Disorders of sexual development (DSD), ranging in severity from genital abnormalities to complete sex reversal, are among the most common human birth defects with incidence rates reaching almost 3%. Although causative alterations in key genes controlling gonad development have been identified, the majority of DSD cases remain unexplained. To improve the diagnosis, we screened 116 children born with idiopathic DSD using a clinically validated array-based comparative genomic hybridization platform. 8951 controls without urogenital defects were used to compare with our cohort of affected patients. Clinically relevant imbalances were found in 21.5% of the analyzed patients. Most anomalies (74.2%) evaded detection by the routinely ordered karyotype and were scattered across the genome in gene-enriched subtelomeric loci. Among these defects, confirmed de novo duplication and deletion events were noted on 1p36.33, 9p24.3 and 19q12-q13.11 for ambiguous genitalia, 10p14 and Xq28 for cryptorchidism and 12p13 and 16p11.2 for hypospadias. These variants were significantly associated with genitourinary defects (P = 6.08×10−12). The causality of defects observed in 5p15.3, 9p24.3, 22q12.1 and Xq28 was supported by the presence of overlapping chromosomal rearrangements in several unrelated patients. In addition to known gonad determining genes including SRY and DMRT1, novel candidate genes such as FGFR2, KANK1, ADCY2 and ZEB2 were encompassed. The identification of risk germline rearrangements for urogenital birth defects may impact diagnosis and genetic counseling and contribute to the elucidation of the molecular mechanisms underlying the pathogenesis of human sexual development.
Citation: Tannour-Louet M, Han S, Corbett ST, Louet J-F, Yatsenko S, Meyers L, et al. (2010) Identification of De Novo Copy Number Variants Associated with Human Disorders of Sexual Development. PLoS ONE 5(10): e15392. doi:10.1371/journal.pone.0015392
Editor: Syed A. Aziz, Health Canada, Canada
Received: August 17, 2010; Accepted: September 1, 2010; Published: October 26, 2010
Copyright: © 2010 Tannour-Louet, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by Grants 1R01DK078121 from the National Institute of Kidney and Digestive Diseases to DJL, the American Urological Association Foundation (SC and DJL), and by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (P01HD36289) to DJL. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
The acquisition of a sexual phenotype depends on critical embryonic steps, which initially commit the bipotential gonad to either a testis or an ovary and direct normal morphogenesis of external genitalia. Disruption of these developmental processes occurs frequently in humans as reflected by the high prevalence in newborns of disorders of sexual development (DSD) ranging in severity from genital abnormalities to complete sex reversal. Failure of testis descent or cryptorchidism is found in 2% of full-term males . Hypospadias or defects in the growth and closure of the external genitalia affect nearly 1 in 125 live male births . Genital phenotypes that are not clearly male or female are estimated to occur in about 1 of 2000 to 4500 babies . Despite their incidence, the molecular basis underlying the pathology of congenital genitourinary (GU) defects is surprisingly poorly understood. Fetal exposure to environmental toxicants , , as well as point mutations in a small subset of genes (see for review , ) can affect human urogenital tract development, but these known causes do not account for all of the large number of GU birth defects. Interestingly, as referenced in the Online database of Mendelian Inheritance in Man (http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim), a significant number of these urogenital inborn errors are associated with major congenital malformations or multiple minor anomalies, a trait that is highly suggestive of a causative chromosomal abnormality. However, routine cytogenetic methods had led to earlier reports of low rates of structural defects associated with disorders of sexual development , .
The finding that several common syndromes (including mental retardation, developmental delay and autism) are caused by specific submicroscopic chromosomal rearrangements, opened up new avenues for dissecting complex human phenotypes , . The development of comparative genomic hybridization (CGH) into a microarray format allowed the identification and diagnosis of cryptic deletions or duplications of genomic regions that were once invisible using traditional cytogenetic methods, including karyotype analysis and fluorescence in situ hybridization (FISH). Several of these subtle rearrangements occur in regions flanked by low-copy repeats and likely result from non-allelic homologous recombination between different copies of these repeats during meiosis. Such submicroscopic imbalances lead to copy number changes of DNA segments and can influence gene expression levels by directly disrupting genes or regulatory sequences, creating fusion genes or altering gene dosage. These structural chromosomal defects can cause disease as occurs in the microdeletion and microduplication syndromes , , , ,  or confer risk of complex disorders , .
