- Research article
- Open Access
- Open Peer Review
Identification of ANKDD1B variants in an ankylosing spondylitis pedigree and a sporadic patient
BMC Medical Genetics volume 19, Article number: 111 (2018)
Ankylosing spondylitis (AS) is a debilitating autoimmune disease affecting tens of millions of people in the world. The genetics of AS is unclear. Analysis of rare AS pedigrees might facilitate our understanding of AS pathogenesis.
We used genome-wide linkage analysis and whole-exome sequencing in combination with variant co-segregation verification and haplotype analysis to study an AS pedigree and a sporadic AS patient.
We identified a missense variant in the ankyrin repeat and death domain containing 1B gene ANKDD1B from a Han Chinese pedigree with dominantly inherited AS. This variant (p.L87V) co-segregates with all male patients of the pedigree. In females, the penetrance of the symptoms is incomplete with one identified patient out of 5 carriers, consistent with the reduced frequency of AS in females of the general population. We further identified a distinct missense variant affecting a conserved amino acid (p.R102L) of ANKDD1B in a male from 30 sporadic early onset AS patients. Both variants are absent in 500 normal controls. We determined the haplotypes of four major known AS risk loci, including HLA-B*27, 2p15, ERAP1 and IL23R, and found that only HLA-B*27 is strongly associated with patients in our cohort.
Together these results suggest that ANKDD1B variants might be associated with AS and genetic analyses of more AS patients are warranted to verify this association.
Ankylosing spondylitis (AS) is a severe, debilitating and incurable autoimmune disease affecting multi millions of people in the world . AS is the major subtype of spondyloarthritis, a spectrum of inter-related rheumatic diseases that also includes reactive arthritis (ReA), psoriatic arthritis (PsA), juvenile spondyloarthritis (JSpA), enteropathic arthritis (spondylitis/arthritis associated with inflammatory bowel disease), and undifferentiated spondyloarthritis (USpA) (https://www.spondylitis.org) [2, 3].
The symptoms of AS often appear gradually and progress from stiffness and chronic dull pain in the lower back to severe pain felt from the sacroiliac joint. In severe cases, AS can cause a complete fusion (ankylosis) of the spine. Many AS patients suffer severe loss of mobility and as a consequence lose working capabilities.
The average AS prevalence varies among different populations, with 0.24% in Europe, 0.17% in Asia, 0.3% in North America, 0.1% in Latin America and 0.7% in Africa. Based on these ratios, it is estimated that the number of AS cases in Europe and Asia alone could reach 1.30–1.56 million and 4.63–4.98 million, respectively .
AS is highly inheritable. The recurrence risks in monozygous twins and first-degree relatives are 63 and 8.2%, respectively [4, 5]. Most AS is presented in sporadic cases, probably reflecting the oligogenic nature of this disease. The human leukocyte antigen B27 (HLA-B*27) genotype was found strongly associated with AS [6,7,8]. Specifically HLA-B*27 carriers could have a 20-fold increase in the risk of developing spondylarthropathy-related diseases , which is exemplified by the fact that most AS patients are HLA-B*27 positive in the general population. However the presence of HLA-B*27 genotype is not sufficient for AS pathogenesis, as only 1–5% HLA-B*27 carriers eventually develop AS [8, 10, 11].
Recently large-scale genome-wide association studies on patients with European ancestry and of the Han Chinese have identified at least 31 non-HLA-B genetic loci associated with AS [11,12,13,14,15,16,17]. Among these loci, IL23R, 2p15, ERAP1 exhibit the most significant association [12, 15,16,17]. Nevertheless these loci, together with HLA-B*27, could explain only 24.4% of the heritability of AS . Therefore the major genetic causes of AS remain to be identified. Ideally, AS cases from consanguinity inheritance or large pedigrees could provide a simpler inheritance pattern compared to sporadic cases, which might facilitate the identification of more elusive risk genes of AS.
To further understand the genetics of AS, we employed a combination of genome-wide linkage analysis and next-generation sequencing (NGS) in a three-generation Han Chinese pedigree with five AS patients. The analysis revealed a missense variant affecting a conserved amino acid in the novel gene ANKDD1B that segregates with the disease. We further identified a distinct ANKDD1B missense variant in a male by surveying a group of sporadic AS patients using exome sequencing. These findings suggest that ANKDD1B variants might be related with the pathogenesis of AS.
