLASTN). A second approach used for encoded proteins with one or more specific protein domains was to screen the models using HMMER (hmmer3)42 against the Pfam database (Pfam-A.hmm, release 24.0,, which contains approximately 11,000 conserved domains. Encoded proteins were also analyzed using InterProScan 5.25–64.044 for gene ontology annotations. The mitochondria genome was annotated with GeSeq45.

Mitochondrial gene collection and Phylogenetic tree analysis

Sets of related sequences were subjected to phylogenetic analyses to more precisely determine orthologous relationships between N. decipiens, C. okamuranus, and E. siliculosus. Mitochondrial genomes sequences of 38 brown algae were downloaded from the NCBI database or our genome browsers (Supplementary Table S10). The mitochondrial genomes were annotated using GeSeq, and cDNA sequences of Atp6, Atp8, Atp9, Cox1, Cox3, Cob, Nad1, Nad2, Nad3, Nad4, Nad4l, Nad5, Nad6, Nad7, Nad9, Rpl2, Rpl5, Rpl14, Rpl16, Rpl31, Rps2, Rps3, Rps4, Rps7, Rps8, Rps10, Rps11, Rps12, Rps13, Rps14, Rps19, and Tatc genes from the 38 brown algae were collected. 32 gene sequences were independently aligned using MAFFT46 with default options. Spurious sequences or poorly aligned regions were filtered using trimAl47, then filtered sequences were concatenated. Phylogenetic trees were constructed by the maximum likelihood method (GTR-gamma model) using RAxML version 8.2.1148 with partition analysis excluded third codon and a 1,000 bootstrap replications.

Searching extracellular matrix genes

Data of N. decipiens, C. okamuranus, E. siliculosus, Thalassiosira pseudonana, Phytophthora infestans, Arabidopsis thaliana and Chlamydomonas reinhardtii were downloaded from websites as shown in Supplementary Table S11. Downloaded protein sequences were first analyzed using signalP 4.149, HECTAR50, and TMHMM 2.051 to ensure that proteins contain signal sequences in their N-terminal, extra-membrane domains. Then, intracellular proteins were removed by searching for the endoplasmic reticulum targeting sequence (PDOC00014 in PROSITE database52) using MAST53. Collected proteins were defined as putative extracellular matrix proteins. Upset plots were drawn using UpSetR54.

Identification of the orthologous gene group

Protein sequences of N. decipiens, C. okamuranus, and E. siliculosus were analyzed with OrthoFinder version 2.0.055, using default parameters to identify orthologous gene groups.


cDNA was synthesized from total RNA with SuperScript™ IV First-Strand Synthesis System kit (Thermo Fisher Scientific Inc., Massachusetts, USA). Parts of coding regions of g5468 in the N. decipiens genome were amplified with PrimeSTAR GXL DNA Polymerase (Takara Bio Inc., Shiga, Japan). Primer sequences for the RT-PCR were 5′-TCTCCAAGACCGCCAAGG-3′ (Fw-primer) and 5′-TCAGCATCTTTCGCAGCC-3′ (Rv-primer). Blast analysis showed that these primers sequences were unique to the N. decipiens genome. PCR products were observed with an Agilent Bioanalyzer DNA 12000 kit (Agilent Technologies, California, USA) (Supplementary Fig. 5).

Genome browser

A genome browser has been established for the assembled genome sequences using the JavaScript-based Genome Browser (JBrowse) 1.11.656. The assembled sequence and gene models are accessible at