Cryptic chromosomal rearrangements are involved in the etiology of human reproductive disorders since Y chromosome microdeletions are associated with human male infertility. Based on this, we tested the hypothesis that submicroscopic chromosomal alterations, too small to be detected by routine cytogenetic methods, may exist in patients with human disorders of sexual development. We studied probands presenting with hypospadias, cryptorchidism and ambiguous genitalia, the most common genital defects seen in pediatric urology clinics. We compared the resolution of clinical detection of such cryptic abnormalities by microarray-based chromosomal screening and by the routinely used karyotype. We further analyzed the contribution of these structural anomalies to the observed GU phenotypes by studying their association with the genital traits, as well as their inheritance and their recurrence. For the first time, findings revealed the presence of frequent microdeletions and microduplications in the genome of children born with urogenital disorders and established de novo germline rearrangements as significant risk factors for developmental defects of human urogenital tract.
Ethics Statement, Human Subjects and Sample Collection
This study was approved by the Institutional Review Board Committee at the Baylor College of Medicine, Houston TX. Probands affected with unexplained syndromic and non-syndromic congenital genitourinary disorders including hypospadias, cryptorchidism or ambiguous genitalia were enrolled through Texas Children's Hospital and Ben Taub General Hospital, Houston TX. Known causes of these birth defects such as anomalies in the synthesis of testosterone or adrenal steroid hormones or exogenous modifiers were ruled out after examination by pediatric urologists or neonatologists. Written informed consents were obtained for infant/child subjects and from their parents. Blood was collected from the children during surgery for correction of the GU defects. Parents provided saliva specimens. Based on the novel CMA findings, additional cases were then identified through an existing database from Kleberg Cytogenetics Laboratory (Baylor College of Medicine, Houston TX). These additional probands were referred patients, mostly presenting with external genital ambiguity with or without subclinical phenotypes. Clinical indications at the time of the referral were taken from crude clinical comments on laboratory requisitions.
CGH based Microarray Analysis (CMA)
High molecular weight genomic DNA isolated from peripheral blood or saliva was submitted for chromosomal microarray analysis (CMA) to the Clinical Cytogenetics Laboratory at Baylor College of Medicine. CMA is a clinically validated targeted CGH array that covers over 150 distinct human clinically relevant chromosomal loci , . Three different versions of CMA have been used depending on the time of sample submission. The versions 5 and 6 contain 3 to 10 BAC/PAC clones per genomic disorder specific locus and subtelomeric regions, with CMA V.5.0 consisting of 853 BAC clones and CMA V.6.1 consisting of 1475 BAC clones with inclusion of 1 clone per band at 650 cytogenetic banding resolution. The newer version Oligo V.6 uses 42,640 oligonucleotides of 60 base pairs with an average of 20 to 40 oligonucleotides corresponding to each CMA V.6.1 BAC clone genomic locus. Importantly, data acquired from the array platforms CMA V.6.1 and CMA Oligo V6 were shown to be qualitatively comparable, allowing for cross comparison analysis . One unique DNA reference served as a control for CMA analysis and was from a pregnancy-proven fertile, gender-matched individual without any familial history of congenital genitourinary defects. CMA procedures and data analyses were performed as previously described , , .
All data are MIAME compliant and have been deposited in a MIAME compliant database.
Interpretation of CNV significance
Clinically significant CNVs included detection of well-characterized deletion/duplication syndromes, deletion/duplication >3 Mb in size or cytogenetically visible, and de novo deletions or duplications <1 Mb. Imbalances that were not associated with well-characterized human syndromes were defined as “likely benign” when the variant was well documented to occur in the normal population on the basis of public databases (http://projects.tcag.ca/variation) or internal lab experience which includes analysis of about 16,000 individuals. In cases in which non-polymorphic defects were <1 Mb in size and parental samples were unavailable, variants were considered to be CNVs of uncertain clinical significance. Maternally inherited copy changes were included in this latter category as the rearrangements may be causative without necessarily translating into similar abnormal GU traits in the female genitourinary tract.
