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Association of hypoxia inducible factor-1 alpha gene polymorphism with both type 1 and type 2 diabetes in a Caucasian (Hungarian) sample
- Geza Nagy†1,
- Reka Kovacs-Nagy†2,
- Eva Kereszturi2,
- Aniko Somogyi1,
- Anna Szekely3,
- Nora Nemeth2,
- Nora Hosszufalusi4,
- Pal Panczel4,
- Zsolt Ronai2 and
- Maria Sasvari-Szekely2Email author
© Nagy et al; licensee BioMed Central Ltd. 2009
Received: 5 March 2009
Accepted: 19 August 2009
Published: 19 August 2009
Hypoxia inducible factor-1 alpha (HIF-1α) is a transcription factor that plays an important role in neo-vascularisation, embryonic pancreas beta-cell mass development, and beta cell protection. Recently a non synonymous single nucleotide polymorphism (g.C45035T SNP, rs11549465) of HIF-1α gene, resulting in the p.P582S amino acid change has been shown to be associated with type 2 diabetes (T2DM) in a Japanese population. Our aim was to replicate these findings on a Caucasian (Hungarian) population, as well as to study whether this genetic effect is restricted to T2DM or can be expanded to diabetes in general.
A large Caucasian sample (N = 890) was recruited including 370 T2DM, 166 T1DM and 354 healthy subjects. Genotyping was validated by two independent methods: a restriction fragment analysis (RFLP) and a real time PCR using TaqMan probes. An overestimation of heterozygotes by RFLP was observed as a consequence of a nearby SNP (rs34005929). Therefore genotyping results of the justified TaqMan system were accepted. The measured genotype distribution corresponded to Hardy-Weinberg equilibrium (P = 0.740)
As the TT genotype was extremely rare in the population (0.6% in clinical sample and 2.5% in controls), the genotypes were grouped as T absent (CC) and T present (CT and TT). Genotype-wise analysis showed a significant increase of T present group in controls (24.0%) as compared to patients (16.8%, P = 0.008). This genetic effect was demonstrated in the separated samples of type 1 (15.1%, P = 0.020), and also in type 2 (17.6%, P = 0.032) diabetes. Allele-wise analysis gave identical results showing a higher frequency of the T allele in the control sample (13.3%) than in the clinical sample (8.7%, P = 0.002) with similar results in type 1 (7.8%, P = 0.010) and type 2 (9.1%, P = 0.011) diabetes. The odds ratio for diabetes (either type 1 or 2) was 1.56 in the presence of the C allele.
We confirmed the protective effect of a rare genetic variant of HIF-1α gene against type 2 diabetes in a Caucasian sample. Moreover we demonstrated a genetic contribution of the same polymorphism in type 1 diabetes as well, supporting a possible overlap in pathomechanism for T2DM and a T1DM.
Type 1 (T1DM) and type 2 diabetes (T2DM) both result from the metabolic consequences of insufficient insulin effect, and have similar complications but appear to be due to completely distinct pathogenetic mechanisms. T1DM results from autoimmune β-cell destruction leading to insulin deficiency, whereas T2DM is the end point of a progressive insulin secretory defect on a background of insulin resistance .
The genetic background of both types of diabetes is undeniable and is being widely investigated. Both common forms are considered to be complex diseases caused by multiple environmental and genetic risk factors [2, 3]. Previously genes such as the PPARγ, Kir6.2, Calpain-10, TCF7L2 and class 1 HLA genes, the CTLA-4, INS, PTPN22 have been proved to be related to the manifestation of T2 and T1DM respectively [4, 5]. Due to previously observed differences in the clinical and pathogenic properties of T1 and T2DM, candidate gene studies rarely consider T2 candidate genes as potential T1 candidate genes and vice versa.
