Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments
© Liu et al. 2016
Received: 23 July 2015
Accepted: 31 October 2015
Published: 11 November 2015
The Erratum to this article has been published in Human Genomics 2016 10:5
Absence of the anterior (ACL) or posterior cruciate ligament (PCL) are rare congenital malformations that result in knee joint instability, with a prevalence of 1.7 per 100,000 live births and can be associated with other lower-limb abnormalities such as ACL agnesia and absence of the menisci of the knee. While a few cases of absence of ACL/PCL are reported in the literature, a number of large familial case series of related conditions such as ACL agnesia suggest a potential underlying monogenic etiology. We performed whole exome sequencing of a family with two individuals affected by ACL/PCL.
We identified copy number variation (CNV) deletion impacting the exon sequences of CEP57L1, present in the affected mother and her affected daughter based on the exome sequencing data. The deletion was validated using quantitative PCR (qPCR), and the gene was confirmed to be expressed in ACL ligament tissue. Interestingly, we detected reduced expression of CEP57L1 in Epstein–Barr virus (EBV) cells from the two patients in comparison with healthy controls. Evaluation of 3D protein structure showed that the helix-binding sites of the protein remain intact with the deletion, but other functional binding sites related to microtubule attachment are missing. The specificity of the CNV deletion was confirmed by showing that it was absent in ~700 exome sequencing samples as well as in the database of genomic variations (DGV), a database containing large numbers of annotated CNVs from previous scientific reports.
We identified a novel CNV deletion that was inherited through an autosomal dominant transmission from an affected mother to her affected daughter, both of whom suffered from the absence of the anterior and posterior cruciate ligaments of the knees.
KeywordsCopy number variation Rare disease Whole exome sequencing
Congenital absence of the anterior (ACL)/posterior cruciate ligaments (PCL) is an extremely unusual condition with a prevalence of 1.7 per 100,000 live births and was first reported in 1956 in a radiographic study of the knee [1–3]. The symptom of this disease usually associated with serious malformation or dislocation of the knees. ACL is the most common disorder, and it can be associated with hypoplasia or total PCL.
There is little knowledge of the genetics information related to this disease, but a previous study in a large number of families suggested autosomal dominant inheritance of ACL . In this study, we uncovered two individuals (mother and her daughter) in a large cohort of subjects with rare diseases, and we confirmed the underlying sequence copy number variations (CNVs) that predisposes to this disease.
Among 662 individuals from 212 families with Mendelian disease phenotypes, there was one family with two affected patients, including a mother (ID#4779933454) and her 13-year-old daughter (ID#1993197298), suffering from an absence of bilateral ACL and PCL ligaments. Their history was notable for joint instability and difficulty with ambulation. Absence of ACL and PCL was confirmed on MRI and by arthroscopy. The proband (daughter) has an unaffected younger sister and unaffected father, for both of whom DNA was not obtainable. However, the pattern of inheritance suggests it is autosomal dominant ; no other extended family members have a history of joint or lower-limb disorders.
Exome capture and sequencing
Following the manufacturer’s protocols, we used Agilent SureSelect Human All Exon Kit (in solution) (Agilent Technologies, Santa Clara, CA, USA) to perform exome capture for the family included in this study. We used Covaris AFA (Covaris, Woburn, MA, USA) to randomly fragment genomic DNA samples with an average size of 150–200 bp and then attached adapters to both ends. We applied AgencourtAMPure SPRI beads (Beckman Coulter, Brea CA, USA) to purify the adapter-ligated templates with an insert size of around 250 bp. We employed ligation-mediated polymerase chain reaction (LM-PCR) and SureSelect Biotinylated RNA Library (BAITS) (Agilent Technologies, Santa Clara, CA, USA) to amplify, purify, and hybridize DNA for enrichment. We then washed out non-hybridized fragments after 24 h and estimated the magnitude of enrichment through capture LM-PCR products by using an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). The Hiseq2000 platform (Illumina, San Diego, CA, USA) started paired-end sequencing with read lengths of 90 bp. We applied Illumina base-calling software V.1.7 at its default parameters to process raw image files for base-calling.
