The draft genome of a socially polymorphic halictid bee, Lasioglossum albipes
- Sarah D Kocher1, 2, 7Email author,
- Cai Li†2, 3,
- Wei Yang2,
- Hao Tan2,
- Soojin V Yi4,
- Xingyu Yang4,
- Hopi E Hoekstra1, 5,
- Guojie Zhang2, 6,
- Naomi E Pierce1 and
- Douglas W Yu7, 8Email author
© Kocher et al.; licensee BioMed Central Ltd. 2013
Received: 17 July 2013
Accepted: 20 December 2013
Published: 20 December 2013
Taxa that harbor natural phenotypic variation are ideal for ecological genomic approaches aimed at understanding how the interplay between genetic and environmental factors can lead to the evolution of complex traits. Lasioglossum albipes is a polymorphic halictid bee that expresses variation in social behavior among populations, and common-garden experiments have suggested that this variation is likely to have a genetic component.
We present the L. albipes genome assembly to characterize the genetic and ecological factors associated with the evolution of social behavior. The de novo assembly is comparable to other published social insect genomes, with an N50 scaffold length of 602 kb. Gene families unique to L. albipes are associated with integrin-mediated signaling and DNA-binding domains, and several appear to be expanded in this species, including the glutathione-s-transferases and the inositol monophosphatases. L. albipes has an intact DNA methylation system, and in silico analyses suggest that methylation occurs primarily in exons. Comparisons to other insect genomes indicate that genes associated with metabolism and nucleotide binding undergo accelerated evolution in the halictid lineage. Whole-genome resequencing data from one solitary and one social L. albipes female identify six genes that appear to be rapidly diverging between social forms, including a putative odorant receptor and a cuticular protein.
L. albipes represents a novel genetic model system for understanding the evolution of social behavior. It represents the first published genome sequence of a primitively social insect, thereby facilitating comparative genomic studies across the Hymenoptera as a whole.
Social behavior holds special distinction in evolutionary biology because it represents a major transition from an individual to a coordinated group . Despite this additional layer of complexity, the same genetic and genomic methods used to study complex behaviors in model systems can be applied to the study of sociality.
One such approach is to combine genetic and ecological studies to understand how genes and the environment shape the striking diversity of behaviors that occur within and between species. Taxa harboring natural variation in a trait of interest - whether it be morphological, physiological, or behavioral - are ideal because they enable quantitative and population genetic studies to elucidate some of the underlying genetic components [2, 3]. Over the past few years, this approach has helped to illuminate some of the genetic and ecological factors associated with repeated evolution of both morphological and behavioral traits: examples include benthic and limnetic forms in sticklebacks [4, 5], coat color in mice [6, 7], mimicry rings in Heliconius butterflies , and song performance in crickets [9, 10].
Halictid bees (Hymenoptera: Halictidae) or ‘sweat bees’ are small- to medium-sized bees with a cosmopolitan distribution and over 4,000 described species. They are mass provisioners and pollen feeders, and nest primarily in the ground. Most species are solitary, but many are primitively eusocial (as defined by ). These species produce colonies composed of a facultatively sterile worker caste and only one or a few reproductive individuals that are not morphologically distinguishable from each other [11, 12].
Halictids are particularly useful models for behavior because they harbor extensive variation in social behavior both within and between species [13, 14]. Within the Halictidae, eusociality has evolved at least twice, with many subsequent reversions [15, 16]. The origins of eusociality in this group are relatively young (approximately 22 to 35 millions of years ago; [15, 16]), and perhaps because of this, a great deal of variation in social behavior exists, ranging from solitary to communal to eusocial (reviewed in [13, 14]). Interestingly, some of these species are socially polymorphic, and females are capable of producing either solitary or social nests. These social polymorphisms can occur across geographical gradients or even within populations [17–20].