Despite the clear differences between T1 and T2DM there are indications of common etiological factors contributing to their manifestation. Investigations focusing on the pathogenesis of β cell dysfunction in T2DM have uncovered factors classically associated with T1DM. Latent autoimmune diabetes of adults (LADA) initially has a clinical presentation similar to T2DM and may comprise up to 15% of the patients originally diagnosed as having T2DM [6, 7]. These patients, however, like in T1DM, exhibit anti β cell autoimmunity and develop a progressive β cell failure suggesting an overlap in etiology . It is hypothesized that an accelerated β cell loss may be the link between T1DM and T2DM as post mortem examinations of human pancreatic tissue suggest that increased apoptosis is responsible for decreased pancreatic β cell mass in T2DM . This notion is supported by in vitro and in vivo animal experiments, revealing apoptosis in incubated rodent β cells  and also in cultured human islets incubated in glucose concentrations similar to those seen in plasma of patients with T2DM , and also in the desert gerbil, during the progression to hyperglycaemia induced by a high-energy diet .
This growing evidence suggests that classification of diabetes into two distinct diseases may not reflect the true nature of the disorder . Clearly, β cell dysfunction is a hallmark of both types of diabetes and a genetic variant that predisposes an individual toward reduced insulin secretion potentially could increase the risk of developing diabetes .
Hypoxia inducible factor 1 (HIF-1) is a key early mediator of the response to ischemia. The heterodimer of HIF-1α and β subunits is a potent transcription factor that promotes cell survival, glycolysis, and angiogenesis . The transcriptional activity is primarily controlled by the oxygen-regulated breakdown of the α subunit . The HIF-1α protein contains five functional domains. The basic helix-loop-helix (bHLH) domain is specifically required for the binding of DNA , the Per/Arnt/Sim (PAS) domain is involved in dimerisation of the α and β subunits. Transcriptional activation and interaction with coactivators are mediated by two transactivation domains in the C terminal half of HIF-1α, termed as N-terminal (N-TAD) and C-terminal (C-TAD) transactivation domains . Negative regulation of HIF-1α under normoxic conditions occurs via the oxygen-dependent degradation (ODD) domain, which partly overlaps with N-TAD.[19, 20] Under normoxic conditions, HIF-1α is hydroxylated on proline residues (P402, P564) by a family of oxygen-dependant prolyl hydroxylases which mediate high affinity binding to the von-Hippel-Landau (VHL) protein, a component of the E3 ubiquitin-protein ligase complex that ubiquitinates HIF-1α, thereby targeting it for degradation.
The HIF-1α gene is located at chromosome 14q21-q24, where the susceptibility locus to T2DM was localized in Finns . In a recent study Yamada and colleagues  examined all regions of the HIF-1α gene in a Japanese population and found 32 SNPs, two of them located in exons. They found a significant association between T2DM and a non synonymous SNP in exone 12 (rs11549465) causing a change of proline to serine (p.P582S) in the expressed protein. Our aim was to replicate Yamada's study in a diabetic sample with a different ethnic origin, and investigate whether this genetic variant in the HIF-1α gene, as a shared genetic contributor plays a role in the development of not only T2DM but T1DM as well.
Diabetic patients were recruited randomly from the inpatient and outpatient services of the 2nd and 3rd Department of Internal Medicine at the Semmelweis University. The diagnosis of DM was based on fasting plasma glucose levels or 75 g oral glucose tolerance test according to the criteria of the WHO. The study was approved by the Local Ethics Committee (TUKEB). Every patient provided written informed consent for their participation.
The demographic variables of the samples were as follows. T1DM sample N = 166; age: 36.9 ± 13.1; 54.8% male and 45.2% female. T2DM sample N = 370, age: 64.0 ± 12.0; 41.9% male and 58.1% female. Control subjects without DM history were recruited at the Institute of Psychology, Eötvös Loránd University, N = 354; age: 25.1 ± 8.5; 32.5% male and 67.5% female. Both the clinical and the control samples were ethnically homogenous, of Caucasian origin, and consisted of unrelated individuals.
Non-invasive DNA sampling was applied as described elsewhere . DNA was isolated from buccal cells using the DNA-purification kit obtained from Gentra (Minneapolis, US).
