To explore the origins and consequences of tetraploidy in the African clawed frog, we sequenced the Xenopus laevis genome and compared it to the related diploid X. tropicalis genome. We characterize the allotetraploid origin of X. laevis by partitioning its genome into two homoeologous subgenomes, marked by distinct families of ‘fossil’ transposable elements. On the basis of the activity of these elements and the age of hundreds of unitary pseudogenes, we estimate that the two diploid progenitor species diverged around 34 million years ago (Ma) and combined to form an allotetraploid around 17–18 Ma. More than 56% of all genes were retained in two homoeologous copies. Protein function, gene expression, and the amount of conserved flanking sequence all correlate with retention rates. The subgenomes have evolved asymmetrically, with one chromosome set more often preserving the ancestral state and the other experiencing more gene loss, deletion, rearrangement, and reduced gene expression.
Ancient polyploidization events have shaped diverse eukaryotic genomes1, including two rounds of whole-genome duplication at the base of the vertebrate radiation2. While polyploidy is rare in amniotes, presumably owing to constraints on sex chromosome dosage3,4, it is common in fish5, amphibians6,7, and plants8. Polyploidy provides raw material for evolutionary diversification because gene duplicates can support new functions and networks9. However, the component subgenomes of a polyploid must cooperate to mediate potential incompatibilities of dosage, regulatory controls, protein–protein interactions and transposable element activity.
The African clawed frog X. laevis is one of a polyploid series that ranges from diploid to dodecaploid, and is therefore ideal for studying the impact of genome duplication10, especially given its status as a model for cell and developmental biology11. X. laevis has a chromosome number (2n = 36) nearly double that of the Western clawed frog Xenopus (formerly Silurana) tropicalis (2n = 20) and most other diploid frogs12, and is proposed to be an allotetraploid that arose via the interspecific hybridization of diploid progenitors with 2n = 18, followed by subsequent genome doubling to restore meiotic pairing and disomic inheritance10,13 (see Supplementary Note 1 and Extended Data Fig. 1 for discussion of the Xenopus allotetraploidy hypothesis).
Here we provide evidence for the allotetraploid hypothesis by tracing the origins of the X. laevis genome from its extinct progenitor diploids. The two subgenomes are distinct and maintain separate recombinational identities. Despite sharing the same nucleus, we find that the subgenomes have evolved asymmetrically: one of the two subgenomes has experienced more intrachromosomal rearrangement, gene loss by deletion and pseudogenization, and changes in levels of gene expression and in histone and DNA methylation. Superimposed on these global trends are local gene family expansions and the alteration of gene expression patterns.
Assembly, annotation and karyotype
We sequenced the genome of the X. laevis inbred ‘J’ strain by whole-genome shotgun methods in combination with long-insert clone-based end sequencing, (Supplementary Note 2) and organized the assembled sequences into chromosomes using fluorescence in situ hybridization (FISH) of 798 bacterial artificial chromosome clones (BACs) and in vivo and in vitro chromatin conformation capture analysis (Supplementary Note 3 and Methods). These complementary methods produced a high-quality chromosome-scale draft that includes all previously known X. laevis genes and assigns >91% of the assembled sequence (and 90% of the predicted protein-coding genes) to a chromosomal location.
We annotated 45,099 protein-coding genes and 342 microRNAs using RNA sequencing (RNA-seq) from 14 developmental stages (including the oocyte stage) and 14 adult tissues and organs (Supplementary Note 4), analysis of histone marks associated with transcription, and homology with X. tropicalis and other tetrapods (Supplementary Note 5 and Methods). Of the X. laevis protein-coding genes, 24,419 can be placed in 2:1 or 1:1 correspondence with 15,613 X. tropicalis genes, defining 8,806 homoeologous pairs of X. laevis genes with X. tropicalis orthologues and 6,807 single copy orthologues. The remaining genes are members of larger gene families (such as olfactory receptor genes) whose X. tropicalis orthology is more complex.
