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Open Access Research article

The SWI/SNF protein ATRX co-regulates pseudoautosomal genes that have translocated to autosomes in the mouse genome

Michael A Levy14, Andrew D Fernandes12, Deanna C Tremblay14, Claudia Seah34 and Nathalie G Bérubé134*

Author Affiliations

1 Department of Biochemistry, University of Western Ontario, London, N6A 4L6, Canada

2 Applied Mathematics, University of Western Ontario, London, N6A 4L6, Canada

3 Paediatrics, University of Western Ontario, London, N6A 4L6, Canada

4 Children's Health Research Institute, Lawson Health Research Institute, 800 Commissioners Road East, London, N6C 2V5, Canada

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BMC Genomics 2008, 9:468  doi:10.1186/1471-2164-9-468

The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2164/9/468


Received:2 April 2008
Accepted:8 October 2008
Published:8 October 2008

© 2008 Levy et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Pseudoautosomal regions (PAR1 and PAR2) in eutherians retain homologous regions between the X and Y chromosomes that play a critical role in the obligatory X-Y crossover during male meiosis. Genes that reside in the PAR1 are exceptional in that they are rich in repetitive sequences and undergo a very high rate of recombination. Remarkably, murine PAR1 homologs have translocated to various autosomes, reflecting the complex recombination history during the evolution of the mammalian X chromosome.

Results

We now report that the SNF2-type chromatin remodeling protein ATRX controls the expression of eutherian ancestral PAR1 genes that have translocated to autosomes in the mouse. In addition, we have identified two potentially novel mouse PAR1 orthologs.

Conclusion

We propose that the ancestral PAR1 genes share a common epigenetic environment that allows ATRX to control their expression.

Background

The sex chromosomes in modern placental mammals (eutherians) are highly dimorphic but initially evolved from a homologous pair of autosomes [1]. Over millions of years of mammalian evolution, the sex chromosomes have lost most of their homology due to chromosome Y attrition [2]. The remaining homology between the sex chromosomes exists in the pseudoautosomal regions (PARs), located at the ends of the X and Y chromosomes [3] and was generated when genetic material from the tips of autosomes translocated to the ancient sex chromosomes [4]. Gene dosage between XX females and XY males is usually achieved by the silencing of one X chromosome in every female cell, a process known as X chromosome inactivation (XCI) [5]. Because both males and females have two copies of all PAR genes there is no requirement for dosage compensation and these genes therefore escape this inactivation process [6].

Comparison of human PARs with those of other primates, carnivores (dogs and cats) and artiodactyls (cattle, sheep, pigs; representing the common evolutionary ancestor between humans and mice) has revealed that gene content is mostly conserved in eutherians, including the existence of PARs at both ends of the X and Y chromosomes [4]. However, rodents are strikingly different in that they have a single, dissimilar and considerably shorter PAR region [7]. Fewer than half of the 24 PAR1 genes identified so far in humans have also been found in the mouse genome, and all have diverged considerably [7]. This divergence is largely due to the increased recombination rates in the PARs during male meiosis [8]. In addition, the PARs comprise a unique chromosomal environment that is rich in repetitive sequences [9,10]. For these reasons, the identification of human PAR genes and orthologs has been difficult. Interestingly, in the mouse, all human PAR1 orthologs identified to date are located on autosomes. For example, colony stimulating factor 2 receptor, alpha (Csf2ra) is located on mouse chromosome 19 [11] and CD99 antigen (Cd99) and Dehydrogenase/reductase short-chain dehydrogenase/reductase family, X chromosome (Dhrsxy) are located on chromosome 4 [9,12]. Human orthologs of acetylserotonin O-methyltransferase-like (ASMTL) and several members of the arylsulfatase (ARS) family of genes (ARSE, ARSD, ARSF, and ARSH) located just outside the PAR1, have not yet been reported in the mouse (Figure 1). Due to their location in the PAR region of evolutionary ancestors, and their current autosomal location, we will refer to these genes in the mouse as "ancestral PAR genes".

thumbnailFigure 1. Evolution of PAR genes in humans and mice. PAR genes that are downregulated in the ATRX-null mouse forebrain are clustered together within the PAR1 region of common evolutionary ancestors of humans and mice but have translocated to autosomes in the mouse. Vertical lines and arrows represent individual genes. The position of the first nucleotide of each gene is as follows: SHOX (505,079), CSF2RA (1,347,701), ASMTL (1,482,032), DHRSXY (2,147,553), CD99 (2,619,553), ARSD (2,848,421), ARSE (2,832,011) (Human reference sequence NCBI Build 36.1). PAR1, pseudoautosomal region 1; PAR2, pseudoautosomal region 2. PAR regions are highlighted in orange.

The α thalassemia mental retardation, X linked (ATRX) protein, transcribed from Xq13.3 belongs to the Sucrose non-fermenting 2 (Snf2) family of enzymes that use the energy of adenosine tri-phosphate (ATP) hydrolysis to disrupt nucleosome stability [13,14]. Mutations in ATRX result in moderate to profound cognitive deficits, facial dysmorphisms, as well as skeletal and urogenital abnormalities, among other symptoms [15]. The chromatin remodeling properties of ATRX have been demonstrated in vitro [16]. In addition to a conserved ATPase/helicase domain, ATRX has an N-terminal zinc finger ATRX-DNMT3A/B-DNMT3L (ADD) domain that is shared with de novo methyltransferases. Several lines of evidence have also linked ATRX to highly repetitive genomic regions including pericentromeric heterochromatin in mouse and human cells [17]. Moreover, ATRX mutations in humans result in aberrant DNA methylation patterns at several repetitive elements, including ribosomal DNA (rDNA) repeats, subtelomeric repeats and Y-specific satellite repeats [18]. These repetitive sequences usually form heterochromatic structures and seem to be specifically targeted by the ATRX protein.

To assess the role of ATRX in brain development, we previously used Cre-loxP recombination to remove Atrx specifically in the forebrain beginning at E8.5. Loss of ATRX in the embryonic forebrain caused hypocellularity and a reduction in forebrain size and loss of the dentate gyrus [19].

Genes that are directly regulated by the ATRX protein have not yet been identified in either humans or mice. To identify potential genes that are controlled by ATRX, we performed a screen of gene expression and found that a subset of ancestral PAR1 genes is consistently downregulated in the absence of ATRX in the developing mouse brain. Among them are two potentially novel mouse orthologs of Arse and Asmtl. The only common link between ancestral PAR genes is their adjacent location and shared chromatin environment in the ancestral PAR region. We propose that conserved sequences and/or chromatin features targeted by ATRX were maintained upon translocation of these genes from the PAR1 on the ancestral X chromosome to their current location on mouse autosomes, and allow ATRX to modulate their expression.