Restriction fragment length polymorphism
A PCR-RFLP technique developed by Percy et al.  was applied with small modifications. Amplification was carried out using 1 μM of each primer (forward: 5' GTG TGG CCA TTG TAA AA 3', reverse: 5' AAC ACG TTA GGG CTT CTT 3'), 1× buffer and Q-solution (Qiagen), 200 μM dATP, dCTP, dGTP and dTTP, 0.1 U HotStarTaq DNA polymerase and approximately 5 ng genomic DNA in a final volume of 10 μL. Thermocycle: 95°C for 15 minutes, followed by 40 cycles of 94°C, 30 sec denaturation, 52°C, 30 sec annealing and 72°C 1 min extension, with the final polymerization at 72°C for 10 minutes.
For the genotype dependent digestion 1× NEBuffer 1, 0.1 mg/mL BSA, 0.7 U Tsp45 I restriction endonuclease (New England Biolabs) and 5 μL PCR-product were used in a total volume of 50 μL. Samples were incubated at 65°C overnight and the generated DNA fragments were separated on 1.5% agarose-2% Metaphor agarose composite gel matrix. For controlling the complete digestion, a non-polymorphic cleavage site was applied producing a 194-bp-long fragment. A 260-bp-long product was observed in case of the T allele, while a 139 bp and 121 bp fragments were generated in the presence of the C variant.
The C__25473074_10 SNP genotyping kit obtained from Applied Biosystems contained the two flanking primers and the C- and T-specific probes labeled with VIC and FAM fluorescent dyes, respectively. 1× of this genotyping kit, 1× TaqMan® PCR Master Mix, No AmpErase® UNG and approximately 5 ng genomic DNA was employed in a final volume of 5 μL. A 7300 Real-Time PCR System was used for the amplification, the first step of the thermocycle was an initial denaturation and activation at 95°C for 10 minutes, followed by 40 cycles of 95°C for 15 seconds and 60°C for 1 minute.
Comparison of the genotyping methods
150 healthy individuals were investigated using the two independent techniques. In more than 10% of the heterozygotes the Tsp45 I PCR-RFLP and the TaqMan method gave controversial results. Direct sequencing of the PCR products clearly demonstrated that there was a misgenotyping of rs11549465 SNP by PCR-RFLP. The misgenotyping was fully explained by the presence of another SNP (rs34005929) located in a 4 bp distance thus disturbing the correct genotyping of the studied polymorphism.
The allele discrimination of TaqMan system proved to be reliable based on direct sequencing data. Genotypes could be unambiguously determined on the observed ΔC T (C T VIC - C T FAM) values. ΔC T values between -5.0 and -2.4 corresponded to the CC genotype, values from -1.9 to 0.7 demonstrated the heterozygote form, whereas ΔC T-s in the range of 1.2–3.8 were characteristic to the TT variation. Therefore the TaqMan system was used for large scale genotyping. Obtained genotype frequencies were compared to the calculated frequencies based on the Hardy-Weinberg equilibrium and no significant differences were observed (P = 0.740 for all participants, P = 0.444 for the control group, P = 0.853 for the total patient group. Within the patient group P = 1.000 for the DM1 and P = 0.808 for the DM2 groups).
The pGL3-Control luciferase reporter vector (Promega, Madison, WI) was used as a control. The pHRE vector – which is a modified pGL3-Control plasmid (figure 1A) – containing five contiguous hypoxia responsive elements (5'-GATCTGAGACAGCACGTAGGGC-3') in front of the luciferase reporter gene, was a generous gift from Dr. M. Geiszt (Institute of Physiology, Semmelweis University, Budapest, Hungary). The wild type and p.P582S mutant HIF-1α expression vectors were a kind gift of Dr. Yukio Horikawa, Department of Diabetes and Endocrinology, Gifu University School of Medicine, Gifu, Japan.