The X. laevis karyotype (Fig. 1a) reveals nine pairs of homoeologous chromosomes1,14,15. Each of the first eight pairs is co-orthologous to and named for a corresponding X. tropicalis chromosome, appending an L and S for the longer and shorter homoeologues, respectively16. XLA2L is the Z/W sex chromosome17, for which we determined a W-specific sequence in the q-subtelomeric region that includes the sex-determining gene dmw17 and a corresponding Z-specific haplotype. The homoeologous XLA2Sq, by contrast, has no such locus, and neither does XTR2 (Extended Data Fig. 2a and Supplementary Note 6). The ninth pair of homoeologues is a q–q fusion of proto-chromosomes homologous to XTR9 and XTR10, which probably occurred before allotetraploidization (Extended Data Fig. 2b–d and Supplementary Note 6). The S chromosomes are, on average, 13.2% shorter karyotypically16 and 17.3% shorter in assembled sequence than their L counterparts. The single nucleotide polymorphism rate in X. laevis is approximately 0.4%, far less than the approximately 6% divergence between homoeologous genes (Extended Data Fig. 1c and Supplementary Note 8.8).
Subgenomes and timing of allotetraploidization
We reasoned that dispersed relicts of transposable elements specific to each progenitor would mark the descendent subgenomes in an allotetraploid (Fig. 2c and Extended Data Fig. 1). Three classes of DNA transposon relicts appeared almost exclusively on either the L or S chromosomes (Supplementary Note 7). Xl-TpL_harb and Xl-TpS_harb are subfamilies of miniature inverted-repeat transposable elements (MITE) of the PIF/harbinger superfamily18,19 whose relicts were almost completely restricted to L or S chromosomes, respectively (Fig. 1b and Extended Data Fig. 3a). Similarly, sequence relicts of the Tc1/mariner superfamily member Xl-TpS_mar (closely related to the fish MMTS subfamily20) were found almost exclusively on the S chromosomes (Fig. 1b), as confirmed by FISH analysis using Xl-TpS_mar as a probe (Fig. 1c and Supplementary Note 7.4; see Supplementary Note 7.3 for details on the rare elements that map to the opposite subgenome).
The L and S chromosome sets therefore represent the descendants of two distinct diploid progenitors, confirming the allotetraploid hypothesis despite the absence of extant progenitor species. Analysis of synonymous divergence of protein-coding genes suggests that the L and S subgenomes diverged from each other around 34 Ma (T2) and from X. tropicalis around 48 Ma (T1) (Fig. 2a), consistent with prior gene-by-gene estimates from transcriptomes21,22,23,24 (Supplementary Note 8, Extended Data Fig. 4 and Methods). L- and S-specific transposable elements were active around 18–34 Ma, indicating that the two progenitors were independently evolving diploids during that period (Fig. 2a, Supplementary Note 7.5 and Extended Data Fig. 3). More recent transposon activity is more uniformly distributed across the L and S chromosomes (not shown). Finally, consistent with a common origin for tetraploid Xenopus species, we can clearly identify orthologues of L and S genes in whole-genome sequences of a related allotetraploid frog, X. borealis, and estimate the X. laevis–X. borealis divergence to be around 17 Ma (T3). These considerations constrain the allotetraploid event to around 17–18 Ma (T*). This timing is consistent with other estimates of the radiation of tetraploid Xenopus species, which are presumed to emerge from the bottleneck of a shared allotetraploid founder population23,24.
With the exception of the chromosome 9–10 fusion, X. laevis and X. tropicalis chromosomes have maintained conserved synteny since their divergence around 48 Ma (Fig. 1a, b). The absence of inter-chromosomal rearrangements is consistent with the relative stability of amphibian and avian karyotypes compared to those of mammals25, which typically show dozens of inter-chromosome rearrangements26. It also contrasts with many plant polyploids, which can show considerable inter-subgenome rearrangement27. The distribution of L- and S-specific repeats along entire chromosomes implies the absence of crossover recombination between homoeologues since allotetraploidization, presumably because the two progenitors were sufficiently diverged to avoid meiotic pairing between homoeologous chromosomes, though we cannot rule out very limited localized inter-homoeologue exchanges (Supplementary Note 7).
The extensive collinearity between homologous X. laevis L and X. tropicalis chromosomes (Fig. 1a) implies that they represent the ancestral chromosome organization. In contrast, the S subgenome shows extensive intra-chromosomal rearrangements, evident in the large inversions of XLA2S, XLA3S, XLA4S, XLA5S and XLA8S, as well as shorter rearrangements (Fig. 1a). The S subgenome has also experienced more deletions. For example, the 45S pre-ribosomal RNA gene cluster is found on X. laevis XLA3Lp, but its homoeologous locus on XLA3Sp is absent (Extended Data Fig. 5a). Extensive small-scale deletions (Extended Data Fig. 5b) reduce the length of S chromosomes relative to their L and X. tropicalis counterparts (see below).