FISH analysis was used to validate selected CMA findings >150 Kb in size, using the standard clinical cytogenetics laboratory protocol . Briefly, BAC clone DNA probes were labeled directly with Spectrum Orange-dUTP or Spectrum Green-dUTP using a commercially available kit (Abbot Molecular/Vysis). At least 10 metaphase and/or 50 interphase cells were scored for each hybridization. A control probe, labeled in the opposite color, was included in the same hybridization in order to confirm that cells were diploid (ploidy control).
Quantitative TaqMan copy number variant (CNV) assays (Applied Biosystems) were used as an alternate secondary confirmation to FISH analysis. All reactions with TaqMan CNV assays were performed in triplicate using the FAM dye label-based assay for the target of interest and the VIC dye label-based TaqMan CNV RNaseP for the internal controls. The targets were custom designed in the areas where most significant changes in the probes were detected. QPCR was performed with 20 ng gDNA according to the manufacturer's protocol in an Applied Biosystems One Step Plus Real-Time PCR System using the default universal cycling conditions. Relative quantitation analysis was done to estimate copy number for each sample by using the Copy Caller Software V1.0 (Applied Biosystems).
Concurrent G-banding Karyotype
Metaphase preparations from PHA-stimulated patient lymphocyte cultures followed a standard protocol to obtain chromosomes at ≥600–50-band level . Briefly, after being cultured for ~72 hours in RPMI 1640 with 20% fetal bovine serum, lymphocytes were synchronized by the addition of thymidine for 24 hours of culture, followed by the addition of ethidium bromide and colcemid for the last 45 minutes and 25 minutes of culture, respectively. The cells were treated for 20 minutes with 0.075 M KCl and were fixed in 3:1 methanol–acetic acid prior to staining. The chromosomes were GTG-banded, and ≥20 chromosomal spreads were examined.
To analyze the frequency of de novo copy number changes in affected GU patients compared to unaffected GU individuals (non-GU controls), two-tailed Fisher's exact test was performed and statistical significance determined using SPSS software. Since (i) de novo events were only observed in GU patients run on CMA V.6.1 and CMA Oligo V6 (n = 90 out of the total of 116 analyzed GU children) and (ii) data acquired from the array platforms CMA V.6.1 and CMA Oligo V6 were shown to be qualitatively comparable , comparison of frequencies was done for cases and non-GU controls run only on CMA V.6.1 and CMA Oligo V6. P values were also determined for each of the spontaneous events to evaluate their association with the GU phenotype as compared to their specific occurrence in individuals without GU defects (n = 8951). Significance threshold was set at P = 5.0×10−2.
Detection of Non-Polymorphic Imbalances Leading to Variations in Copy Number in the Genome of Children Born With Disorders of Sex Development
High molecular weight genomic DNA was isolated from peripheral blood of 116 children presenting with unexplained cases of disorders of sexual development ranging in severity from penile growth or testicular descent anomalies to genitalia ambiguity or complete sex reversal. Since the primary goal of this study was to improve the diagnosis of these urogenital defects and rapidly translate the findings to the clinic, DNA was analyzed using an established CGH microarray platform available for clinical diagnosis (chromosome microarray assay, CMA) , . This targeted array specifically assesses relative copy number changes for over 150 human clinically relevant chromosomal loci. One unique DNA reference served as a control for CMA analysis and was from a pregnancy-proven fertile, gender-matched individual without any familial history of congenital genitourinary defects. Copy number variants (CNVs) were classified based on their clinical significance (see Methods). Basically, CNV pathogenicity depended on whether a given CNV overlapped with a known genomic syndrome that includes urogenital defects among the clinical features, or was present in a patient with similar phenotype, was not a copy number variant in healthy individuals, arose de novo (but not exclusively) and contained at least one gene.
Chromosomal imbalances were detected in 37 (31.9%) of the 116 patients analyzed (Table 1). When compared to the polymorphisms documented in public CNV databases (http://projects.tcag.ca/variation) or based on internal lab experience, which included analysis of about 16,000 individuals, 83.8% (31 of 37) of these defects were non-polymorphic (Table 1). FISH or qPCR secondarily validated these structural variants. They spanned the genome and affected sex chromosomes, as well as autosomal regions (Figure 1 and Tables 2–5), an observation consistent with the fact that male sexual development is governed by genes not restricted to the Y chromosome . Most of the genomic rearrangements (25 of 37 i.e. 72.9%) were clinically significant copy number variants (Table 1 and Tables 2–4). Detection rates of these clinically relevant aberrations were slightly comparable between the three studied genital conditions (25% for ambiguous genitalia, 17.2% for hypospadias and 18.5% for cryptorchidism) (Table 1). Interestingly, these genomic abnormalities were noted in patients presenting with both syndromic, as well as non-syndromic genitourinary disorders (Table 1), with no statistically significant difference in their respective detection rates. From a clinical perspective, this latter observation stresses the importance of screening children presenting with isolated hypospadias or cryptorchidism, who usually are not referred for genetic testing.
