- Research article
- Open Access
Genetic association between germline JAK2polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case–control study
BMC Genetics volume 15, Article number: 147 (2014)
Myeloproliferative neoplasms (MPNs) are a group of haematological malignancies that can be characterised by a somatic mutation (JAK2V617F). This mutation causes the bone marrow to produce excessive blood cells and is found in polycythaemia vera (~95%), essential thrombocythaemia and primary myelofibrosis (both ~50%). It is considered as a major genetic factor contributing to the development of these MPNs. No genetic association study of MPN in the Hong Kong population has so far been reported. Here, we investigated the relationship between germline JAK2 polymorphisms and MPNs in Hong Kong Chinese to find causal variants that contribute to MPN development. We analysed 19 tag single nucleotide polymorphisms (SNPs) within the JAK2 locus in 172 MPN patients and 470 healthy controls. Three of these 19 SNPs defined the reported JAK2 46/1 haplotype: rs10974944, rs12343867 and rs12340895. Allele and haplotype frequencies were compared between patients and controls by logistic regression adjusted for sex and age. Permutation test was used to correct for multiple comparisons. With significant findings from the 19 SNPs, we then examined 76 additional SNPs across the 148.7-kb region of JAK2 via imputation with the SNP data from the 1000 Genomes Project.
In single-marker analysis, 15 SNPs showed association with JAK2V617F-positive MPNs (n = 128), and 8 of these were novel MPN-associated SNPs not previously reported. Exhaustive variable-sized sliding-window haplotype analysis identified 184 haplotypes showing significant differences (P < 0.05) in frequencies between patients and controls even after multiple-testing correction. However, single-marker alleles exhibited the strongest association with V617F-positive MPNs. In local Hong Kong Chinese, rs12342421 showed the strongest association signal: asymptotic P = 3.76 × 10−15, empirical P = 2.00 × 10−5 for 50,000 permutations, OR = 3.55 for the minor allele C, and 95% CI, 2.59-4.87. Conditional logistic regression also signified an independent effect of rs12342421 in significant haplotype windows, and this independent effect remained unchanged even with the imputation of additional 76 SNPs. No significant association was found between V617F-negative MPNs and JAK2 SNPs.
With a large sample size, we reported the association between JAK2V617F-positive MPNs and 15 tag JAK2 SNPs and the association of rs12342421 being independent of the JAK2 46/1 haplotype in Hong Kong Chinese population.
Myeloproliferative neoplasms (MPNs) are a group of clonal diseases originating from the bone marrow. The present study focuses on three main MPNs: polycythaemia vera (PV), essential thrombocythaemia (ET), and primary myelofibrosis (PMF) . These three non-leukaemic MPNs are characterised by their BCR-ABL-negativity and recurrent genetic aberrations, particularly a somatic mutation, JAK2V617F (hereafter V617F). This point mutation leads to the Val-to-Phe substitution at the amino acid position 617 and constitutively activates the JAK-STAT signalling pathway that is essential for homeostatic processes including proliferation and survival of haematopoietic cells ,. It was detected in almost all PV patients and about half of ET and PMF patients, but not in healthy individuals -. In 2008, World Health Organization included V617F as one of the diagnostic criteria for this group of MPNs . Subsequently, disease anticipation was first reported in Swedish families with an increased risk of developing MPNs among the first-degree relatives of MPN patients . Thereafter, more MPN predisposition loci were revealed by several independent groups around the same time. It was found that the JAK2 germline haplotype 46/1 increased the likelihood of developing MPNs, mainly in patients with the JAK2 mutation -. Association of JAK2 alleles and/or haplotypes with MPNs has now been reported in Caucasians -,-, Japanese ,, Chinese - and Brazilians . However, work remains to be done to identify the causal variants in or flanking the JAK2 locus and to delineate the mechanism by which such casual variants contribute to MPN development.
The aim of this study was to evaluate the association between JAK2 germline polymorphisms and MPNs in the Chinese population of Hong Kong. Our primary hypothesis was that the disease might have possible association with other variants spanning the JAK2 gene. Our case–control association study was carried out in two stages on the same sample set (n = 642): an initial direct genotyping of 19 SNPs including the reported JAK2 46/1 risk-haplotype-tagging SNPs and other tag SNPs selected from HapMap , and an imputation study of additional 76 SNPs in an attempt to narrow down the targeted region involved in the development of MPNs. Among Asian studies, we have the largest sample size of controls (n = 470) and the second largest total sample size (n = 642).
We recruited 172 MPN patients and 470 healthy control subjects, all Chinese. The patients included 61 with PV, 93 with ET, 17 with PMF, and 1 with unclassified MPN, and 86 males (50.0%) and 86 females (50.0%). Their mean age was 57 years (ranges: 18–88 years). For the healthy controls, the mean age was 51 years (ranges: 16–75 years), and there were 236 males (50.2%) and 234 females (49.8%).
Detection of JAK2V617Fmutation in Hong Kong Chinese
All cases and controls were first screened for V617F mutation. Overall, 128 (74.4%) MPN patients were positive and 44 (25.6%) negative for V617F. Age differed significantly between V617F-positive MPN cases and healthy controls (P < 0.0001) whereas there was no difference in age between V617F-negative MPNs and controls (P = 0.7342). However, there was still statistically significant difference in age between all MPN cases (both V617F-positive and -negative) and controls (P < 0.0001). Fisher’s exact test suggested no significant difference in sex ratio between the two groups (P > 0.3). The prevalence of V617F in our cohort was 87% (53/61) in PV, 68% (63/93) in ET, 65% (11/17) in PMF, and 100% (1/1) in unclassified MPN. The mutation frequency did not differ by sex and age in our patient group. Overall, the data suggested that MPNs can affect anyone regardless of sex and age, in our Hong Kong Chinese population. The mutation was not detected in the 470 healthy controls.