Results

Effects of ATRX deletion on forebrain gene expression

The ability of ATRX to remodel chromatin [16] suggests that ATRX can regulate gene expression. To identify possible gene targets of the ATRX protein in the developing mouse brain, we used the previously described AtrxFoxg1Cre mice that lack ATRX in the forebrain [19]. In this model system, Atrx deletion is achieved by crossing AtrxloxP "floxed" mice to mice that express cyclization recombinase (Cre) under the control of the forebrain-specific forkhead box G1 (Foxg1) promoter [20]. We performed microarray analysis to compare the expression profiles of the AtrxFoxg1Cre and control telencephalon at embryonic day 13.5 (E13.5) (n = 3 pairs) using an Affymetrix mouse genome expression array representing approximately 39,000 transcripts [21]. Only probe sets showing a significant difference (p < 0.05) were included in all subsequent studies. By setting a threshold of 1.5 fold change we identified 202 disregulated probesets, and at a threshold of 2 fold change we identified only 22 altered probe sets. Approximately two-thirds of the probe sets demonstrating altered expression were upregulated (Additional file 1).

Additional file 1. Summary of microarray results. cRNA was generated from total forebrain RNA from three pairs of littermate-matched ATRX-null and wild type forebrain tissue and hybridized to an Affymetrix Mouse Genome 430 2.0 Array. Data was analyzed using GeneSpring. Probe sets were filtered by fold change (1.5 and 2 fold at E13.5 and P0.5) and confidence, P < 0.05, and duplicate genes were removed. (A) Venn diagrams to categorize probe sets according to developmental timepoint and fold change in expression levels. (B) Hierarchical clustering of differentially expressed probe sets. Approximately two-thirds of the misregulated genes are upregulated. Ancestral PAR genes are consistently downregulated at both timepoints and are indicated by blue text. Probe sets were filtered by 1.5 fold or 2 fold change, P < 0.05, at either E13.5 or P0.5. Normalized expression levels are displayed.

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We next compared gene expression patterns in control and Atrx-null forebrain tissue at postnatal day 0.5 (P0.5) (n = 4 pairs). At a threshold of 1.5 fold change, we identified 304 probe sets and at a threshold of 2 fold change, we identified 57 probe sets showing altered transcript levels. When we compared the microarray results at E13.5 and P0.5 we identified 14 common probe sets that were upregulated and 13 that were downregulated more than 1.5 fold, and one increased and three decreased more than 2 fold (Additional file 1).

We used GeneSpring to identify significantly overrepresented Gene Ontology (GO) categories in the Atrx-null mouse forebrain. Several statistically and biologically significant categories of upregulated genes were related to the immune response. This could be an indirect response to the increased apoptosis that characterizes the Atrx-null forebrain at E13.5 in the developing cortex and to a lesser extent at P0.5 in the hippocampus [19]. In particular, categories and genes involved in phagocytotic clearing of apoptotic cells, such as complement activation [22], were enriched at both E13.5 and P0.5. Several genes involved in cell adhesion processes were upregulated at P0.5 and, consistent with the abnormal forebrain development described in the Atrx-null forebrain[19], genes involved in neurogenesis and nervous system development were downregulated at both timepoints (Additional file 2).

Additional file 2. Significantly misregulated GO categories. GeneSpring was used to identify significantly overrepresented GO categories. Probe sets were filtered by 1.5 fold change, P < 0.05 and categorized as either up or downregulated. When there were multiple probe sets for a gene, duplicates were removed. P < 0.001 was used as the significance cutoff.

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Ancestral pseudoautosomal genes are downregulated in the Atrx-null mouse forebrain

Five of the most downregulated transcripts identified in the microarray analysis were unidentified cDNA clones (Affymetrix IDs 1436320_at, 1448057_at, 1443755_at, 1429730_at and 1453066_at; Accessions [GenBank:W45978], [GenBank:BI202412], [GenBank:BE457721], [GenBank:AK007409] and [GenBank:BI320076] respectively). To further investigate these probe sets, their NCBI nucleotide sequences were used for a Basic Local Alignment Search Tool nucleotide (BLASTn) search of the nr database. The expressed sequence tag (EST) [GenBank:W45978] has similarity to Mus musculus Dhrsxy ([GenBank:NM_001033326], score = 120, E value 5e-24). The EST [GenBank:BI202412] displayed similarity to several unidentified mouse cDNA clones. Interestingly, a BLAST-like Alignment Tool (BLAT) search of this clone showed similarity to intron 1 of mouse Dhrsxy and it could represent an unknown splice variant of Dhrsxy. The EST [GenBank:BE457721] is annotated as similar to human Arse and a BLASTn search revealed high similarity to Rattus norvegicus Arse ([GenBank:NM_001047885], score 197, E value 6e-28). BLASTn of [GenBank:AK007409] showed high similarity to Asmtl in cow ([GenBank:BT02626], score = 248, E value = 6e-62) as well as dog, human, the putative rat Asmtl, and numerous other species. The EST [GenBank:BI320076] displayed no significant hits to any sequences by either BLASTn or BLAT. Interestingly, while Dhrsxy, Arse and Asmtl do not display an obvious connection, they do share a common link in that they are all pseudoautosomal genes in eutherians. In addition, the microarray data showed decreased expression of Cd99, Shox2 and Csf2ra, that also lie within the pseudoautosomal region in most eutherians. Therefore, while GO analysis identified a subset of downregulated genes involved in brain development at both timepoints, a more in depth analysis of downregulated targets revealed that many are orthologs of PAR1 genes residing on the tip of the X and Y chromosomes in most placental mammals. Overall, our transcriptional screen identified six of these genes, constituting approximately half of all PAR1 orthologs discovered in the mouse genome so far. The more intriguing aspect of this finding is that in the mouse, these genes no longer reside within the PAR1 region but have translocated to autosomes (Figure 1). It also identified two potential novel PAR1 orthologs–Arse and Asmtl–not previously identified in the mouse genome. At E13.5, these genes represent 6 of the 15 most downregulated transcripts identified by microarray analysis. Strikingly, they constitute 4 of the top 5 most downregulated genes in the microarray performed on P0.5 forebrain tissue (Arse and Shox2 were not significantly decreased in the microarray at P0.5) (Table 1, Additional file 1). These results suggest that ATRX normally participates in the transcriptional activation of these genes during both the proliferative (E13.5) and more differentiative (P0.5) stages of forebrain development.

Table 1. Downregulated genes in the ATRX-null forebrain at E13.5 and P0.5.