On the right, CMA detected imbalances were shown for each clinical condition (asterisks). To gain insight into the genomic distribution of the identified imbalances, all published single gene mutations associated with cryptorchidism (blue), hypospadias (green) and ambiguous genitalia (red) were reviewed and indicated on the left side of the chromosomes. References are available upon request.
Regardless of the GU condition, the size of CMA detected anomalies ranged from 50 kilobases to 57.4 Mb with an average defect size of 5.5 Mb, which is at the limit of the resolution of routine karyotype (Tables 2–5). Importantly, none of the imbalances smaller than 5 Mb, which represent about 70% of the identified CMA defects, were detected by concurrent high-resolution karyotype analysis (Tables 2–5). For the cases of imbalances larger than 5 Mb, CMA analysis had proven to provide a better definition of the structural defect than the karyotype (patients 6, 9, 12, 13, 18- see Tables 2–5). Moreover, most of the detected imbalances (70.6%) were subtelomeric defects (Tables 2–5), which are known to be difficult to characterize by G-banding due to their location in the distal G-negative staining regions of the chromosomes. The most illustrative finding was seen in patient 15 with a referring diagnosis of ambiguous genitalia (Table 2). A large deletion of 57.4 Mb spanning the subtelomeric 10q26 was only suspected by karyotype, but was successfully detected by CMA analysis. Interestingly, this deletion encompassed FGFR2, a particularly noteworthy candidate gene in light of recent studies in rodents that found evidence for its role in testis formation and male sex determination , . While gene variants of FGFR2 may influence the risk of hypospadias in humans , conditional inactivation of FGFR2 in mouse models resulted in blockade of the XY-specific gonad growth and disruption of testis differentiation, leading to a male-to-female sex reversal phenotype. The characterization of FGFR2 as a sex-determining gene in the mouse suggests that the CMA detected human haploinsufficiency of FGFR2 is a strong candidate defect underlying the phenotype of abnormal male genital development in patient 15.
Interestingly, in three unrelated CMA screened patients (27, 28 and 30; Table 2), a low-level mosaic state became apparent after CMA screening and retrospective analysis of the karyotype. Interphase FISH performed on blood smears in which multiple cell lineages coexist, was requested after CMA testing, to verify mosaicism in these children. The conventional karyotype was normal since it examined only the cell population of stimulated T lymphocytes. The fact that CMA analysis performed on DNA from uncultured blood cells was able to improve the detection of low level mosaicism missed by cytogenetic analysis, is of significant clinical importance, especially for the diagnosis of genital ambiguity.
Strong Association of De Novo Copy Variants with Human Disorders of Sex Development
The inheritance of the FISH-confirmed CMA defects was investigated by CMA testing. Parental samples were not available for all patients, leading to an underestimation of the clinically significant abnormalities in the present evaluation. De novo occurrences were noted for: (i) deletions in 1p36.33, 9p23p24 and 19q12-q13.11 for probands presenting with a referring diagnosis of ambiguous genitalia; (ii) duplications in 10p14 and Xq28 for cryptorchid children; (iii) and deletions in 12p13.31-p13.2 and 16p11.2 for patients with hypospadias (Table 6). Importantly, these de novo copy number changes were found to be more frequent in patients with congenital genitourinary defects than in control individuals without GU abnormalities (28 out of 8951), with an association that is statistically significant (P = 6.08×10−12; Fisher's exact test) (Tables 6 and 7).
To a lesser extent, imbalances inherited from a phenotypically normal maternal parent were also considered since the rearrangements may be causative without necessarily translating into similar abnormal GU traits in the female genitourinary tract. Thus, maternally inherited copy changes were considered as of unclear clinical significance and noted as: (i) deletion in 7p22.1 for ambiguous genitalia; (ii) duplications in 4q35.2 and 5p15.31 for hypospadias; (iii) duplication in 5p15.2 and in the androgen receptor insensitivity region, Xq12 for cryptorchidism (Table 5).