Genetic association study of genotyped SNPs
In total, 19 tag SNPs were selected, capturing the genetic information of 95 SNPs in the study region (148.7 kb) with a mean r2 of 0.96. All of them are intronic SNPs except rs3808850 (5’ upstream). As explained in the section of Materials and methods, JAK2 risk-haplotype-tagging SNPs were forced to be included. The SNPs were also called S1, S2, …., and S19 in the sequential order from the 5’ end to the 3’ end of the JAK2 sense strand for ease of discussion.
The genotypes were in Hardy-Weinberg equilibrium (Fisher’s exact test P > 0.05) for all SNPs in the control group. In general, linkage disequilibrium (LD) among the 19 SNPs in the combined group of V617F-positive MPN cases and healthy controls was not strong except for those tagging the JAK2 risk-haplotype (Figure 1). The same applied to the LD measures (r2) for the combined group of V617F-negative MPN cases and healthy controls (details not shown).
As a difference in age was observed between cases and controls, we sought to minimise the influence of age. To be consistent with previous studies ,, we also adjusted for sex in the analyses although the difference in sex ratio between cases and controls did not reach statistical significance. Among the five genetic models tested (genotypic, additive, allelic, dominant and recessive) for the 19 directly genotyped SNPs, the allelic model generated the most significant results. Therefore, we increased the stringency of our allelic test by comparing the 19 SNPs between V617F-positive MPNs and controls with adjustment for sex and age, and with correction for multiple comparisons by 50,000 permutations. All 19 SNPs were associated with V617F-positive MPNs before permutation except rs1536798 (S5; P asym = 0.0765) and rs10974947 (S11; P asym = 0.1414) while 2 other SNPs (rs10815148 (S6) and rs3824432 (S16)) did not survive after 50,000 permutations with P emp > 0.05 (Table 1); asymptotic P value is denoted as P asym and empirical P value as P emp . Moreover, 8 of these 15 MPN-associated SNPs were novel and have not been reported previously: rs2149555 (S4), rs2149556 (S7), rs10119004 (S10), rs12343065 (S14), rs7857730 (S15), rs7847294 (S17), rs3780378 (S18) and rs10815162 (S19) (see footnote a of Table 1).
The results agreed with the findings of Caucasian studies: the minor alleles of the JAK2 risk-haplotype-tagging SNPs (allele G of rs12340895 (S13), allele G of rs10974944 (S9) and allele C of rs12343867 (S12)) were strongly associated with V617F-positive MPNs with descending odds ratios (ORs; 3.27, 2.87, and 2.60, respectively, with P asym ≤ 3.80 × 10−9). All 3 SNPs statistically survived the 50,000 permutations with P emp = 2.00 × 10−5, which is the lowest P emp value achievable with 50,000 permutations. These results suggested that S9, S12, and S13 were strongly associated with V617F-positive MPNs. Intriguingly, we identified rs12342421 (S8) as the most significantly MPN-associated SNP (P asym = 3.76 × 10−15 and P emp = 2.00 × 10−5, Table 1) among the 19 SNPs in Hong Kong Chinese population. The corresponding OR for the minor allele C was 3.55 (95% CI, 2.59-4.87).
Given the significant difference between V617F-positive MPNs and healthy controls, we then examined V617F-negative MPN patients for the same 19 SNPs. Overall, comparison of V617F-negative MPNs and controls did not produce any significant association (P emp >0.05) after 50,000 permutations with rs12342421 (S8) still being the strongest SNP (P emp = 0.0621) (Additional file 1: Table S1). Likewise, haplotype analysis of V617F-negative MPNs did not yield any significant results either (P emp ≥ 0.2298; data not shown). Nonetheless, a comparison of the SNP allele frequencies between V617F-positive and V617F-negative patients also did not reveal any significant difference except for rs12342421 (S8; P asym = 0.0031 and P emp = 0.0303) and rs12340895 (S13; P asym = 0.0075 and P emp = 0.0380).
We then performed haplotype analysis by comparing V617F-positive MPNs and controls with adjustment for sex and age. Exhaustive variable-sized sliding-window haplotype analysis was done on the 19 genotyped SNPs. PLINK  examined 190 windows with 1 to 19 SNPs per window, and identified 184 haplotype windows (96.8%) showing significant differences (P emp < 0.05) in frequencies between patients and controls even after 50,000 permutations (Table 2). Of all the sliding haplotype windows of a given size, the haplotype window with the most significant omnibus test is shown in the third column from the right of Table 2. We examined such most significant haplotype windows for all possible window sizes, and noted that all these most significant haplotype windows always included rs12342421 (S8) as a constituent SNP. Of all these most significant haplotype windows, the 1-SNP window rs12342421 (S8) itself achieved the strongest association with V617F-positive MPNs (P asym = 3.76 × 10−15 and P emp = 2.00 × 10−5) (Table 2). These results were comparable to those (data not shown) based on haplotype blocks generated from Haploview (Figure 1).