Patients and subjects
The study protocol was approved by the Review Board of the Second Xiangya Hospital of the Central South University in China with informed consent from each study participant. The proband (AS9_1) (Fig. 1) was diagnosed with ankylosing spondylitis in 2009 at the Department of Rheumatology of the Second Xiangya Hospital. A follow up of the proband identified a 16-member, three-generation AS9 pedigree (Fig. 2a). The disease history of the five AS9 patients and the sporadic patient sAS_P1 is shown in Additional file 1: Table S1. Medical images of two other patients are also shown in Fig. 1.
Genomic DNA was extracted from peripheral blood of the family members using a DNeasy Blood & Tissue Kit (Qiagen, Valencia, CA) on the QIAcube automated DNA extraction robot (Qiagen, Hilden, Germany).
Genome-wide linkage analysis
Genomic DNA samples of the AS9 family members were adjusted to a final concentration of 50 ng/μl. The Infinium OmniZhongHua-8 v1.3 Beadchip (Illumina Inc., San Diego, USA) and the Illumina BeadScan genotyping system (Beadstation Scanner) were employed to obtain the signal intensities of SNP probes. The Infinium OmniZhongHua-8 v1.3 Beadchip contains 887,270 SNPs that cover common, intermediate and rare variants specific to Chinese populations. The GenomeStudio V1.0 Genotyping Module was used to analyze the genotypes (human genome build 37/Hg19) and evaluate the experimental quality. The call rates of the samples were greater than 99.5%. After no call SNPs, SNPs with minor allele frequency < 0.05, and mismatched SNPs between parents and children were excluded, we chose one SNP per 0.5 cM (7079 SNPs across the genome with an average gap of 379 kb) for multi-point parametric linkage analysis using the merlin (v1.1.2) software based on an autosomal dominant inheritance disease model. Specifically we excluded all females of the third generation from the linkage analysis, since females have a penetrance much lower than males . We treated AS9_6 as patient because she has a symptomatic son.
Four members of the AS9 family (AS9_1, AS9_2, AS9_3 and AS9_4) were subjected to whole-exome sequencing analysis. Each individual paired-end Agilent SureSelect library was prepared according to manufacturer’s instructions (Agilent) from 1.0 μg genomic DNA sheared with a Covaris S220 sonicator (Covaris, Inc., Woburn, USA). Exome capture was performed with Agilent’s SureSelect Human All Exon kit V5, which resulted in ~ 50 Mb DNA sequences of 334,378 exons from 20,965 genes being captured. Paired-end sequencing (150-bp reads) was carried on HiSeq 4000 platform (Illumina). After demultiplexing, paired-end sequences were mapped to the human genome (UCSC hg19) using Burrows-Wheeler Aligner (BWA) . The mean coverage of the target regions obtained for the four samples was 99.9, 99.9, 99.8 and 99.9%, with average sequencing depth of 90.86X, 83.27X, 76.24X and 83.87X for AS9_1, AS9_2, AS9_3 and AS9_4, respectively (Additional file 2: Table S2). Downstream processing was performed using the Genome Analysis Toolkit (GATK), varscan2 and Picard, and variant calls were made with the GATK HaplotypeCaller. Variant annotation was based on Ensembl release 82, and filtering was performed with ANNOVAR Documentation.
127,303, 122,644, 115,062 and 126,720 confidence variants in AS9_1, AS9_2, AS9_3 and AS9_4, respectively, were identified from the exome sequencing (Additional file 3: Table S3). Non-synonymous SNPs or frameshift-causing INDELs with an alternative allele frequency > 0.005 in the NHLBI Exome Sequencing Project Exome Variant Server (ESP6500), dbSNP (build 138) (http://www.ncbi.nlm.nih.gov/projects/SNP/index.html), the 1000 Genomes Browser (released May 2012) (http://www.1000genomes.org/) or the ExAC Browser (http://exac.broadinstitute.org) were excluded prior to analysis. The called SNVs and INDELs were filtered and those predicted by HapMap Genome Browser (release #28) (http://hapmap.ncbi.nlm.nih.gov/), SIFT (http://sift.jcvi.org/), Polyphen2 (http://genetics.bwh.harvard.edu/pph2/) and MutationTaster (http://www.mutationtaster.org/) to be non-deleterious were excluded. By this approach, six candidate variants distributed in five genes were identified in all four patients (Additional file 3: Table S3 and Additional file 4: Table S4), which include GBP5 (containing two distinct variants), ANKDD1B, TMEM30B, CACNA1H and RFPL3.