Hence, the present analysis shed light on spontaneous chromosomal rearrangements affecting novel and unsuspected gene-enriched regions that have potential to contribute to the pathogenesis of human genital development.
Unrelated Patients Presenting with Similar Genital Traits Shared Common Affected Loci
The causal link of the CMA defects to the GU phenotype was further strengthened by the fact that common overlapped loci were shared by unrelated probands having similar genital defects. Spontaneous deletion of the 9p23p24 region was found in patients 9, 12, and 13, all with gonadal dysgenesis (Table 2). A minimal common region of overlap included 260 kb of 9p24.3 (Figure 2A). This smallest reported sex-reversing 9p deletion appears therefore as a hotspot for the pathogenesis of sex determination. It encompasses KANK1, DOCK8 and DMRT genes. The testis specific DMRT1 is worthy of mention, since it encodes a protein-sharing domain homology with the doublesex (Dsx) of Drosophila and Mab3 of Caenorhabditis. Both of these genes are crucial for the normal sexual development of these organisms. Genetic inactivation of DMRT1 demonstrated its requirement for the development of the male gonad , but did not lead to sex reversal in XY mice, suggesting the involvement of additional interacting factors in order to phenocopy the human phenotype. One of such gene candidates could be KANK1 since it is highly expressed in the mouse embryonic genital tract (http://www.genepaint.org) and is able to physically interact and regulate the subcellular localization of beta catenin whose activation in normal XY mice has been shown to disrupt the male program and result in male-to-female sex-reversal , .
A. Delineation of a minimal human 9p sex reversal deletion. Schematic representation of the overlapping CMA detected 9p deletions in three unrelated 46,XY patients presenting with gonadal dysgenesis. A minimal common 260 Kb region was defined. Map showing the BAC clones covering the critical sex determination region and the normal flanking clones (RP11-459D20 and GS-43N6). A UCSC genome browser view (May 2006 Human Assembly) of the RefSeq genes encompassing the minimal 9p24.3 sex-reversing region was presented. B. Structural variation shared by unrelated patients presenting with distinct urogenital defects, may affect master regulator(s) of human genital development. A common genomic interval of 65 Kb in the cytoband 5p15.31 was deleted in patient 6 with genital ambiguity and duplicated in patient 5 with hypospadias. CMA detection of the 65 Kb duplication in patient 5 and a UCSC genome browser view (May 2006 Human Assembly) of the encompassed ADCY2 gene were presented.
In addition to the 9p region, the locus Yp11.31 was an expected recurrent hit in patients with ambiguous genitalia, since it encompasses SRY, the testis-determining gene (Table 2).
Unique Similar Loci were Abnormal in Patients Presenting with Different Urogenital Traits
Identical unique loci were affected in patients presenting distinct genital phenotypic traits, which suggest that structural perturbations within these segments may alter master regulator(s) of multiple processes of human sexual development. Indeed, a large deletion of the subtelomeric cytoband 5p15 detected in the patient 6 with genital ambiguity overlapped a region duplicated in patient 5 with hypospadias (Figure 2B). The fact that the shared genomic interval spanned the locus of the Cri-du-Chat syndrome, which includes hypospadias among its various clinical features, provides support for a causative link of the 5p15 defect to the GU phenotype. The encompassed gene, ADCY2, appeared as an ideal candidate controlling genitourinary development since it presents a high and specific expression pattern in the testis as well as in the developing genital tract (http://www.genepaint.org). Moreover, the ADCY2 encoding protein regulates the intracellular levels of cyclic AMP, a crucial second messenger in major regulatory pathways involved in the biogenesis of the genital system such as Sonic Hedgehog signaling.
The DiGeorge syndrome critical region 22q11.2 was also found duplicated in patients with ambiguous genitalia, while its deletion was seen in patients presenting with GU abnormalities in association with Smith-Lemli-Opitz syndrome or Wilms tumor (Table 2). This region may have a dosage sensitive gene(s) that plays a role in the development of the genitourinary system in humans.
