Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region
© Skinner et al.; licensee BioMed Central Ltd. 2013
Received: 3 September 2012
Accepted: 8 January 2013
Published: 15 January 2013
Sex chromosomes are subject to evolutionary pressures distinct from the remainder of the genome, shaping their structure and sequence content. We are interested in the sex chromosomes of domestic pigs (Sus scrofa), how their structure and gene content compares and contrasts with other mammalian species, and the role of sex-linked genes in fertility. This requires an understanding of the XY-homologous sequence on these chromosomes.
To this end, we performed microarray-based comparative genomic hybridisation (array-CGH) with male and female Duroc genomic DNA on a pig X-chromosome BAC tiling-path microarray. Putative XY-homologous BACs from regions of interest were subsequently FISH mapped.
We show that the porcine PAR is approximately 6.5-6.9 Mb at the beginning of the short arm of the X, with gene content reflective of the artiodactyl common ancestor. Our array-CGH data also shows an XY-homologous region close to the end of the X long arm, spanning three X BACs. These BACs were FISH mapped, and paint the entire long arm of SSCY. Further clones of interest revealed X-autosomal homology or regions containing repetitive content.
This study has identified regions of XY homology in the pig genome, and defined the boundary of the PAR on the X chromosome. This adds to our understanding of the evolution of the sex chromosomes in different mammalian lineages, and will prove valuable for future comparative genomic work in suids and for the construction and annotation of the genome sequence for the sex chromosomes. Our finding that the SSCYq repetitive content has corresponding sequence on the X chromosome gives further insight into structure of SSCY, and suggests further functionally important sequences remain to be discovered on the X and Y.
KeywordsX-chromosome Genome Porcine Evolution Microarray Pseudoautosomal
Domestic pigs (Sus scrofa) are agriculturally important animals, as well as important model organisms for many human diseases. The genome sequencing effort associated with the domestic pig has recently been published , with the current Sscrofa10.2 assembly available on the Ensembl database (http://www.ensembl.org/Sus_scrofa/Info/Index). However, this sequence information is limited to the autosomes and the X chromosomes; little sequence data is available for the Y chromosome.
Pig genomes are comprised of 18 autosome pairs, and the sex chromosomes . The X chromosome shows a small interstitial C-band on the short arm and a large G-band on the long arm, thought to correlate with repetitive content [3, 4]. A single known pseudoautosomal region (PAR) lies at the terminus of the X short arm. Several genes have been mapped to the pig PAR - for example, KAL1 and STS. Though not in PAR1 of humans, these may be PAR-related in some other mammalian species (e.g. cow and dog ). However, the pseudoautosomal boundary (PAB), and thus the gene complement of the pig PAR, remains imprecisely defined. Evidence from the cow, a relatively closely related species, suggests that the PAR may be 5-9 Mb in size .
The Y chromosome is the smallest of the pig chromosomes, and information about its structure and gene content has remained elusive since the identification of the pig sex chromosomes . Cytogenetic investigation has shown the pig Y to be a metacentric chromosome, estimated to be about 50 Mb in length by flow cytometry . Early studies looking at the banding pattern of the Y noted that the long arm (Yq) contains a large C band, indicating that this arm contains a substantial proportion of constitutive heterochromatin [3, 10]. Subsequent physical mapping of bacterial artificial chromosome (BAC) clones containing Y chromosome content by fluorescence in-situ hybridisation (FISH) has revealed that the long arm can be almost entirely painted by a single BAC clone, while most, if not all, of the single copy sequences are found on the short arm . This level of repetitive sequence further complicates attempts to sequence this chromosome, a problem common to mammalian Y chromosomes (e.g. mouse; [11–15]).
Some clues as to the structure of the pig Y have come from the search for male specific DNA sequences. These yielded short repetitive sequences [16–19], which appear male-specific (or at a very high copy number on the Y relative to the autosomes). The sequence identity between these different repeats ranges from 80-91%. Together these sequences presumably partially explain the repetitive nature of SSCYq. The broad organisation of SSCYq seems complex, but it is apparent that it contains an expanding and diverging group of repeats. It remains unknown however whether there are regions of XY homology on the long arm of the Y chromosome interspersed amongst the repetitive content.