Cell cultures, hypoxic treatment, transient transfection
SK-N-FI (neuroblastoma) cell line was grown in Dulbecco's modified Eagle's medium, high Glucose (Gibco, Carlsbad, CA) supplemented with 10% fetal bovine serum and 1% nonessential amino acids. Normoxic cultures were kept in 21% O2, 74% N2 and 5% CO2 in humidified atmosphere. Hypoxic samples were incubated in a humidified atmosphere of 1% O2, 94% N2 and 5% CO2 in a modular incubator chamber (Billups-Rothenberg, USA). A mixture of 0.1 μg pHRE reporter construct, 0.1 μg HIF-1α expression vector and 0.1 μg pCMV-β-gal and 6 μl Lipofectamine 2000 (Invitrogen, Carlsbad, CA) was used to transfect 1.2 × 106 SK-N-FI cells plated 24 hours before transfection in six-well plates. Luciferase and β-galactosidase activities were detected using the Luciferase Assay System kit (Promega, Madison, WI) and by ONPG (O-nitrophenyl-β-D-galactopyranoside) cleavage rate, respectively. Three parallels were used in all transfections and all experiments were performed in triplicates.
The SPSS program for Windows (13.0 version) was used for the statistical analyses. The Hardy-Weinberg equilibrium and differences in allele and genotype distribution of controls and patient groups (or males and females) was tested by Chi-square analysis. Risks were examined by odds ratios (ORs) with 95% confidence intervals (CIs), using unconditional logistic regression models adjusted for age (years) and sex. Possible effects of genotypes on age or BMI were tested by t-tests. G*Power 3.1.0  has been used for computing a post hoc test for achieved power. Input parameters included the population effect size = 0.1 (as a conventionally small effect size), alpha = 0.05, df = 1 for our 2 × 2 and df = 2 for our 2 × 3 analyses. Power estimates were 85% for the 2 × 2 contingency tables and 77% for the 2 × 3 contingency tables, which are generally considered acceptable .
Distribution of Hypoxia inducible factor-1 alpha (HIF-1α) genotypes (rs11549465) between males and females
CT + TT
Type 1 Diabetes
Type 2 Diabetes
Hypoxia inducible factor-1 alpha (HIF-1α) allele and genotype frequencies in the studied groups
P = 0.005
P = 0.044
P = 0.023
CT + TT
P = 0.008
P = 0.020
P = 0.032
P = 0.002
P = 0.010
P = 0.011
Separation of diabetic patients to type 1 (T1DM) and type 2 (T2DM) gave identical results demonstrating that the effects of HIF-1α gene variants are similar in type 1 and type 2 diabetes (Table 2). As the T allele is relatively rare especially among patients (8.7%), TT homozygotes do not reach the criteria of Pearson Chi-Square test in some cases (P values are in parentheses in Table 2). Therefore it was necessary to group the genotype categories as T absent (CC) and T present (CT and TT) for genotype-wise statistical analysis. As it is shown in Table 2, the allele and genotype distributions between type 1 and type 2 patients are approximately equal and both groups show a statistically significant difference if compared to the control group. The values of significance (P) are given in Table 2 regarding the comparison between the patients and the controls. It is important to note that comparison of either allele or genotype distribution among patients with type 1 and type 2 diabetes did not result in any significant differences.
The presented data demonstrated an under representation of the T allele in all patient groups suggesting a protective effect of the T allele against diabetes. It is worth mentioning that -although the numbers are rather small – TT homozygotes are extremely rare among patients (0.6%), while their incidence is more than 4 fold higher in the control group (2.5%). With other words, the C allele is a risk factor for both type 1 and type 2 diabetes (OR = 1.56, CI: 1.41–1.71). The above risk estimate was based on unconditional logistic regression adjusted for age (years) and sex using data from a total of 879 participants with all data available (535 patients and 344 controls).
In the present genetic association analysis performed on a Caucasian sample, we investigated the HIF-1α gene rs11549465 SNP, a C→T non synonymous SNP (g.C45035T) resulting in a substitution of proline to serine (P582S) in exon 12. Our result demonstrated a statistically significant decrease in frequencies of T allele containing genotypes (CT + TT), as well as in the T allele frequencies among individuals with diabetes (see Table 2). Of note, allele and genotype distribution was very similar between subjects with T1DM and those with T2DM. On the other hand both the T2DM and T1DM groups showed a statistically significant difference in allele and genotype distribution when compared to the control. In summary, a protective effect of the rare HIF-1α gene variant was proven against both, type 1 and type 2 diabetes, in a Caucasian sample.
