Sequencing, assembly and annotation of the D. albomicans genome

The availability of 12 Drosophila genomes helps us to optimize the assembly. We inferred that conserved syntenic protein-coding gene pairs whose order and orientation are the same among all the 12 Drosophila genomes should have experienced few rearrangements in the D. albomicans genome. We then collected scaffolds that aligned to the same gene or to regions consisting of conserved syntenic gene pairs [20], and merged 1,433 scaffolds into 701 super-scaffolds. The final female reference genome assembly of D. albomicans has an improved scaffold N50 from 31.9 kb to 49.0 kb (Table 1). To validate the assembly accuracy, we designed primer pairs for 154 fragments randomly selected throughout the genome, about half of which span at least one gap region. 148 pairs (96%) successfully produced unique PCR products with expected lengths, with the remaining 4% all spanning a gap region that may be too long to be amplified. We also aligned the assembly against 820 EST sequences derived from a male of another strain of D. albomicans [9], and 88.5% of ESTs aligned to the genome assembly with an overall identity of 98.8%. Contamination is low: only 289 scaffolds, comprising 739 kb (0.3% of the total sequence) showed evidence for human or bacterial sources. These results show that we have produced a high-quality draft assembly of the D. albomicans genome.

We annotated 14,042 protein-coding genes on non-B scaffolds and 272 genes in male-specific scaffolds (and thus candidate B-linked genes), using both de novo gene prediction and homology-based methods. We found that 5.5% of the D. albomicans genome consists of repetitive elements (compared to 5.35% of D. melanogaster [21], Additional File 4), suggesting that our short-read assembly has captured a sizeable fraction of repeat sequences. Finally, previous analysis of 12 Drosophila genomes has shown that 95% of genes exhibit no movement between chromosome arms (called 'Muller elements' in Drosophila species) across species [20]. This allowed us to assign 11,949 (85.1%) D. albomicans protein-coding genes or 5576 scaffolds (109 Mb, 52.8%) into chromosome arms based on their alignments with the D. virilis genome.

Genomic divergence between the neo-sex chromosomes

To investigate the divergence between the neo-sex chromosomes after recombination ceased, we mapped male and female reads separately to the female genome and characterized the level of variation for each chromosome. SNP and short indel (< 6 bp) densities calculated from female reads against the neo-X reference reflect segregating variation among different neo-X chromosomes, whereas those derived from the less inbred males reflect both neo-X/Y divergence and segregating variation among different neo-X chromosomes. Sequence coverage is similar across chromosomal arms and thus should not bias comparisons across chromosomes (Additional File 5).

Females generally show lower levels of variation relative to males (Figure 2, Additional File 6 and 7), consistent with the more severe inbreeding of the females used for sequencing. The neo-X reveals a similarly low level of SNP density as the ancient X chromosome relative to autosomes, either due to the bottleneck effect of inbreeding or very recent selective sweeps [22, 23]. In contrast, SNP density of the neo-sex chromosome calculated from male data is much higher than that of the ancient X (P < 10^-3, Chi-square test, Table 2, Figure 2A). Elevated SNP density levels on the neo-sex chromosomes of males can mainly be attributed to sequence divergence between the neo-X and neo-Y chromosome. Indeed, the ratio of SNP density in males versus females is significantly higher for the neo-sex chromosomes (which in males includes both segregating neo-X variants and neo-X/neo-Y divergence) relative to the ancient X and the autosomes (Table 2, Fisher's exact test, P < 0.01). Fixed neo-X/neo-Y differences are necessarily present in the male reads pool at a roughly 1:1 ratio whereas segregating variation on either chromosome may be found at a variety of frequencies. Consistent with many neo-sex-linked SNPs in males reflecting fixed differences between the neo-X and neo-Y alleles, the fraction and density of SNPs present at a ratio around 1 is the highest on the neo-sex chromosomes in males (17.7% and 0.7 sites/kb; Additional File 8). Thus, these data demonstrate that the neo-X/neo-Y chromosome pair has already started to diverge within only 0.12 MY. However, the non-recombining fourth chromosome shows similarly increased levels of diversity in males relative to females, indicating that some sampling effects on chromosome-specific differences in levels of diversity between the sexes cannot be ruled out. Interestingly, although both neo-X polymorphisms and neo-X/neo-Y divergence contribute to the overall SNP density of the neo-sex chromosomes in males, it is still lower than that of autosome 2 (Figure 2A, but not within coding regions, see below). This could be explained by longer coalescent times for autosomes than neo-sex chromosomes, or by demographic factors or selective sweeps reducing neo-X diversity as mentioned above. Also, excessive inversion polymorphisms of autosome 2 (see [24] and also Additional File 9) could result in a higher overall SNP density [25]. It will be of great interest to study patterns of diversity of the various chromosomes in more detail using a larger population sample.

