http://orcid.org/0000-0001-9533-1993
Figures
Abstract
Background
Ebstein anomaly (EA) is a rare congenital defect characterized by apical displacement of the septal tricuspid leaflets and atrialization of the right ventricle. The etiology of EA is unclear; however, recurrence in families and the association of EA with genetic syndromes and copy number variants (CNVs) suggest a genetic component.
Objective
We performed a population-based study to search for recurrent and novel CNVs in a previously unreported set of EA cases.
Methods
We genotyped 60 EA cases identified from all live births (2,891,076) from selected California counties (1991–2010) using the Illumina HumanOmni2.5–8 array. We identified 38 candidate CNVs in 28 (46%) cases and prioritized and validated 11 CNVs based on the genes included.
Results
Five CNVs (41%) overlapped or were close to genes involved in early myocardial development, including NODAL, PDLIM5, SIX1, ASF1A and FGF12. We also replicated a previous association of EA with CNVs at 1p34.1 and AKAP12. Finally, we identified four CNVs overlapping or in close proximity to the transcription factors HES3, TRIM71, CUX1 and EIF4EBP2.
Citation: Giannakou A, Sicko RJ, Zhang W, Romitti P, Browne ML, Caggana M, et al. (2017) Copy number variants in Ebstein anomaly. PLoS ONE 12(12): e0188168. https://doi.org/10.1371/journal.pone.0188168
Editor: Diego Fraidenraich, Rutgers University Newark, UNITED STATES
Received: September 18, 2017; Accepted: November 1, 2017; Published: December 7, 2017
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: The data are publicly available from the Office of Statewide Health Planning and Development (OSHPD). The data are not available for replication because specific approvals from OSHPD and the California Committee for the Protection of Human Subjects have to be obtained in order to access them. Requests for data may be sent to: Healthcare Information Resource Center 400 R Street, Suite 250 Sacramento, CA 95811-6213 Tel: (916) 326- 3802 HIRCNonPublic@oshpd.ca.gov.
Funding: This work was funded by the Intramural Research Program of the National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development (contract numbers HHSN275201100001I and HHSN27500005; NICHD contract N01-DK-73431). This study was internally funded by the investigators’ institution. No outside funding was involved and the investigators had total control over data collection and analysis, decision to publish and preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Ebstein anomaly (EA) is a rare congenital malformation of the tricuspid valve and right ventricle characterized by apical displacement of the origin of septal tricuspid leaflets and atrialization of the right ventricle [1]. Additional cardiac defects such as patent foramen ovale (PFO), atrial septal defect, ventricular septal defect, pulmonary outflow obstruction, patent ductus arteriosus (PDA), accessory conduction pathways, bicuspid aortic valve and left heart lesions like mitral valve prolapse and left ventricular noncompaction have been associated with EA [1–4]. In fact, in 39% of EA cases, a left heart defect has been reported [4]. The estimated prevalence of EA is 1 in 20,000 live births [5–7]. Although diagnosis and treatment for EA have improved greatly, still many symptomatic neonates with EA do not survive beyond the first decade of life [2, 8].
The majority of infants with EA appear to occur sporadically; however, reports of familial recurrence, [9–15] as well as of genetic mutations associated with EA, [16] show evidence of a genetic background. Mutations in sarcomeric protein, myosin heavy chain cardiac muscle beta (MYH7) have been linked with EA and cardiomyopathy [17]. EA has also been identified in association with rare mutations, various syndromes, chromosomal abnormalities and copy number variants (CNVs) [18]. In our previous study we linked EA with CNVs, specifically, duplication of 1p34.1 and 8q21.13, genes related to myocardial development, BMP signaling, histone modification and cardiomyocyte differentiation, supporting the involvement of the developing myocardium in the etiology of EA [18].
Although a genetic factor has been identified in a small percentage of EA cases, the number of studies examining genetic factors in association with EA is limited; thus, the genetic components contributing to the development of EA remains largely unclear. In this population-based study, we searched for potentially causal CNVs in EA cases without accompanying major defects.
Materials and methods
Ethics statement
The California Department of Public Health (IRB 13-03-1164), the New York State Department of Health (IRB 07–007), and the NIH Office of Human Subjects Research (OHSRP 11631) reviewed and approved this study. Prior to genotyping and analysis, cases were given a random identification number and all personally identifying information was removed.
Cases
EA cases were identified via the California Birth Defects Monitoring Program (CBDMP), a population-based, active ascertainment birth defects surveillance program. The methods have been described in detail previously [19]. In brief, trained staff collected diagnostic and demographic information. Each diagnosis was coded using a modification of the British Paediatric Association (BPA) Classification of Diseases. Modifications to the BPA codes were developed by the CDC and the CBDMP [19]. A study performed on the CBDMP registry determined that the completeness of ascertainment exceeded 93% [20].