One species in particular represents an ideal system for exploring the genetic mechanisms underlying social behavior: Lasioglossum albipes. This socially polymorphic species is solitary in inland localities in France and Germany, but eusocial in southwestern France where the climate is warmer and nests are initiated earlier in the summer [11, 18]. The life cycle of the social females is typical for a eusocial species with a univoltine life history (that is, one generation per year). Females found a nest in the spring and rear a first brood of workers that then help rear a second brood of reproductive males and females that subsequently mate and diapause through the winter to repeat the cycle the following spring. The life cycle of the solitary populations is the same except that the first, eusocial worker brood is not produced. Common-garden experiments were conducted with L. albipes in which both social forms were reared in the laboratory under the same conditions and also under complementary photoperiods; the typical behaviors for each population remained the same in the lab as in the field, suggesting that this behavioral polymorphism is likely to have an underlying genetic component . This system thus provides an excellent model for studying the ecological and genetic factors associated with the evolution of social behavior.
Here we present the draft genome of this socially polymorphic bee, the first halictid for which genomic resources have been developed. We compare its genome sequence to other published insect genomes and identify a number of interesting patterns that can be tested in future studies.
Results and discussion
Genome sequencing and assembly
Data used for genome assembly and scaffolding
Insert size (bp)
Read length (bp)
Raw data (Gb)
Data after filtering (Gb)
GC content (%)
Genome assembly statistics
Largest contig (bp)
Scaffolds >1 kb (n)
N50 scaffolds (bp)
Scaffolds >N50 (n)
Largest scaffold (bp)
Ultra-conserved core eukaryotic genes
RNA sequencing was performed on four pooled adult females collected from field sites in France and Switzerland (Additional file 1). RNA was extracted and a 2 × 100 paired-end library was sequenced on an Illumina HiSeq 2000. The resulting 35,207,669 reads were mapped back to the reference genome (approximately 230× coverage assuming a 30 Mb transcriptome) using Tophat , and 23,308 transcript models were generated using Cufflinks . These data were incorporated into the gene annotation pipeline (see below for details) to refine gene annotation.
Gene family expansion
We also characterized over- and under-represented IPR domains in the L. albipes gene set in comparison to A. mellifera. IPR domains with >2-fold difference between L. albipes and A. mellifera were considered as over- or under-represented. There were 92 IPR domains overrepresented in L. albipes (Additional file 10), including some associated with the expanded gene families discussed above, such as IPR017933 and IPR000760. Additionally, the MADF domain (IPR006578) has 42 copies in L. albipes but only nine in A. mellifera. This domain is associated with transcription factor Adf-1 in Drosophila, and is known to play a role in the regulation of alcohol dehydrogenase expression . There are also several fatty acid-related domains over-represented in L. albipes (IPR015876, IPR005804 and IPR020842). Previous studies in H. saltator found expression of a fatty acid synthase to be upregulated in reproductive females relative to workers .
Gene family contraction
Several genes appear to be lost in L. albipes but present in the six other sequenced hymenopterans (Additional file 11), and 36 IPR domains are under-represented in the L. albipes gene set when compared with A. mellifera (Additional file 12). One under-represented domain of interest is IPR017996 (‘Major Royal Jelly’ protein (MRJP)). Yellow and royal-jelly-like proteins control expression of genes affecting cuticular pigmentation, development, sexual maturation and behavior , and are associated with caste determination in the honey bee . We manually curated the yellow and MRJP gene families, and found 10 yellow genes in L. albipes, the same number as in A. mellifera. In contrast, only two credible MRJP genes were found in L. albipes, similar to the number found in the ant species C. floridanus and H. saltator. The ML tree of yellow genes and MRJP genes is shown in Additional file 13.
Epigenetic mechanisms can play an important role in gene regulation and phenotypic plasticity. DNA methylation appears to be one of the key mechanisms underlying transgenerational epigenetic effects. DNA methylation is widespread across Hymenoptera  and has been implicated in caste differentiation in honey bees and ants [31, 35, 36].