Verification of gene expression changes

To validate the microarray results, we performed real-time quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) analysis of Dhrsxy, Cd99, Csf2ra, Shox2 and also the putative new orthologs of Asmtl and Arse in Atrx-null and control E13.5 and P0.5 forebrain (n = 3 at each time point). Since Arse and Asmtl have not yet been identified in the mouse, we sequenced the PCR products to ensure they corresponded to the transcripts identified on the microarray, and not to other contaminating sequences. The qRT-PCR results confirmed that five of the six genes exhibit decreased expression in the Atrx-null forebrain at E13.5, and that these genes remain downregulated at P0.5 (Figure 2A). In addition, analysis at P17 demonstrated decreased expression of ancestral PAR genes at this later time point as well (Figure 2A). One exception was Shox2 which exhibited highly variable expression differences between the Atrx-null and control tissue at E13.5, P0.5 and P17, ranging from a 170 fold decrease to a 90 fold increase (Figure 2B). Therefore, while the expression of Shox2 is clearly affected by the loss of ATRX protein, the outcome on expression levels appears to be highly variable and does not validate the consistent downregulation observed by microarray analysis.

thumbnailFigure 2. Relative expression of ancestral PAR genes in ATRX-null mouse forebrains. (A) Real-time quantitative RT-PCR of the indicated PAR1 genes showed a decrease in expression in the Atrx-null mouse forebrain. RNA was isolated from littermate-matched Atrx-null and control embryos/mice at E13.5, P0.5 and P17. Results were normalized to β-actin expression levels. Error bars represent standard error of the mean between biological replicates (n = 3). (B) Expression of Shox2 in seven (E13.5) or three (P0.5 and P17) littermate-matched pairs. Error bars represent standard error of the mean for technical replicates. In (A) and (B) expression levels for the control forebrains were set to one for each reaction (represented by the black bars).

Our discovery that the expression of several ancestral PAR1 genes is controlled by ATRX throughout the early developmental period of the mouse brain reveals an unexpected association between the levels of ATRX protein and the expression of these ancestral PAR1 genes.

Identification of a novel ARS family mouse homolog

In humans, a cluster of ARS genes are located approximately 115 kilobases centromeric to the PAR1 region on the X chromosome, but still possess the ability to escape XCI in females [23]. Located outside the PAR1, these genes do not have an identical homolog on the Y chromosome but have pseudogenes, and in the evolutionary past it is believed that they were true pseudoautosomal genes with identical copies on both the X and Y chromosome [24].

A multiple alignment of amino acid sequences of [GenBank:BE45772] suggested that it is a fragment of the full length ARSE protein, aligning in the middle of the approximately 600 amino acid ARSE protein of multiple other species (Additional file 3). The putative mouse ARSE is 65% identical to rat and 47% identical to human.

Additional file 3. Amino acid alignment of a small portion of ARSD/E between multiple species. Sequences were aligned using T-Coffee 5.56 [47] using default parameters, edited using JalView [46] and shaded using Boxshade [51]. Mouse ARSD/E has highest identity to rat ARSE (65%). Accession numbers are ARSE: chicken [GenBank:XP_416856], cow [GenBank:ABS45001], dog [GenBank:NP_001041587], horse [GenBank:XP_001495573], macaque [GenBank:Q60HH5], human [GenBank:CAA58556], platypus [GenBank:XP_001514429], opossum [GenBank:XP_001362844], pufferfish [GenBank:CAG09268], rat [GenBank:CAI84983]. ARSD: dog [GenBank:XP_548838], horse [GenBank:XP_001495553], human [GenBank:CAA58555], macaque [GenBank:XP_001092405], opossum, [GenBank:XP_001362931], platypus [GenBank:XP_001507106], chicken [GenBank:XP_416855], zebrafish [GenBank:XP_700386]. Mouse Arsd/e translated from [GenBank:BE457721].

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Phylogenetic analysis demonstrated that the mouse ARSE sequence clusters with near certainty with the rat ARSE, however, this putative ARSE clustered within the ARSD proteins, not ARSE as expected (Figure 3). Therefore, we propose that we have identified a member of the PAR1 ARS family but at this time cannot determine the exact identity and will refer to this sequence as Arsd/e. We note that the long branch-length between the rodent ARS sequences and the remaining ARSD clade may be an artifact due to the short mouse sequence and its high similarity to the rat sequence, which has undergone seemingly accelerated evolutionary change.

thumbnailFigure 3. Phylogenetic tree of ARS proteins. Human ARSE [GenGank:NP_000038] was used as a seed to search the GenBank NR database for orthologs and an approximate maximum-likelihood tree was generated. The putative ARS family gene downregulated in the Atrx-null forebrain clusters closely with rat ARSE but with the ARSD proteins. Entries are annotated with species, chromosome (where known) and GenBank Accession number.

Comparisons to available mouse Ars gene family members shows that [GenBank:BE457721] is more similar to Arse genes in rat than to other mouse arylsulfatase family members (Additional file 4), suggesting that we have identified Arse. This data, combined with our ability to specifically amplify this transcript from mouse brain cDNA and also from a commercially available E15 cDNA library (data not shown), indicates that we have likely identified the mouse homologue of a previously unidentified mouse Ars gene rather then a gene fragment from a known mouse family member.

Additional file 4. Comparisons of Ars family members. The transcript identified as a putative mouse Arse ortholog is more similar to rat Arse then to any other Ars family members. Pairwise percent identities were calculated using Jalview [46]. Accession numbers are: Arse [GenBank:BE45772], Arsa [GenBank:NM_009713], Arsb [GenBank:NM_009712.3], Arsc/Sts [GenBank:NM_009293.1], Arsg [GenBank:NM_028710.2], Arsi [GenBank:NM_001038499.1], Arsj [GenBank:NM_173451.2], Arsk [GenBank:NM_029847.4], rat Arse [GenBank:NM_001047885.1], rat Arsc/Sts [GenBank:NM_012661.1].