In the 1000 Genomes Project, rs12342421 (S8) is in perfect LD (r2 = 1; Additional file 2: Figure S1A) with JAK2 risk-haplotype-tagging SNPs (rs10974944, rs12343867 and rs12340895, i.e. S9, S12 and S13) for Han Chinese in Beijing (CHB), and in very strong LD (r2 ≥ 0.94; Additional file 2: Figure S1B) with these three SNPs in Caucasians of European ancestry (CEU). All LD plots were constructed based on solid spine of linkage disequilibrium (SSLD). The LD was moderately strong (r2 ≥ 0.76; Figure 1) for the corresponding pairs of SNPs in our study cohort of 128 V617F-positive MPN cases and 470 controls. We found that rs12342421 (S8) was not in the same LD block with JAK2 risk-haplotype-tagging SNPs in the CEU population (Additional file 2: Figure S1B). When we further divided the sample groups and constructed LD plots, we found that the LD patterns, in descending order of LD strength (from the most correlated to the least correlated), were: the controls only ≈ the combined group of V617F-negative MPNs and controls (Additional file 3: Figures S2 and S3, respectively), the combined group of all MPNs and controls (Additional file 3: Figure S4), the combined group of V617F-positive MPNs and controls (Figure 1), all MPN cases only (Additional file 3: Figure S5), and the V617F-positive MPN cases only (Additional file 3: Figure S6). Overall, a higher degree of correlation was observed among these few SNP pairs in the 1000 Genomes Project data of CHB and CEU populations (Additional file 2: Figure S1A, B) and in our controls (Additional file 3: Figure S2) when compared with our V617F-positive MPN cases (Additional file 3: Figure S6).
Genetic association of genotyped and imputed SNPs
With these significant findings, we further performed imputation for 76 additional SNPs (selected using Tagger with minor allele frequency or MAF of 0.01) with Beagle to examine the 148.7-kb region encompassing the JAK2 locus. Manual quality control check on Beagle indicated an accuracy of >95% in imputing the missing (removed) genotypes. Consistent trends were identified when all 95 SNPs (19 directly genotyped and 76 imputed) were analysed together by logistic regression adjusted for sex and age: single-marker analysis generated the strongest association signal for rs12342421 (S8) as in our initial study. Of these 95 SNPs, 67 showed association exceeding the significance of 8 × 10−8 (P asym ). The strongest association was detected for rs12342421 (S8; P asym = 3.76 × 10−15, P emp = 2.00 × 10−5 and OR = 3.55) while SNPs in high LD with S8 showed similar levels of association (see Table 3 for the top 20 SNPs).
To have an overall picture, we examined the LD structure (Figure 2) for all 95 SNPs (19 directly genotyped and 76 imputed). We realised that rs12342421 (SNP no. 43 in Figure 2) also tagged (r2 = 0.85) rs4495487 (SNP no. 49 in Figure 2) that was reported to be the additional variant contributing to MPN predisposition in Japanese population . All the SNPs within this haplotype block showed very strong extent of LD (r2 close to 1; bottom panel of Figure 2).
Likewise, exhaustive haplotype analysis was performed on these 95 SNPs to further restrict the linked region and identify the most probable MPN-predisposing variants or haplotypes (Additional file 4: Table S2). Age and sex were adjusted as covariates. The SNP rs12342421 (S8) again topped the 1634 haplotype windows as a 1-SNP window (S8 itself): P asym = 3.76 × 10−15 and P emp = 2.00 × 10−5 for 50,000 permutations (Additional file 4: Table S2). Adjacent SNPs spanning across rs12342421 formed the most significantly associated haplotypes among the rest as in the sliding windows for the 19 directly genotyped SNPs. The SNP rs12342421 (S8) was obviously important because almost all the statistically significant haplotypes carried this SNP.
Conditional logistic regression
Based on the results from PLINK, we tested the individual effect on disease association of the strongest MPN-associated SNP (rs12342421, i.e. S8) and the risk-haplotype-tagging SNPs (rs10974944, rs12343867 and rs12340895, i.e. S9, S12 and S13) in the corresponding sliding window. The shortest and most significant sliding haplotype window containing these four SNPs was the 6-SNP window S8…S13 (P asym = 2.75 × 10−12; Table 2), which was therefore selected for conditional logistic regression analysis. Conditional analysis for the independent effect of one SNP at a time suggested that only rs12342421 (S8) contributed an independent effect to the significant association between the 6-SNP window and V617F-positive MPN cases (P = 0.0005 for omnibus test of independent effect, Table 4). Logically, controlling for all the single SNPs except rs12342421 (S8) yielded a reduced but still statistically significant P value of ≤0.0072 while controlling for rs12342421 (S8) demolished the significance (P = 0.4360) (Table 4). In other words, we could not detect any significant association when rs12342421 (S8) was removed from the combination, and the original risk-haplotype-tagging SNPs (S9, S12 and S13) did not explain all the association signals.
Our data suggested that JAK2 germline polymorphisms, especially rs12342421 (S8), were significantly associated with V617F-positive MPN in Hong Kong Chinese population.
There has been evidence suggesting that JAK2 46/1 haplotype contributed to the development of V617F-positive MPNs, but the findings for V617F-negative MPNs are inconsistent and less convincing. While most of the studies detected no association between the risk-haplotype and V617F-negative MPNs ,,,-, significant association with V617F-negative MPN patients was reported in two studies with bigger sample size (n = 108 and 53) ,. In the light of recent Chinese studies that the JAK2 haplotype poses a higher risk of developing V617F-positive MPNs ,, we employed a case–control study design to explore the described genetic susceptibility to MPNs in the Hong Kong Chinese population. To avoid missing any potential causal variant in the region, we investigated not only the risk-haplotype-tagging SNPs but also a total of 95 SNPs in two stages with an increased sample size. In the first stage, we genotyped 19 tag SNPs of the JAK2 locus. In the second stage, we carried out genotype imputation on additional 76 JAK2 SNPs. We then combined the 19 directly genotyped SNPs and the 76 imputed SNPs (95 in total), and carefully examined both datasets by both single-marker and haplotype analyses.
