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Volume 2012 (2012), Article ID 826323, 4 pages
DNase1: No Association with Crohn's Disease in a New Zealand Population
1Discipline of Nutrition, Faculty of Medical and Health Sciences (FMHS), The University of Auckland, 85 Park Road, Grafton, 1142 Auckland, New Zealand
2Nutrigenomics New Zealand, New Zealand
3Department of Medicine, Faculty of Medical and Health Sciences (FMHS), The University of Auckland, 85 Park Road, Grafton, 1142 Auckland, New Zealand
Received 29 February 2012; Accepted 10 April 2012
Academic Editors: G. Barbaro, J. C. Hoffmann, L. Rodrigo, and I. Takeyoshi
Copyright © 2012 Angharad R. Morgan et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
DNase1 has been implicated in a number of immune disorders and is an excellent candidate gene for Crohn's disease (CD). We investigated whether DNase1 SNPs rs1053874 and rs8176938 were associated with CD in a well-characterized New Zealand dataset consisting of 447 cases and 716 controls. Furthermore, we measured serum DNase1 activity levels in a number of CD patients and controls. We did not find any evidence of association for either DNase1 genetic variation or DNase1 activity levels with CD. The lack of association indicates that DNase1 does not play a significant role in predisposing to CD in the New Zealand population.
Deoxyribonuclease 1 (DNase1) is an endonuclease that facilitates chromatin breakdown. Deficiency in DNase1 and the resulting difficulty of removing DNA from nuclear antigens promote susceptibility to immune disorders such as systemic lupus erythematosus (SLE) [1, 2], Sjogren’s disease , and thyroid autoimmunity . A recent report has also provided some evidence for a role in Crohn’s disease (CD) .
Genetic variation in DNase1 has been associated with SLE . Studies of associations between DNase1 genetic variants and CD have not been reported to date.
We investigated whether DNase1 SNPs rs1053874 and rs8176938 were associated with CD in a well-characterized case-control New Zealand dataset. Furthermore, we measured serum DNase1 activity levels in a number of CD patients and controls.
A total of 1163 subjects from New Zealand were included in the study: 447 cases and 716 controls. All participants self-reported European ancestry.
Clinical records were analysed to confirm diagnosis, and IBD status was defined using standard diagnostic criteria . Cases were phenotyped according to the Montreal classification systems.
Participants consented to collection of peripheral blood or a buccal swab for DNA extraction and genotyping, and DNA was extracted from the blood/buccal samples using Qiagen’s DNA extraction kit and following the manufacturer’s instructions.
The study was conducted under ethical protocol MEC/04/12/011, authorised through the New Zealand Multiregion Human Ethics Committee. All study subjects gave informed consent.
We searched for SNPs in the DNase1 gene in the hapmap database and identified 2 common (MAF > 5%) SNPs: rs1053874 and rs8176938. We genotyped these SNPs using the ABI TaqMan MGB diallelic discrimination system and predesigned assays on demand (Applied Biosystems, Melbourne, Australia). The polymerase chain reaction amplification was performed using the ABI Prism 7900 HT sequence-detector machine using the following conditions: 10 minutes at 95°C, followed by 40 cycles at 92°C for 15 seconds and 60°C for 1 minute. The allelic discrimination results were determined after the amplification by performing an endpoint read.
All sample plates contained cases, controls, blanks, hapmap, and duplicate samples. Quality control measures included independent double genotyping, blind to sample identity, and comparison of our hapmap sample genotypes to those in the hapmap database (http://www.hapmap.org/).
2.3. Measurement of DNase1 Activity Levels
DNase1 activity levels were measured in the serum of 213 CD patients and 209 controls using a commercially available validated enzyme-linked immunosorbent assay (ELISA) kit (Orgentec, Germany), and the protocol was followed as described by the manufacturer. All samples were analyzed in duplicate. Activity levels were determined from a standard curve using a 4-parameter-fit with lin-log coordinates for optical density and concentration.
2.4. Statistical Analysis
SNPs were tested for deviation from HWE in both cases and controls using a chi-square goodness-of-fit test. To determine if there were differences between cases and controls, genotype and allele frequencies for each SNP were analyzed by 2 × 3 and 2 × 2 Chi-square tables, respectively.
Genotype and phenotype associations were assessed by comparing allele frequencies between controls and patient subgroups defined using the clinical characteristics. These analyses were carried out using R (R: a language and environment for statistical computing, R Foundation for Statistical Computing, Vienna, Austria. ISBN 3-900051-07-0, URL http://www.r-project.org/) and SAS (V9.1 SAS Institute., Cary, NC, USA).
Across-group comparisons of serum DNase 1 activity were tested using a generalized linear model for mean differences.