Early degeneration of neo-Y coding regions

The divergence between the neo-X and neo-Y is likely caused by the accumulation of deleterious mutations on the neo-Y after the inhibition of homologous recombination [2]. To investigate this process, we compared patterns of SNP densities in the coding regions of neo-X- and neo-Y-linked sequences. We found that the male to female ratio of exonic SNP density is higher on neo-sex chromosomes than on any other chromosome (Table 2), suggesting an excess of mutations accumulating in coding regions of neo-Y-linked genes. To evaluate their deleterious effects, we characterized putative pseudogenes on the neo-Y chromosome whose coding regions contain premature stop codons or frame-shift mutations. We first identified ancestral pseudogenes (i.e. those shared between the neo-X and neo-Y chromosome) by mapping female reads to the reference genome and keeping only those genes that were not found to be pseudogenized in the female data. After applying the same procedure to all chromosomes, we identified a total of 80 putative pseudogenes that mapped to the neo-sex chromosome in males, a significantly higher fraction than on any other chromosome (P < 0.05, Fisher's exact test, Table 2). These pseudogenized presumably neo-Y-linked alleles did not show any significant enrichment for specific gene ontology (GO) terms, suggesting that genes are inactivated randomly during early neo-Y degeneration [5]. Additionally, the neo-sex chromosome genes show slightly higher levels of pairwise nonsynonymous diversity (Table 2) and slightly relaxed constraint on synonymous sites (as measured by codon usage indices; Additional File 10).

Together, these data suggest that deleterious mutations have already begun to accumulate at some neo-Y protein-coding genes. The proportion of pseudogenized neo-Y loci in D. albomicans (2% of total neo-X loci in 0.12 MY) is much lower than that in D. miranda (46% of genes have become non-functional [5]), a species where a neo-sex chromosome originated about 1 MY ago. The neo-X chromosome of D. miranda shows partial dosage compensation [26], which can render some genes on the neo-Y functionally redundant and speed up Y degeneration of genes that are dosage compensated on the neo-X. Also, the rate of degeneration is expected to be highly non-uniform over the course of Y evolution, and different evolutionary processes causing mutation accumulation show different temporal dynamics [27]. In particular, Muller's ratchet and background selection are more likely to dominate degeneration of Y chromosomes at very early stages, such as that of D. albomicans, while genetic hitchhiking of deleterious mutations together with beneficial alleles is more likely to contribute to Y degeneration at later stages [27]. It will be of great interest to test the role of these evolutionary models of Y degeneration using population genomic studies of the D. albomicans neo-sex chromosomes.

The neo-Y has an excess of tandem duplications

We also investigated structural variants (SVs) in the D. albomicans genome, including duplications, inversions and large-scale insertion/deletion events (> 150 bp). To identify SVs, we took advantage of abnormally aligned read mate-pairs mapped against our reference genome. For example, sequence reads from the same insert are supposed to have opposite orientations when aligned to the reference genome. However, reads surrounding the breakpoint of tandem duplications would instead face the same orientation [28] (Additional File 11). Since females are more inbred and were used for the initial genome assembly, many fewer reads derived from females showed mate-pair violations (31.8% of male pairs versus only 4.5% of female pairs).

By characterizing all the abnormally aligned mate-pairs against the reference genome, we detected a total of 86,890 SVs (each SV event is supported by at least 3 mate-pairs, see Methods). We found deletions to be more common than insertions on all chromosomes (50% to 70.3% SV sites, Additional File 9 and 12), consistent with a previous report in other Drosophila species [29]. Intriguingly, we found the male-to-female ratio of tandem duplications to be highest on the neo-sex chromosome among all the chromosomes and types of SVs investigated (Figure 3A and Additional File 9), suggesting an accumulation of tandem duplications on the neo-Y. The lack of recombination on the neo-Y implies that it is mechanistically harder to remove pre-existing duplicated sequences through a recombination event. In addition, reduced efficiency of purifying selection on the neo-Y could lead to less efficient elimination of slightly deleterious duplicated sequences. Notably, neo-Y chromosomes have the highest proportion of tandem duplicates overlapping with coding regions, supporting the notion that slightly deleterious effects of extra gene or exon doses associated with these tandem duplications are not being effectively purged from the neo-Y (Figure 3B). Interestingly, we found no bias in the chromosomal distribution of dispersed duplications (Additional File 13). Unlike for tandem duplications, the removal of dispersed duplications probably does not rely on homologous recombination between alleles, and thus their distribution may be less influenced by differences in the recombination environments of the neo-sex chromosomes.