Response of subgenomes to allotetraploidy
Redundant functional elements in a polyploid are expected to rapidly revert to single copies through the fixation of disabling mutations and/or loss28 unless prevented by neofunctionalization8, subfunctionalization26, or selection for gene dosage29. Differential gene loss between homoeologous chromosomes is sometimes referred to as ‘genome fractionation’30,31,32 (Supplementary Note 1). At least 56.4% of the protein-coding genes duplicated by allotetraploidization have been retained in the X. laevis genome (Supplementary Note 10; 60.2% if genes on unassigned short scaffolds are included). Previous studies that relied on cDNA21 and expressed sequence tag (EST) surveys22,33,34 observed far lower rates of retention, probably owing to sampling biases from gene expression (Supplementary Note 8.2).
Even higher retention rates were found for homoeologous microRNAs (156 out of 180, 86.7%), similar to the salmonid-specific duplication5, and both primary copies are expressed for intergenic homoeologous microRNAs (Supplementary Note 8.6 and Extended Data Fig. 5e). Pan-vertebrate putatively cis-regulatory conserved non-coding elements (CNEs)35 were also highly retained (541 out of 550, 98.4%; Supplementary Note 8.7 and Table 1). CNEs conserved between X. laevis and X. tropicalis, however, were retained at a significantly lower rate (49%, P ≤ 1 × 1050; Table 1 and Supplemental Table 3). Longer genes (by genomic span, exon number or coding length) were more likely to be retained (Wilcoxon signed-rank test, P ≤ 10−5; Supplementary Note 10.5 and Extended Data Fig. 5 h–j), broadly consistent with the idea that longer genes have more independently mutable functions and are therefore more susceptible to subfunctionalization and subsequent retention36.
Genes have been lost asymmetrically between the two subgenomes of X. laevis. Similar results have been reported for some plant polyploids30 but not in rainbow trout5. For X. laevis protein-coding genes with clear 1:1 or 2:1 orthologues in X. tropicalis, we found that significantly more genes were lost from the S subgenome (31.5%) than from the L subgenome (8.3%; χ2 test P = 2.23 × 10−50; Supplementary Table 2), with the same trend for other types of functional elements, such as histone H3 lysine 4 trimethylation (H3K4me3)-enriched promoters and p300-bound enhancers (Table 1). Across most of the genome, genes appeared to be lost independently of their neighbours, as runs of gene losses were nearly geometrically distributed (Fig. 3a, right). We did observe some large block deletions (for example, several olfactory clusters (Extended Data Fig. 5b) and a few unusually long blocks of functionally unrelated genes that were retained in two copies without loss (Fig. 3a, left)).
Many lost genes were simply deleted, as demonstrated by significantly shorter distances between conserved flanking genes in the other subgenome and in X. tropicalis. Both the size and number of deletions were greater on the S subgenome (Extended Data Fig. 5c). We identified 985 ‘unitary’ (that is, non-retrotransposed) pseudogenes out of 1,531 loci examined in detail. This 64% detection rate was similar between subgenomes in X. laevis and comparable to that reported in trout5. Based on the accumulation of non-synonymous mutations37 we estimated that most of these pseudogenes escaped evolutionary constraint around 15 Ma (Fig. 2a and Extended Data Fig. 6), consistent with the onset of extensive redundancy in the allotetraploid, although the precision of our pseudogene age estimates is low (Supplementary Note 9). Most pseudogenes showed no evidence of expression, but of 769 pseudogenes longer than 100 bp, 133 (17.2%) showed residual expression (Extended Data Fig. 6). Conversely, among homoeologous gene pairs, we found 760 for which one member had little to no expression across our 28 sampled conditions. Although these retained some gene structure (start and stop codon, no frame shifts, good splice signals), they showed increased rates of amino acid change and appeared to be under relaxed selection (Extended Data Fig. 5f). We called these nominally dying genes ‘thanagenes’ (Supplementary Note 12.5). Reduced expression may be due to mutated cis-regulatory elements, as exemplified by the six6 gene pair (Fig. 4e, Extended Data Fig. 8 g–i and Supplementary Note 13.1).
Although tetraploidy created two ‘copies’ of nearly every gene, additional gene copies were continually produced by tandem duplication (Fig. 3d and Extended Data Fig. 7). The number of tandem clusters was greater in X. tropicalis than in the X. laevis L subgenome, which in turn was greater than in the S subgenome (Supplementary Note 11.1). Although tandem duplication was faster in X. tropicalis than in X. laevis, there was also a higher rate of loss. Since tandem duplications and deletions occur by unequal crossing over during meiosis, these differing rates were consistent with the shorter generation time of X. tropicalis (Extended Data Fig. 7 f, g). The mean time to loss of an old tandem duplicate is around 40 Ma in X. laevis (on either subgenome) compared to around 16 Ma in X. tropicalis. Homoeologous gene loss and tandem duplication can combine to yield complex histories for some gene families. We discuss how these families contribute to the literature on whole-genome duplication evolution in Supplementary Notes 10 and 13.