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To further confirm the identity of [GenBank:BE457721], we assessed the outcome of ATRX depletion on Arsd/e expression by RNA interference in the Neuro-2a cultured neuroblastoma cell line. Small interfering RNAs (siRNAs) were used to transiently deplete ATRX, as was done previously [25]. Cells transfected with a non-specific siRNA or no siRNA ("Mock") were used as controls. At 72 hours following siRNA transfection, we monitored the effectiveness of ATRX depletion by indirect immunofluorescence using an ATRX-specific antibody (H300) and qRT-PCR analysis of Atrx expression levels using primers that simultaneously amplify both the full length isoform and the reported truncated isoform [26]. In the siATRX-treated samples, approximately 95% of cells were negative for ATRX (Figure 4A) and Atrx transcript levels were depleted by approximately 5 fold (Figure 4B). We then used qRT-PCR to determine the outcome of ATRX silencing on the expression level of the Arsd/e. Similar to the results obtained in the Atrx-null forebrain, the expression of Arsd/e was decreased two fold (Figure 4B). These findings support that we have identified the mouse Arsd/e and confirm the regulation of this ancestral PAR gene by ATRX, and that this outcome on gene expression can be recapitulated in two different systems: in vivo in the ATRX-null developing forebrain and in vitro in ATRX-depleted cultured neuronal cells.

thumbnailFigure 4. Arsd/e transcriptional downregulation is recapitulated in ATRX-depleted cells. (A) RNA interference was used to deplete ATRX in Neuro-2a neuroblastoma cells. Cells were transfected with 8 nM siRNA, fixed after 72 h and processed for immunofluorescence staining using an anti-ATRX primary antibody (H300) and anti-rabbit Alexa 488 secondary antibody, then counterstained with DAPI to detect nuclei. In the siATRX treated samples, approximately 95% of cells were negative for ATRX. Scale bar = 20 μM. (B) Total RNA was isolated for quantitative real-time PCR of Atrx and Arsd/e gene expression at 72 hours post-transfection. Mock (transfection reagent only) expression levels were set to one and a non-specific siRNA was used as a control. Results were normalized to β-actin expression levels. Error bars represent standard error of the mean (n = 3).

Identification of an ASMTL-like gene

[GenBank:AK007409] is the RIKEN cDNA 1810009N02 gene and contains a musculoaponeurotic fibrosarcoma (MAF) domain. A multiple sequence alignment of amino acid sequences was used to further determine the identity of [GenBank:AK007409] (Additional file 5). [GenBank:AK007409] aligns to the N terminus of ASMTL from multiple other species. The N terminal portion of ASMTL also contains a MAF domain. Human ASMTL was generated by a fusion of a duplicated acetylserotonin O-methyltransferase (ASMT) with the bacterial maf gene [27]. While [GenBank:AK007409] contains a MAF domain, it lacks the ASMT domain. However, this is similar to the putative rat ASMTL (Accession [GenBank:NP_001099385]) which also lacks the ASMT domain. The putative mouse ASMTL is 54% identical to rat, and 51% identical to the human protein.

Additional file 5. Amino acid alignment of the N terminal of ASMTL between multiple species. Sequences were aligned using T-Coffee 5.56 [47] using default parameters, edited using JalView [46] and shaded using Boxshade [51]. The putative mouse ASMTL aligns within the N terminal MAF domain and is most similar to rat ASMTL (54% identity) which also contains only the MAF domain. Accession numbers are: human [GenBank:XP_001133965], orangutan [GenBank:CAH90398], chimpanzee [XP_001137696], cow [GenBank:AAI03000], dog [GenBank:XP_851655], frog [GenBank:NP_001085814], chicken [GenBank:XP_001231914], zebrafish [GenBank:NP_998676], platypus [GenBank:XP_001506357], mouse [GenBank:NP_081215].

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In contrast to ARSE, ASMTL has fewer discernable high-similarity full-length orthologs, and its evolution appears tied to the pseudoautosomal region [27]. Therefore fewer sequences were available for analysis. Figure 5 shows the inferred phylogeny of the ASMTL family, with the primate branches collapsed for clarity. With fairly high bootstrap support, the tree mirrors the known branching of the placental mammals, marsupials, monotremes, birds, amphibians, and fish. The mouse sequence displays the only anomalous placement in the tree, clustering well outside the mammalian clade. Both the placement and the branch-length of the mouse sequence indicate that it is of considerably evolutionarily derived character compared to the putative ancestor, and it appears to have followed an evolutionary path quite different from its paralogs. The lack of the ASMT domain in the mouse sequence may also be responsible for the placement of the mouse sequence in the tree. As with ARSE, some of this divergence may be due to the availability of a partial mouse sequence, but the sequence remains quite unique, nonetheless.

thumbnailFigure 5. Phylogenetic tree of ASMTL proteins. Human ASMTL [GenBank:NP_004183] was used as a seed to search the GenBank NR database for orthologs and an approximate maximum-likelihood tree was generated. The putative mouse ASMTL lacks the ASMT domain and clusters well outside the mammalian clade, indicating that it has considerably diverged compared to the putative ancestor. Entries are annotated with species, chromosome (where known) and GenBank Accession number.

Discussion

Mutations in the ATRX gene result in profound cognitive deficits, facial dysmorphisms, as well as skeletal and urogenital abnormalities [15]. Global deletion of Atrx in mouse embryonic stem cells results in a growth disadvantage [28], and conditional loss of Atrx beginning at the 8–16 cell stage leads to embryonic lethality by E9.5 [28]. To bypass early embryonic lethality, we have previously used a conditional approach to delete Atrx in the mouse forebrain beginning at E8.0. These mice have significantly increased cortical progenitor cell apoptosis, causing a reduction in forebrain size and hypocellularity in the neocortex and hippocampus [19]. ATRX is a chromatin remodeling protein [16] and has been proposed to regulate gene expression by modulating chromatin structure, but gene targets of ATRX have not yet been reported. We used a microarray approach to perform large-scale analysis of gene expression changes in the ATRX-null versus wild type mouse forebrain at E13.5 and P0.5. The fact that relatively few genes display altered expression indicates that ATRX is not a global regulator of gene expression but likely controls specific gene loci. It is not clear at this point if ATRX acts by binding directly to DNA or through other unidentified factors to upregulate the ancestral PAR genes identified in our study. The only target of ATRX identified to date is α globin which is downregulated in patients with germline or somatic ATRX mutations [29], including α-thalassemia myelodysplastic syndrome [30], although evidence that ATRX directly binds to the α globin locus is still lacking.

Through global transcriptional profiling we have now identified a distinct group of genes, the ancestral PAR genes, that are controlled by ATRX in the mouse brain. The human PAR1 contains 24 genes, but only 10 of these have been reported in the mouse genome. Arsd/e, Asmtl, Cd99, Csf2ra, Dhrsxy and Shox2 were among the most downregulated genes identified in the ATRX-null embryonic forebrain. Although these genes are unrelated in function, they share a common ancestral location in the PAR1 of the X chromosome millions of years ago. Our findings demonstrate that they have maintained a mechanism of co-regulation that was conserved in evolution and that requires ATRX, even after their dispersal to autosomes in the mouse genome.

The PAR1 region exhibits recombination rates approximately 10 times higher than the rest of the human genome [8]. Consequently, genes in this region undergo rapid evolution leading to high interspecies divergence [9,31] making positive identification of homologs difficult. Using multiple sequence alignments and phylogenetic analysis we have identified Arsd/e and Asmtl as putative novel mouse ancestral PAR transcripts. Identity between mouse and human sequences are 47%, 40% and 51% for ARSE [GenBank:NM_000047], ARSD [GenBank:NM_001669] and ASMTL [GenBank:NM_004192], respectively, which is similar to what was reported for other PAR1 genes. For example, DHRSXY exhibits 59% protein identity between humans and mice [9], CD99 46% identity [32], and 35% for CSF2RA [33].