After single-marker analysis, we adopted a variable-sized sliding-window strategy to examine haplotypic effects in an unbiased manner. This exhaustive approach is best suited for capturing the haplotypes of all possible sliding-widow sizes (including single markers) that are most significantly associated with MPNs . This comprehensive approach identified from the 19 directly genotyped SNPs 184 haplotype windows that showed significant association (~97% of all 190 haplotype windows; P emp < 0.05, Table 2) even after correction for multiple comparisons. However, single-marker analyses of both the 19 SNPs and the 76 imputed SNPs showed that V617F-positive MPNs were associated more significantly with the single SNP rs12342421 (S8, also tagging the risk haplotype) than the haplotypes (Table 1 vs Table 2, and Table 3 vs Additional file 4: Table S2)) although strong association between the risk-haplotype-tagging SNPs (rs10974944, rs12343867 and rs12340895, i.e., S9, S12 and S13) and V617F-positive MPNs was also evident. The C allele rs12342421 (S8) was enriched in V617F-positive MPN patients when compared with controls. Our conditional logistic regression further demonstrated that this single SNP contributed an independent effect to the most significant association between haplotypes and MPNs (Table 4) – a novel finding not previously reported. Analysis showed that rs12342421 (S8) had stronger association when it was not combined with other SNPs, i.e. as a single marker (Table 2). This means that the effect of rs12342421 (S8) became less significant when it was combined with other SNPs. The results also imply that the original risk-haplotype-tagging SNPs (S9, S12 and S13) do not explain all the association signals; this finding is intriguing because many studies only focused on one or more of these three risk-haplotype-tagging SNPs.
Although rs12342421 (S8) was analysed in an early study, the results were never reported explicitly . Two other studies indeed reported the association of rs12342421 (S8) with MPNs in Caucasians ,. However, both studies did not investigate whether rs12342421 (S8) contributed an effect independent of the JAK2 46/1 haplotype ,. In addition, Pardanani et al.  is so far the only study that reported opposite effects (high-risk vs protective) for PV and ET for SNPs found to be associated with these MPN subtypes. Zerjavic et al.  is so far also the only study that failed to demonstrate association between MPNs and rs12343867 (S12) – the SNP most commonly used for tagging the 46/1 haplotype, while other risk-haplotype tagging SNPs still showed association with MPNs. Zerjavic et al.  also reported a less significant association for rs12342421 (S8) than for rs10974944 (S9) – a finding different from ours (Table 1).
Overall, 19 tag SNPs were genotyped in this study and 15 found to be associated with V617F-postive MPNs (see footnote a of Table 1). Of these, 7 have been previously reported to be associated with MPNs in one or more studies -, including the most three commonly studied risk-haplotype-tagging SNPs rs10974944, rs12343867 and rs12340895 (i.e. S9, S12 and S13). The remaining eight SNPs are novel MPN-associated SNPs and have not been reported previously. In contrast, four SNPs that have been reported to be associated MPN or its subtypes were not genotyped experimentally or by imputation in the current study: rs10758677 in a European study , rs10758669 in an American study , rs11999802 in another American study  and rs10118930 in a Chinese study . Of particular interest is rs11999802, a genome-wide significant SNP (P = 1.8 × 10−8) associated with PV with an allelic OR of 4.41 in a small-scale genome-wide association study involving 34 PV patients and 3,278 control subjects of European ancestry .
Our results show that the significant association between JAK2 polymorphisms and MPNs in Hong Kong Chinese is comparable to the results in other populations. However, we found that rs12342421 (S8) was not in the same LD block with JAK2 risk-haplotype-tagging SNPs in the CEU population (Additional file 2: Figure S1B) although it is still in strong LD (r2 close to 1) with JAK2 risk-haplotype-tagging SNPs. This may explain why rs12342421 (S8), rather than the JAK2 risk-haplotype-tagging SNPs, exhibits a stronger association with MPNs in our population. When we examined the effect of V617F on the extent of LD, we found that the r2 between rs12342421 (S8) and other JAK2 risk-haplotype-tagging SNPs decreased in a V617F-dependent manner. We observed that controls had stronger LD (r2) among these SNPs than cases, and that cases without V617F mutation had stronger LD than cases with V617F mutation (Additional file 3: Figures S2-S6 and Figure 1). The r2 values were much lower when V617F-positive cases were included to construct the LD plot. It has been demonstrated that there can be extensive variation in the extent of LD between cases and controls in a region of genetic association . The variation in LD patterns observed in our cases (especially cases with V617F) and controls suggests that the region surrounding rs12342421 (S8) is associated with MPNs. While current genetic maps can be used to examine the LD structure, fine mapping at higher resolution may still be required to sufficiently examine the region because recombination occurs not only in hot spots .
We explored the potential biological functions of the genotyped genetic markers with several web-based SNP prediction tools that are supported by regularly updated databases and software tools: SNPnexus , SNP Function Prediction (FuncPred) , F-SNP  and MaInspector . In silico analysis predicted no known function for rs12342421 (S8) and other genotyped SNPs except that one 5’-upstream SNP (rs3808850 (S1)) and two intronic SNPs (rs7849191 (S2) and rs3780378 (S18)) were predicted by FuncPred to be involved in transcription factor binding sites. Experimental functional studies may be required to clarify this issue.
We then conducted an analysis of expression quantitative trait loci (eQTL) across the JAK2 gene (142.8 kb) with several online tools: eQTL resources @ the Pritchard lab , seeQTL , and UCSC Genome Browser . This analysis did not detect any regulatory regions within the two recombination hotspots encompassing the JAK2 gene .