Variant validation and co-segregation analysis
Sanger sequencing was used to validate the candidate variants found in exome sequencing. Segregation analyses were performed on the family members. The two ANKDD1B variants were also examined in the exome sequences of 500 healthy adults of both sexes and different ages, who were recruited by the genome sequencing company Novogene (Beijing) and used as an internal control for genetic variants potentially specific for the Han Chinese. Primer pairs used to amplify fragments encompassing individual variants were designed using an online tool (PrimerQuest, IDT) (http://www.idtdna.com/Primerquest/Home/Index) and the primer sequences for ANKDD1B are listed in Additional file 5: Table S5.
The genomic sequence for each SNP was obtained from dbSNP database (https://www.ncbi.nlm.nih.gov/projects/SNP/). The genomic DNAs from patients were amplified by PCR using primers listed in Additional file 6: Table S6 and the sequences of the amplified fragments were determined.
The AS9 ankylosing spondylitis pedigree
Using the modified New York criteria for ankylosing spondylitis , a diagnosis of AS was made on three individuals (AS9_1, AS9_2, AS9_9) of a three-generation pedigree of the Han Chinese (Fig. 1, Fig. 2a and Additional file 1: Table S1). The family history suggests an autosomal dominant pattern of inheritance, which predominantly affects male members (Fig. 2a). The shared symptoms include: the onset of chronic lower back pain before the age of 20 years, symptomatic sacroiliitis (persistent pain and stiffness lasting > 3 months) and improvement on exercise and worsening with rest. In the proband AS9_1, the symptom was limited to sacroiliitis on both sides, which was verified by radiology (Fig.1a, left). Joint replacement surgery was performed on the right sacroiliac joint of the proband in 2010 (Fig. 1a, right). The proband described that his deceased father also had similar symptoms. For patient AS9_2, the progression of the disease has led to severe deformation of the spine (Fig. 1b, left) and the formation of the “bamboo”-like vertebral joints due to ankylosis (Fig. 1b, right). Patient AS9_9 is the son of patient AS9_2 and began to show mild signs of sacroiliitis before the age of 20 years, which was confirmed by radiology (Fig. 1c).
The other two patients (AS9_3 and AS9_4) were diagnosed based on symptoms that include teenage onset of chronic back pain and symptomatic sacroiliitis (Additional file 1: Table S1). However these symptoms were not verified by radiology due to personal reasons (Additional file 1: Table S1). AS9_3 was not tested for HLA-B*27 positivity as well. We later genotyped rs13202464, a SNP associated with the HLA-B locus in the Han Chinese  and rs116488202, another verified SNP strongly associated with both Europeans and the Han Chinese  (Table 1). We found that AS9_3 shares identical haplotypes at these loci with other HLA-B*27-positive patients of the family, suggesting that AS9_3 is likely HLA-B*27-positive as well.
Genome-wide linkage analysis identified seven risk chromosomal regions in the AS9 pedigree
AS is an oligogenic disease  and most AS patients are identified as sporadic cases. The heritability of AS in the AS9 pedigree might provide a rare opportunity for identifying new AS-associated genetic variants.
To identify the potential genetic variants, we performed genome-wide linkage analysis on 10 AS9 family members (six third-generation females were excluded due to the incomplete penetrance of AS in females) based on an autosomal dominant inheritance model (see Methods). Multi-point parametric linkage analysis identified seven regions on five chromosomes with maximum multi-point parametric LOD (logarithm of odds) scores between 1.275 and 1.4608 (Fig. 2b and Table 2). We also identified seven other regions distributed on seven chromosomes, with the maximal LOD scores between 0.2322 and 0.8175 (Fig. 2b).