As it was pointed out by earlier studies, it is highly relevant to replicate genetic association studies, because it is well known that there are significant differences in the frequencies of certain genetic variations among different ethnic groups. Our results regarding T2DM patients are in line with the first demonstration of association between the T allele in exon 12 of the HIF-1α gene and T2DM by Yamada and his colleagues. The frequency of the rare T allele in our control sample (13.3%) was comparable to previous reports on the European population , and indicated that the T allele is almost twice as frequent among Caucasians, than observed in Yamada's Japanese study group.
Due to the substantially different pathophysiological features of T1 and T2DM, candidate genes of T2DM have rarely been examined as candidate genes modifying the risk of T1DM [31, 32]. However recently an overlap has been proposed by Wilkin and coworkers . Their "accelerator hypothesis" suggests that T1 and T2 diabetes are the same disease of hyperglycemia-induced beta cell damage in which T1DM has the added effect of autoimmunity. Other findings have also strengthened this hypothesis from a genetic point of view by demonstrating familiar clustering of type 1 and type 2 diabetes mellitus [34–36]. There is also evidence that for selected susceptibility gene variants, there might be a shared genetic contribution to the pathogenesis of T1DM and T2DM. For example, the common variant of the peroxisome proliferator activated receptor γ gene isoform 2 (PPARγ2) Pro12Ala that has been consistently reported to associate with T2DM was recently shown to be associated with T1DM, as well . Moreover, Galanakis and coworkers just recently have shown that the intron 4 a/b polymorphism of the endothelial nitric oxide synthase gene (eNOS) is associated with both type 1 and type 2 diabetes . Our new finding that indicates a decreased number of the minor allele in the T1DM sample is another example for the possible shared genetic background of T2 and T1 diabetes.
The polymorphism investigated in our study causes a proline to serine change in the 582 position which is within the N-TAD near the ODD domain of the HIF-1α protein . Proline 582 has not been proven to be a HIF-1α hydroxylation site, and it is not known whether it mediates VHL binding. Moreover, the serine-proline substitution in this position does not appear to alter VHL binding in vitro to a fragment of HIF-1α after hydroxylation at proline 564 .
Previous in vitro functional analysis of this HIF-1α mutation gave conflicting results. First Yamada and his colleagues  indicated that the mutant variant has a consistently higher level of HIF-1α transcriptional activity than the wild-type. Since the enhanced transactivation capacity of the mutant was observed with statistical significance only under hypoxic condition, the authors suggested that this genetic variant, by enhancing the transcriptional activity of target genes, could be a protective factor against the onset of type 2 diabetes by its activities in the pancreatic developmental stage. Hlatky and coworkers  could not replicate these findings. We also attempted to demonstrate the functional importance of HIF-1α variants, however, we did not find any significant differences in the transcriptional activity of the HIF-1α variants using a luciferase reporter system (see Figure 1). One possible reason of this contradiction might be a relatively high endogenous HIF-1α activity in our cell line as measured in the presence of the luciferase vector with hypoxia responsive elements (Figure 1, pHRE) in the absence of any HIF-1α expression vector.
Tanimoto and colleagues suggested that the conformational changes caused by the amino acid substitution either might alter protein stability, or could enhance recruitment of transcriptional cofactors that interact with HIF-1α. Since, the authors could not detect any differences in degradation, the altered transactivational properties was taken into consideration as a possible molecular effect of Pro582Ser change . Further investigations in the field of cancer research demonstrated the rs11549465 variant to have enhanced transcription activities in in-vitro studies under both normoxic and hypoxic conditions [40, 41] associated with increased tumor microvessel density in head and neck cancer, and in prostate cancer. In conclusion, changes in the transactivational properties of the studied genetic variants could be hypothesized, however, their effect probably depends on the specific coactivators of various cell types.