DNA methyltransferases (DNMTs) are the genes that perform DNA methylation; all share a conserved catalytic domain, suggesting a common and ancient origin . Studies of mammalian systems have established that different DNMTs undertake distinct functions (reviewed in ). For example, human genomes contain two DNMT1s, one DNMT2, and one DNMT3 (DNMT3a/b). DNMT1 is responsible for maintaining the patterns of DNA methylation between DNA replications and is referred to as the ‘maintenance methyltransferase’. The role of DNMT2 is still not completely resolved, but recent studies suggest that it may act as a tRNA methyltransferase. Finally, DNMT3s mediate de novo methylation of previously unmethylated cytosines.
We investigated whether L. albipes exons contain a complete repertoire of putative DNMTs. Using a homology-based search (Additional files 14 and 15), we found strong evidence that the L. albipes genome encodes two putative xDNMT1s (Lalb_01810 and Lalb_06290), one putative DNMT2 (Lalb_08279), and one putative DNMT3 (Lalb_11571). These results demonstrate that L. albipes appears to have an intact DNA methylation system.
CpG content in and around genes
DNA methylation patterns show a high degree of conservation across insect taxa. Methylation appears to occur primarily in exons and in 5′ UTRs (untranslated regions) and has been implicated in alternative splicing [39–42]. In animal genomes, DNA methylation occurs primarily at CpG dinucleotides (cytosine followed by guanine). Because methylated cytosines undergo frequent deamination and tend to mutate to thymines, methylated CpG regions tend to have lower frequencies of CpG dinucleotides . To investigate the presence of DNA methylation and its influence, we examined normalized CpG content (CpG O/E) across different genomic regions in L. albipes. Regions with lower CpG content than expected are interpreted as a signal of methylation .
Somewhat surprisingly, GpC O/E values also varied significantly between CDS and the genomic background (P <10-160), though these differences were less pronounced than they are for CpG O/E (Figure 4B). This was caused by G+C content skew in CDS, which are particularly GC-enriched in L. albipes (Additional file 16). Interestingly, there is a strong negative correlation between GpC O/E and GC content as well as between CpG O/E and GC content (Additional file 17). After controlling for underlying GC content variation, only CpG O/E ratios exhibit clear and substantial differences from the genomic background (Additional file 18), providing strong support for DNA methylation in L. albipes exons.
Based on these results, we propose that DNA methylation occurs in the L. albipes genome, although experimental validation will be necessary. A subset of 1,801 genes harbor extreme differences in CpG and GpC O/E values and are likely to reflect methylation in these regions (Additional file 19). The negative correlation between normalized CpG and GpC content versus GC content is unique in the L. albipes genome and appears to be opposite to the pattern observed in the honey bee , suggesting that additional, unknown evolutionary forces are acting on the nucleotide composition of L. albipes.
L. albipes is the first bee whose genome has been characterized that does not belong to the corbiculate bees (Hymenoptera: Apidae) and, as such, represents a novel lineage for comparative studies aimed at identifying the molecular toolkit associated with the evolution of social behavior. To identify genes showing signatures of accelerated evolution in L. albipes (halictid bees) and/or Apoidea (all bees), we conducted branch-specific tests in PAML . We chose six species representative of the sequenced Hymenopteran genomes to perform these analyses. These taxa include two bees (L. albipes and A. mellifera), two ants (H. saltator and S. invicta), the parasitoid wasp, N. vitripennis, as an outgroup to the social Hymenoptera, and the fruit fly, D. melanogaster, as an outgroup to the Hymenoptera as a whole. We used the ‘branch’ model in PAML to search for signatures of accelerated evolution in focal lineages using a likelihood-ratio test (LRT) to calculate significance. Following correction for multiple testing, 615 genes showed signatures of accelerated evolution in the L. albipes lineage when compared to the remaining branches (FDR <0.05; Additional file 20), and 899 in Apoidea when contrasted to the remaining branches (FDR <0.05; Additional file 21).