Exome data analysis
We used two independent analysis pipelines to perform alignment, variant calling, and annotation. Pipeline (1). Sequencing reads were aligned to the human reference genome (UCSC hg19) with Burrows–Wheeler Aligner (BWA, version 0.6.2) . Optical and PCR duplicates were marked and removed with Picard (version 1.73). Local realignment of reads containing indel sites and base quality score recalibration (BQSR) were performed with the Genome Analysis Tool Kit (GATK, version 2.3) . Single nucleotide variation (SNV) and small indels were called with GATK UnifiedGenotyper. Variants were marked as potential sequencing artifacts if the filters on the following annotations were evaluated to be true: (1) for SNVs, “DP < 10,” “QD < 2.0,” “MQ < 40.0,” “FS > 60.0,” “HaplotypeScore > 13.0,” “MQRankSum < −12.5,” “ReadPosRankSum < −8.0,” (2) for small indels, “DP < 10,” “QD < 2.0,” “ReadPosRankSum < −20.0,” “InbreedingCoeff < −0.8,” “FS > 200.0.” The kinship coefficient was calculated for each sample using KING  to confirm reported relationships and identify cryptic relationships among samples. ANNOVAR  and SnpEff (version 2.0.5)  were used for annotating variants. Human gene mutation database (HGMD)  was used for annotating known genes and mutations for human inherited diseases. Prediction scores from SIFT , Polyphen2 , LRT , and MutationTaster  along with conservation scores PhyloP  and GERP++  for every potential nonsynonymous SNV in the human genome were retrieved from dbNSFP (database for nonsynonymous SNPs’ functional predictions) .
Pipeline (2). Fastq files were aligned to the human reference genome (UCSC hg19) with the short oligonucleotide analysis package (SOAP, version 2.2.1) . SOAPsnp (version 1.05)  was used for single nucleotide variant (SNV) detection and GATK for small insertion-deletion (indel) detection, followed by BGI’s self-developed programs to perform variant functional annotation.
SNV detection, variant filtering, and prioritization
A series of common filtering criteria were applied to all candidate variants in both pipelines as described below. First we excluded variants that were (1) not within an exon, a predicted splice site, or an UTR; (2) synonymous changes, and (3) with minor allele frequency (MAF) >0.5 % in either the 1000 Genomes Project (http://www.1000genomes.org/), the Exome Sequencing Project (ESP6500; http://evs.gs.washington.edu/EVS/), or our internal exome datasets. Variants near splicing donor/recipient sites and frameshift indels were given particular attention as they could cause pathogenic changes such as exon-skipping, premature truncation, stop loss, or stop gain, as well as frameshifts.
We considered a number of possible genetic models in variant prioritization, which included filtering out of variants based on (1) evolutionary conservation, i.e., variants of PhyloP  value <0.95 were considered to be in non-conserved regions thus discarded; (2) prediction of pathogenicity by both PolyPhen  and SIFT ; and (3) biological and clinical relevance of identified variants with emphasis on pathways and interaction networks of known genes and/or proteins pertinent to the disease.
Given that congenital absence of ACP/PCL is thought to be a dominantly inherited syndrome, we used a de novo dominant model of Mendelian inheritance in our variant prioritization and filtering methodology . Specifically, we focused on variants found to be heterozygous and strongly deleterious in the proband and affected parents. SNVs and indels were selected as potential pathogenic variants if they met all the following criteria: (1) heterozygous in proband and in the affect maternal sample; (2) not previously described or rare (MAF < 0.5 %) in a control cohort of more than 9000 control individuals (1000 genomes project, April 2012 release; 6503 exomes from NHLBI GO Exome Sequencing Project (ESP6500SI) and 1200 in-house whole-exomes; (3) nonsynonymous, or splice acceptor and donor site SNVs, or frame shift coding indels (NS/SS/I); (4) predicted to be deleterious by at least three prediction methods, i.e., SIFT, PolyPhen2, MutationTaster, and LRT; and (5) conserved PhyloP score and GERP++ score >2.0. Variants were also analyzed using the ingenuity variant analysis web-based application. As both affected were female, we also included in our analysis all variants on the chr X, considering both heterozygous dominant and hemizygous dominant scenarios. SNVs and indels fulfilling these criteria were retained as potential pathogenic variants if they also then met all the criteria 2–5 (above).
CNV analysis for exon sequencing
CNV analysis was performed by using the standard exome hidden Markov model (XHMM) pipeline that consisting of six steps . The depth of coverage for all targets and all 662 samples used for case/control comparison for this study was performed using GATK. (2) Target regions with extreme GC content (<10 % or >90 %) and low complexity regions are filtered out from further analysis. (3) PCA normalization of read depth is performed for all samples to remove inherent biases in sample preparation and sequencing. (4) Samples with extreme variability in normalized read depth are removed. (5) Per-sample CNV Detection with a HMM is performed. (6) Quality metrics are assigned to all samples for discovered CNVs.