ARSD and ARSE are members of the arylsulfatase gene family and are located just outside the human PAR1 in a cluster of four arylsulfatase genes [24]. ARSE gene mutations cause X-linked chondrodysplasia punctata, a disorder characterized by abnormalities in cartilage and bone development [34]. ARSE may therefore play a role in the skeletal defects seen in patients with the ATR-X syndrome if it is also regulated by ATRX in humans. The role of ARSD is unknown and it has no demonstrated sulfatase activity despite its high conservation of the N-terminal domain important for catalytic sulfatase activity [35]. ARSE exhibits a restricted pattern of expression [23] while ARSD is ubiquitously expressed [36].

The function of human ASMTL is unknown. The gene was generated by the duplication of the PAR1 gene Asmt which then fused with the bacterial orfE/maf gene [27]. While other ASMT genes involved in the serotonin/N-acetylserotonin/melatonin pathway are expressed specifically in the human brain, pineal gland and retina [37], ASMTL has a wider expression pattern and may not be involved in this pathway but could still have methyltransferase activity since it retains the necessary domain [27].

We have also identified the mouse Shox2 gene as a potential target of ATRX, and we observed that Shox2 expression levels are highly sensitive to ATRX deficiency in the developing mouse brain. Two SHOX genes, SHOX and SHOX2 have been identified in the human genome, on chromosomes X and 3, respectively. Only one mouse homolog has been identified and is mapped to chromosome 3. Like ARSE, SHOX genes are involved in skeletal development: mutations and deletions in SHOX lead to Leri-Weill dyschondrosteosis [38,39] and non-syndromic idiopathic short stature [40,41], and deletions cause the short stature phenotype seen in Turner syndrome [41,42]. SHOX2 is involved in craniofacial and limb development [43] and SHOX2 mutations lead to cleft palate [44]. Along with ARSE, the SHOX genes provide an intriguing correlation with the skeletal phenotype of ATR-X patients, and future work should address whether these genes are regulated by ATRX in humans.

Conclusion

Collectively, our findings suggest that even though they are now located on different chromosomes, a large subset of ancestral PAR genes might share a common sequence or factor that was conserved upon translocation from the pseudoautosomal region on the X chromosome to their current autosomal locations in the mouse genome (Figure 6). Uniform regulation of gene expression may be due to similar regulatory features such as common sequences or epigenetic modifications (e.g. CpG islands). Despite the sequencing of the human X chromosome, gaps remain, most notably in the PAR1 region [45]. The repetitive nature of the PARs likely explains the paucity of sequence data for these regions, and the lack of genomic sequence data for the PAR1 genes that have translocated to autosomes in the mouse. However, we speculate that ATRX could be targeted to repetitive sequences surrounding these genes. One indication that ATRX would preferentially target repetitive sequences comes from studies done in human ATR-X syndrome patients. The analysis of blood samples revealed altered DNA methylation of several highly repeated sequences including ribosomal DNA arrays, the Y-specific repeat DYZ2 and subtelomeric repeats [18]. Conservation of repetitive elements in the PAR1 region of eutherians may have been maintained with the PAR1 genes as they moved to autosomes, and perhaps allow ATRX to target these genes in their modern chromosomal locations.

thumbnailFigure 6. Proposed model for the co-regulation of ancestral PAR genes by ATRX. Mice and humans diverged from a common ancestor approximately 50 million years ago. In humans, genes have remained in the PAR region (orange) while in mice and rats they have translocated to autosomes (grey). Our data suggest that despite the translocation of these genes to autosomes (numbered), they still share a common sequence or chromatin environment that allows ATRX (green circles) to keep these genes active. We propose that this common feature was conserved upon translocation from the pseudoautosomal region on the X and Y chromosomes in the ancestral PAR to their current autosomal locations in the mouse genome. mya, millions of years ago.

Future work should focus on identifying the molecular mechanisms by which ATRX can co-regulate this diverse set of genes linked by their ancestral localization in the PAR1 region. This will lead to a better understanding of ATRX function in the regulation of chromatin structure and its effects on gene expression in general.

Methods

Mouse husbandry

Mice conditionally deficient for ATRX in the forebrain were generated by crossing AtrxloxP females with heterozygous Foxg1Cre male mice, as previously described [19]. Pregnant females were sacrificed at E13.5, embryos were recovered and yolk sac DNA was genotyped by PCR using the primers 17F, 18R and neoras described previously [19]. For newborns (P0.5) and juveniles (P17), pups were sacrificed and tail DNA was used for genotyping as previously described [19].

Microarray analysis

Total forebrain RNA (10 μg) was isolated from three E13.5 and four P0.5 pairs of littermate-matched ATRX-null and control embryos using the RNeasy Mini kit (Qiagen). cRNA was generated and hybridized to an Affymetrix Mouse Genome 430 2.0 Array at the London Regional genomics Center (London, Canada). For the analysis at E13.5, RNA from two forebrains was pooled for each array. Probe signal intensities were generated using GCOS1.4 (Affymetrix Inc., Santa Clara, CA) using default values for the Statistical Expression algorithm parameters and a Target Signal of 150 for all probe sets and a Normalization Value of 1. Gene level data was generated using the RMA preprocessor in GeneSpring GX 7.3.1 (Agilent Technologies Inc., Palo Alto, CA). Data were then transformed (measurements less than 0.01 set to 0.01), normalized per chip to the 50th percentile, and per gene to control samples. Probe sets representing Atrx transcripts were removed (10 sets). Remaining probe sets were filtered by fold change of either ≥1.5 or 2 between control and Atrx-null samples, and by confidence level of P < 0.05. Heatmaps were generated using the GeneSpring hierarchical clustering gene tree function. Significantly overrepresented GO categories were determined using GeneSpring: at E13.5 and P0.5, probe sets were filtered by 1.5 fold change, P < 0.05 and categorized as either up or downregulated. Where there were multiple probe sets for a gene, duplicates were removed. P < 0.001 was used as the significance cutoff.

qRT-PCR

Total RNA was isolated using the RNeasy Mini kit (QIAGEN). First-strand cDNA was synthesized from 3 μg of total RNA using the SuperScript™ II Reverse Transcriptase kit (Invitrogen) with 25 mM dNTPs (GE Healthcare), 1 μL porcine RNAguard (GE Healthcare) and 3 μL random primers (GE Healthcare). PCR reactions were performed on a Chromo4 Continuous Fluorescence Detector in the presence of iQ™ SYBR Green Supermix and recorded using the Opticon Monitor 3 software (Bio-Rad Laboratories, Inc.). Samples were amplified as follows: 95°C for 10 seconds, annealed for 20 seconds, 72°C for 30 seconds (See Additional file 6 for primer sequences and annealing temperatures). After amplification a melting curve was generated, and samples were run on a 1.5% agarose gel (75 V for 1 h) to visualize amplicon purity. Standard curves were generated for each primer pair using three fold serial dilutions of control cDNA. Primer efficiency was calculated as E = [10(-1/slope)-1]*100, where a desirable slope is -3.32 and r2 > 0.99. Samples were normalized to β-actin expression and relative gene expression levels were calculated using GeneX software (Bio-Rad Laboratories, Inc.).