HIF-1 is a major determinant in the expression and secretion of vascular endothelial growth factor (VEGF) by cells [42–44]. It has been shown that VEGF increases the survival of pancreatic islets and thus β cell sparing after islet transplantation by stimulating angiogenesis and improving islet revascularization [45, 46]. Moreover, transgenic mice that over-express VEGF are characterized by islet hyperplasia, suggesting that VEGF modulates endocrine pancreatic differentiation . Recent findings suggest that VEGF protects also against the development of T1DM and may play a role as a specific "pancreatic protector" . Therefore, one might speculate that the studied genetic variant of the HIF-1α, by enhancing the transcriptional activity of target genes, could be a protective factor against the onset of not only type 2 diabetes  but also that of type 1 diabetes by its activities in the pancreatic developmental stage.
In the presented genetic association study we determined the genotype of the HIF-1α gene rs11549465 SNP, a C→T non synonymous SNP (g.C45035T) resulting in a substitution of proline to serine (P582S) in exon 12 on a large Caucasian sample of diabetic patients (N = 536) and controls (N = 354). In accordance with a recent study of Yamada and colleagues , we found a statistically significant decrease in frequencies of CT and TT genotypes, as well as in the T allele frequencies among individuals with diabetes suggesting the protective effect of the T allele in type 2 diabetes. Moreover, the same genetic effect was found in type 1 diabetes, as well, pinpointing the possibility of shared genetic contributors in the development of diabetes mellitus.
This work was supported by Hungarian funds ETT – 448/2006 and the Scientific Grant of the Hungarian Diabetes Association (A. Somogyi), ETT 55105 and OTKA T048576 (M. Sasvari-Szekely). The authors thank for G. Kollman for her valuable technical assistance.
- Qu HQ, Grant SF, Bradfield JP, Kim C, Frackelton E, Hakonarson H, Polychronakos C: Association analysis of type 2 diabetes Loci in type 1 diabetes. Diabetes. 2008, 57 (7): 1983-1986. 10.2337/db08-0270.View ArticlePubMedPubMed CentralGoogle Scholar
- Todd JA: Genetic control of autoimmunity in type 1 diabetes. Immunol Today. 1990, 11 (4): 122-129. 10.1016/0167-5699(90)90049-F.View ArticlePubMedGoogle Scholar
- Zimmet P, Alberti KG, Shaw J: Global and societal implications of the diabetes epidemic. Nature. 2001, 414 (6865): 782-787. 10.1038/414782a.View ArticlePubMedGoogle Scholar
- Freeman H, Cox RD: Type-2 diabetes: a cocktail of genetic discovery. Human molecular genetics. 2006, 15 (Spec No 2): R202-209. 10.1093/hmg/ddl191.View ArticlePubMedGoogle Scholar
- Alizadeh BZ, Koeleman BP: Genetic polymorphisms in susceptibility to Type 1 Diabetes. Clin Chim Acta. 2008, 387 (1–2): 9-17. 10.1016/j.cca.2007.09.021.View ArticlePubMedGoogle Scholar
- Naik RG, Palmer JP: Latent autoimmune diabetes in adults (LADA). Rev Endocr Metab Disord. 2003, 4 (3): 233-241. 10.1023/A:1025148211587.View ArticlePubMedGoogle Scholar
- Lowe CE, Cooper JD, Brusko T, Walker NM, Smyth DJ, Bailey R, Bourget K, Plagnol V, Field S, Atkinson M, et al: Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes. Nat Genet. 2007, 39 (9): 1074-1082. 10.1038/ng2102.View ArticlePubMedGoogle Scholar
- Mathis D, Vence L, Benoist C: beta-Cell death during progression to diabetes. Nature. 2001, 414 (6865): 792-798. 10.1038/414792a.View ArticlePubMedGoogle Scholar