The raw outputs of XHMM were further processed by selecting the region with “Y” annotation, which indicates the CNV region existed in the proband. The selected regions were then compared with the clinical phenotypes; the regions were further selected if the clinical phenotype matches the existence of the CNV. In other words, if the individual in this family has the disease, CNV presence in the individual is required and CNV absence if the individual is healthy.
Computational validation for CNVs
Since CNVs are common across the human genome, it is important to determine CNV specificity during the CNV validation processes. In this study, multiple validations were applied in order to increase the confidence of the CNV hits. First, we checked whether the CNV hit is presented in 274 healthy individuals; second, we checked whether the CNV hit existed in any of the 147 families with different monogenic diseases, including 388 individuals also called at the same time for this study (Additional file 1: Table S1); finally, we checked whether the CNV hit is present in the database of genomic variations (DGV), which contains annotated CNVs from previous scientific reports . If a CNV hit presented only in the patients but not in other populations and had not been reported in other previous studies, it is more confident to conclude that the CNV may be relevant or potentially associated with the target disease.
qPCR validation for CNVs
CNV Validation by quantitative PCR (qPCR) with the Universal Probe Library (UPL): CNV validation by qPCR was performed roughly as described previously [23, 24]. UPL probes (Roche, Indianapolis, IN) and corresponding primers were selected using the ProbeFinder v2.49 software (Roche, Indianapolis, IN). Probes used and primer sequences are provided in Table 2. All primers were tested to ensure that they generated a PCR product of the correct approximate size. All primer probe combinations were also tested on a dilution series of control DNA to determine PCR efficiencies. All assays achieved PCR efficiency between 95 and 105 %. Quantitative PCR was performed on an ABI Prism™ 7900HT Sequence Detection System (Applied Biosystems, Foster City, CA). Each sample reaction was performed in triplicate, in 10 ul of reaction mixture containing 10 ng genomic DNA, 100 nM of the UPL probe, 400 nM of each PCR primer, and 1× TaqMan Gene Expression Master Mix containing UDG and ROX (Life Technologies, Carlsbad, CA). Male and female genomic DNAs (Promega, Madison, WI) were included in the analysis as positive controls for subjects with expected normal copy number. Data were evaluated using the Sequence Detection Software v2.4 (Applied Biosystems, Foster City, CA). Data was further analyzed by the ∆ΔCT method. The geometric mean of the CT values for the two control sequences (GAPDH and SNCA) was calculated and used as the reference value for ∆ΔCT calculations. The Promega female DNA sample was considered the reference 2N sample for ∆ΔCT calculations. Hemizygous deletions were determined when the relative copy number value for a specific sample normalized to the reference sample was less than 0.75.
Epstein–Barr virus (EBV) cells were developed from the proband and affected family member (mother), together with cells from four healthy controls described in next section. The EBV-transformed cell lines from the six individuals were cultured into exponential growth, and 5 million cells were harvested for RNA isolation. Thus, two of the EBV cell lines were from the individuals harboring the hemizygous deletion in CEP57L1, whereas the other four cell lines were from randomly selected individuals from the CAG bio-repository representing normal CEP57L1 genotypes and expression. Expression of G6PD was observed to be variable between EBV cell lines, so for the analysis of expression from the EBV cells, only ACTB and B2M were used as controls. In addition, for analysis of expression in EBV-transformed cells, a sample from an individual not carrying the predicted deletion was used as the control sample for calculations.
qPCR validation for EBV cells and ligament tissues from knee surgery
Samples of anterior cruciate ligament (ACL) tissue were isolated from four individuals undergoing ACL surgeries. Samples were stored at −80C prior to RNA isolation. RNA was isolated from homogenized tissue samples or cell lysates using the RNeasy Mini Kit (Qiagen, Venlo, Netherlands) with optional on-column DNAse digestion, following the manufacturer’s instructions. ACL samples (approximately 200 mg tissue) were homogenized in buffer RLT using a PowerGen 125 Homogenizer (Fisher Scientific, Waltham, MA). EBV-transformed cell lines (5 × 106 cells) were homogenized in buffer RLT using QiaShredder columns (Qiagen).