Whole-exome sequencing identified six candidate variants in the AS9 pedigree
The linkage analysis only provided information concerning the genomic locations of potential genetic variants associated with the AS9 pedigree. To narrow down the genetic variants, we performed exome sequencing on four patients (AS9_1, AS9_2, AS9_3 and AS9_4). In total we obtained on average 4.6 Gbp, 4.2 Gbp, 3.8 Gbp and 4.2 Gbp sequences that covered more than 99% of the exonic regions for AS9_1, AS9_2, AS9_3 and AS9_4, respectively (Additional file 2: Table S2). The sequencing depth for each patient was from 76X for AS9_3 to 90X for AS9_1.
From the exome sequencing (see Methods), we identified six candidate variants distributed in five genes that are shared by all four patients (Additional file 3: Table S3 and Additional file 4: Table S4). These genes include GBP5 (containing two different variants), ANKDD1B, TMEM30B, CACNA1H and RFPL3.
We examined co-segregation of these variants with individuals of the AS9 pedigree and found that the CACNA1H variant was absent in the AS9_9 patient, suggesting that CACNA1H is probably not a risk locus. MutationTaster (www.mutationtaster.org) prediction indicates that the variants in GBP5 and RFPL3 are likely non-disease causing polymorphisms. The variant in TMEM30B was reported in the ExAC database (http://exac.broadinsitutute.org) at a frequency of 0.002 and is predicted by the SIFT software (www.sift.jcvi.org) to be a highly tolerated change. We currently could not conclude whether this variant confers any risk for AS. Together these analyses suggest that the genetic variant in ANKDD1B is worthy of further consideration.
ANKDD1B variants might be associated with ankylosing spondylitis
We next compared the genomic positions of the five candidate genes (Additional file 4: Table S4) with the whole-genome linkage results (Fig. 2b and c). Interestingly only ANKDD1B is contained within one of the seven linkage regions with MAX_LOD score above 1.275 (Table 2), which is between rs3112483 and rs13161885 on Chr. 5 (Fig. 2c and Table 2). This result is consistent with the bioinformatics analysis described above and suggests that ANKDD1B is potentially associated with the AS9 pedigree.
We examined the coding exons of ANKDD1B in all 16 members of the AS9 family by Sanger sequencing. The L87V variant (Fig. 2d) was verified in the four patients analyzed by exome sequencing and also patient AS9_9 (Fig. 2a), who was not included in our initial exome analysis. The variant was found in AS9_6, who is non-symptomatic but has a symptomatic son. We further detected the L87V variant in three non-symptomatic members of the family (Fig. 2a). Two are daughters of patient AS9_2 and one is the daughter of the non-symptomatic AS9_6. This variant was not detected in seven other non-symptomatic family members (Fig. 2a and Table 1).
ANKDD1B encodes a novel conserved protein with multiple ankyrin repeats and a death domain (Additional file 7: Figure S1). The variant found in the AS9 pedigree changes a conserved leucine to valine at position 87 within the first ankyrin repeat and is predicted to cause a partially deleterious effect on the protein function (www.predictprotein.org).
To further examine the association of ANKDD1B with AS, we surveyed the coding exons and splice sites of ANKDD1B in 30 sporadic AS patients previously analyzed by whole-exome sequencing (Z. Tan and H. Zeng, unpublished observations). From a 21-year old male patient (sAS_P1, Additional file 1: Table S1), we identified a distinct missense variant that changes a conserved arginine to leucine at position 102 (exon3:c.G305T:p.R102L) within the second ankyrin repeat (Fig. 2e, Table 1 and Additional file 7: Figure S1). This variant is predicted to cause strongly deleterious effect on the protein function (www.predictprotein.org).