Origin and evolution of B chromosomes

To understand the genomic composition and functional significance of B chromosomes in D. albomicans, we attempted to isolate B chromosome sequences and identify B-linked genes. We first randomly selected scaffolds from the 17 Mb of male-specific sequence and performed PCR amplification using females of different D. albomicans strains with and without Bs. However, none of the 25 scaffolds tested showed clear linkage to B chromosomes, suggesting that B chromosomes either largely share sequences with standard chromosomes or that the identified scaffolds are either male-specific (neo-Y or Y-linked), located in heterochromatic sequences that could not be mapped or assembled with the lower-coverage female data, or represent polymorphisms segregating in the less inbred male data. We thus took advantage of a previously identified 260 bp B-linked fragment, which was cloned using subtractive hybridization (W.W., unpublished data, Figure 4A), to bait B-specific sequences. Four scaffolds showed high levels of sequence similarity to this probe, with scaffold S51440 giving the best match (Additional File 14). To validate the assembly of this scaffold and confirm that it is indeed B-specific, we designed ten primer pairs spanning and surrounding the aligned region on this scaffold. One pair of primers amplified a fragment of the expected length in all B-containing isofemale strains but not in strains lacking B chromosomes (in a total of 8 lines tested), thereby confirming that the amplified sequence is B-specific (Figure 4B). All other primer pairs amplified products in both B and non-B strains, indicating that this scaffold is largely composed of sequences highly similar to standard chromosomes. This high level of sequence homology would explain why our genomic approach failed to identify B-linked sequences based on presence/absence of DNA scaffolds in samples with and without B chromosomes. Interestingly, we were able to successfully detect transcription from this B-linked fragment using an RT-PCR assay. This fragment carries a transcribing unit homologous to the gene shg on chr2R and contains a diagnostic SNP in all the four B-containing strains but not in the four non-B strains, implying that functional genes may exist on this B chromosome.

Intriguingly, almost all the sequences of the four scaffolds that show homology to the B-derived sequence are homologous to regions that are located on the ancient X and/or the neo-X chromosome of D. albomicans, and the scaffold with the highest sequence similarity to the B-specific probe (scaffold S51440) contains sequence mapping to both chromosomes (Additional File 15). Notably, different portions of S51440 mapped to sub-centromeric and sub-telomeric regions of the ancient X and neo-sex chromosomes, respectively, and this mapping holds across a range of Drosophila species (Additional File 15). In addition, S51440 shows three-fold elevation in simple repeat content compared to the rest of the genome (20.86% versus 6.69%; Table S2). We also aligned male reads containing B sequences and female reads without B sequences to the reported Drosophila centromeric sequences [30]. The proportion of male reads that align to these centromeric sequences is much higher than that of female reads (1.2 × 10^-5 vs. 3.2 × 10^-6), although it is unclear how much of this can be attributed to sequences contained in the neo-Y or the ancestral Y chromosome. Taken together, these characteristics of candidate B-linked sequences suggest that D. albomicans B chromosomes may have originated as a byproduct from (sub-)centromeric/telomeric fragments created by the fusion of the ancient third autosome and the ancestral sex chromosomes. Consistent with an association between the formation of B and neo-sex chromosomes, all close relatives of D. albomicans within the D. immigrans species group lack the 'neo-sex' fusion [7, 9] as well as B chromosomes. B chromosomes may have subsequently acquired some unique sequences or genes after their origination by mutations or rearrangements.