EA cases were identified from all live births (N = 2,891,076) from 1991 to 2002 with maternal residence in San Francisco, Los Angeles, Santa Clara and San Joaquin Valley County (Fresno, Kern, Kings, Madera, Merced, San Joaquin, Stanislaus and Tulare), excluding births at military facilities. Infants with co-occurring syndromes, other major congenital heart defects (CHD) defects or other major non-CHD defects were excluded. Infants with PDA, PFO and bicuspid aortic valve were not excluded from the case group. These exclusions were done to establish a more homogeneous phenotypic EA group for genetic interrogation. A total of 60 cases met the inclusion criteria and we located archived newborn screening dried blood spots (DBS) for the all 60 cases along with eight unaffected live births to serve as controls.
To ensure that the identified CNVs were rare in the unaffected population, we investigated their frequencies in an unaffected group of infants. We randomly selected 165 infants without birth defects derived from the same population (county and year of birth) as the cases, obtained their bloodspots, and performed qPCR copy-number assays using at least one probe per CNV region. Demographic data for all live births in the study counties from 1991 to 2002 were obtained from birth records and compared with the 60 EA cases using Fisher’s exact test or t test.
DNA extraction
GenSolve DNA recovery kit (GenTegra, Pleasanton, CA) was used to extract DNA from two 3 mm punches from each infant’s dried blood spot. Punches were incubated at 56°C in 620μL freshly prepared GenSolve Recovery Solution A (1% LiDS, Solution A and Proteinase K) with gentle shaking for 1 hour. Following incubation, the blood spots were transferred to a spin basket in a tube containing 20μL of GenSolve Recovery Solution B and centrifuged to collect extracted DNA from the punches. The flow through containing extracted DNA was purified using a QIAamp DNA Mini Kit (QIAGEN, VALENCIA, CA) following the manufacturer's standard protocol. Final elution volume was 50μL.
CNV detection, selection, and validation
The 60 EA cases, 42 cases of unrelated phenotype, eight controls, (one in duplicate), and one HapMap sample were batched and genotyped. The methods have been described previously [21]. In brief, samples were genotyped using the Illumina HumanOmni2.5-8v1-3_A1 bead arrays and the Infinium LCG assay protocol. The mean sample call rate ± SD (range) was 99.85 ± 0.25 (97.31–99.93). The mean log R ratio deviation was 0.103 ± 0.026 (0.078–0.291). Single nucleotide polymorphism genotype reproducibility was 100% for the duplicated control. Genotype clusters were defined based on the data generated in this project. Genotypes and clusters were manually reviewed and cleaned by re-clustering, editing, and excluding where appropriate. A total of 2,303,118 autosomal markers were included in the CNV analysis. CNVs were called and annotated using pennCNV (version 2011/05/03).
CNVs were excluded if they were shorter than 20 kb, contained fewer than ten SNP probes, overlapped more than 20% with common CNVs in HapMap or CHOP, or overlapped more than 20% with same-type CNVs in an in-house reference CNV database compromised of unaffected controls and cases of other unrelated birth defects. The remaining CNVs were uploaded to DGV (build37/hg19, DGV release date 2016-05-15, and date accessed 2016-12-10) and analyzed for overlap. A CNV was selected for further analysis if it had minimal overlap with variants present in DGV or if the CNV overlapped a gene with no DGV entries significantly overlapping it. Although the DGV is a very valuable resource, some studies in the database have very small sample sizes and all could potentially include false positives. Furthermore, breakpoint determination is not precise. For these reasons, we chose to ignore overlap with low confidence in the DGV browser and overlap with variants from studies using similar methods.
In total, 38 CNVs were considered candidate CNVs for EA. We selected 11 CNVs for validation based on whether they contained biologically relevant genes, or overlapped CNVs that had been previously reported in EA cases. CNV validation studies were performed using one to three quantitative real-time polymerase chain reaction (qPCR) TaqMan assays (Applied Biosystems, Carlsbad, CA, USA) per CNV region. Validations were performed as previously described. [21] All 60 EA cases and four control subjects were included in each assay. We subsequently screened all validated CNVs against an additional 165 control samples from unaffected California live births using at least one assay targeting each area of interest. Therefore, a total of 169 unaffected controls were screened using at least one assay in each candidate CNV region.