The two ANKDD1B variants were not found in 500 internal (local) control exomes sequenced. The L87 V variant identified in the pedigree was not identified in NHLBI Exome Sequencing Project Exome Variant Server (ESP6500), the 1000 Genomes Browser as well as the ExAC database. The variant identified in the sporadic male patient (sAS_P1) (c.G305 T:p.R102L) has a SNP number (rs191940699) and is presented in the dbSNP database (www.ncbi.nlm.nih.gov) with a global MAF of 0.0016/8. In addition this SNP is presented in the ExAc database (http://exac.broadinsitutute.org) as a c.G305A:p.R102H variant with an allele frequency of 7.477e-05 (1 out of 13,374 alleles from 6687 individuals in total). In the South Asian population in which this SNP was identified, its allele frequency is 0.0001422 (1 out of 7030 alleles from 3515 individuals). The low values of these frequencies imply a selection against these variants in the general population.
Haplotype analysis of the ANKDD1B variant carriers
Besides the linkage region on Chr. 5 that contains ANKDD1B, we also identified six other regions (Table 2 and Fig. 2b) with MAX-LOD scores above 1.275. Interestingly, one region on Chr. 6 contains the HLA-B locus (Fig. 2c), prompting us to examine the haplotype of HLA-B*27 in our cohort. We found that the SNP rs13202464 previously reported to tag HLA-B*27 in Asian populations  also predominantly tags the patients (6/6 in patients vs 3/11 in non-AS individuals) (Table 1). However the SNP rs116488202 reported to tag HLA-B*27 more significantly in both Asian and European populations  is presented identically among the patients and normal individuals (Table 1), with the risk minor allele (T) absent in all individuals.
The linkage region on Chr. 2 does not contain the major AS risk locus 2p15 but is at a close distance, with 0.97 Mb between the left outline of this region and the SNP rs6759298 reported to tag 2p15 . We genotyped rs6759298 and found that the risk allele of this SNP does not exhibit an apparent association with AS patients (3/6) vs non-AS individuals (6/11) (Table 1).
The ERAP1 locus is also significantly associated with AS in the general population . The ERAP1-tagging SNP rs30187  is 0.3 Mb apart from the right outline of the linkage region on Chr. 5 (Fig. 2c). 3/6 patients carry the risk allele of rs30187 while 9/11 non-AS individuals are also positive (Table 1), suggesting that the genotype of ERAP1 might not be associated with AS in our cohort.
No linkage region on Chr. 1 with a MAX-LOD score above 1.0 was identified. However since the AS risk locus IL23R is located on Chr. 1, we also genotyped the SNP rs11209026 that tags IL23R . We found that all individuals in our cohort are homozygous for the risk allele (Table 1). Therefore we could not evaluate the contribution of the IL23R locus to the pathogenesis of our patients.
We compared the other four linkage regions (Table 2, in blue) with all the AS risk loci identified to date  and found that none are located within these regions. We postulate that these linkage regions might contain new risk loci for AS or are merely associated with the AS9 family by coincidence.
In this study, we combined genome-wide linkage analysis and exome sequencing to identify the ANKDD1B gene as a potential locus related ankylosing spondylitis in a Chinese AS pedigree.
AS is an oligogenic disease with over 75% of the heritability unexplained . Of the 32 identified loci associated with AS [11, 15], HLA-B*27 is the most significant risk factor, followed by IL23R, 2p15 and ERAP1 . Among the seven linkage regions we identified in AS9 pedigree (Fig. 2b), one contains the HLA-B locus and two others are closely linked to the 2p15 and ERAP1 loci, respectively (Fig. 2c). This correlation does not appear to be a random coincidence. Instead, it suggests that these linkage regions more or less correspond to the risk loci of AS and could be useful for distinguishing other genetic variants related to AS, e.g., those variants derived from exome sequencing. Indeed, among the six candidate variants that we identified from exome sequencing of the AS9 pedigree, only ANKDD1B is contained within a linkage region on Chr. 5 (Fig. 2c). Furthermore, a different ANKDD1B variant (R102L) was identified in a sporadic AS patient, emphasizing the potential correlation between ANKDD1B variants and AS in the Chinese patients.