Given the above, the aims of this study were therefore to determine the boundary and size of the porcine PAR, and to identify any other regions of XY homology through the use of microarray-based comparative genomic hybridisation to give insights into sex chromosome evolution in mammals in general and pigs in particular.
Results and discussion
Regions of XY homology identified by array-CGH
Two regions of XY-homology were found: the PAR, described in greater detail below, and a region towards the q-terminus of Xq. The 3 BACs in this region (CH242-139K22, CH242-115P19 and CH242-96N5) painted the entire long arm of the Y chromosome (Figure 2A) in addition to their discrete X signals. These were flanked proximally by CH242-390A7 and distally by CH242-305A15 (see also Additional file 2: Table S2). Although the microarray results suggest that the XY-homology may continue to the SSCX q-terminus, FISH mapped clones surrounding the XY-homology block appear X-specific.
Pig Yq is known to be highly repetitive . A number of male-specific repetitive sequences have been previously identified [16–19], which must contribute to Yq. However, a comparison by BLAST of these repetitive sequences with the three X BAC clones found in this study failed to show significant matches. That is, whatever sequence underlies the XY homology is not one of the previously identified repeats. Moreover, no BLAST matches were found against any of the clones on the array for which sequence is available. Very little sequence appears to be shared between these 3 BACs in a BAC-BAC BLAST comparison. Those short (~40 bp) sequences that are shared are also found in the surrounding X-specific BACs. Consequently, the precise sequence underlying the XY homology remains undetermined. It does however confirm that the organisation of SSCYq is more complex than tandemly repeated copies of the already-identified male-specific repeats. Further work will be required to determine whether the repetitive long arm of SSCY contains ampliconic genes, as found in the male-specific regions of Y chromosomes of other species (e.g. [13, 14, 20, 21]).
X-autosomal, autosomal and repetitive clones
One clone, CH242-34G16, showed homology between the X chromosome and the autosome pair SSC3 (Figure 2B). Some pig satellite DNAs are already known to be present on X and autosomes, primarily centromeric satellites – for example, SSCSR1A found at the centromeres of chromosomes 3 and X . Given the position of the clone in a repetitive portion of Xq it seems likely that a similar satellite underlies the homology.
Two other clones that appeared of interest from the microarray experiments physically mapped to autosomes - CH242-100A10 on SSC18 and CH242-131F14 on SSC5p (Figure 2C). These are likely clones miss-assigned during the construction of the library, as they show no evidence for X or Y signal.
Many clones within regions of interest along the X chromosome, for example CH242-9O15, appear to contain a high amount of repetitive content from FISH mapping, despite blocking with Hybloc (Cot-1) DNA (Figure 2D – background thresholding is deliberately reduced). Signals from these probes paint many of the repetitive regions of the pig genome, and this presumably explains their high log2 ratios. Supporting this idea, the repetitive region on SSCXp appears to coincide with a known heterochromatic C-band, and the region on SSCXq correlates with a prominent G-band [3, 4].
Boundary and gene content of the porcine PAR
The PAR size of ~6.7 Mb is comparable to that of other mammalian PARs that have been sequenced. It is most similar to cattle (5-9 Mb ; by Ensemble, about 5.5-6 Mb) and dog (6.6 Mb ). It is longer than the PARs of horse (1.8 Mb ), human PAR1 (2.7Mb ) chimp (2.7 Mb [26–28]) or mouse (700 kb ). Although the sizes and gene content of PARs change over time as sex-specific regions expand, and autosomal regions are acquired onto the sex chromosomes (e.g. [24, 30]), it appears that gross changes to the PAB may have occurred infrequently in the cetartiodactyl lineages.
A PAB proximal to SHROOM2-like in pig is consistent with mapping of PABs in cow and dog; these species PABs are in the interval between SHROOM2 and GPR143 in cow  and distal to SHROOM2 in dog . Furthermore, evidence also indicates that SHROOM2 and GPR143 are pseudoautosomal in porpoise  suggesting that the pig has retained much, but not all, of the ancestral cetartiodactyl PAR.