These circumstantial findings suggest that the causal variants driving the disease development may not be the SNPs or haplotypes reported here, but some untyped variants in LD with these markers. However, it is also possible that the potential functions of the associated SNPs are some biological processes that are not well captured by current functional annotation software. Owing to limited eQTL studies on different tissues or cell types, eQTL studies might provide only limited knowledge for linking regulatory variants to specific genes in different tissues or cell types. There might be some other eQTLs that have not been curated, leading to the limited information .
The distribution of V617F in our Hong Kong MPN patients (PV, ET and PMF) is similar to those in other studies -. This justified our comparable findings to those in other populations. Taken together, our results corroborate the findings that JAK2 variants are predisposing factors for MPN development dependent on V617F in Hong Kong Chinese, especially rs12342421 (S8). Conceivably, the failure to detect, in our study, the association between V617F-negative MPNs and controls as reported elsewhere , can be ascribed to the small sample size of the cases (n = 44). Larger sample size would probably be needed to detect an association for V617F-negative MPNs.
To the best of our knowledge, we are the first to perform genotype imputation in genetic association studies of MPNs. Being an essential component in genetic association study, imputation enabled us to test many untyped markers for associations with MPNs and hence increased the chance to identify causal variants. Although we failed to find the causal variant, imputation together with conditional logistic regression indeed further strengthens our confidence to conclude that rs12342421 (S8) contributed an independent effect to the most significant association between JAK2 risk haplotype and MPNs.
Fifteen JAK2 germline polymorphisms were associated with MPN patients with V617F mutation in Hong Kong Chinese population. The single JAK2 SNP rs12342421 (S8) was associated with predisposition to the development of V617F-positive MPN by 3.55 fold for the minor allele C, but independent of the JAK2 46/1 haplotype. No significant association was found between V617F-negative MPN patients and the JAK2 risk alleles. We have presented some plausible arguments that S8 is likely to be involved in the pathogenesis of MPN. However, further functional validation is necessary to prove its involvement in the disease development.
Subjects and DNA samples
Participants were Hong Kong Chinese MPN patients diagnosed according to the WHO 2008 criteria  and recruited from six local hospitals. Every patient signed a written informed consent. Both blood and saliva samples were collected from patients. Blood DNA was extracted with FlexiGene DNA Kit (Qiagen) and used for V617F detection. Saliva samples were collected using the Oragene DNA self-collection kit (DNA Genotek), and saliva DNA was extracted according to the manufacturer’s instructions and used for SNP genotyping. As for controls, 470 blood samples from anonymous healthy Chinese donors were collected from the Hong Kong Red Cross Blood Transfusion Service and these donors were matched to the MPN patients for sex and age as much as possible. DNA extracted from control blood samples were used for both V617F detection and SNP genotyping. Assuming a prevalence of 0.00002, MAF of 0.1, genotypic relative risk of 2.5 for Aa and 5.0 for AA, we estimated that a sample size of 128 cases and 460 controls would have 80% power (Genetic Power Calculator) . This study was approved by the Human Subjects Ethics Sub-Committee of the University (reference numbers: 20090801001 and 20111118001) and Research Ethics Committees of the hospitals, according to the guideline of the Declaration of Helsinki. The Research Ethics Committees of the hospitals under Hospital Authority included the following: Kowloon West Cluster Clinical Research Ethics Committee (reference number: KW/EX/09-076); Research Ethics Committee, Kowloon Central/Kowloon East Clusters (KC/KE-09-0120/FR-3); Joint The Chinese University of Hong Kong–New Territories East Cluster Clinical Research Ethics Committee (reference number: CRE-2009.423); and Ethics Committee, Hong Kong Easter Cluster (HKEC-2009-069). All experiments were performed in the research laboratories of Department of Health Technology and Informatics, The Hong Kong Polytechnic University.
DNA from all blood samples of patients and controls were tested for V617F by amplification refractory mutation system modified from Jones et al. . PCR products were analysed by electrophoresis on 5% polyacrylamide gels. Details are provided in Additional file 5.
SNP selection and genotyping
First, we attempted to identify JAK2 germline variants that are associated with the development of MPNs in our Hong Kong Chinese population in addition to the JAK2 risk haplotypes. Tag SNPs were selected using the Tagger software from a 148.7-kb region encompassing the JAK2 locus and its potential regulatory regions (3 kb upstream and downstream of JAK2) with MAF ≥0.1 and pairwise tagging algorithm, r2 ≥ 0.8, based on HapMap CHB database (release #24/phase I) . In line with previous studies, we force-included the reported risk-haplotype-tagging SNPs (rs10974944, rs12343867, and rs12340895; i.e. S9, S12 and S13) -,. To avoid the complication from loss of heterozygosity resulting from somatic isodisomy in clonal myeloid cells, DNA from patients’ saliva samples (instead of blood samples) was used for SNP genotyping. In this study, two methods were used for genotyping SNPs (Additional file 5): 14 SNPs by restriction fragment length polymorphism analysis and 5 SNPs by unlabelled probe melting analysis -. Details of primer sequences and reaction conditions are given in (Additional file 6: Table S3). For illustration, the restriction fragments and the banding patterns of a SNP are shown in (Additional file 7: Figure S7), and the melting curves of another SNP in (Additional file 8: Figure S8).