The genetic location of ANKDD1B is 5q13.3 (www.ensembl.org), which is 0.1 cM away from 5q14.3, a previously identified risk locus in Asian populations . The significance of 5q14.3 locus was not replicated in the study of European populations . Therefore it is unclear whether 5q14.3 represents an Asian-specific locus or the association of this locus with AS  was in fact caused by its closeness with ANKDD1B. The linkage region on Chr. 5 identified in this study is also close to but does not contain the risk locus ERAP1 (Fig. 2c). Whether the haplotype of ERAP1 affects the identification of this linkage region is unknown. The linkage region that we identified on Chr. 2 is close to another major AS risk locus, 2p15  (Fig. 2c). Currently we could not determine whether the identification of this linkage region is caused by its closeness to 2p15 or it represents a different risk locus for AS. The other linkage regions (Table 2, in blue) do not contain any of the AS risk loci identified so far .
ANKDD1B encodes a novel protein containing 10 tandem ankyrin repeats and a death domain and is conserved from zebrafish to human (Additional file 7: Figure S1). Ankyrin repeats are found in proteins involved in inflammatory response, transcription, cell-cycle regulation, cytoskeleton integrity development, cell-cell signaling and protein transport . Death domains are usually regulators of inflammation, innate immune response and cell death through their interactions with TNF (tumor necrosis factor) receptors and Toll-like receptors [21,22,23].
A protein expression database (www.proteinatlas.org) indicates that the ANKDD1B protein is expressed in muscles, distinct cells of the lymph node and tonsil, a chronic myeloid leukemia cell line (K-562), a multiple myeloma cell line (LP-1) and an ovarian cystadenocarcinoma cell line (EFO-21). In addition the ANKDD1B transcript was detected in multiple human tissues including the lymph node and spleen (www.genecards.org). In mouse, the ANKDD1B transcript is expressed in higher levels in multiple B- and T-cell lines and in various parts of the nervous system (www.biogps.org). The site of expression and the domain structure of ANKDD1B suggest a function in the immune system.
The complex oligogenic nature of AS hinders the genetic analysis of AS pathogenesis. A previous analysis of AS recurrence in relation to genetic distances estimated that multiplicative interactions involving ~five genetic loci could partially explain the occurrence of AS in the general population . In our pedigree and the sporadic male patient, the presence of the ANKDD1B variant and HLA-B*27 are the most significant factors predicting whether an individual develops AS (Table 1), while the roles of three other GWAS-derived significant loci (IL23R, 2p15, ERAP1) could not be evaluated, probably due to the limited size of our cohort.
In the AS9 pedigree, all four male carriers are HLA-B*27 positive and developed AS (Fig. 2a and Table 1). Four of the five female carriers are HLA-B*27 positive, while only one developed AS (Fig. 2a and Table 1). This phenomenon is consistent with AS epidemiology in the general population, in which males are three times more frequently affected than females .
Besides the AS9 pedigree described in our study, three other Han Chinese AS pedigrees were also described recently , in which the 2q36.1-36.3 locus was found to be associated with disease transmission in addition to HLA-B*27. This locus has not been associated with AS in other association studies . It is possible that a combination of genome-wide linkage analysis and genome sequencing would narrow down the potential AS-related genetic variants in these pedigrees.
In short, we found that a novel missense variant of the ANKDD1B gene might be associated with patients in a rare AS pedigree of the Han Chinese. We also found a different ANKDD1B missense variant in a sporadic AS patient. ANKDD1B was identified with the combination of genome-wide linkage analysis and exome sequencing and verified to be co-segregated with the patients in a similar manner as the HLA-B*27 locus, implying that this gene might be related to AS pathogenesis and is worth to be considered for understanding the genetics of AS. Future studies, including verification of this association in more AS patients and analysis of animal models carrying ANKDD1B mutations, might provide novel insights into the pathogenesis of AS.
Dean LE, Jones GT, MacDonald AG, Downham C, Sturrock RD, Macfarlane GJ. Global prevalence of ankylosing spondylitis. Rheumatology (Oxford). 2014;53(4):650–7. Epub 2013/12/11. https://doi.org/10.1093/rheumatology/ket387. PubMed PMID: 24324212.
Braun J, Sieper J. Ankylosing spondylitis. Lancet. 2007;369(9570):1379–90. Epub 2007/04/24. https://doi.org/10.1016/S0140-6736(07)60635-7. PubMed PMID: 17448825.