Many of the genes that are seen in the pig PAR have clear homologues in other mammalian species. However, variation is seen; there appears to have been an expansion of odorant-binding genes in pig in a cluster - multiple orthologous genes are also seen in mouse and rat, and perhaps cow, but not in the other species. The gene SHOX, seen in the PARs of pig, dog and human only here, has been secondarily lost from the sex chromosomes in mice and rats , and presumably from cow also. The horse SHOX cDNA, together with cDNA sequences for predicted X-genes PLCXD1 and PPP2R3B, is found on the unmapped sequence chromosome Un0036. These genes have been confirmed PAR associated in horse . This suggests that the horse X assembly is lacking a region at the tip of the short arm, corresponding to Un0036.
There are two novel protein-coding genes in pig shown in Figure 4. When the protein sequences for these genes are compared to the NCBI nr database by BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi), they both most closely match neuroligin-4-X or X-like variants. Since NLGN4X currently covers 465.6 kb of genomic sequence, these may represent errors in the current X assembly. Otherwise, they may reflect transcript variants or gene expansions unique to the suid lineage. NLGN4X is not found within PAR1 of humans, nor is it within the PARs of chimp, horse or mouse. It is however within the PARs of cattle and dog. This reflects the differences in PAR boundary locations in these species, and the broadly conservation of gene order on mammalian X chromosomes. Given the importance of neuroligins in synaptogenesis, and their association with human mental disorders such as autism , any functional effects of these genes in pigs would be of interest.
Human PAR genes and their pig orthologues
Pig closest match by BLAT
phosphatidylinositol-specific phospholipase C, X domain containing 1
GTP binding protein 6 (putative)
protein phosphatase 2, regulatory subunit B”, beta
short stature homeobox
cytokine receptor-like factor 2
colony stimulating factor 2 receptor, alpha, low-affinity (granulocyte-macrophage)
interleukin 3 receptor, alpha (low affinity)
solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6
F2Z565_PIG - SSCX, 96.7 Mb
purinergic receptor P2Y, G-protein coupled, 8
PAR sequence ~446 kb, no gene
A kinase (PRKA) anchor protein 17A
dehydrogenase/reductase (SDR family) X-linked
SSCX, 89 Mb. SSC5, 2
zinc finger, BED-type containing 1
SSC9, 1, 8, no gene
Xg blood group
It is likely that as the pig X sequence annotation improves, some of the ‘missing’ genes will be found, and some of the novel sequences will be found to be errors in the automated annotation, or assigned homologues. Those that remain represent interesting targets for future studies in pig development and evolutionary history. Of equal interest will be genes that are within the PAR in some mammalian species, and not in others (e.g. NLGN4X). These may be subject to rapid divergence between the X and Y variants, and hence have acquired important functional differences.
This study has identified regions of XY homology in the pig genome, and defined the boundary of the PAR on the X chromosome. This adds to our understanding of the evolution of the sex chromosomes in different mammalian lineages, and will prove valuable for future comparative genomic work in suids and for the construction and annotation of the genome sequence for the sex chromosomes. Our finding that the SSCYq repetitive content has corresponding sequence on the X chromosome gives further insight into structure of SSCY, and suggests the potential for other, perhaps functional, material embedded within.
Microarray construction followed the protocol of Fiegler et al. . Briefly, the BAC clones of the tiling path were grown overnight from glycerol stocks in LB in 96 well deep-well plates. BAC DNA was extracted by mini-prep, purified via 96-well filter-plates and eluted in ddH2O. The purified products were amplified by DOP-PCR. Amplified DOP-PCR products were tagged with an aminolinker by PCR, filter-purified and eluted in spotting buffer. Amino-linked products were spotted onto CodeLink microarray slides using an MGII610 (BioRobotics).