Results
Demographic data
Of the 2,891,076 live births, 60 met our case definition and inclusion criteria. Maternal age, maternal race/ethnicity or parity did not differ statistically between cases and the general population. Mothers of cases (44.66%) were more likely than mothers of controls (34.16%) to have more than a high school education (P = 0.04). Cases had significantly shorter gestation (mean of 268 vs. 274 days; P = 0.012). Select demographic characteristics of mothers and EA cases and the California source population are shown in Table 1.
Genetic analysis
The 60 EA cases genotyped resulted in 2864 PennCNV calls in the microarray analysis. After applying the selection criteria described in the Material and Methods section, we identified 38 CNVs in 28 (46%) cases. We selected 11 CNVs in 10 cases for qPCR confirmation based on the genes included and their functions. All 11 CNVs were validated: seven duplications and four heterozygous deletions ranging from 22 Kb to 331 Kb (Table 2). One validated duplication at 3q28 had overlap with a heterozygous deletion detected in one control, the validated heterozygous deletion at 7q22.1 had overlap with a heterozygous deletion detected in two control samples and the validated deletion at 10q22.1 had overlap with a heterozygous deletion detected in one control sample. Precise breakpoint studies were not performed, so it is unknown whether the CNVs detected in controls are the same size as those detected in our cases.
Genes implicated in cardiac development were present in five validated CNVs. Four CNVs previously associated with cardiac defects were also identified. Two variants identified in this study, a duplication overlapping AKAP12 in one case and a duplication at 1p34.1 in another case, had also been identified in cases with EA in our previous study [18].
Four CNVs were identified that overlapped or were close to transcription factors HES3, TRIM71, CUX1 and EIF4EBP2 which are important in cardiac development. HES3 and CUX1 have been reported to interact with Notch and Wnt pathways [22, 23] and dysregulation of these signaling pathways is known to lead to congenital heart defects [24, 25]. In case 1 a 22 Kb deletion was identified at 10q22.1, 19 Kb upstream of NODAL, which is a factor in cardiac progenitor differentiation [26] and an inducer of Sox17, an endoderm-specific gene regulating paracrine signals in cardiogenesis [27]. A 240 Kb duplication intersecting PDLIM5 was identified at 4q22 in case 4. PDLIM5 is involved in cardiomyocyte development, differentiation and survival as well as heart development in general [28, 29]. Loss of PDLIM5 has also been associated with dilated cardiomyopathy [30]. In case 9 a 238 Kb duplication was identified at 14q23.1 encompassing SIX1, a gene that is transiently expressed in cardiac progenitor cells and has been reported to function as a regulator of cardiovascular morphogenesis [31]. In case 8 a 122 Kb deletion was identified at 6q22 downstream of ASF1A, a factor required for heart development [32]. In case 5 a 190 Kb duplication at 3q28 intersected FGF12, a gene that has been suggested to perform embryonic functions during atrial development [33]. FGF12 is a candidate gene for Brugada syndrome [34] and has been described in association with posterior urethral valves with duplication/triplication in FGF12 [35]. In case 7 a 331Kb duplication was identified overlapping AKAP12, a gene that we have previously linked to EA and cardiomyopathy after identifying a deletion intersecting AKAP12 in one EA case. [18] A 156 Kb duplication at 1p34.1 was identified in case 10. This duplication overlaps with the 234 Kb duplication at 1p34.1 that we have previously described in association with EA [18]. A 161Kb duplication in case 3 was detected at 22q11, a genetic locus where variations have previously been reported in some congenital heart defect cases [36, 37]. The validated CNVs are described in more detail in Table 2 and the other candidate CNVs that were not selected for validation are reported in Table 3.
Discussion
To our knowledge, this is only the second study to perform a genome wide investigation on CNVs in infants with isolated, non-syndromic, EA, following only our previous work. Thus, our study contributes meaningfully to supporting the role of genetic factors in EA. We identified rare, potentially pathogenic CNVs in almost one half of the EA cases. The candidate CNVs that were identified and validated were prioritized because they included genes linked to early heart development and cardiomyocyte differentiation.
In 5 out of 10 cases with rare CNVs, we identified CNVs overlapping, or being in close proximity to, genes linked to early cardiac development including NODAL, PDLIM5, SIX1, ASF1A and FGF12. Each of these genes plays an important role in cardiomyocyte differentiation, cardiac development and morphogenesis.