In parallel, alterations occurring on 2q22 and Xq28 loci were found in patients with cryptochidism and hypospadias (Tables 3–4). These genomic regions may contain candidate genes that regulate a common protagonist(s) or pathway(s) controlling both testicular descent and formation of the male urethra. The deletion 2q22 in patient 2 presenting with cryptorchidism and hypospadias was in the region associated with Mowat-Wilson syndrome (MWS). Among anomalies frequently observed in MWS are urogenital anomalies including hypospadias and undescended testis. MWS is a genetic condition caused by heterozygous mutations or deletions of ZEB2 (zinc finger E-box binding homeobox 2 gene), a protein that interacts with a receptor-mediated, activated full-length SMAD. ZEB2 is strongly expressed in the developing murine genital tract (http://www.genepaint.org). Knockout mice models of ZEB2 presented reproductive system defects (, http://www.informatics.jax.org). Moreover, ZEB2 has been shown to modulate Wnt signaling, a critical pathway for the development of the genital tract . Hence, ZEB2 appears as a potential candidate involved in the male urogenital development.
Taken together, our findings highlight for the first time the presence of previously unrecognized chromosomal imbalances as potential genetic risks factors in disorders of sexual development and illustrate how a microarray-based technology provides a powerful alternative to traditional cytogenetic and gene-mapping approaches for discovering contributing factors in disease of complex etiology.
The development of male reproductive system is a complex process controlled by delicate networks that specify sex-specific differentiation, organogenesis and endocrine function. The fragility of these regulatory cascades is illustrated by the high prevalence of genitourinary defects in newborns. These inborn urogenital anomalies present difficult challenges for the parents and the physicians, as care of these children is complicated by surgical, psychological, social and sexual concerns. The gold standard for genetic diagnosis remains a karyotype analysis and an endocrine profile but findings in intersex cases are not always informative. Indeed, only a small portion of these developmental aberrations can be attributed to defects in the synthesis of testosterone or adrenal steroid hormones, receptor alterations, exogenous modifiers or obvious numerical and structural chromosomal alterations, such as Klinefelter syndrome. The underlying causes of the majority of “idiopathic” cases remain to be discovered. In this study, the use of a clinically validated microarray (CMA) revealed the existence of cryptic imbalances strongly associated with defects of urogenital development or recurrently found in patients with DSD. These chromosomal aberrations were mostly too small to be detected by the routinely ordered karyotype, which has a limited resolution of 5–10 Mb, depending on the quality of chromosome preparations. Many of these genomic anomalies went also largely undetected because they were located in subtelomeric loci, which are notoriously difficult to characterize by G-banding. Moreover, mild or isolated cases of hypospadias and cryptorchid patients are usually not referred for genetic testing, while this study proved that this subset of patients harbored structural variation that may convey defective urogenital traits.
Most of the detected chromosomal aberrations encompassed one to a few hundred genes including known gonad-determining genes (SRY and DMRT1) as well as novel candidate genes such as FGFR2, KANK1, ADCY2 and ZEB2. Changes in dosage or structure of genes within the affected DNA segments might lead to haploinsufficiency or altered transcription profiles, which may disturb the intricate fine-tuned network of genes controlling the human genital development. Clinically relevant examples of gene dosage alterations have already been documented for factors controlling mammalian sex development. For instance, deletion of the sex-determining gene WNT4 is responsible for the masculinization of XX mouse pups, while its duplication and overexpression in humans leads to XY sex reversal , . Duplications of large segments of DNA containing DAX1 or SOX9 also cause sex reversal , . Thus, our findings contribute in a coherent manner to strengthen the emerging concept that sex determination and differentiation are dosage sensitive at multiple steps of their pathways. In addition to dosage effects, imbalances may lead to disruption of regulatory sequences that control the expression of neighboring genes; thus, in some cases, a gene related to genital development may lie adjacent to the detected deletion or duplication. For instance, a submicroscopic 258 Kb deletion, detected 11,320 bp upstream of DAX1 in a 21-year-old 46,XY female, may lead to a loss of regulatory sequences and position-effect upregulation of DAX1 expression .