Probe labelling and hybridisation
Genomic DNAs from male and female Duroc pigs were labelled with Cy3 and Cy5 by random priming following  with the following modifications: 1 μg Porcine Hybloc DNA (a Cot-1 equivalent - Applied Genetics Laboratories, Florida) was used as a competitor DNA with 0.15 μg genomic DNA. Genomic DNA was extracted using a Qiagen Blood and Tissue Kit. Male DNA was obtained from muscle provided by Genus, from a Duroc boar being routinely culled. Female gDNA was extracted from Duroc sow fibroblast cell line 2–14 provided by Fengtang Yang at the Wellcome Trust Sanger Institute. Hybridisation was performed in a moist chamber for 48 hours. Post-hybridisation washes followed .
Imaging and analysis
Each microarray slide was scanned using a GenePix Personal 4100A Scanner (Axon Instruments) at a 5 μm resolution. Cy3 and Cy5 fluorescence intensities of each DNA spot was quantified in BlueFuse for Microarrays v3.2 (Blue-Gnome Ltd, Cambridge, UK). The Cy3/Cy5 fluorescence ratios were calculated and transformed into log2 values. The ratios were normalized using block median normalization for each of the sixteen blocks to account for any block-block variation. The results from the four experiments were exported from the software for further analysis using Inforsense 5.0.1. Each hybridization was treated as a separate experiment. Clones with a confidence score < 0.7 in each experiment were excluded. An average was taken of the log2 ratios for each clone across the experiments. Clones were further filtered to leave only those 586 clones with surviving log2 ratios in 2 or more experiments. Full results from the array experiments are available on GEO with accession GSE40244; the average log2 ratios for each clone are also presented in Additional file 1: Table S1. At time of writing, most clones are sequenced and at least partially assembled. Information may be found on clone status at NCBI (http://www.ncbi.nlm.nih.gov/nuccore).
Approximate start and stop positions were downloaded from the Sscrofa10.2 assembly on Ensemble for each clone to enable ordering of the clones. A 5-clone average was taken along the length of the chromosome to assist visualisation. Clone position was plotted against log2 ratio using gnuplot (http://www.gnuplot.org). The SSCX ideogram was adapted from the Pre-Ensemble cytogenetic map (http://pre.ensembl.org/Sus_scrofa_map/Location/Genome Ensemble).
Fluorescent in-situ hybridisation (FISH)
Chromosome preparations were made from a fibroblast cell line derived from a skin biopsy of the same male Duroc used for array-CGH experiments. The cell line was established at the Well come Trust Sanger Institute. Chromosome preparation followed standard protocols [35, 36]: mitostatic treatment with colcemid at a final concentration of 0.1 μg/ml for 1 h at 37°C, hypotonic treatment with 75 mM KCl for 15 min at 37°C and fixation with 3:1 methanol:acetic acid.
BACs of interest from array-CGH were labelled by nick translation with biotin-16-dUTP (Roche) following standard protocols. Slides with metaphase preparations were aged overnight at 37°C then treated with 4 mg/ml RNase A for one hour at 37°C. The chromosomes were denatured for 1 minute 30 seconds in 70% formamide in 2 × SSC at 70°C. BACs were applied to slides and sealed under coverslips with rubber cement. Hybridization was carried out in a humidified chamber for 24 hours at 37°C. Following post-hybridization washes (40% formamide in 2 × SSC for 20 minutes; 1 minute in 2 × SSC/0.1% Igepal at RT; 15 minutes in 4 × SSC/0.05% Tween 20 at RT; 25 minutes in 4 × SSC/0.05% Tween 20/2% BSA at RT), probes were detected with 1:200 streptavidin-Cy3 (Amersham) in 4 × SSC, 0.05% Igepal, 1.25% BSA for 35 minutes. Slides were washed in 4 × SSC, 0.05% Igepal for 2 × 5 minutes then counterstained using Vectashield with DAPI (Vector Labs). Slides were analyzed on Nikon Microphot-SA epifluorescence microscope equipped with a cooled CCD camera and appropriate filters. Images were captured using SmartCapture 2 (Digital Scientific UK).
We wish to thank the Wellcome Trust Sanger Institute Pig X and Y sequencing group for providing the X chromosome tiling path library and deriving fibroblast cell lines, Genus for providing the Duroc boar, and the array team with Cambridge Genomic Services for assistance with the microarray experiments. This work was funded by BBSRC grant BB/F021372/1.
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