Assay design for qRT-PCR analysis of gene expression in ACL tissue or EBV LCLs
Gene symbol—probe name
UPL probe #
Centrosomal protein 57 kDa-like 1
Spans exons 4 and 5 of human CEP57L1 transcript variant 1
Centrosomal protein 57 kDa-like 1
Spans exons 5 and 6 of human CEP57L1 transcript variant 1
Centrosomal protein 57 kDa-like 1
Contained within exon 1 of human CEP57L1 transcript variant 1
Spans exons 4 and 5 of human ACTB transcript
Spans exons 1 and 2 of human B2M transcript
Spans exons 4 and 5 of human G6PD transcript
Centrosomal protein 57 kDa-like protein 1 (CEP57L1) is a protein-coding gene that aids in (1) microtubule binding through filaments composed of tubulin monomers, (2) identical protein binding, and (3) γ-tublulin binding with the microtubule constituent protein of the same name. Each function interacts selectively and non-covalently. A three-dimensional (3D) model of CEP57L1 was rendered using Phyre2 . The structure created by Phyre2 was chosen due its high confidence, and model quality estimations were done for structural validation [26–28]. The sequence of the wild-type (wt) CEP57L1 was obtained from the UniProt database (accession number Q7IYX8). Models and quality estimations were done through the protein model portal (PMP), which is part of the Structural Biology Knowledgebase (SBKB, sbkb.org), Protein Structure Initiative (PSI), and Nature Publishing Group (NPG). PEP-FOLD was used to determine the structure of residues 1 to 18, which resulted in an α-helical motif (Fig. 3c) . A Monte Carlo simulation of CEP57L1 was performed using PELE from the Barcelona Supercomputing Center (BSC) . The simulation generated 67 low-energy conformations out of 100 steps in less than 24 h using one central processing unit (CPU) as requested by the BSC for searching protein local motion.
Discoveries and computational validation of rare variants underlying ACL/PCL
Besides the exclusions of the CNVs in healthy controls, it is important that the CNV regions are exclusive to other rare diseases, implying that the CNV should be unique to the ACL/PCL phenotypes in this instance. In order to further validate the results, we collected additional 388 individuals who have wide ranges of rare disease (147 different diagnoses). Again, the CNV region is not identified in any of those individuals. We expanded the culprit CNV region to include 50k base pairs up/downstream at the CNV locus. The region is still exclusive and different from any CNVs identified in the healthy control or the different disease groups. We additionally evaluated the CNVs through DGV, which is a genome variation database based on published CNV regions. Many of the studies reported in DGV contain very large populations with large number of CNVs . No genome variations have been reported before in DGV for the culprit region, indicating that there is a novel CNV.
The computational validation enhances the specificity of the CNV regions we identified. Based on multiple filters we applied, the results show that the CNV region could be a potential variation that is responsible for the absence of ACL/PCL phenotypes.
qPCR validation for CNVs
qPCR validation primer information for EBV cells genomic DNA
UPL probe #
Centrosomal protein 57 kDa-like 1
Amplicon located in intronic genomic DNA between exons 6 and 7 (chr6:109474636-109474742) chr6:109474636-109474742
Glyceraldehyde 3-phosphate dehydrogenase
qPCR validation for CEP57L1 expression profiling in EBV cells
To determine if CEP57L1 is expressed in anterior cruciate ligament (ACL) tissue, we extracted RNA from ACL tissue samples from four individuals who had undergone surgeries on their ACLs. These subjects were unrelated to the individuals who contained CEP57L1 deletions. RNA from ACL tissues was converted to cDNA and subjected to qPCR using a series of assays targeting three different regions of the CEP57L1 messenger RNA (mRNA) or one of three control mRNAs (B2M, ACTB, G6PD). Amplification of CEP57L1 mRNA was observed in all four RNA samples, to variable degrees depending on the assay used. Each of the assays completely failed to amplify anything from RNA samples that had been subjected to control reverse transcriptase reactions from which the reverse transcriptase enzyme had been excluded. We conclude that CEP57L1 is expressed in ACL tissue.
To determine if the hemizygous deletion affected expression of CEP57L1, we extracted RNA from cell lines generated by EBV transformation of peripheral blood mononuclear cells from the proband, her mother, and four healthy controls. RNA from the two deletion containing subjects was compared to RNA from four subjects randomly selected from the CAG bio-repository (Fig. 2b). Exon 1 of the CEP57L1 mRNA lies outside the detected deletion so the expression of exon 1 is expected to be unaltered. Detection of CEP57L1 mRNA with an assay targeted exon 1 showed that the t levels of expression of CEP57L1 mRNA in the cases and controls were similar. Exons 4 through 6 are contained within the detected deletion. Using assays that detect the junction of exons 4 and 5 or the junction of exons 5 and 6 revealed relatively similar levels of expression of these more 3′ regions of the CEP57L1 mRNA in all four of the control subjects. In comparison, both deletion subjects showed lower expression of these regions of the mRNA, at approximately 40–50 % of the control subjects. We interpret these data to indicate that the deletion subjects possess approximately half the amount of functional, full length CEP57L1 mRNA as control subjects.