These insights allow us to further develop a model of neo-sex and B chromosome evolution in D. albomicans. It has been hypothesized that centromere-fused chromosomes may be favored during asymmetrical female meiosis if the excess of centromeric satellites facilitates their entry into oocytes [31, 32]. Such a selective advantage would apply to the neo-X fusion, i.e., the fusion of the third autosome (chr3) to the ancestral X chromosome (chrX) but not the male-limited neo-Y. Indeed, the neo-X chromosome remains polymorphic within experimental hybrid populations from female D. albomicans and male D. nasuta, which contain both the fused chrX and chr3 (i.e. the neo-X) and unfused chrX and chr3 (i.e. the ancestral conditions), but no neo-Y chromosomes [33]. Further, the neo-X can increase in frequency in such a hybrid population in a background with neo-Y chromosomes [33]. In contrast, a polymorphic neo-Y is excluded within a few generations in hybrids without the neo-X fusion. The formation of the neo-X could result in centromeric imbalances between paired chromosomes in males [34], which could have been remedied by a second fusion producing the neo-Y [33] or by loss of centromeric fragments of the neo-X. Indeed, a polymorphic neo-Y can reach fixation within a few generations in hybrids containing the neo-X [33]. The lost centromeric fragments from these fusions could have given rise to the B chromosomes found in D. albomicans. This, of course, does not exclude the possibility that genes or genomic regions derived from other chromosomes also contributed to the formation of B chromosomes, and they may be maintained within the population because of newly acquired functions. This might explain the fact that D. albomicans strains with 1-2 B's produce significantly more offsprings than strains with no or more B chromosomes (Additional File 16) [18]. Further identification of B-linked scaffolds and the genes they carry will help to understand the phenotypic effects of B chromosomes in D. albomicans.

Fly strains and karyotyping

We collected D. albomicans individuals from the wild in Kunming, China, and established isofemale strains for genome sequencing. We karyotyped a total of 15 strains following the method described in [35]. In brief, ganglions were dissected from third stage instar larvae and treated with 0.065 mg/ml of colchicine solution, followed by hypotonic treatment with 0.075 mol/l KCL solution. After fixation by Carnoy solution, we dried the slides and stained them with Giemsa solution (Fluka) for 1.5 h and then washed them in water. Metaphase images were then captured under a microscope (Nikon). B-chromosome number in the Kunming D. albomicans population ranges from 0 to 7 (Additional File 2). We selected one strain, KM55-5, containing 1-2Bs in about 70% investigated karyotypes, since carrying 1-2 Bs has been shown to maximize offspring number in D. albomicans [18]. The strain was karyotyped every 2 generations to assure B-chromosome maintenance, and reared for 13 generations before DNA extraction. We picked around 40 males and extracted their genomic DNA with a PUREGENE DNA Isolation Kit (Gentra System). To screen individuals without Bs from this strain, we inbred pairs of one single male and one virgin female for four generations and karyotyped their offspring (at least 20 larvae).

We established a primary cell line using early stage embryos (4-6 h) of the KM55-5 strain to estimate the genome size of D. albomicans [36]. About 5 × 10⁵ cells were harvested and washed twice with PBS solution. Cells were then transferred to FACS tubes kept on ice, and 50 μl RNase A (1 mg/ml) and 100 μl propidium iodide (PI, 1 mg/ml) were added to each sample. Samples were analyzed on a FACScan flow cytometer (Becton Dickinson). The result was then compared with chicken red blood cells and Drosophila S2 cells which were prepared at the same time.

Sequencing and assembling

Solexa library preparation and sequencing followed the manufacturer's standard instructions (Illumina). Briefly, we prepared 5 ug genomic DNA from outbred virgin B-containing males and inbred virgin females without Bs, shearing them with Nebulizer (Invitrogen). Paired-end libraries were prepared and subject to Solexa sequencing, with read sequencing from both ends. Lanes yielding an abnormal GC content or read bases with low Q20 length (< 30 bp) were removed from the raw data before assembly or mapping. We used EST sequences generated from a cDNA library derived from males of another D. albomicans strain (strain 15112-1751.4) [9] for assembly quality assessment.

We used SOAPdenovo http://soap.genomics.org.cn/[37] and tried different k-mer parameters and combinations of read lanes of male and female reads. Female reads, although adding up to a much lower genomic coverage than male reads (28.5 fold vs. 124.5 fold), consistently produced a higher contig and scaffold N50 size under the same assembly parameters. This suggests that sequence coverage of 30-fold is sufficient to produce a decent-quality assembly, and that male-limited neo-Y or Y-linked sequences or B chromosomes deteriorate the assemblies. We therefore assembled the reference genome using all the female reads (28.5-fold) to construct contigs, and part of the male reads (70.4-fold, selected according to their read qualities) to link contigs into scaffolds (these were not used in the contig assembly to prevent the introduction of sex-linked and B-linked heterozygous sites that would deteriorate the quality of the assembly). Short reads were then mapped back to the scaffolds to fill in gaps. All of the assemblies used a k-mer value of 31, and the low quality first and last 5 bp of all reads were trimmed. Scaffolds assembled solely from male or female reads were also produced to extract candidate B-linked sequences (male-specific sequences that were not part of the ancestral Y). We aligned scaffolds assembled from male reads only to those assembled from female reads and selected male-specific scaffolds as candidate B regions using a blast E-value cutoff of 10^-5 and a maximum GenBlastA alignment span size of 25% of the query [38]. A total of 63 Mb of male scaffolds, for which less than 20% of their length could be aligned to female scaffolds were considered as candidate B scaffolds.