NODAL is a TGFβ family member and a key factor in cardiac progenitor differentiation [26]. NODAL induces SOX17 which is an endoderm-specific gene that regulates paracrine signals in cardiogenesis [27]. Studies in mice have shown that lack of Nodal co-receptor results in failure of embryonic stem (ES) cells to differentiate into cardiomyocytes [38, 39]. Nodal has also been shown to activate heart formation in both avian and amphibian embryos [40–46]. In humans, high levels of Activin, a mimic of NODAL, have been demonstrated to activate endoderm formation in ES cells [47–50]. Thus, a deletion causing dysregulation of NODAL expression could result in defective differentiation of cardiomyocytes and myocardial defects contributing to the cardiac anomaly seen in EA.
PDLIM5, also known as Enigma homolog 1 (ENH1/PDLIM5), is a member of the PDZ-LIM protein group that is highly expressed in the myocardium and plays an important role in differentiation via activation of protein kinases and transcription factors [29]. Specifically, ENH1 overexpression has been shown to upregulate MyoD and myogenin as well as myogenic transcription factors such as bHLH [29]. Previous studies in mice and C2C12 cells suggest that ENH1 is involved in cardiomyocyte development and differentiation, heart development in general and embryonic survival [28, 29]. These studies suggest that ENH1 has an important role in normal development and differentiation of cardiomyocytes; therefore, defective expression could lead to myocardial defects that are associated with EA.
In addition to its importance in development and differentiation, loss of ENH1 has been linked to dilated cardiomyopathy [30]. The proposed mechanism is destabilization of the ENH-CypherS-Calsarcin protein complex at the Z-line [30]. Recent studies also show that ENH1, acting at cardiomyocytes through binding partners, has a pivotal role in the cardiovascular system as a modulator in sustaining contractile activity [51]. All these findings suggest a complex, yet unclear, role of ENH1 in the developing heart at the level of cardiomyocytes that could potentially explain abnormal myocardial and structural development similar to what is seen in EA.
SIX1 is a transcription factor that is transiently expressed in cardiac progenitor cells. Together with its canonical coactivator EYA1, it is active in mammalian organogenesis [52] and is linked to congenital cardiac abnormalities [53–55]. The SIX1/EYA1 transcription complex has been suggested to function as a regulator of cardiovascular morphogenesis working as part of the Tbx1-Six1/Eya1-Fgf8 regulatory cascade [31]. TBX1 and FGF8 are well established regulators of heart morphogenesis [56, 57]. A variant affecting expression of SIX1 could result in dysregulation of the Tbx1-Six1/Eya1-Fgf8 regulatory cascade and lead to cardiac structural malformations.
ASF1A is a conserved histone chaperone that interacts with histones H3 and H4 [58]. Previous studies have reported the crucial role of histone chaperone activity in normal heart development and our previous work has also underscored the potential role of histone-modifying genes in CHD and EA [18, 32]. ASF1A is a member of the HIRA/UBN1/ASF1a complex, a chromatin remodeling complex that interacts with NKX2-5 and regulates gene expression dynamics in ES cells [32]. NKX2-5 is a well-established transcription factor, vital for cardiac development and morphogenesis, especially of the right heart [59]. A deletion affecting ASF1A could result in an ineffective HIRA/BUN1/ASF1a complex formation that could lead to defective expression of transcription factors and genes necessary for normal heart development.
Finally, Fgf12 is a gene that is highly expressed in the mouse myocardium, especially the atrium, during embryogenesis [33]. FGF12 has also been suggested as a candidate gene for Brugada syndrome, a cardiac arrhythmia channelopathy [34].
Our results extend previous reports indicating a genetic component to EA [16–18, 60–62]. Several theories have been proposed to explain the cause of the tricuspid valve abnormality in EA. Suggested mechanisms include failure of the valve to delaminate from the myocardium and abnormal myocardial development or myocardial arrest leading to valve anomalies [2, 63–65].
In our study, 5 out of the 11 validated CNVs identified include genes related to cardiomyocyte development, differentiation and myocardial morphogenesis which may contribute to abnormal right heart development. These findings show that early myocardial development could in fact play a very important role in EA.
Interestingly, a 331 Kb duplication was identified in case 7 overlapping AKAP12. We have previously identified a deletion in one EA case in this region overlapping the duplication identified in this study (Fig 1) [18]. AKAP12 (Gravin) is an A-kinase anchoring protein that targets protein kinase A, protein kinase C, calcineurin and other signaling molecules to the beta2-adrenergic receptor. It has been shown that disruption of Gravin leads to augmented contractility and increased baseline cardiac function [66]. In mice homozygous for an Akap12 mutation, there was increased phosphorylation of Cardiac myosin-binding protein C (cMyBPC) [66] which is a known factor in cardiomyopathy in humans [67].
