CREBBP is a target of epigenetic, but not genetic, modification in juvenile myelomonocytic leukemia

Background Juvenile myelomonocytic leukemia (JMML) is a myeloproliferative neoplasm of childhood whose clinical heterogeneity is only poorly represented by gene sequence alterations. It was previously shown that aberrant DNA methylation of distinct target genes defines a more aggressive variant of JMML, but only few significant targets are known so far. To get a broader picture of disturbed CpG methylation patterns in JMML, we carried out a methylation screen of 34 candidate genes in 45 patients using quantitative mass spectrometry. Findings Five of 34 candidate genes analyzed showed recurrent hypermethylation in JMML. cAMP-responsive element-binding protein-binding protein (CREBBP) was the most frequent target of epigenetic modification (77 % of cases). However, no pathogenic mutations of CREBBP were identified in a genetic analysis of 64 patients. CREBBP hypermethylation correlated with clinical parameters known to predict poor outcome. Conclusions This study supports the relevance of epigenetic aberrations in JMML pathophysiology. Our data confirm that DNA hypermethylation in JMML is highly target-specific and associated with higher-risk features. These findings encourage the development of prognostic markers based on epigenetic alterations, which will be helpful in the difficult clinical management of this heterogeneous disease. Electronic supplementary material The online version of this article (doi:10.1186/s13148-016-0216-3) contains supplementary material, which is available to authorized users.

Risk assessment in juvenile myelomonocytic leukemia (JMML) is important for clinical decision-making as this aggressive myeloproliferative neoplasm is generally unresponsive to conventional chemotherapy and most (but not all) patients need early allotransplantation [1,2]. Several clinical parameters have been well-established to predict poor outcome [2], but the picture is less clear at the molecular level. Specifically, if and how the set of genetic mutations in leukemic cells contributes to clinical risk remains a matter of ongoing debate [2][3][4]. Recent research on epigenetic dysregulation in JMML has provided a growing body of evidence that high-risk cases of JMML are characterized by specific CpG island hypermethylation which integrates the clinical and genetic risk factors identified so far [5][6][7]. To provide a broader picture of epimutations in JMML, we carried out a DNA methylation analysis of 34 candidate genes in leukemic cells from 45 children with JMML. myeloid leukemia published previously [8]. Considering that monosomy 7 is the most frequent cytogenetic abnormality observed in JMML cells [2], and reasoning that a two-hit mechanism of tumor suppressor inactivation might involve hypermethylation of the second allele after deletion of one allele, we selected an additional nine genes because of their location in a~2.5 mega base pair region on chromosome segment 7q22 which is commonly deleted in myeloid malignancies [9]. In the cohort used here, monosomy 7 was present in 11/45 cases (24 %). Detailed information on the DNA regions interrogated by the mass spectrometry assays is given in Additional file 1: Table S1.
We defined a gene as hypermethylated in a JMML sample if the average CpG methylation in the region of analysis exceeded three standard deviations above the mean observed in granulocytes of 11 healthy control subjects. Using this definition, 34 of 44 JMML cases (77 %) showed hypermethylation of the cAMP-responsive element-binding protein-binding protein (CREBBP) gene (the assay was uninformative in one case), 20 of 45 (44 %) were hypermethylated in the MPO gene, and 19 of 45 (42 %) carried a hypermethylated SLC12A8 gene (Fig. 1b). Most CpG units analyzed in the HIC1 and TCF4 genes had normal methylation in JMML, but each region contained a single CpG unit near its border with significant hypermethylation in JMML (Fig. 1c). This observation may hint at aberrant methylation in neighboring regions not covered by the assay. A group-wise comparison of methylation levels using Mann-Whitney test with Bonferroni correction showed for each gene a highly   The significance of differences was calculated using the Mann-Whitney test and is indicated as follows: *p ≤ 0.0014 (Bonferroni threshold for significance level p ≤ 0.05 after correction for 36 tests, i.e., 34 genes plus HIC1 CpG 3359 and TCF4 CpG 1515); ns, p > 0.0014. c The HIC1 and TCF4 genes had normal methylation in JMML when averaging all CpG units in the region of analysis, but each region contained a single CpG unit with significant hypermethylation in JMML significant difference between the "hypermethylated JMML" group and healthy controls but no difference between "normal methylation JMML" and controls (Fig. 1b, c). The DNA methylation level of the remaining 29 genes was similar between JMML samples and healthy granulocytes or the difference was so small that no biological significance would be expected (Additional file 1: Table S1). The analysis demonstrates that CpG hypermethylation in JMML is highly locus-specific. Although a significant proportion of JMML cases are characterized by aberrant DNA methylation, the hypermethylation events are confined to a limited array of genetic regions. This observation fits well with three previous studies where 11 of 15 candidate regions did not show any aberrant methylation in 127 cases analyzed [5], or where hypermethylation was restricted to only one of two CpG islands of the RASA4 locus [6] or one of three CpG islands of the AKAP12 locus [10]. Contrary to the two-hit hypothesis formulated above, none of the nine 7q22 genes exhibited frequent hypermethylation in JMML, whether monosomy 7 was present or not.