Our findings provide support for the genomic basis of human disorders of sexual development and call for genome-wide CNV screenings which may, due to their extended coverage, reveal a higher proportion of germline mutations associated with urogenital defects. Enrichment in candidate genes for human sexual development is subsequently bound to increase. Our present study using the clinically established CMA platform was motivated by a rapid translation of our findings to the clinical arena. Molecular testing, such as with CMA, could significantly impact patient care by assisting the pediatric urologists and neonatologists in diagnosis. Genetic counseling offered to families based on the identification of pathogenic rearrangements may provide parents with essential clinical information pertaining to the child's diagnosis and permit proper estimates of the risk of recurrence for subsequent pregnancies. De novo imbalances are expected to have a very low risk of recurrence but it may be useful in future pregnancies to check for gonadal mosaicism in the parents. An unbalanced translocation identified by CMA may reveal a balanced translocation in a carrier parent and thus chances for a chromosomally abnormal future pregnancy would be as high as 25%. In vitro fertilization and pre-implantation genetic diagnosis could provide these couples with a possible alternative path to parenthood, specifically in case of severe genital ambiguity.
In conclusion, this study presented structural DNA variation as a potential underlying etiology for human disorders of sexual development. Frequent disease-causing submicroscopic gains and losses of DNA segments were detected across the genome and strongly associated with defective urogenital traits. This has been achieved with significantly higher resolution and greater clinical yield than standard routine karyotype, thus making this array-based CGH screen as a genetic test of choice in diagnosis. While GU defects cases arise among newborns without clear etiology, this study offers novel loci to dissect for determining key genes involved in the human sexual development.
We would like to thank all the referring physicians and especially Drs. Edmond T. Gonzales, Lars Cisek, David R. Roth and Eric Jones, the affected individuals and their family members who participated in this study. We thank Dr. Kenneth McElreavy (Pasteur Institute, Paris, France) who provided two patient samples with gonadal dysgenesis for this study. We thank Drs. John Belmont, Lisa White and Hao Liu for their cooperation. We also thank Matthew Folsom for his excellent technical assistance.
Conceived and designed the experiments: MTL SH DJL. Performed the experiments: MTL SH STC SY LM JFL. Analyzed the data: MTL SH DJL JFL. Contributed reagents/materials/analysis tools: CAS SHK SWC. Wrote the paper: MTL.
- 1. Virtanen HE, Bjerknes R, Cortes D, Jorgensen N, Rajpert-De Meyts E, et al. (2007) Cryptorchidism: classification, prevalence and long-term consequences. Acta Paediatr 96: 611–616.
- 2. Pohl HG, Joyce GF, Wise M, Cilento BG Jr (2007) Cryptorchidism and hypospadias. J Urol 177: 1646–1651.
- 3. Hughes IA (2007) Early management and gender assignment in disorders of sexual differentiation. Endocr Dev 11: 47–57.
- 4. Foresta C, Zuccarello D, Garolla A, Ferlin A (2008) Role of hormones, genes, and environment in human cryptorchidism. Endocr Rev 29: 560–580.
- 5. Wang MH, Baskin LS (2008) Endocrine disruptors, genital development, and hypospadias. J Androl 29: 499–505.
- 6. Matzuk MM, Lamb DJ (2008) The biology of infertility: research advances and clinical challenges. Nat Med 14: 1197–1213.
- 7. Wilhelm D, Koopman P (2006) The makings of maleness: towards an integrated view of male sexual development. Nat Rev Genet 7: 620–631.
- 8. Cox MJ, Coplen DE, Austin PF (2008) The incidence of disorders of sexual differentiation and chromosomal abnormalities of cryptorchidism and hypospadias stratified by meatal location. J Urol 180: 2649–2652. discussion 2652.
- 9. Moreno-Garcia M, Miranda EB (2002) Chromosomal anomalies in cryptorchidism and hypospadias. J Urol 168: 2170–2172. discussion 2172.
- 10. Wain LV, Armour JA, Tobin MD (2009) Genomic copy number variation, human health, and disease. Lancet 374: 340–350.
- 11. Lupski JR (2007) Genomic rearrangements and sporadic disease. Nat Genet 39: S43–47.
- 12. Shaw-Smith C, Pittman AM, Willatt L, Martin H, Rickman L, et al. (2006) Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability. Nat Genet 38: 1032–1037.
- 13. Sharp AJ, Hansen S, Selzer RR, Cheng Z, Regan R, et al. (2006) Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nat Genet 38: 1038–1042.
- 14. Koolen DA, Vissers LE, Pfundt R, de Leeuw N, Knight SJ, et al. (2006) A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet 38: 999–1001.