Functional patterns of gene retention and loss
We found preferential retention or loss of many functional categories (Fig. 4a, Extended Data Figs 4e, 9, 10 and Supplementary Note 13). DNA binding proteins, components of developmentally regulated signalling (TGFβ, Wnt, Hedgehog and Hippo) and cell cycle regulation pathways were retained at a substantially higher rate (>90%) than average (Extended Data Fig. 10). Genes retained in multiple copies after the ancient vertebrate genome duplication were also more likely to be retained as homoeologues in X. laevis (Supplementary Note 10.4), similar to teleost and trout genome duplications5. We found nearly complete retention of 37 out of 38 duplicated genes in the four pairs of homoeologous Hox clusters, with a single pseudogene (Fig. 3c). High rates of homoeologue retention in most genes in these categories suggest that stoichiometrically controlled expression levels may be needed, or subfunctionalization of homoeologues may have occurred, either in their expression domain or in their target specificity.
Conversely, homoeologous genes in other functional categories have been lost at a higher rate, presumably because of a corresponding lack of selection for dosage. For example, genes involved in DNA repair were lost at a high rate (79%) (Supplementary Note 10.1). This is consistent with relaxed selection for repair in the immediate aftermath of allotetraploidy, when all genes were present in four copies per somatic cell5. Other metabolic categories were also prone to loss, presumably because single loci encoding enzymes were sufficient38. Genomic regions with notable loss include the major histocompatibility complex genes on the S subgenome (Fig. 3b) and several olfactory receptor clusters (Extended Data Fig. 5b). We hypothesize that homoeologous genes may be functionally incompatible in these cases, leading to en bloc deletion in response to selection pressure. Specific case studies of duplicate gene retention and loss are detailed in Extended Data Figs 9, 10 and Supplementary Note 13.
Evolution of gene expression
Gene expression is also a predictor of retention, whereby more highly expressed genes are more likely to be retained (Extended Data Fig. 8b), similar to results seen in Paramecium39,40. Developmentally regulated genes whose expression levels peak at the maternal zygotic transition (MZT) or during neural differentiation were retained at higher levels (P < 0.01), based on gene expression networks constructed from developmental and adult tissue expression (Methods, Fig. 4a (right), Extended Data Fig. 10e and Supplementary Note 12.3). We speculate that the exceptional retention of developmentally regulated genes is due to selection for stoichiometric dosage of these factors, and in some cases higher expression in the physically larger allotetraploid cells and embryos relative to those of diploid frogs, although a propensity36 of these genes for sub- or neofunctionalization could also have contributed. In the adult, genes whose expression peaks in the brain and eye were also retained at higher levels (Fig. 4b).
In X. laevis, the expression of homoeologues was highly correlated (Extended Data Fig. 8a), showing that the overall expression of homoeologues diverged similarly to that of orthologues between Xenopus species41. Many homoeologous pairs, however, were differentially expressed throughout development or across adult tissues, either in a spatiotemporal pattern (a form of subfunctionalization36; Supplementary Note 12.4 and Extended Data Fig. 8d–f) or in the same pattern but with differing expression levels. When homoeologous gene pairs were both expressed, the average L copy expression level was approximately 25% higher than that of the S copy consistently across adult tissues and after the MZT42 (Fig. 4b and Supplementary Note 12.2). Excess L expression, however, averaged only around 12% in oocyte and early pre-MZT stages, suggesting that the two subgenomes were more evenly expressed as maternal transcripts but developed an increased asymmetry after the MZT. Strikingly, we found 391 cases in which one homoeologue had no detectable maternal mRNA (oocytes, egg and stage 8; Fig. 4c, d and Extended Data Fig. 8c). Compared to similar transcript data from X. tropicalis, we found cases of an apparent loss of expression (‘maternal subfunctionalization’, that is, X. tropicalis and one X. laevis gene was expressed, whereas the other X. laevis gene was silenced pre-MZT) in 238 genes (for example numbl.S). We also found gains of expression (‘maternal neofunctionalization’, that is, the X. tropicalis gene was not expressed maternally, but one X. laevis gene was expressed) in 153 genes (for example hoxb4.L). We did not see such a large divergence in other expression domains (Supplementary Note 12.2 and Extended Data Fig. 8c), suggesting a higher level of plasticity of maternal mRNA regulation between X. laevis homoeologues, similar to the trend seen between Xenopus species41.