An important finding of this study is a 156 Kb duplication at 1p34.1 in one CA EA case that overlaps a 234 Kb duplication at the same locus, previously detected in a NY EA case (Fig 2) [18]. Both cases were Black/African American. This finding narrows down the region of interest and the genes overlapped by the intersection of the CNVs at 1p34.1 in both studies include ST3GAL3, ARTN and IPO13. IPO13, also known as importin13, is highly expressed in heart tissue and it has been shown to act as a carrier of myopodin [68]. Myopodin is a synaptopodin gene family member that is expressed in heart muscle and has been suggested to function as a regulatory protein in signaling pathways between nucleus and the Z-disc during development [69]. According to the integrated regulation from ENCODE tracks in UCSC, the locus of interest is rich in DNaseI hypersensitivity clusters suggesting that 1p34.1 is a regulatory region functionally related to transcriptional activity [70]. Various transcription factors that act at the duplicated part of 1p34.1 including MAX, C-Fos, YY1, SIX5, FOSL2, EGR-1, and AP-2 gamma, have been suggested to play important roles in development and differentiation. In fact, Ap-2 gamma and SIX5 act during embryogenesis and organogenesis. Replicating the association between duplication of 1p34.1 and EA adds additional evidence of a strong association between this region and EA and suggests that 1p34.1 represents an important locus for follow-up genetic and functional studies.
This study has several strengths and weaknesses. First, it is a population-based study, with a representative set of cases from California live births. The data available through the California Birth Defects Monitoring Program (CBDMP) registry have been collected and coded by well-trained staff and provide excellent and unbiased ascertainment of cases. Another strength is our validation of 11 CNVs ensuring that no false positives are present in our final candidate EA-associated CNV list. Our CNV selection criteria included filtering against the DGV database to assure that the detected CNVs were absent or extremely rare in unaffected subjects. Furthermore, to rule out CNVs specific to our study population, we screened the CNVs in 165 control subjects from the California population. Due to the nature of the CNV validation method (TaqMan copy-number assays), we are unable to determine the exact breakpoints of CNVs. Using one assay per CNV region, we are effectively ruling out the presence of CNVs with breakpoints matching those detected in the cases in the 165 control subjects. The study population included only liveborn infants and thus fetuses with EA that were spontaneously lost or electively terminated were not represented. Such EA cases might have a different genetic etiology. The CNVs identified in EA cases could not be further explored for their origin, i.e., inherited or arose de novo, owing to a lack of data from parents. EA phenotypic presentation and severity can vary considerably, however clinical and treatment data are rarely available from such birth defects registries. Moreover, stratifying based on phenotype and severity, if such data were available, would lead to a very small sample size, inadequate to estimate risk. Our objective was to examine a possible genetic profile in an initial set of EA patients and lay the foundation for larger and more refined investigations.
Conclusion
Our study identified CNVs affecting crucial signaling pathways for cardiomyocyte differentiation and cell-fate determination. In addition, CNVs were identified in loci that overlap, or are in close proximity to, transcription factors. We also replicated, in an independent population, associations of EA with AKAP12 as well as with 1p34.1duplication. Abnormal differentiation of cardiomyocytes, AKAP12 and duplication of 1p34.1 are important areas for future investigation into the etiology of EA.
Acknowledgments
This research was supported by the Intramural Research Program of the Eunice Kennedy Shriver National Institute of Child Health and Human Development of the National Institutes of Health.
We thank the California Department of Public Health, Maternal Child and Adolescent Health Division for providing surveillance data from California for this study. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the California Department of Public Health.
We would like to thank Ahmad Shabbir, DMV, MS, PhD from California Maternal Quality Care Collaborative for his valuable assistance. We thank Michael Tsai and Natalie Weir at the Minnesota Core Laboratories and the staff at the Biomedical Genomics Center Facility at the University of Minnesota for microarray genotyping; and Nathan Pankratz, University of Minnesota, and Karl G. Hill, Social Development Research Group, University of Washington, for generously sharing population B-allele frequency and GC content files for pennCNV software. This study makes use of data generated by the DECIPHER Consortium. A full list of centers that contributed to the generation of the data is available from http://decipher.sanger.ac.uk and via email from decipher@sanger.ac.uk. Those who carried out the original analysis and collection of the data bear no responsibility for the further analysis or interpretation. Some data used for comparison in this article were obtained from the International Standards for Cytogenomic Arrays Consortium database (http://www.iscaconsortium.org), which generates this information using the National Center for Biotechnology Information’s database of genomic structural variation (dbVar, http://www.ncbi.nlm.nih.gov/dbvar/), study nstd37. Specimens and associated phenotype data were provided by International Standards for Cytogenomic Arrays Consortium member laboratories.
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