Imputation of genotypes for 76 JAK2SNPs
Genotypes of 76 additional SNPs within the 148.7-kb region under study were imputed by Beagle v3.2 . One of the imputed SNPs was rs4495487, which was recently reported to contribute to MPN development in the Japanese population . The genotype data of the 1000 Genomes Project (phase 1) based on 97 CHB subjects were used as the reference panel. We manually performed a quality control check by removing some of the known genotypes of the 19 directly genotyped SNPs, and imputed them with Beagle v3.2. The post-imputation results were merged with the original data to check for the imputation accuracy.
Genotypes were tested for Hardy-Weinberg equilibrium (HWE) by Fisher’s exact test using PLINK (ver.1.07)  prior to data analysis. PLINK was used for statistical analysis for all the 19 directly genotyped SNPs and the 76 imputed SNPs, and also the haplotype association tests. Single-marker and haplotype analyses were conducted between cases and controls with logistic regression adjusted for sex and age (age at diagnosis for MPN patients) as covariates; the respective asymptotic P value was denoted as P asym . Correction for multiple comparisons was achieved by generating empirical P values (P emp ) based on 50,000 permutations, i.e., swapping of the case–control status 50,000 times. Haplotypes were defined by a variable-sized sliding-window approach based on all possible sizes of SNPs spanning the whole genomic region. Subsequently, we studied the contribution of individual SNPs to significant haplotype association with disease by conditional logistic regression analysis. Haploview v4.2  was used to generate the linkage disequilibrium (LD) map of the JAK2 gene based on an algorithm called solid spine of linkage disequilibrium (SSLD) .
Single nucleotide polymorphism
- JAK2 :
Janus kinase 2
Minor allele frequency
Caucasians with European ancestry
Han Chinese in Beijing
Solid spine of linkage disequilibrium
Tefferi A, Vardiman JW: Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms. Leukemia. 2008, 22 (1): 14-22. 10.1038/sj.leu.2404955.
Tefferi A: Novel mutations and their functional and clinical relevance in myeloproliferative neoplasms: JAK2, MPL, TET2, ASXL1, CBL, IDH and IKZF1. Leukemia. 2010, 24 (6): 1128-1138. 10.1038/leu.2010.69.
Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ, Boggon TJ, Wlodarska I, Clark JJ, Moore S, Adelsperger J, Koo S, Lee JC, Gabriel S, Mercher T, D'Andrea A, Frohling S, Dohner K, Marynen P, Vandenberghe P, Mesa RA, Tefferi A, Griffin JD, Eck MJ, Sellers WR, Meyerson M, Golub TR, Lee SJ, Gilliland DG: Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis. Cancer Cell. 2005, 7 (4): 387-397. 10.1016/j.ccr.2005.03.023.
Jones AV, Kreil S, Zoi K, Waghorn K, Curtis C, Zhang L, Score J, Seear R, Chase AJ, Grand FH, White H, Zoi C, Loukopoulos D, Terpos E, Vervessou EC, Schultheis B, Emig M, Ernst T, Lengfelder E, Hehlmann R, Hochhaus A, Oscier D, Silver RT, Reiter A, Cross NC: Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders. Blood. 2005, 106 (6): 2162-2168. 10.1182/blood-2005-03-1320.
Baxter EJ, Scott LM, Campbell PJ, East C, Fourouclas N, Swanton S, Vassiliou GS, Bench AJ, Boyd EM, Curtin N, Scott MA, Erber WN, Green AR: Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders. Lancet. 2005, 365 (9464): 1054-1061. 10.1016/S0140-6736(05)71142-9.
James C, Ugo V, Le Couedic JP, Staerk J, Delhommeau F, Lacout C, Garcon L, Raslova H, Berger R, Bennaceur-Griscelli A, Villeval JL, Constantinescu SN, Casadevall N, Vainchenker W: A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera. Nature. 2005, 434 (7037): 1144-1148. 10.1038/nature03546.
Kralovics R, Passamonti F, Buser AS, Teo SS, Tiedt R, Passweg JR, Tichelli A, Cazzola M, Skoda RC: A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med. 2005, 352 (17): 1779-1790. 10.1056/NEJMoa051113.
Landgren O, Goldin LR, Kristinsson SY, Helgadottir EA, Samuelsson J, Bjorkholm M: Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24,577 first-degree relatives of 11,039 patients with myeloproliferative neoplasms in Sweden. Blood. 2008, 112 (6): 2199-2204. 10.1182/blood-2008-03-143602.
Olcaydu D, Harutyunyan A, Jager R, Berg T, Gisslinger B, Pabinger I, Gisslinger H, Kralovics R: A common JAK2 haplotype confers susceptibility to myeloproliferative neoplasms. Nat Genet. 2009, 41 (4): 450-454. 10.1038/ng.341.
Jones AV, Chase A, Silver RT, Oscier D, Zoi K, Wang YL, Cario H, Pahl HL, Collins A, Reiter A, Grand F, Cross NC: JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms. Nat Genet. 2009, 41 (4): 446-449. 10.1038/ng.334.
Kilpivaara O, Mukherjee S, Schram AM, Wadleigh M, Mullally A, Ebert BL, Bass A, Marubayashi S, Heguy A, Garcia-Manero G, Kantarjian H, Offit K, Stone RM, Gilliland DG, Klein RJ, Levine RL: A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms. Nat Genet. 2009, 41 (4): 455-459. 10.1038/ng.342.
Pardanani A, Lasho TL, Finke CM, Gangat N, Wolanskyj AP, Hanson CA, Tefferi A: The JAK2 46/1 haplotype confers susceptibility to essential thrombocythemia regardless of JAK2V617F mutational status-clinical correlates in a study of 226 consecutive patients. Leukemia. 2010, 24 (1): 110-114. 10.1038/leu.2009.226.