Additional file 6. Conditions for quantitative real-time PCR. Primer sequences and annealing temperatures used for quantitative real-time PCR confirmation of downregulated ancestral PAR genes.

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For Arsd/e and Asmtl, the PCR products were gel extracted using the QIAquick Gel Extraction Kit (QIAGEN) according to the manufacturer's instructions and sequenced at the DNA Sequencing Facility at Robarts Research Institute (London, Canada).

Bioinformatics analysis of novel ancestral PAR genes

Probeset sequences were obtained from the Netaffx website http://www.affymetrix.com/analysis/netaffx webcite and used for BLASTn searches http://www.ncbi.nlm.nih.gov/BLAST webcite. For calculation of interspecies similarity, sequences were obtained from NCBI RefSeq http://www.ncbi.nlm.nih.gov/RefSeq webcite or Ensemble http://www.ensembl.org webcite where RefSeq sequences were not available, and pairwise comparisons made using Jalview [46].

For generation of trees and sequence alignments, human ARSE (SwissProt P51690, RefSeq NP_000038) and human ASMTL (SwissProt O95671, RefSeq NP_004183) were used as seeds and the GenBank NR database was searched for high-similarity, full-length orthologs and paralogs. Fifty-nine ARSE and twenty-two ASMTL sequences met or exceeded the similarity cutoff, with resultant species spanning the metazoa from anemone and urchin to a diverse set of vertebrates. Sequences were aligned using T-Coffee 5.56 [47] using default parameters. Alignments were manually adjusted via inspection prior to further analysis. Approximate maximum-likelihood trees were built using PHYML 2.4.5 [48] using the WAG model of protein evolution [49] and a seven-category Gamma-plus-invariant model of rate heterogeneity. All rate parameters were estimated from the data. One hundred bootstrap replicates were performed to assess support for the inferred tree topology. All trees are presented as midpoint-rooted phylograms. Since the given mouse sequences were quite short compared to the full protein length, two sets of trees were built for each family to assess if the mouse sequences were long enough to definitively support their taxonomic clustering. One set utilized a "trimmed" alignment where all alignment columns outside the mouse sequence domain were removed. The trees produced with this trimmed alignment were compared with the set of trees produced from the alignment of the mouse sequences to their respective full-length proteins. For both ARSD/E and ASMTL, very little difference was observed between full-length and trimmed-alignment trees. The trimmed alignments tended to exaggerate sequence divergence and modestly lower bootstrap support levels. Overall topology did not appear significantly different, however, and the text references the full-length sequence phylogeny exclusively.

Cell culture and RNA interference

Neuro-2a cells were grown at 37°C with 5% CO2 in EMEM supplemented with 10% fetal bovine serum (Sigma-Aldrich). For siRNA treatment, 1.5 × 104 cells were plated in a plastic six well dish (Corning Incorporated) on glass coverslips and allowed to grow to 15% confluency (approximately 24 hours). Cultures were transfected using Lipofectamine 2000 (Invitrogen) with 8 nM siATRX (Dharmacon), a non-specific control siRNA (Sigma-Aldrich), or with no siRNA ("Mock") according to the manufacturers' instructions (for siRNA sequences refer to [25]). Total RNA was extracted from cells after 72 hours, cDNA was generated and qPCR analysis performed as described above. Alternatively, cells were processed for immunofluorescence staining as described below.

Immunofluorescence

Neuro-2a cells were fixed using 3:1 methanol:ethanol, incubated for 1 h with the primary antibody (H300 anti-ATRX, 1:100 dilution; Santa Cruz) followed by the secondary antibody (goat-anti rabbit Alexa 594, 1:1500 dilution; Molecular Probes), then counterstained with 4',6-diamidino-2-phenylindole (DAPI) (Sigma-Aldrich) for 5 min. Coverslips were mounted with Vectashield (Vector Laboratories), Z-stack images were captured using a Leica DMI6000b inverted microscope and Openlab software (v5.0, Improvision) and processed using Volocity software (v4.0, Improvision); deconvolution was performed using iterative restoration set with a confidence limit of 95%.

Abbreviations

PAR: Pseudoautosomal region; SWI/SNF: Switching/Sucrose non-fermenting; ATRX: α thalassemia mental retardation: X linked; XCI: X chromosome inactivation; Csf2ra: Colony stimulating factor 2 receptor: alpha; Cd99: CD99 antigen; Dhrsxy: dehydrogenase/reductase (SDR family) X chromosome; Ars: Arylsulfatase; Asmtl: acetylserotonin O-methyltransferase-like; ADD: Atrx Dnmt3a/b Dnmt3L; rDNA: ribosomal DNA; Foxg1: forkhead box G1; Cre: cyclization recombinase; EST: Expressed Sequence Tag; BLASTn: Basic Local Alignment Search Tool nucleotide; BLAT: BLAST-like Alignment Tool; E: embryonic; P: postnatal; Sts: steroid sulfatase; siRNA: Small interfering RNA; RT-PCR: reverse-transcriptase polymerase chain reaction; MAF: musculoaponeurotic fibrosarcoma; ASMT: acetylserotonin O-methyltransferase; SDR: Short-chain dehydrogenase/reductase; SHOX: short stature homeobox; ATR-X: alpha thalassemia mental retardation: X linked (referring to the syndrome); Neuro-2a: Neuroblastoma-2a; DAPI: 4',6-diamidino-2-phenylindole; GO: Gene Ontology.

Authors' contributions

ML performed animal husbandry, isolated RNA from E13.5 forebrains for microarray and qRT-PCR analysis, analyzed microarray results, carried out qRT-PCR analysis, cell culture and immunofluorescence, initial bioinformatics analysis and wrote the manuscript. AF performed the phylogenetic analysis of Arsd/e and Asmtl and provided expertise on the bioinformatics analysis. DT performed animal husbandry and extracted RNA from P0.5 forebrains for microarray and qRT-PCR analysis. CS performed animal husbandry and provided technical expertise. NB provided technical expertise, intellectual direction and assisted with the writing of the manuscript.