Overall, thousands of homoeologue pairs have either divergent spatiotemporal patterns or similar patterns with differing expression levels. Such homoeologue pairs differed in substitution rate and coding sequence length difference more than those that were similar in expression (Supplementary Note 12.4 and Extended Data Fig. 8d–f), a pattern that was also found in trout homoeologous pairs5. These expression differences can largely be attributed to changes in epigenetic regulation (Random Forest classification; ROC area under the curve 0.78), with changes in H3K4me3 and DNA methylation contributing the most explanatory power among our epigenetic variables (Supplementary Note 14). Detailed comparison of the two subgenomes will facilitate identification of specific sequences that control cis-regulatory differences between homoeologues.
The two subgenomes of Xenopus laevis have evolved asymmetrically, with the L subgenome more consistently resembling the ancestral condition and the S subgenome more disrupted by deletion and rearrangement. Asymmetric gene loss has been observed in allopolyploid plants30 and yeast43 at the segmental level, but it has not been shown directly that similarly fractionated segments derive from the same progenitor (Fig. 1c). Our results are consistent with the idea that optimized gene expression levels are an important force affecting gene retention following polyploidy39,40. The asymmetry between the L and S subgenomes could have been the result of an intrinsic difference between their diploid progenitors. Alternately, the remodelling of the S genome could have been a response to the L–S merger itself, a ‘genomic shock’44 resulting from the activation of transposable elements (Fig. 2a and Supplementary Note 8.5). The popularity of Xenopus as a model for the study of vertebrate development, cell biology and immunology is now extended to a model for vertebrate polyploidy.
No statistical methods were used to predetermine sample size. The experiments were not randomized. The investigators were not blinded to allocation during experiments and outcome assessment.
Notation and terminology
‘Homoeologous’ chromosomes are anciently orthologous chromosomes that diverged by speciation but were reunited in the same nucleus by a polyploidization event. They are a special case of paralogues. Homoeologous genes are sometimes called ‘alloalleles’ to emphasize their role as alternate forms of a gene, but since homoeologues are unlinked and assort independently, we do not use this terminology. Similarly, loss of homoeologous genes is sometimes referred to as ‘diploidization’. We prefer the simpler and more descriptive term ‘gene loss’. Note that an allotetraploid such as Xenopus laevis has two related subgenomes, but these subgenomes are each transmitted to progeny via conventional disomic inheritance. So immediately after allotetraploidization, the new species is already genetically diploid. This is clearly the case for X. laevis, since we find no evidence for recombination between homoeologous chromosomes, which would create new sequences with mixed ‘L’ and ‘S’ type transposable elements.
Sequencing and assembly
DNA was extracted from the blood of a single female from the inbred J-strain for whole-genome shotgun sequencing. We generated 4.6 billion paired-end Illumina reads from a range of inserts and used Sanger dideoxy sequencing to obtain fosmid- and bacterial artificial chromosome (BAC)-end pairs and full BAC sequences. We used meraculous45 as the primary genome assembler. See supplementary notes for more detailed information.
Chromosome scale organization
We identified 798 BACs containing genes of interest distributed across the Xenopus genome and performed fluorescence FISH to assign these BACs to specific chromosomes based on Hoechst 33258-stained late-replication banding patterns (Supplementary Table 1). Tethered chromatin conformation capture (TCC)46 and in vitro chromatin conformation capture47 were performed as previously described, and assembled with HiRise47.
Characterization of sex locus
Sex determination in X. laevis follows a female heterogametic ZZ/ZW system48. We fully sequenced BAC clones representing both W and Z haplotypes, and identified both W- and Z-specific sequences (Extended Data Fig. 2a). The existence of the Z-specific sequence was unexpected and therefore verified by PCR analysis using specific primer sets and DNA from gynogenetic frogs having either W or Z loci.
We made use of extensive previously generated transcriptome data for X. laevis and X. tropicalis, including 697,015 X. laevis EST sequences49. In addition, more than 1 billion RNA-seq reads were generated for this project from 14 oocyte/developmental stages and 14 adult tissues from J-strain X. laevis (Supplementary Note 4). These data were combined with homology and ab initio predictions using the Joint Genome Institute’s integrated gene call pipeline (see Supplementary Notes 4 and 8 for more details).