3.1. Comparison of DNase1 Genotypes in CD Patients and Healthy Controls
Both SNPs were in Hardy-Weinberg equilibrium. Neither was found to be associated with CD (Table 1). We undertook a phenotype analysis, and there were no associations with any of the different clinical characteristics of CD (Table 2).
3.2. Comparison of DNase1 Activity Levels in CD Patients and Healthy Controls
DNase1 activity levels were measured in the serum. Activity in the controls ranged from 43 to 100%. Activity in the cases ranged from 39 to 100%. The mean serum DNase1 activity for CD patients was 80% and that for the controls was also 80%. Thus, there was no difference in activity levels between cases and controls. We also compared DNase1 activity levels across the different CD phenotypes, but there were no significant findings (Table 3). Neither there were any differences when comparing by gender.
DNase1 is known to be involved in a number of immune disorders, but research into its role in CD has been rare. There have been no previous studies investigating associations between genetic variation in DNase1 and CD, and only one published study examined DNase1 activity levels in CD.
We were unable to replicate the association reported in previous research in which DNase1 activity in CD patients was significantly lower than in healthy individuals . In our study there was no difference in the DNase1 activity levels. All of the CD patients in the previous study had active severe disease. Our sample set was larger and contained a range of different phenotypes but when we stratify by these different phenotypes, including severity, we were still unable to see any associations with DNase1. Nonreproducibility does not necessarily demonstrate that the original association reported was spurious and should not discourage further research in this promising field. True associations may not replicate across different data sets for a number of reasons.
As well as investigating DNase1 activity levels, we also undertook an analysis of genetic variation in DNase1 and compared the genotype and allele frequencies of 2 SNPs in CD patients and controls. Genetic variation in DNase1 has previously been associated with SLE  but in the study we report here we were not able to find any evidence for association between DNase1 SNPs and CD. Data from a recent CD genomewide meta-analysis  also does not provide support for DNase1 being associated with CD: SNP rs1053874 was included in the analysis, and the allele frequencies did not differ between cases and controls.
To summarise, although DNase1 is a good candidate for CD, in the present study we failed to detect any significant associations. The absence of association between DNase1 and CD indicates that DNase1 does not play a significant role in predisposing to CD in the New Zealand population.
The authors would like to thank the many patients with IBD who participated in this study, and also the control subjects. Nutrigenomics New Zealand is collaboration between AgResearch Ltd., Plant & Food Research and The University of Auckland with funding through the Ministry of Science and Innovation (MSI).
- F. Martinez Valle, E. Balada, J. Ordi-Ros, and M. Vilardell-Tarres, “DNase 1 and systemic lupus erythematosus,” Autoimmunity Reviews, vol. 7, no. 5, pp. 359–363, 2008.
- F. Martinez-Valle, E. Balada, J. Ordi-Ros, S. Bujan-Rivas, A. Sellas-Fernandez, and M. Vilardell-Tarres, “DNase 1 activity in patients with systemic lupus erythematosus: relationship with epidemiological, clinical, immunological and therapeutical features,” Lupus, vol. 18, no. 5, pp. 418–423, 2009.
- S. Belguith-Maalej, H. Hadj-Kacem, N. Kaddour, Z. Bahloul, and H. Ayadi, “DNase1 exon2 analysis in Tunisian patients with rheumatoid arthritis, systemic lupus erythematosus and Sjögren syndrome and healthy subjects,” Rheumatology International, vol. 30, no. 1, pp. 69–74, 2009.
- M. Dittmar, C. Bischofs, N. Matheis, R. Poppe, and G. J. Kahaly, “A novel mutation in the DNASE1 gene is related with protein instability and decreased enzyme activity in thyroid autoimmunity,” Journal of Autoimmunity, vol. 32, no. 1, pp. 7–13, 2009.
- K. Malíčková, D. Duricová, M. Bortlík, et al., “Impaired deoxyribonuclease I activity in patients with inflammatory bowel diseases,” Autoimmune Diseases, vol. 2011, Article ID 945861, 5 pages, 2011.
- K. Yasutomo, T. Horiuchi, S. Kagami et al., “Mutation of DNASE1 in people with systemic lupus erythematosus,” Nature Genetics, vol. 28, no. 4, pp. 313–314, 2001.
- J. E. Lennard-Jones, “Classification of inflammatory bowel disease,” Scandinavian Journal of Gastroenterology, Supplement, vol. 24, no. 170, pp. 2–6, 1989.
- A. Franke, D. P. McGovern, J. C. Barrett, et al., “Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci,” Nature Genetics, vol. 42, no. 12, pp. 1118–1125, 2010.