Stolwijk C, Boonen A, van Tubergen A, Reveille JD. Epidemiology of spondyloarthritis. Rheum Dis Clin N Am 2012;38(3):441–76. Epub 2012/10/23. https://doi.org/10.1016/j.rdc.2012.09.003. PubMed PMID: 23083748; PubMed Central PMCID: PMC4470267.
Brown MA, Kennedy LG, MacGregor AJ, Darke C, Duncan E, Shatford JL, et al. Susceptibility to ankylosing spondylitis in twins: the role of genes, HLA, and the environment. Arthritis Rheum 1997;40(10):1823–8. https://doi.org/10.1002/1529-0131(199710)40:10<1823::AID-ART15>3.0.CO;2%2D1. PubMed PMID: 9336417.
Brown MA, Laval SH, Brophy S, Calin A. Recurrence risk modelling of the genetic susceptibility to ankylosing spondylitis. Ann Rheum Dis. 2000;59(11):883–6. PubMed PMID: 11053066; PubMed Central PMCID: PMCPMC1753017
Brewerton DA, Hart FD, Nicholls A, Caffrey M, James DC, Sturrock RD. Ankylosing spondylitis and HL-A 27. Lancet. 1973;1(7809):904–7. Epub 1973/04/28. PubMed PMID: 4123836
Schlosstein L, Terasaki PI, Bluestone R, Pearson CM. High association of an HL-A antigen, W27, with ankylosing spondylitis. N Engl J Med. 1973;288(14):704–6. Epub 1973/04/05. https://doi.org/10.1056/NEJM197304052881403. PubMed PMID: 4688372.
Reveille JD. An update on the contribution of the MHC to AS susceptibility. Clin Rheumatol 2014;33(6):749–757. Epub 2014/05/20. doi: https://doi.org/10.1007/s10067-014-2662-7. PubMed PMID: 24838411; PubMed Central PMCID: PMC4488903.
Braun J, Bollow M, Remlinger G, Eggens U, Rudwaleit M, Distler A, et al. Prevalence of spondylarthropathies in HLA-B27 positive and negative blood donors. Arthritis Rheum. 1998;41(1):58–67. https://doi.org/10.1002/1529-0131(199801)41:1<58::AID-ART8>3.0.CO;2-G. PubMed PMID: 9433870.
Bowness P. Hla-B27. Annu Rev Immunol 2015;33:29–48. Epub 2015/04/12. https://doi.org/10.1146/annurev-immunol-032414-112110. PubMed PMID: 25861975.
O'Rielly DD, Uddin M, Rahman P. Ankylosing spondylitis: beyond genome-wide association studies. Curr Opin Rheumatol. 2016;28(4):337–345. https://doi.org/10.1097/BOR.0000000000000297. PubMed PMID: 27224740.
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007;39(11):1329–37. Epub 2007/10/24. https://doi.org/10.1038/ng.2007.17. PubMed PMID: 17952073; PubMed Central PMCID: PMC2680141.
Danoy P, Pryce K, Hadler J, Bradbury LA, Farrar C, Pointon J, et al. Association of variants at 1q32 and STAT3 with ankylosing spondylitis suggests genetic overlap with Crohn's disease. PLoS Genet. 2010;6(12):e1001195. Epub 2010/12/15. https://doi.org/10.1371/journal.pgen.1001195. PubMed PMID: 21152001; PubMed Central PMCID: PMC2996314.
Evans DM, Spencer CC, Pointon JJ, Su Z, Harvey D, Kochan G, et al. Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Nat Genet. 2011;43(8):761–7. Epub 2011/07/12. https://doi.org/10.1038/ng.873. PubMed PMID: 21743469; PubMed Central PMCID: PMC3640413.
International Genetics of Ankylosing Spondylitis C, Cortes A, Hadler J, Pointon JP, Robinson PC, Karaderi T, et al. Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nat Genet. 2013;45(7):730–8. https://doi.org/10.1038/ng.2667. PubMed PMID: 23749187; PubMed Central PMCID: PMCPMC3757343.