Characterization of subgenome-specific transposable elements
We found subgenome-specific repeats using a RepeatMasker50 result. The repeats were used to reconstruct full-length subgenome specific transposon sequences. The specific transposons, Xl-TpL_harb, Xl-TpS_harb and Xl-TpS_mar, were classified on the basis of their target site sequence and terminal inverted repeat (TIR) sequences. The coverage lengths of the transposons on each chromosome were calculated from the results of BLASTN search (E < 10−5) using the consensus sequences of the transposons as queries. The chromosomal distribution of the Xl-TpS_mar was revealed by a FISH analysis (Supplementary Note 7.4).
Phylogeny, divergence time, and evolutionary rates
We used Hymenochirus boettgeri, Pipa carvalhoi and Rana pipiens sequences as outgroups to estimate the evolutionary rate of duplicated genes in X. laevis and their relationship to X. tropicalis. See Supplementary Notes 7 and 8 for more detail.
Deletions and pseudogenes
Pseudogene sequences contain various defects including premature stop codons, frameshifts, disrupted splicing, and/or partial coding deletions. 985 pseudogenes were identified among 1,531 ‘2-1-2 regions’, with the others deleted or rendered unidentifiable by mutation. 368 out of 985 could be timed, based on the accumulation of non-synonymous and synonymous substitution between a pseudogene, its homoeologue and its orthologue in X. tropicalis, providing a time since the loss of constraint for each pseudogene37. See Supplementary Note 9 for additional details.
Functional annotation of genes
We used several bioinformatic methods and high-throughput datasets to assign functional annotations to Xenopus genes. Protein domains were assigned using InterPro (including PFAM and Panther)51 and KEGG52. Gene Ontology was assigned using InterPro2Go51. We identified genes that encode mitochondrial proteins by mapping the MitoCarta53 database from mouse to the most recent X. tropicalis proteome. Xenopus genes associated with germ plasm were manually curated using the extensive Xenopus literature (Supplementary Note 13).
We analysed transcriptome data generated for 14 oocyte/developmental stages and 14 adult tissues in duplicate except for oocyte stages (see Supplementary Note 4). Expression levels were measured by mapping paired-end RNA-seq reads to predicted full length cDNA and reporting transcripts per one million mapped reads (TPM). We consider the limit of detectable expression to be TPM >0.5. Co-expression modules were defined by weighted gene correlation network analysis (WGCNA) clustering54 (Supplementary Note 12).
We determined DNA methylation levels (DNAme) by whole genome bisulfite sequencing and used ChIP–seq to generate profiles of the promoter mark histone H3 lysine 4 trimethylation (H3K4me3), the transcription elongation mark H3K36me3, as well as RNA polymerase II (RNAPII) and the enhancer-associated co-activator p300. To test which regulatory features would contribute most to the L versus S expression differences, we applied a Random Forest machine learning algorithm to analyse differential expression between the L and S homoeologues (See Supplementary Note 14).
The XENLAv9.1 genome assembly and annotation are deposited at NCBI (accession LYTH00000000. The DNA read libraries of X. laevis and X. borealis were deposited at the Sequence Read Archive under accessions SRP071264 and SRP070985, respectively. Datasets of the X. laevis RNA-seq short reads were deposited in NCBI Gene Expression Omnibus (accession number GSE73430 for stages, GSE73419 for tissues). Datasets of the Hymenochirus RNA-seq short reads were deposited in NCBI GEO (accession number GSE76089). The epigenetic data have been deposited in NCBI’s Gene Expression Omnibus and are accessible through GEO Series accession numbers GSE76059 for ChIP–seq. MethylC-seq data are accessible through GEO Series accession number GSE76247. The sequence data from BAC and fosmid clones have been deposited to DDBJ/GenBank/EMBL under the accession numbers: (i) GA131508–GA227532, GA228275–GA244139, GA244852–GA274229, GA274976–GA275712, GA277157–GA344957, GA345673–GA350926 and GA351685–GA393223 for the XLB1 end-sequences; (ii) GA720358–GA756840 for the XLB2 end-sequences; (iii) GA756841–GA867435 for the XLFIC end-sequences and (iv) AP012997–AP013026,AP014660–AP014679, AP017316 and AP017317 for the finished BAC/fosmid sequences.
Please see Supplementary Note 15 for funding information.
Extended data figures
This zipped file contains Supplementary Table 1-11.