To further optimize the D. albomcians assembly, we blasted [39] all the D. virilis proteins ftp://flybase.net/genomes/Drosophila_virilis/current/fasta/ against our raw assembly, using an E-value cutoff of 10^-3. When several scaffolds that aligned to a D. virilis protein overlapped with each other, only the scaffold with the highest alignment score was kept. We then merged scaffolds into larger ones according to their order along the query gene. We also extracted D. virilis proteins that have syntenic relationship, which are conserved across other 11 Drosophila species [20]. D. virilis scaffolds encompassing these proteins were concatenated into superscaffolds as reference. We then aligned exon-level merged D. albomicans scaffolds with sensitive parameters (- = r 1 -q -1 -G 1 -E 2 -W 9 -F "m D" -U -e 1e-5) to D. virilis sequences and only retained hits spanning over 50% of the query. Aligned scaffolds were ordered and concatenated with 500 interval Ns.

Annotations

We downloaded the protein sequence annotations of 8 Drosophila species (all species available on ftp://ftp.flybase.net/releases/ excluding D. sechellia, D. simulans, D. persimilis and D. erecta because their sister species were used instead). We removed redundant proteins (proteins that share orthologous relationships) and our final set of annotation queries consisted of 66,877 proteins that were blasted against the D. albomicans mosaic scaffolds. The top two query proteins (ranked by alignment span sizes) were chosen to represent D. albomicans loci and fed to GeneWise [40], in order to determine their gene structures. GeneID and SNAP [41, 42] were used to check the GeneWise predictions and results were reconciled by GLEAN [43]. We only retained proteins on non-B sequences that have more than 50 amino acids and were supported by both GeneWise and GeneID/SNAP. For candidate B sequences, we did not require the predicted proteins to be supported by GeneWise. All the proteins and scaffolds were then subjected to a blast search against the NCBI nt/nr database ftp://ftp.ncbi.nih.gov/blast/db/20090216/. We removed proteins/scaffolds showing high sequence similarities (at least 50% sequence identity over 80% length) with human or bacteria sequences. We also narrowed down the candidate B scaffolds, assuming that B chromosomes would not show sequence similarities with known sequences, and removed all candidate B scaffolds that had protein-coding sequences annotated that showed homology to any published sequences. After this screening procedure, we retained a total of 17 Mb candidate B sequences. We annotated repetitive elements (Table S2) using two well-established libraries built from the 12 Drosophila genomes, one from Repbase and one from ReAS ftp://ftp.genomics.org.cn/pub/reas/drosophila/[44, 45] by RepeatMasker http://www.repeatmasker.org/. We also annotated simple tandem repeated sequences using the Tandem Repeat Finder (Table S2) [46].

We ordered and oriented D. virilis scaffolds to build chromosomal sequences based on the results of [47]. We established reciprocally-best orthologous relationship between predicted D. albomicans and D. virilis proteins ftp://ftp.flybase.net/releases/. We also aligned D. albomicans scaffolds with D. virilis chromosomes by ranking the ratio of identical bases to aligned span size and picked the highest ranked scaffold to assign D. albomicans proteins to different chromosomes.

Identifications of SNP, indel and structural variation

We used the Short Oligonucleotide Alignment Program (SOAP) [48] to separately align male and female reads back to the genome assembly using the 'paired-end' mode and allowing for a maximum of 2 nucleotide mismatches per read. Using these parameters, reads were only aligned when their relative orientations are correct and their inferred distance along the assembly (the aligned span size) was consistent with the estimated library insert size. We then identified SNPs using SOAPsnp http://soap.genomics.org.cn/soapsnp.html, which showed a 99% consistency for SNP identification compared with Illumina HapMap 1 M BeadChip Duo data [49]. SOAPsnp identifies SNPs based on Bayes' theorem, taking into account both sequencing and alignment qualities. Heterozygosity levels for each chromosome were then calculated using customized Perl scripts.