Differences between social forms
To look for gross genetic differences between social forms, individual females from one solitary and one social population were sequenced to approximately 15× coverage. Remapping of these reads to the reference genome revealed that these individuals vary as much from each other as they do from the reference sequence, with 499,486 SNPs unique to the solitary female (compared to the social female and the reference sequence) and 493,579 SNPs unique to the social female (compared to the reference and solitary female). Per-site Watterson’s ΘW was calculated using four-fold degenerate nucleotides, and is estimated at 0.003. Comparisons with A. mellifera (ΘW approximately 0.09 for non-coding sites) () suggest potentially reduced level of genetic diversity of L. albipes compared to the honey bee.
The numbers of synonymous (Ks) and non-synonymous (Ka) substitutions and their ratio (Ka/Ks) were calculated for each gene to search for loci showing signatures of accelerated evolution between social forms. Sliding window analyses did not reveal any large genomic regions that appear to be differentiated between social forms, but six genes had Ka/Ks values >1, indicating that these sequences could be diverging rapidly between these two populations (FDR <0.1; Additional file 25). Two of these genes encode a putative odorant receptor (Lalb_14702) and a cuticular protein similar to apidermin-3 (Lalb_0725) (), perhaps indicating that differences in chemical signaling and/or pheromone production are associated with shifts in sociality. The remaining genes include: a metalloendopeptidase similar to neprilysin 1, which is associated with modulation of neurotransmitter levels and expressed in the brain mushroom bodies in Drosophila, and a receptor-type tyrosine-protein phosphatase associated with the regulation of axon guidance and also with autism in humans . These genes provide an interesting set of candidates for further examination, but given that these genetic differences were characterized between two individuals, further work examining multiple individuals from a number of solitary and social populations is needed to fully characterize signatures of selection between the solitary and social behavioral forms within L. albipes.
Its intraspecific behavioral variation makes L. albipes ideal for population and ecological genomic studies to characterize the underlying genetic components associated with solitary and social behavior. Our results suggest that mechanisms associated with DNA methylation and nutrient storage may play a role in modulating social behavior in this species, and future research will examine these pathways in more detail. The addition of L. albipes to the published hymenopteran genomes establishes a framework for further phylogenetic comparisons that we can use to investigate forces that have shaped the evolution of social behavior.
Materials and methods
Sample preparation and library construction
Whole bodies were first rinsed in ethanol then ground in liquid nitrogen to facilitate extraction of genetic material. DNA extractions were performed using a Qiagen Genomic-tip 20/G kit (Valencia, CA, USA) and standard protocol. Genomic DNA extracted from the samples Albi-2 and Albi-3 was used to generate non-amplified DNA libraries of 200 and 500 bp. To obtain sufficient genomic DNA, we performed a multiple displacement amplification on the Albi-2 sample using the REPLI-g Midi kit (Qiagen, Valencia, CA, USA) prior to library construction. This may have contributed to lower GC content within these libraries, and as such, additional 200, 500, and 800 bp libraries were constructed from unamplified genomic DNA from the Albi-3 sample. To improve genome assembly, genomic DNA from 20 pooled females was also used to construct an amplification-free 10 kb library.
For library construction, DNA was sheared to fragments of size 200 to 500 bp. Ends were repaired, A-tailed, and ligated to paired-end adapters (Illumina, San Diego, CA, USA). A size selection was then performed by agarose gel, and fragments were amplified with LM-PCR. Long-insert libraries were constructed by shearing genomic DNA to the appropriate insert size with nebulization (2 kb library) or HydroShear (5 kb and 10 kb libraries; Covaris, Woburn, MA, USA). Fragments were end-repaired with biotinylated nucleotide analogues (Illumina, San Diego, CA, USA), and size-selected fragments (2 kb, 5 kb, and 10 kb) were circularized via intramolecular ligation, sheared to 500 bp with Adaptive Focused Acoustic (Covaris, Woburn, MA, USA), and purified on magnetic beads (Invitrogen, Carlsbad, CA, USA). These purified fragments were then end-repaired, A-tailed, and ligated to paired end adapters (Illumina). A final size selection step and LM-PCR purification was conducted prior to sequencing.