Lin Z, Bei JX, Shen M, Li Q, Liao Z, Zhang Y, et al. A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis. Nat Genet 2012;44(1):73–7. Epub 2011/12/06. https://doi.org/10.1038/ng.1005. PubMed PMID: 22138694.
Reveille JD, Sims AM, Danoy P, Evans DM, Leo P, Pointon JJ, et al. Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Nat Genet. 2010;42(2):123–7. Epub 2010/01/12. https://doi.org/10.1038/ng.513. PubMed PMID: 20062062; PubMed Central PMCID: PMC3224997.
Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics. 2009;25(14):1754–60. https://doi.org/10.1093/bioinformatics/btp324. PubMed PMID: 19451168; PubMed Central PMCID: PMCPMC2705234.
van der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. A proposal for modification of the New York criteria. Arthritis Rheum. 1984;27(4):361–8. Epub 1984/04/01. PubMed PMID: 6231933
Mosavi LK, Cammett TJ, Desrosiers DC, Peng ZY. The ankyrin repeat as molecular architecture for protein recognition. Protein Sci. 2004;13(6):1435–48. Epub 2004/05/21. https://doi.org/10.1110/ps.03554604. PubMed PMID: 15152081; PubMed Central PMCID: PMC2279977.
Feinstein E, Kimchi A, Wallach D, Boldin M, Varfolomeev E. The death domain: a module shared by proteins with diverse cellular functions. Trends Biochem Sci. 1995;20(9):342–4. Epub 1995/09/01. PubMed PMID: 7482697
O'Neill LA, Dunne A, Edjeback M, Gray P, Jefferies C, Wietek C. Mal and MyD88: adapter proteins involved in signal transduction by toll-like receptors. J Endotoxin Res. 2003;9(1):55–9. Epub 2003/04/15. https://doi.org/10.1179/096805103125001351. PubMed PMID: 12691620.
Wajant H. Death receptors. Essays Biochem. 2003;39:53–71. Epub 2003/10/31. PubMed PMID: 14585074
Gu J, Huang J, Li C, Zhao L, Huang F, Liao Z, et al. Association of chromosome 2q36.1–36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families. J Med Genet. 2009;46(10):657–62. https://doi.org/10.1136/jmg.2009.066456. PubMed PMID: 19416804; PubMed Central PMCID: PMCPMC2748191.
We thank the AS9 family members and other individuals for their cooperation. We thank Qiong Fu, Chunyu Liu and Qing Zhou for suggestions.
The study is supported by a Natural Science Foundation of China grant to ZT (No. 81470445), a MOST grant (2016YFC1201805) and Natural Science Foundation of China grants (No. 31371253 and 31571045) to LM. This study is also partially supported by Key Projects of Changsha Science and Technology (K1306005–31-1). The funding bodies have no roles in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
The study protocol was approved by the Review Board of the Second Xiangya Hospital of the Central South University in China with written, informed consent from each study participant to participate in this study.
Consent for publication
Written informed consent for publication was obtained from the participants. The participant whose images were included in this manuscript consented for them to be published.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Table S1. List of patients from the AS9 pedigree and sAS_P1. (PPTX 45 kb)
Table S2. Exome sequencing quality metrics. (PPTX 46 kb)
Table S3. NGS summary. (PPTX 54 kb)
Table S4. List of candidate genes. (PPTX 46 kb)
Table S5. ANKDD1B PCR and sequencing primers. (PPTX 40 kb)
Table S6. PCR primers for haplotype genotyping. (PPTX 41 kb)
Figure S1. ANKDD1B protein domains and sequence alignment. Upper panel: human ANKDD1B domain structure. AR: ankyrin repeat. Lower panel: ANKDD1B protein sequence alignment from zebrafish to human. The two variants identified in the AS9 pedigree and the sAS_P1 patient are indicated. (TIFF 6077 kb)
About this article
Cite this article
Tan, Z., Zeng, H., Xu, Z. et al. Identification of ANKDD1B variants in an ankylosing spondylitis pedigree and a sporadic patient. BMC Med Genet 19, 111 (2018). https://doi.org/10.1186/s12881-018-0622-9
- Ankylosing spondylitis
- Ankyrin repeat