High-resolution DNA methylation analysis of the CREBBP CpG island in JMML
The CREBBP gene was hypermethylated in 77 % of JMML cases. CREBBP is a histone acetyltransferase and functions as transcriptional co-activator of a large number of regulatory proteins [11]. Mice with a null mutation in one CREBBP allele develop a myelodysplastic/ myeloproliferative neoplasm [12]. Decreased expression of CREBBP facilitates Ras-induced transformation [13]. The CREBBP methylation assay used here covered 13 CpG units in a 437-base pair region located 1.5 kilobases upstream of the transcription start site. Most CREBBP CpG units were characterized by remarkable baseline methylation in healthy controls which increased to even higher levels in JMML (Fig. 2a). However, three CREBBP CpG units (containing CpG sites #8, #9, #10, and #22) were virtually unmethylated in healthy granulocytes. Of these, CpG sites #8 to #10 acquired particularly high hypermethylation in JMML (Fig. 2b), raising the possibility of specific functional importance. In silico analysis using  TFBIND [14] revealed that CpG sites #8 to #10 may interfere with binding motifs for the transcription factors GATA1/2 and GTF3A (Fig. 2c).

Somatic CREBBP mutations are uncommon in JMML
We next studied if the CREBBP locus was not only subject to epigenetic modification in JMML, but also to genetic mutation. We analyzed leukemic granulocyte DNA from 64 children with JMML (17 of which overlapped with the 44-patient series used for epigenetic analysis) for CREBBP exon sequence variants using the Agilent SureSelect v4.0 capture technique and deep-sequencing, resulting in an average CREBBP exon depth of 82 reads. Eighty percent of CREBBP exons were covered by at least 50 reads. No insertions or deletions in the CREBBP gene were found in any JMML sample. After removing common nonpathogenic single-nucleotide polymorphisms documented in public databases such as dbSNP, we identified 10 nonsynonymous sequence variants in 11 cases of JMML (Additional file 1: Table S2). All except one (c.A493G) were listed in at least one of four exome variation resources (Exome Variant Server, ExAC browser, 1000 Genomes, dbSNP) with minor allele frequencies of less than 0.1 %. Three variants (c.A5933G, c.A2728G, c.G2941A) corresponded to alterations associated with Rubinstein-Taybi syndrome [15,16]. However, indicative clinical features (facial dysmorphism, thumb or toe malformation, intellectual disability) were documented in none of the 11 children. Importantly, we did not detect any of the CREBBP histone acetyltransferase domain mutations described as pathogenic somatic events in lymphoblastic leukemia or lymphoma [17][18][19][20]. DNA from paired non-hematopoietic tissue was available in 5 of 11 JMML cases with non-synonymous CREBBP sequence variants, enabling us to test the germline status. In all cases, the variants were present in non-leukemic tissue. The pathogenic significance of these germline CREBBP variants in JMML patients without syndromic features remains unclear. Taken together, the data indicate that the coding sequence of CREBBP is not a relevant target of somatic alteration in JMML, in agreement with the absence of CREBBP mutations from myeloproliferative neoplasms in adults [21].
CREBBP methylation is associated with established hematologic and clinical parameters indicating an aggressive JMML phenotype It was repeatedly shown that DNA hypermethylation at specific target genes in JMML is associated with clinical parameters indicating poor prognosis [5][6][7]10]. To test if this relationship was also true for CREBBP methylation, we focused on CpG sites #8 to #10 because these sites were unmethylated in healthy individuals but had high methylation variation in JMML. The level of methylation at these sites was significantly associated with older age and elevated fetal hemoglobin at diagnosis (Fig. 2d and Additional file 1: Table S3), two main predictors of reduced survival [1,2]. In addition, methylation at CpG sites #8 to #10 was associated with the category of Ras pathway mutation (Additional file 1: Table S3), being considerably higher in JMML cases with PTPN11 mutation or neurofibromatosis type 1 (NF1) than in JMML with KRAS, NRAS, or CBL mutation. The relevance of the mutation category to disease course and outcome of JMML remains controversial [2][3][4]22], but higher CREBBP methylation in JMML with PTPN11 mutation or NF1 is consistent with the prevailing opinion that these subgroups are more aggressive. Variable correlation with age, high fetal hemoglobin, mutation, or karyotype but no other parameters was also found for MPO, SLC12A8, and HIC1 CpG 3359. The small group size and heterogeneous treatment precluded meaningful outcome analyses. However, we noted that five events of death occurred in the CREBBP hypermethylation group (5/34 patients, 15 %) compared to no such event in the group with normal CREBBP methylation (0/10 patients); the median followup time was 6.0 years for all 44 patients. In summary, the data strengthen the concept that higher-risk cases of JMML carry a distinct DNA methylation phenotype. Future studies are needed to elucidate the functional role of coordinated DNA hypermethylation at specific loci in the JMML-initiating cell.

Patient samples
We used clinical material from German JMML patients registered in the European Working Group of MDS in Childhood (EWOG-MDS) studies "98" and "2006" after obtaining informed consent and ethics approval (University of Freiburg, reference number EK247/05). Patients with Noonan syndrome (PTPN11 or KRAS germline mutation) were excluded. Clinical characteristics are given in Additional file 1: Table S3.

High-resolution quantitative DNA methylation analysis
Leukemic granulocytes from 45 patients (bone marrow, N = 36; peripheral blood, N = 9) were enriched by Ficoll centrifugation (Biochrom). Genomic DNA was isolated using the Gentra Puregene kit (Qiagen) and bisulfite converted using the EZ DNA methylation kit (Zymo Research). The MassARRAY EpiTYPER assay (Agena Bioscience) was used to assess CpG island methylation at 34 target regions ( Fig. 1a and Additional file 1: Table S1). Primer sequences are listed in Additional file 1: Table S4.