Tefferi A, Lasho TL, Patnaik MM, Finke CM, Hussein K, Hogan WJ, Elliott MA, Litzow MR, Hanson CA, Pardanani A: JAK2 germline genetic variation affects disease susceptibility in primary myelofibrosis regardless of V617F mutational status: nullizygosity for the JAK2 46/1 haplotype is associated with inferior survival. Leukemia. 2010, 24 (1): 105-109. 10.1038/leu.2009.225.
Ohyashiki JH, Yoneta M, Hisatomi H, Iwabuchi T, Umezu T, Ohyashiki K: The C allele of JAK2 rs4495487 is an additional candidate locus that contributes to myeloproliferative neoplasm predisposition in the Japanese population. BMC Med Genet. 2012, 13: 6-10.1186/1471-2350-13-6.
Tanaka M, Yujiri T, Ito S, Okayama N, Takahashi T, Shinohara K, Azuno Y, Nawata R, Hinoda Y, Tanizawa Y: JAK2 46/1 haplotype is associated with JAK2 V617F-positive myeloproliferative neoplasms in Japanese patients. Int J Hematol. 2013, 97 (3): 409-413. 10.1007/s12185-013-1295-y.
Pardanani A, Fridley BL, Lasho TL, Gilliland DG, Tefferi A: Host genetic variation contributes to phenotypic diversity in myeloproliferative disorders. Blood. 2008, 111 (5): 2785-2789. 10.1182/blood-2007-06-095703.
Trifa AP, Cucuianu A, Petrov L, Urian L, Militaru MS, Dima D, Pop IV, Popp RA: The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms. Ann Hematol. 2010, 89 (10): 979-983. 10.1007/s00277-010-0960-y.
Wang K, Swierczek S, Hickman K, Hakonarson H, Prchal JT: Convergent mechanisms of somatic mutations in polycythemia vera. Discov Med. 2011, 12 (62): 25-32.
Hu TT, Zhang XJ, Guan M: The association between jak2 46/1 haplotype and the susceptibility of PV and ET in Chinese Han population. Zhonghua Yixue Jianyan Zazhi. 2011, 34 (8): 717-721.
Zhang X, Hu T, Wu Z, Kang Z, Liu W, Guan M: The JAK2 46/1 haplotype is a risk factor for myeloproliferative neoplasms in Chinese patients. Int J Hematol. 2012, 96 (5): 611-616. 10.1007/s12185-012-1169-8.
Wang J, Xu Z, Liu L, Gale RP, Cross NC, Jones AV, Qin T, Ai X, Xu J, Zhang T, Sun X, Li Q, Zhang P, Zhang Y, Xiao Z: JAK2V617F allele burden, JAK2 46/1 haplotype and clinical features of Chinese with myeloproliferative neoplasms. Leukemia. 2013, 27 (8): 1763-1767. 10.1038/leu.2013.21.
Hsiao HH, Liu YC, Tsai HJ, Lee CP, Hsu JF, Lin SF: JAK2V617F mutation is associated with special alleles in essential thrombocythemia. Leuk Lymphoma. 2011, 52 (3): 478-482. 10.3109/10428194.2010.542260.
Pagliarini-e-Silva S, Santos BC, Pereira EM, Ferreira ME, Baraldi EC, Sell AM, Visentainer JE: Evaluation of the association between the JAK2 46/1 haplotype and chronic myeloproliferative neoplasms in a Brazilian population. Clinics. 2013, 68 (1): 5-9. 10.6061/clinics/2013(01)OA02.
The International HapMap Consortium: The International HapMap Project. Nature. 2003, 426 (6968): 789-796. 10.1038/nature02168.
Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC: PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet. 2007, 81 (3): 559-575. 10.1086/519795.
Guo Y, Li J, Bonham AJ, Wang Y, Deng H: Gains in power for exhaustive analyses of haplotypes using variable-sized sliding window strategy: a comparison of association-mapping strategies. Eur J Hum Genet. 2009, 17 (6): 785-792. 10.1038/ejhg.2008.244.
Zerjavic K, Zagradisnik B, Lokar L, Krasevac MG, Vokac NK: The association of the JAK2 46/1 haplotype with non-splanchnic venous thrombosis. Thromb Res. 2013, 132 (2): e86-e93. 10.1016/j.thromres.2013.06.021.
Zaykin DV, Meng Z, Ehm MG: Contrasting linkage-disequilibrium patterns between cases and controls as a novel association-mapping method. Am J Hum Genet. 2006, 78 (5): 737-746. 10.1086/503710.
Shifman S, Kuypers J, Kokoris M, Yakir B, Darvasi A: Linkage disequilibrium patterns of the human genome across populations. Hum Mol Genet. 2003, 12 (7): 771-776. 10.1093/hmg/ddg088.
Dayem Ullah AZ, Lemoine NR, Chelala C: SNPnexus: a web server for functional annotation of novel and publicly known genetic variants (2012 update). Nucleic Acids Res. 2012, 40 (Web Server issue): W65-W70. 10.1093/nar/gks364.
Xu Z, Taylor JA: SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. Nucleic Acids Res. 2009, 37 (Web Server issue): W600-W605. 10.1093/nar/gkp290.
Lee PH, Shatkay H: F-SNP: computationally predicted functional SNPs for disease association studies. Nucleic Acids Res. 2008, 36 (Database issue): D820-D824.