For transcriptome sequencing, RNA was extracted from four individual females using a Qiagen RNeasy extraction kit (Valencia, CA, USA) and standard protocol. RNA was then pooled and cDNA libraries constructed.
First strand cDNA was synthesized using random hexamers and Superscript II reverse transcriptase (Invitrogen, Carlsbad, CA, USA). E. coli DNA PolI (Invitrogen) was used for second strand synthesis, and double stranded cDNA was then purified using the Qiaquick PCR purification kit (Qiagen, Valencia, CA, USA). Purified cDNA was sheared to 100 to 500 bp fragments with a nebulizer (Invitrogen), end-repaired, and a 3′ dA overhang added to the ends. Illumina adapters were ligated to the cDNA and size selected to 200 ± 20 bp on an agarose gel. Fifteen cycles of PCR amplification were conducted prior to sequencing. Gel-purification of 18 to 30 nt RNA was used for smRNA-seq. 5′ and 3′ Illumina RNA adapters were ligated to these fragments, and products were size-selected on a denaturing polyacrylamide gel. These purified products were then reverse transcribed with small RNA RT primers and amplified with small RNA PCR primers 1 and 2 (Illumina) with 15 cycles of PCR prior to sequencing.
SOAPdenovo  was used for genome assembly. We constructed a de Bruijn graph using the parameter ‘-K 47’. Then, default parameters were used to simplify the graph and generate contigs by removing tips, merging bubbles and solving repeats. All sequenced reads were then realigned onto the contig sequences with the parameters: ‘-k 47 -f’. Finally, scaffolds were constructed by weighting the rates of consistent and conflicting paired-end relationships with parameter: ‘-F -u’. All usable reads were realigned to contigs and paired-end information was used to assemble scaffolds and close gaps. Raw sequencing reads were mapped back to the scaffolds using SOAPaligner  with options ‘-m 0 -x 1000 -v 5’ for 200 bp, 500 bp, and 800 bp libraries, ‘-m 0 -x 10000 -R -v 3’ for 2 kb and 5 kb libraries, and ‘-m 0 -x 20000 -R -v 3’ for the 10 kb library. The results were used to check for GC bias in the sequencing data. Potential contaminants were filtered using BLASTN to align all assembled sequences against the NCBI nt database (version: 20110312), and sequences with best hits to bacterial or fungal sequences were removed from the assembly and excluded in downstream analyses. Completeness of the assembly was assessed using the CEGMA pipeline .
Known transposable elements (TEs) were identified with RepeatMasker (version 3.2.6) () using the Repbase TE library (v. 15.02) () and default parameters. A consensus sequence for each repeat family was generated and used as the library in RepeatMasker to identify additional high and medium copy repeats (>10 copies) in the genome assembly. Tandem repeats were predicted using TRF , with parameters set to ‘Match = 2, Mismatch = 7, Delta = 7, PM = 80, PI = 10, Minscore = 50, and MaxPeriod = 12’. In total, 107.29 Mb of repetitive sequence were identified, comprising 32.71% of the assembled genome (Additional file 2).
Protein-coding gene annotation
Three different methods were used to predict protein-coding genes: (a) homology-based methods, (b) de novo prediction, and (c) RNA sequencing. Gene sets from four species (C. elegans, D. melanogaster, H. saltator, and A. mellifera) were used for homology-based predictions, one species at a time. TBLASTN was used to search the non-redundant protein sequences of each gene set with an E-value <1e-5. The best hit was then selected, and regions with homologous blocks shorter than 50% of the query protein were excluded. We then used GENEWISE (v. 20.0) () to generate the gene structures. Homology-based repeats were masked in the genome, and AUGUSTUS  and SNAP  were used for de novo gene prediction. Parameters were trained using 2,682 high quality genes with intact ORFs based on homology to A. mellifera. Evidence derived from homology-based predictions (4 sets) and de novo predictions (2 sets) were then integrated in GLEAN to generate a consensus gene set. Based on these analyses, 22,068 genes passed the GLEAN criteria.