CEP57L1 structural analyses
Absence of the ACL/PCL constitutes a rare congenital malformation that results in knee joint instability with a prevalence of 1.7 per 100,000 live births and can be associated with other lower-limb abnormalities such as ACL agnesia and absence of the knee menisci. Previous studies of several families suggested that the potential inheritance pattern is under Mendelian etiology [4, 29, 30]. In this study, we focus on the family with both mother and daughter who are notable for joint instability and difficulty with ambulation. Absence of ACL and PCL were confirmed on MRI and by arthroscopy. Since other family member’s DNA was not obtainable, we applied the analysis in different molecular levels to explore the potential causation of the disease.
We performed a thorough analysis in search for SNVs that may underlie ACL/PCL. No detrimental variant was identified that could explain the disease. We next searched for CNVs to determine if any such variant with detrimental effects segregated in the family. CNVs are structural variations in the genome that lead to either deletions or duplications of chromosome regions of a variable size. CNVs have been proving to associate with susceptibility to disease, such as cancer , autism , and schizophrenia . Previous research also suggests that inherited CNVs are associated with Mendelian diseases . Due to potential underlying Mendelian etiology for the ACL/PCL phenotype, the genetic mechanism could be studied by CNV exploration. Exome sequencing has been shown to enhance Mendelian disease gene identification resulting in improved clinical diagnosis, more accurate genotype-phenotype correlations and new insights into the role of rare genomic variation in disease, both SNVs and CNVs. Therefore, we used WES to explore the potential of identifying SNVs or CNVs that may be associated with ACP/PCL with exome sequencing technology in this study.
Due to the high prevalence of CNVs in human genome , any potential pathogenic CNV needs to be shown to be absent in healthy individuals or patients with other unrelated diseases. We applied several filters to improve the confidences of our results. First, we collected a relatively large number of individuals who were healthy controls (n = 274) as well as 388 individuals that covered a wide range of 144 different rare diseases. By checking the CNVs across those individuals, we make sure the CNVs we identified are not present in healthy controls or in other rare disease group. To overcome the size limitation of the control set, we next examined the CNVs previously reported in the DGV database, which contains many large CNV studies in healthy populations, including over ten thousands individual. If the CNV is absent in the DGV database, it indicates that the CNV is novel and lends support that the CNV may be associated with the disease of interest, which was the case in our study of the ACL/PCL phenotype. Indeed, we identified a novel CNV deletion region on chr6:109466479-109485174, corresponding to gene CEP57L1, we showed the CNV segregated in the family, and we validated the deletion by qPCR.
In order to explore the impact of the CNV deletion we identified, we applied functional studies examining RNA gene expression and the 3D protein structure modeling. We performed qPCR on the corresponding EBV cells of those two individuals. The deletion occurs at region chr6:109466479-109485174, which is corresponding to 10 exons for gene CEP57L1. The rationale is if the CNVs have effects for clinical phenotype, they would cause alternation of expression at the gene level. The results from qPCR show that the CNV deletions possess approximately half the amount of functional, full length CEP57L1 mRNA as control subjects indicates that the de novo CNV deletion would lead to decrease of gene expression. In the protein structure modeling, we prove that the functional sites would lose while the binding site of the protein intact, indicating that with the CNV deletion, the protein could still binding to its targets without available functions.
In conclusion, we discovered a novel CNV associated with ACL/PCL, which has high potential to be the causation of the disease. The confidence is built on the robust discovery set, the novelty of the finding, and strong supports from functional studies in gene and protein levels. In other words, in this project we applied ~700 exome sequencing data for CNV discoveries, the CNVs are validated computationally through multiple filters and database, and the existences of CNV were validated through qPCR experimentally. The corresponding gene expression in tissues were measured and compared to the healthy individuals, and the 3D protein structures were simulated to enhance the confidence of the CNV impact. While interventions at the level of CEP57L1 may not be feasible, the role of this gene in the pathogenesis of ACL/PCLagenesis helps explain disease causality.
This study had been approved by the Children’s Hospital of Philadelphia with IRB# 4886. All the patients who participated in this project have been consented and agree to publish the results.
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