Cartharius K, Frech K, Grote K, Klocke B, Haltmeier M, Klingenhoff A, Frisch M, Bayerlein M, Werner T: MatInspector and beyond: promoter analysis based on transcription factor binding sites. Bioinformatics. 2005, 21 (13): 2933-2942. 10.1093/bioinformatics/bti473.
eQTL resources @ the Pritchard lab [http://eqtl.uchicago.edu/cgi-bin/gbrowse/eqtl/]
Xia K, Shabalin AA, Huang S, Madar V, Zhou YH, Wang W, Zou F, Sun W, Sullivan PF, Wright FA: seeQTL: a searchable database for human eQTLs. Bioinformatics. 2012, 28 (3): 451-452. 10.1093/bioinformatics/btr678.
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM, Haussler D: The human genome browser at UCSC. Genome Res. 2002, 12 (6): 996-1006. 10.1101/gr.229102. Article published online before print in May 2002.
Flutre T, Wen X, Pritchard J, Stephens M: A statistical framework for joint eQTL analysis in multiple tissues. PLoS Genet. 2013, 9 (5): e1003486-10.1371/journal.pgen.1003486.
Purcell S, Cherny SS, Sham PC: Genetic power calculator: design of linkage and association genetic mapping studies of complex traits. Bioinformatics. 2003, 19 (1): 149-150. 10.1093/bioinformatics/19.1.149.
Zhou L, Myers AN, Vandersteen JG, Wang L, Wittwer CT: Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye. Clin Chem. 2004, 50 (8): 1328-1335. 10.1373/clinchem.2004.034322.
Jiang B, Yap MK, Leung KH, Ng PW, Fung WY, Lam WW, Gu YS, Yip SP: PAX6 haplotypes are associated with high myopia in Han Chinese. PLoS One. 2011, 6 (5): e19587-10.1371/journal.pone.0019587.
Mak JY, Yap MK, Fung WY, Ng PW, Yip SP: Association of IGF1 gene haplotypes with high myopia in Chinese adults. Arch Ophthalmol. 2012, 130 (2): 209-216. 10.1001/archophthalmol.2011.365.
Zhu MM, Yap MK, Ho DW, Fung WY, Ng P, Gu YS, Yip SP: Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case–control study in Chinese. BMC Med Genet. 2012, 13: 64-10.1186/1471-2350-13-64.
Yiu WC, Yap MK, Fung WY, Ng PW, Yip SP: Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese. PLoS One. 2013, 8 (4): e61805-10.1371/journal.pone.0061805.
Browning BL, Browning SR: A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals. Am J Hum Genet. 2009, 84 (2): 210-223. 10.1016/j.ajhg.2009.01.005.
Barrett JC, Fry B, Maller J, Daly MJ: Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005, 21 (2): 263-265. 10.1093/bioinformatics/bth457.
This study was supported by grants from the Hong Kong Polytechnic University.
The authors declare that they have no competing interests.
Yip SP designed the research plan, analysed the data, and wrote and revised the manuscript. Koh SP performed experiments, analysed the data, and wrote and revised the manuscript. Lee KK, Chan CC, Lau SM, Kho CS, Lau CK, Lau YM, Lin SY, Wong LG, Au KL, Wong KF, Chu W, Yu PH, Chow ED and Leung KFS recruited and diagnosed the cases. Tsoi WC collected and provided data of the controls. Yung YM revised the manuscript for intellectual content. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Figure S1.: Haploview-generated linkage disequilibrium (LD) map of 19 JAK2 SNPs in Han Chinese in Beijing (A) and Caucasians of European ancestry (B) based on the 1000 Genomes Project data. LD plots were generated utilising the Haploview software. The values in the boxes indicate the r2 values between the respective pairs of SNPs and the empty boxes represent those with r2 = 1.0. Haplotype blocks are defined by solid spine of linkage disequilibrium. (DOC 600 KB)
Additional file 3: Figure S2.: Haploview-generated linkage disequilibrium map of 19 SNPs in the JAK2 gene for only the 470 controls of our study. Figure S3. Haploview-generated linkage disequilibrium map of the 19 SNPs in the JAK2 gene for 44 V617F-negative MPN cases and 470 controls of our study. Figure S4. Haploview-generated linkage disequilibrium map of the 19 SNPs in the JAK2 gene for all the 172 V617F-positive and -negative MPNs patients and the 470 controls of our study. Figure S5. Haploview-generated linkage disequilibrium map of the 19 SNPs in the JAK2 gene for the 172 V617F-positive and -negative MPNs patients of our study. Figure S6. Haploview-generated linkage disequilibrium map of the 19 SNPs in the JAK2 gene for the 128 V617F-positive MPNs patients of our study. (DOC 430 KB)
Additional file 5: JAK2 mutation and single nucleotide polymorphisms (SNPs). (DOC 84 KB)
Additional file 7: Figure S7.: SNP genotyping by restriction fragment length polymorphism. For illustration, rs10119004 (S10) is used as an example. A PCR fragment of 244 bp (see Additional file; Table S3) is amplified to encompass the SNP site. Upper panel: Restriction patterns for the two alleles of rs10119004 (S10) upon restriction digestion by the restriction enzyme HphI. Lower panel: Electrophoresis banding patterns on 8% polyacrylamide gel and stained with SYBR Green I. The DNA ladder is the 1 kb Plus DNA Ladder (lane M) from Invitrogen Life Technologies. (DOC 50 KB)
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Koh, S.P., Yip, S.P., Lee, K.K. et al. Genetic association between germline JAK2polymorphisms and myeloproliferative neoplasms in Hong Kong Chinese population: a case–control study. BMC Genet 15, 147 (2014). https://doi.org/10.1186/s12863-014-0147-y
- Myeloproliferative neoplasms
- Janus Kinase 2 (JAK2)
- V617F mutation
- Single nucleotide polymorphisms
- Genetic susceptibility