To improve gene annotation, RNA sequencing was performed on four pooled adult females collected from field sites in France and Switzerland (Additional file 1). Reads were mapped to the current genome assembly using Tophat , and then Cufflinks  was used to assemble the mapped reads into transcripts with the following parameters for Tophat: ‘-r 20 -mate-std-dev 10 -I 10000’ , and for Cufflinks: ‘-I 50000’. ORFs were predicted in assembled transcripts using BGI’s in-house pipeline, CCG. CCG also integrated the gene models from GLEAN with the transcript-based models in Cufflinks to generate an improved gene set.
Finally, manual curation and visual screening was performed to refine the final gene set. The transcript-based gene models with intact ORFs that had no overlap with the CCG gene set were added. If a transcript-based gene model with an intact ORF covered more than one homology-based gene, the homology-based gene would be replaced by the transcript-based gene model. Gene models supported by more than homology prediction but that had no overlapping genes in the gene set were added. Gene models predicted to be transposable element-related (based on IPRscan and Swiss-Prot annotation) were removed. Furthermore, genes of particular interest (for example, the expanded and contracted gene families) were manually checked. A final gene set of 13,448 genes was used for downstream analysis.
Protein function was assigned using BLASTP best hits to the Swiss-Prot database (E-value <1e-5). Gene motifs and domains were determined using by InterProScan  against the InterPro database . Gene Ontology (GO) annotations for each gene were obtained from the corresponding InterPro entry. The KEGG orthology  annotation was done by KAAS online server  using the SBH method. The pathways in which each gene might be involved were derived from the best KO hit. The statistics of functional annotation is provided in Additional file 11. All functional enrichment analyses were conducted using custom scripts.
ncRNAs were predicted using INFERNAL  and tRNAscan-SE . Four types of ncRNA were annotated: microRNA (miRNA), transfer RNA (tRNA), ribosomal RNA (rRNA), and small nuclear RNA(snRNA). tRNA genes were predicted by tRNAscan-SE with eukaryote parameters. rRNA fragments were identified by aligning the rRNA template sequences from invertebrate animal using BLASTN with an E-value <1E-5. miRNA and snRNA genes were predicted by INFERNAL using the Rfam database (release 9.1). To accelerate the speed, a rough filtering was performed before INFERNAL, by Blastn against the Rfam sequence database with an E-value cutoff of 1. Additional file 12 summarizes the statistics of ncRNA annotation.
Construction of gene families
To gain insight into the evolution of L. albipes gene families, we used Treefam  to cluster protein-coding genes from eight insect species (A. echinatior, S. invicta, C. floridanus, H. saltator, L. albipes, A. mellifera, N. vitripennis, and D. melanogaster) into gene families. Only the longest transcript isoform was used for each gene. BLASTP (with E-value <1e-5) was performed against a blast database including protein-coding sequences for all species. Graph based methods were used to join fragmental alignments for each gene using the solar package in Treefam. We assigned a connection (edge) between two nodes (genes) if more than one-third of the region was aligned in both genes. A H-score ranging from 0 to 100 was used to weigh the similarity (edge). For two genes G1 and G2, the H-score was defined as score (G1G2)/max (score(G1G1), score (G2G2)), (score = BLAST raw score). We used the average distance for the hierarchical clustering algorithm, requiring the minimum edge weight (H-score) to be larger than 10, the minimum edge density (total number of edges/theoretical number of edges) to be larger than 0.34. After clustering, we generated multiple alignments of protein sequences for each gene family using MUSCLE , and converted the protein alignments to CDS alignments. A Venn diagram including the Hymenopteran species is shown as Additional file 13.
Four-fold degenerate sites were used from the single-copy gene family alignments, and used to reconstruct the phylogeny of these eight species in MrBayes  with default parameters. Divergence times of the nodes were inferred using the ‘mcmctree’ package in PAML .