Acknowledgements

We thank Douglas R. Higgs and Richard J. Gibbons for the AtrxloxP mice. We wish to gratefully acknowledge SHARCNET [50] for providing computational resources. M.L. and D.T were supported by Curtis Cadman Foundation and Natural Sciences and Engineering Research Council of Canada (NSERC) fellowships, respectively. This work was funded by the Canadian Institutes for Health Research (MOP-74748) and NSERC (313403) operating grants to N.G.B. N.G.B. is the recipient of a CIHR New Investigator award.

References

  1. Ohno S: Sex chromosomes and sex-linked genes. Berlin: Springer-Verlag; 1967.

  2. Charlesworth B, Charlesworth D: The degeneration of Y chromosomes.

    Philosophical transactions of the Royal Society of London 2000, 355(1403):1563-1572. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  3. Graves JA: Sex chromosome specialization and degeneration in mammals.

    Cell 2006, 124(5):901-914. PubMed Abstract | Publisher Full Text OpenURL

  4. Graves JAM, Wakefield MJ, Toder R: The origin and evolution of the pseudoautosomal regions of human sex chromosomes.

    Hum Mol Genet 1998, 7(13):1991-1996. PubMed Abstract | Publisher Full Text OpenURL

  5. Lyon MF: X-chromosome inactivation as a system of gene dosage compensation to regulate gene expression.

    Prog Nucleic Acid Res Mol Biol 1989, 36:119-130. PubMed Abstract OpenURL

  6. Carrel L, Willard HF: X-inactivation profile reveals extensive variability in X-linked gene expression in females.

    Nature 2005, 434(7031):400-404. PubMed Abstract | Publisher Full Text OpenURL

  7. Perry J, Palmer S, Gabriel A, Ashworth A: A Short Pseudoautosomal Region in Laboratory Mice.

    Genome Res 2001, 11(11):1826-1832. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  8. Lien S, Szyda J, Schechinger B, Rappold G, Arnheim N: Evidence for heterogeneity in recombination in the human pseudoautosomal region: high resolution analysis by sperm typing and radiation-hybrid mapping.

    American journal of human genetics 2000, 66(2):557-566. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  9. Gianfrancesco F, Sanges R, Esposito T, Tempesta S, Rao E, Rappold G, Archidiacono N, Graves JAM, Forabosco A, D'Urso M: Differential Divergence of Three Human Pseudoautosomal Genes and Their Mouse Homologs: Implications for Sex Chromosome Evolution.

    Genome Res 2001, 11(12):2095-2100. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  10. Bacolla A, Collins JR, Gold B, Chuzhanova N, Yi M, Stephens RM, Stefanov S, Olsh A, Jakupciak JP, Dean M, et al.: Long homopurine*homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region.

    Nucleic Acid Res 2006, 34(9):2663-2675. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  11. Disteche CM, Brannan CI, Larsen A, Adler DA, Schorderet DF, Gearing D, Copeland NG, Jenkins NA, Park LS: The human pseudoautosomal GM-CSF receptor alpha subunit gene is autosomal in mouse.

    Nature genetics 1992, 1(5):333-336. PubMed Abstract | Publisher Full Text OpenURL

  12. Bixel G, Kloep S, Butz S, Petri B, Engelhardt B, Vestweber D: Mouse CD99 participates in T-cell recruitment into inflamed skin.

    Blood 2004, 104(10):3205-3213. PubMed Abstract | Publisher Full Text OpenURL

  13. Eisen JA, Sweder KS, Hanawalt PC: Evolution of the SNF2 family of proteins: subfamilies with distinct sequences and functions.

    Nucleic acids research 1995, 23(14):2715-2723. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  14. Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ: ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.

    Human molecular genetics 1996, 5(12):1899-1907. PubMed Abstract | Publisher Full Text OpenURL

  15. Gibbons RJ, Higgs DR: Molecular-clinical spectrum of the ATR-X syndrome.

    American journal of medical genetics 2000, 97(3):204-212. PubMed Abstract OpenURL

  16. Xue Y, Gibbons R, Yan Z, Yang D, McDowell TL, Sechi S, Qin J, Zhou S, Higgs D, Wang W: The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies.

    Proceedings of the National Academy of Sciences of the United States of America 2003, 100(19):10635-10640. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  17. McDowell TL, Gibbons RJ, Sutherland H, O'Rourke DM, Bickmore WA, Pombo A, Turley H, Gatter K, Picketts DJ, Buckle VJ, et al.: Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes.

    Proceedings of the National Academy of Sciences of the United States of America 1999, 96(24):13983-13988. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  18. Gibbons RJ, McDowell TL, Raman S, O'Rourke DM, Garrick D, Ayyub H, Higgs DR: Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.

    Nature genetics 2000, 24(4):368-371. PubMed Abstract | Publisher Full Text OpenURL

  19. Bérubé NG, Mangelsdorf M, Jagla M, Vanderluit J, Garrick D, Gibbons RJ, Higgs DR, Slack RS, Picketts DJ: The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.

    The Journal of clinical investigation 2005, 115(2):258-267. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  20. Hebert JM, McConnell SK: Targeting of cre to the Foxg1 (BF-1) locus mediates loxP recombination in the telencephalon and other developing head structures.

    Developmental biology 2000, 222(2):296-306. PubMed Abstract | Publisher Full Text OpenURL

  21. GeneChip® Mouse Genome 430 2.0 Array [http://www.affymetrix.com/products/arrays/specific/mouse430_2.affx] webcite

  22. Trouw LA, Blom AM, Gasque P: Role of complement and complement regulators in the removal of apoptotic cells.

    Molecular immunology 2008, 45(5):1199-1207. PubMed Abstract | Publisher Full Text OpenURL

  23. Franco B, Meroni G, Parenti G, Levilliers J, Bernard L, Gebbia M, Cox L, Maroteaux P, Sheffield L, Rappold GA, et al.: A cluster of sulfatase genes on Xp22.3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy.

    Cell 1995, 81(1):15-25. PubMed Abstract | Publisher Full Text OpenURL

  24. Meroni G, Franco B, Archidiacono N, Messali S, Andolfi G, Rocchi M, Ballabio A: Characterization of a cluster of sulfatase genes on Xp22.3 suggests gene duplications in an ancestral pseudoautosomal region.

    Human molecular genetics 1996, 5(4):423-431. PubMed Abstract | Publisher Full Text OpenURL

  25. Ritchie K, Seah C, Moulin J, Isaac C, Dick F, Berube NG: Loss of ATRX leads to chromosome cohesion and congression defects.

    The Journal of cell biology 2008, 180(2):315-324. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  26. Garrick D, Samara V, McDowell TL, Smith AJ, Dobbie L, Higgs DR, Gibbons RJ: A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.