We further aligned reads using the 'single-end' mode to identify potential short indels and structural variation. Reads that failed to align before when indels were not permitted were re-aligned and allowing for 1-6 bp short indels (which accounted for more than 80% of short indels in the Drosophila melanogaster genome [50]). Only short indels with at least one supporting read from each strand were retained. To identify structural variation, we utilized aligned read pairs with abnormal span size or orientation (i.e. those showing mate-pair violations) using SOAPsv http://soap.genomics.org.cn/. The experimentally estimated standard deviation of the library insert size from gels is about 50 bp. Long insertion/deletion events were inferred when the distance between the aligned forward and reverse read pairs was larger or shorter than the library insert size by three times the standard deviation. Tandem duplications were called when a pair of reads was aligned as 'reverse-forward' rather than the normal 'forward-reverse' orientation from 5' to 3' along the reference assembly sequence. At least three supporting abnormally aligned reads pairs were required for a structural variant to be kept in our analysis.

Evolutionary analysis

To discriminate neo-X and neo-Y alleles, we first identified SNP or indel sites derived from female reads. We introduced these alleles into the reference scaffolds that mapped to the to neo-sex chromosomes, assuming they represented the neo-X alleles. We then modified these scaffolds by introducing alternative nucleotides and indels found only in males to obtain the homologous neo-Y alleles. We ran GeneWise [40] on the respective allelic sequences and characterized premature stop codons and frameshift mutations at neo-Y-linked genes. GeneWise results indicating different start positions for neo-X and neo-Y coding sequences were checked manually to ensure that such differences were caused by mutations at start codons and not alignment artifacts. Similarly, we characterized putative pseudogenes on the neo-X chromosome based on female reads only. These were taken as ancestral pseudogenes that already existed before the origin of the neo-sex chromosomes, and were thus removed from the analysis.

Since there are no close outgroup sequences available, we could not compare separately substitution rates on the neo-X and the neo-Y chromosome; we therefore compared the rates between the neo-X and neo-Y alleles. We used annotated protein sequences and GeneWise to align homologous neo-sex genes codon by codon. Synonymous and nonsynonymous substitution rates were calculated with the KaKs_calculator [51] using the method of Yang and Nielson [52]. We measured codon bias of neo-X and neo-Y alleles using the codonW http://sourceforge.net/projects/codonw/ and cai programs within the EMBOSS package http://emboss.sourceforge.net/. Different parameters, including effective number of codons (ENC), codon bias index (CBI), frequency of optimal codons index (FOP) and codon adaptation index (CAI) consistently showed a very weak relaxation of selective constraints at synonymous sites of neo-Y-linked genes.

B-linked sequence analysis

We first randomly chose 25 candidate B-linked scaffolds that were identified computationally and designed 100 PCR primer pairs to validate their B-chromosome linkage using genomic DNA of D. albomicans strains with and without B's. None of the primer pairs discriminated between strains with and without B's. We therefore identified scaffolds that had previously been mapped to the B-chromosome by cloning through subtractive hybridization (W.W unpublished). To confirm B-linkage of these sequences, we extracted genomic DNA with PUREGENE DNA Isolation Kit (Gentra) from fly strains with and without B's. Genomic DNA was digested with restriction enzymes, separated on agarose gels and transferred to nylon membranes (Roche Molecular Biochemicals) by Southern blotting. DIG-labeled probes were hybridized to the membrane to confirm the presence/absence of B-sequence in different strains.

We computationally queried the probe sequence against all D. albomicans scaffolds and identified four scaffolds with high sequence similarity to the B-linked sequence. We performed PCR experiments using primers spanning both the probe sequence and the sequence adjacent to it on the candidate scaffolds to exclude assembly artifacts. We also extracted total RNA from D. albomicans adults with and without B's using an RNAeasy Mini Kit (Qiagen) and performed RT-PCR for predicted genes on the B-linked scaffolds. We performed blast searches using these candidate B scaffolds against the genome sequence of other Drosophila species (with searching parameters of relatively low stringency; -r 1 -q -1 -G 1 -E 2 -W 9 -F "m D" -U -e 1e-5, as these species have diverged from D. albomicans more than 40 MY ago [53]). Chromosomal mapping information for the resulting scaffolds in these other species was then retrieved through the UCSC Genome Browser based on their blastz comparison with the D. melanogaster genome [54, 55]. We also downloaded centromeric sequences of Drosophila [30] and mapped male and female reads separately using SOAP.