Gene family expansion and contraction
We used CAFÉ  to identify gene family expansions and contractions in L. albipes. This revealed two gene family expansions: glutathione-S-transferases (Additional file 15), and inositol monophosphatase (Additional file 16). Maximum-likelihood (ML) trees of the expanded families were constructed with PhyML . Roots of the trees were determined using the ‘root’ function in TreeBest .
Genes specific to L. albipes
We performed functional enrichment analyses with custom scripts using chi-squares and Fisher Exact tests (for small sample sizes) to calculate statistical significance. We then performed an FDR  correction to account for multiple testing. The GO/IPR/KEGG enrichment results for L. albipes specific genes are listed in Additional file 7: Tables S7, Additional file 8: Table S8 and Additional file 9: Table S9.
A gene was considered to be lost if it was absent in L. albipes but present in the six other hymenopteran insects (A. echinatior, S. invicta, C. floridanus, H. saltator, A. mellifera and N. vitripennis). To ensure these genes were not due to incorrect clustering or uncompleted annotation, we realigned these genes against the genome assembly. Genes that failed to pass the previous gene prediction criteria, but that had strong evidence of homology (Genewise score > = 70) and were supported by expression data (average coverage depth by RNA-seq data > 1) were reintegrated into the final gene set. Following this, 30 families were found to be lost in L. albipes. Each of the 30 families has only one homolog in A. mellifera (Additional files 11 and 12).
We used the other 11 species, including nine Hymenoptera species A. mellifera, N. vitripennis, H. saltator, C. floridanus, A. echinatior, S. invicta P. barbatus A. cephalotes and L. humile, as well as D. melanogaster and H. sapiens to identify ortholog groups with L. albipes with BLASTP (Additional file 24). For each gene set, we performed all-against-all blasts. Then, we filtered the results by requiring the aligned rates of both target and required that the query must be >50%. We used the reciprocal best hit (RBH) of Blast score to determine orthologs.
Characterization of DNA methyltransferases
We performed a BLASTP search against the human (Homo sapiens), honeybee (A. mellifera), chicken (Gallus gallus), and Nasonia (N. vitripennis) dnmts using all L. albipes proteins as queries. Then potential L. albipes homologs and their query sequences were used to construct a phylogenetic tree using maximum-likelihood using the JTT model.
where P CpG , P c , and P G represent the frequencies of CpG dinucleotides, C nucleotides, and G nucleotides, respectively, estimated from each genomic fragment. Because GpC dinucleotides have the same sequence composition as CpG dinucleotides, but are not subject to DNA methylation, this calculation represents a negative control. See  for further methodological details.
To account for the strong negative correlation between G+C content and both CpG and GpC O/E values, we divided genes and genomic fragments into five groups according to their G+C content, specifically, G+C < 0.35, 0.35 ≤ G+C < 0.45, 0.45 ≤ G+C < 0.5, 0.5 ≤ G+C < 0.55 and G+C ≥ 0.55. This allowed us to compare CpG O/E and GpC O/E of different genomic regions while accounting for G+C content.
Potentially methylated CDS are defined as those with significantly lower CpG O/E than the genomic background while exhibiting not significantly different GpC O/E than the genomic background. We performed a permutation test to determine whether CpG O/E of a specific gene is significantly lower than genome background. P values were determined as the ratio of 1,000 bp genomes fragments whose CpG O/E (GpC O/E) is lower than the focal fragment. The P values were then FDR-adjusted for multiple testing. With FDR <0.2, we observed 1,814 CDs with significantly lower CpG O/E while only 27 CDs with significant lower GpC O/E. Among the 1,814 CDs, 13 of them exhibit both significantly lower CpG O/E and GpC O/E. After discarding those 13 CDs, we considered the remaining 1,801 CDs as potentially methylated.