    Gene 2004, 326:23-34. PubMed Abstract | Publisher Full Text OpenURL

  27. Ried K, Rao E, Schiebel K, Rappold GA: Gene duplications as a recurrent theme in the evolution of the human pseudoautosomal region 1: isolation of the gene ASMTL.

    Hum Mol Genet 1998, 7(11):1771-1778. PubMed Abstract | Publisher Full Text OpenURL

  28. Garrick D, Sharpe JA, Arkell R, Dobbie L, Smith AJ, Wood WG, Higgs DR, Gibbons RJ: Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.

    PLoS genetics 2006, 2(4):e58. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  29. Gibbons RJ, Picketts DJ, Villard L, Higgs DR: Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome).

    Cell 1995, 80(6):837-845. PubMed Abstract | Publisher Full Text OpenURL

  30. Steensma DP, Gibbons RJ, Higgs DR: Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies.

    Blood 2005, 105(2):443-452. PubMed Abstract | Publisher Full Text OpenURL

  31. Ellison J, Franckle LU, Shapiro LJ: Rapid evolution of human pseudoautosomal genes and their mouse homologs.

    Mammalian Genome 1996, 7(1):25-30. PubMed Abstract | Publisher Full Text OpenURL

  32. Park SH, Shin YK, Suh YH, Park WS, Ban YL, Choi HS, Park HJ, Jung KC: Rapid divergency of rodent CD99 orthologs: implications for the evolution of the pseudoautosomal region.

    Gene 2005, 353(2):177-188. PubMed Abstract | Publisher Full Text OpenURL

  33. Park LS, Martin U, Sorensen R, Luhr S, Morrissey PJ, Cosman D, Larsen A: Cloning of the low-affinity murine granulocyte-macrophage colony-stimulating factor receptor and reconstitution of a high-affinity receptor complex.

    Proceedings of the National Academy of Sciences of the United States of America 1992, 89(10):4295-4299. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  34. Daniele A, Parenti G, d'Addio M, Andria G, Ballabio A, Meroni G: Biochemical characterization of arylsulfatase E and functional analysis of mutations found in patients with X-linked chondrodysplasia punctata.

    American journal of human genetics 1998, 62(3):562-572. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  35. Urbitsch P, Salzer MJ, Hirschmann P, Vogt PH: Arylsulfatase D gene in Xp22.3 encodes two protein isoforms.

    DNA Cell Biol 2000, 19(12):765-773. PubMed Abstract | Publisher Full Text OpenURL

  36. Dooley TP, Haldeman-Cahill R, Joiner J, Wilborn TW: Expression profiling of human sulfotransferase and sulfatase gene superfamilies in epithelial tissues and cultured cells.

    Biochem Biophys Res Commun 2000, 277(1):236-245. PubMed Abstract | Publisher Full Text OpenURL

  37. Gauer F, Craft CM: Circadian regulation of hydroxyindole-O-methyltransferase mRNA levels in rat pineal and retina.

    Brain research 1996, 737(1–2):99-109. PubMed Abstract | Publisher Full Text OpenURL

  38. Belin V, Cusin V, Viot G, Girlich D, Toutain A, Moncla A, Vekemans M, Le Merrer M, Munnich A, Cormier-Daire V: SHOX mutations in dyschondrosteosis (Leri-Weill syndrome).

    Nature genetics 1998, 19(1):67-69. PubMed Abstract | Publisher Full Text OpenURL

  39. Shears DJ, Vassal HJ, Goodman FR, Palmer RW, Reardon W, Superti-Furga A, Scambler PJ, Winter RM: Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis.

    Nature genetics 1998, 19(1):70-73. PubMed Abstract | Publisher Full Text OpenURL

  40. Rappold GA, Fukami M, Niesler B, Schiller S, Zumkeller W, Bettendorf M, Heinrich U, Vlachopapadoupoulou E, Reinehr T, Onigata K, et al.: Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.

    J Clin Endocrinol Metab 2002, 87(3):1402-1406. PubMed Abstract | Publisher Full Text OpenURL

  41. Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, et al.: Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

    Nature genetics 1997, 16(1):54-63. PubMed Abstract | Publisher Full Text OpenURL

  42. Clement-Jones M, Schiller S, Rao E, Blaschke RJ, Zuniga A, Zeller R, Robson SC, Binder G, Glass I, Strachan T, et al.: The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome.

    Human molecular genetics 2000, 9(5):695-702. PubMed Abstract | Publisher Full Text OpenURL

  43. Blaschke RJ, Monaghan AP, Schiller S, Schechinger B, Rao E, Padilla-Nash H, Ried T, Rappold GA: SHOT, a SHOX-related homeobox gene, is implicated in craniofacial, brain, heart, and limb development.

    Proceedings of the National Academy of Sciences of the United States of America 1998, 95(5):2406-2411. PubMed Abstract | Publisher Full Text | PubMed Central Full Text OpenURL

  44. Yu L, Gu S, Alappat S, Song Y, Yan M, Zhang X, Zhang G, Jiang Y, Zhang Z, Zhang Y, et al.: Shox2-deficient mice exhibit a rare type of incomplete clefting of the secondary palate.

    Development (Cambridge, England) 2005, 132(19):4397-4406. PubMed Abstract | Publisher Full Text OpenURL

  45. Ross MT, Grafham DV, Coffey AJ, Scherer S, McLay K, Muzny D, Platzer M, Howell GR, Burrows C, Bird CP, et al.: The DNA sequence of the human X chromosome.

    Nature 2005, 434(7031):325-337. PubMed Abstract | Publisher Full Text OpenURL

  46. Clamp M, Cuff J, Searle SM, Barton GJ: The Jalview Java alignment editor.

    Bioinformatics 2004, 20(3):426-427. PubMed Abstract | Publisher Full Text OpenURL

  47. Notredame C, Higgins DG, Heringa J: T-Coffee: A novel method for fast and accurate multiple sequence alignment.

    J Mol Biol 2000, 302(1):205-217. PubMed Abstract | Publisher Full Text OpenURL

  48. Guindon S, Gascuel O: A simple, fast, and accurate algorithm to estimate large phylogenies by maximum likelihood.

    Syst Biol 2003, 52(5):696-704. PubMed Abstract OpenURL

  49. Whelan S, Goldman N: A general empirical model of protein evolution derived from multiple protein families using a maximum-likelihood approach.

    Mol Biol Evol 2001, 18(5):691-699. PubMed Abstract | Publisher Full Text OpenURL

  50. The Canadian Shared Hierarchical Academic Research Computing Network [http://www.sharcnet.ca/] webcite

  51. BoxShade Server 3.21 [http://www.ch.embnet.org/software/BOX_form.html] webcite