- 15. Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, et al. (2004) Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet 36: 955–957.
- 16. Ballif BC, Hornor SA, Jenkins E, Madan-Khetarpal S, Surti U, et al. (2007) Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2. Nat Genet 39: 1071–1073.
- 17. Aitman TJ, Dong R, Vyse TJ, Norsworthy PJ, Johnson MD, et al. (2006) Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans. Nature 439: 851–855.
- 18. Gonzalez E, Kulkarni H, Bolivar H, Mangano A, Sanchez R, et al. (2005) The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility. Science 307: 1434–1440.
- 19. Cheung SW, Shaw CA, Yu W, Li J, Ou Z, et al. (2005) Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genet Med 7: 422–432.
- 20. Lu X, Shaw CA, Patel A, Li J, Cooper ML, et al. (2007) Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases. PLoS ONE 2: e327.
- 21. Ou Z, Kang SH, Shaw CA, Carmack CE, White LD, et al. (2008) Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses. Genet Med 10: 278–289.
- 22. Lu XY, Phung MT, Shaw CA, Pham K, Neil SE, et al. (2008) Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis. Pediatrics 122: 1310–1318.
- 23. Shaffer LG, Kennedy GM, Spikes AS, Lupski JR (1997) Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratory. Am J Med Genet 69: 325–331.
- 24. Bagheri-Fam S, Sim H, Bernard P, Jayakody I, Taketo MM, et al. (2008) Loss of Fgfr2 leads to partial XY sex reversal. Dev Biol 314: 71–83.
- 25. Kim Y, Bingham N, Sekido R, Parker KL, Lovell-Badge R, et al. (2007) Fibroblast growth factor receptor 2 regulates proliferation and Sertoli differentiation during male sex determination. Proc Natl Acad Sci U S A 104: 16558–16563.
- 26. Beleza-Meireles A, Lundberg F, Lagerstedt K, Zhou X, Omrani D, et al. (2007) FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias. Eur J Hum Genet 15: 405–410.
- 27. Raymond CS, Murphy MW, O'Sullivan MG, Bardwell VJ, Zarkower D (2000) Dmrt1, a gene related to worm and fly sexual regulators, is required for mammalian testis differentiation. Genes Dev 14: 2587–2595.
- 28. Wang Y, Kakinuma N, Zhu Y, Kiyama R (2006) Nucleo-cytoplasmic shuttling of human Kank protein accompanies intracellular translocation of beta-catenin. J Cell Sci 119: 4002–4010.
- 29. Maatouk DM, DiNapoli L, Alvers A, Parker KL, Taketo MM, et al. (2008) Stabilization of beta-catenin in XY gonads causes male-to-female sex-reversal. Hum Mol Genet 17: 2949–2955.
- 30. Higashi Y, Maruhashi M, Nelles L, Van de Putte T, Verschueren K, et al. (2002) Generation of the floxed allele of the SIP1 (Smad-interacting protein 1) gene for Cre-mediated conditional knockout in the mouse. Genesis 32: 82–84.
- 31. Miquelajauregui A, Van de Putte T, Polyakov A, Nityanandam A, Boppana S, et al. (2007) Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation. Proc Natl Acad Sci U S A 104: 12919–12924.
- 32. Jordan BK, Mohammed M, Ching ST, Delot E, Chen XN, et al. (2001) Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. Am J Hum Genet 68: 1102–1109.
- 33. Jeays-Ward K, Hoyle C, Brennan J, Dandonneau M, Alldus G, et al. (2003) Endothelial and steroidogenic cell migration are regulated by WNT4 in the developing mammalian gonad. Development 130: 3663–3670.
- 34. Bardoni B, Zanaria E, Guioli S, Floridia G, Worley KC, et al. (1994) A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal. Nat Genet 7: 497–501.
- 35. Huang B, Wang S, Ning Y, Lamb AN, Bartley J (1999) Autosomal XX sex reversal caused by duplication of SOX9. Am J Med Genet 87: 349–353.
- 36. Smyk M, Berg JS, Pursley A, Curtis FK, Fernandez BA, et al. (2007) Male-to-female sex reversal associated with an approximately 250 kb deletion upstream of NR0B1 (DAX1). Hum Genet 122: 63–70.