We used PAML to search for genes showing signatures of accelerated evolution in (a) the L. albipes lineage or (b) the Apoidea lineage. We chose six species (L. albipes, A. mellifera, H. saltator, S.invicta, N. vitripennis, and D. melanogaster) to perform the accelerated evolution analyses. First, the phylogenetic tree was inferred from the four-fold degenerate sites of orthologous groups in the six species. To do LRTs with PAML, we ran one-rate branch models (‘model = 0’ in PAML control file) and two-rate branch models (‘model = 2’ in PAML control file). Two kinds of two-rate branch models were run: one for the L. albipes lineage, the other for the Apoidea lineage. Other parameters set in the PAML control file were ‘codonfreq = 2, kappa = 2.5, initial omega = 0.2, and fix alpha = 1’. P values were FDR-adjusted with a cutoff of 0.05. Functional enrichment analyses were then conducted for the genes that were found under accelerated evolution (Additional files 14, 15, and 16).
Individual resequencing data
Individual females from a solitary and social population were sequenced to approximately 15× coverage on an Illumina HiSeq (2 × 150, paired end) in order to look for large genetic differences between social forms. DNA from each female was extracted using the AutoGen DNA extraction kit (AutoGen, Holliston, MA, USA). Whole bodies were first rinsed in ethanol then ground in liquid nitrogen to facilitate extraction of genetic material. DNA was sheared to approximately 400 bp using HydroShear (Covaris, Woburn, MA, USA). Libraries were constructed using the PrepX ILM DNA Kit for the Apollo 324 system (IntegenX, Pleasanton, CA, USA), and sequenced with a Rapid Run (2 × 150 bp) on an Illumina HiSeq 2500.
Reads were quality checked using FastQC  and were then mapped back to the reference genome using Stampy  using default parameters. Variants were called following the best practices in the Genome Analysis Toolkit v2.7.2 (Broad Institute, Cambridge, MA, USA) and included a local realignment step and variant calling with Haplotype Caller. SNPs were filtered using the following parameters: QD <2.0, FS >60.0, MQ <40.0, HaplotypeScore >13.0, MappingQualityRankSum <-12.5, and ReadPosRankSum <-8.0. Nucleotide diversity was calculated using vcftools , and ΘW was estimated from four-fold degenerate nucleotides using custom scripts (available upon request). Ka/Ks calculations were performed using KaKs calculator using the YN model averaging method , and FDR-corrections were performed with the P adjust package in R (v2.12). Sliding windows were calculated in 100 kb increments across the genome to look for tracts with a high degree of differentiation. Alignments of significant genes were manually checked; one gene (Lalb_07521) was excluded from the list due to uncertainty in read mapping (possibly from a paralogous gene).
This whole genome shotgun project has been deposited at DDBJ/EMBL/GenBankunder the accession SRP016091. The version described in this paper is the first version, SRP016091. The RNA sequencing reads have been deposited in the short read archive under the accession SRX190462, and the individual resequencing data have been deposited in the short read archive under the accessions SAMN02429130 and SAMN02429131.
Naomi E. Pierce and Douglas W. Yu are co-seniors authors.
Core eukaryotic genes
Major royal jelly proteins.
We thank Cecile and Luc Plateaux-Quenu for providing guidance, encouragement, and field assistance throughout this project, D. Michez, P. Rasmont, L. Keller, M. Chapuisat, L. Pellissier, W. Tong, E. Youngsteadt, J. Ayroles, and A. Finklestein for field support and assistance. This work was funded by Yunnan Province (20080A001), the Chinese Academy of Sciences (0902281081, KSCX2-YW-Z-1027), the National Natural Science Foundation of China (31170498), the University of East Anglia, and the State Key Laboratory of Genetic Resources and Evolution at the Kunming Institute of Zoology awarded to DWY, and by a John Templeton Foundation FQEB Prize fellowship, a USDA NIFA Postdoctoral fellowship and two Putnam Expedition grants from the Museum of Comparative Zoology awarded to SDK. NEP and SDK were supported by NSF SES-0750480 and NSF IOS-1257543.
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