- Butler AE, Janson J, Bonner-Weir S, Ritzel R, Rizza RA, Butler PC: Beta-cell deficit and increased beta-cell apoptosis in humans with type 2 diabetes. Diabetes. 2003, 52 (1): 102-110. 10.2337/diabetes.52.1.102.View ArticlePubMedGoogle Scholar
- Efanova IB, Zaitsev SV, Zhivotovsky B, Kohler M, Efendic S, Orrenius S, Berggren PO: Glucose and tolbutamide induce apoptosis in pancreatic beta-cells. A process dependent on intracellular Ca2+ concentration. The Journal of biological chemistry. 1998, 273 (50): 33501-33507. 10.1074/jbc.273.50.33501.View ArticlePubMedGoogle Scholar
- Federici M, Hribal M, Perego L, Ranalli M, Caradonna Z, Perego C, Usellini L, Nano R, Bonini P, Bertuzzi F, et al: High glucose causes apoptosis in cultured human pancreatic islets of Langerhans: a potential role for regulation of specific Bcl family genes toward an apoptotic cell death program. Diabetes. 2001, 50 (6): 1290-1301. 10.2337/diabetes.50.6.1290.View ArticlePubMedGoogle Scholar
- Donath MY, Gross DJ, Cerasi E, Kaiser N: Hyperglycemia-induced beta-cell apoptosis in pancreatic islets of Psammomys obesus during development of diabetes. Diabetes. 1999, 48 (4): 738-744. 10.2337/diabetes.48.4.738.View ArticlePubMedGoogle Scholar
- Donath MY, Ehses JA: Type 1, type 1.5, and type 2 diabetes: NOD the diabetes we thought it was. Proceedings of the National Academy of Sciences of the United States of America. 2006, 103 (33): 12217-12218. 10.1073/pnas.0605480103.View ArticlePubMedPubMed CentralGoogle Scholar
- Florez JC: Newly identified loci highlight beta cell dysfunction as a key cause of type 2 diabetes: Where are the insulin resistance genes?. Diabetologia. 2008, 51 (7): 1100-1110. 10.1007/s00125-008-1025-9.View ArticlePubMedGoogle Scholar
- Wang GL, Semenza GL: General involvement of hypoxia-inducible factor 1 in transcriptional response to hypoxia. Proceedings of the National Academy of Sciences of the United States of America. 1993, 90 (9): 4304-4308. 10.1073/pnas.90.9.4304.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang GL, Jiang BH, Rue EA, Semenza GL: Hypoxia-inducible factor 1 is a basic-helix-loop-helix-PAS heterodimer regulated by cellular O2 tension. Proceedings of the National Academy of Sciences of the United States of America. 1995, 92 (12): 5510-5514. 10.1073/pnas.92.12.5510.View ArticlePubMedPubMed CentralGoogle Scholar
- Jiang BH, Rue E, Wang GL, Roe R, Semenza GL: Dimerization, DNA binding, and transactivation properties of hypoxia-inducible factor 1. The Journal of biological chemistry. 1996, 271 (30): 17771-17778. 10.1074/jbc.271.30.17771.View ArticlePubMedGoogle Scholar
- Pugh CW, O'Rourke JF, Nagao M, Gleadle JM, Ratcliffe PJ: Activation of hypoxia-inducible factor-1; definition of regulatory domains within the alpha subunit. The Journal of biological chemistry. 1997, 272 (17): 11205-11214. 10.1074/jbc.272.17.11205.View ArticlePubMedGoogle Scholar
- Jiang BH, Zheng JZ, Leung SW, Roe R, Semenza GL: Transactivation and inhibitory domains of hypoxia-inducible factor 1alpha. Modulation of transcriptional activity by oxygen tension. The Journal of biological chemistry. 1997, 272 (31): 19253-19260. 10.1074/jbc.272.31.19253.View ArticlePubMedGoogle Scholar
- Huang LE, Gu J, Schau M, Bunn HF: Regulation of hypoxia-inducible factor 1alpha is mediated by an O2-dependent degradation domain via the ubiquitin-proteasome pathway. Proceedings of the National Academy of Sciences of the United States of America. 1998, 95 (14): 7987-7992. 10.1073/pnas.95.14.7987.View ArticlePubMedPubMed CentralGoogle Scholar
- Epstein AC, Gleadle JM, McNeill LA, Hewitson KS, O'Rourke J, Mole DR, Mukherji M, Metzen E, Wilson MI, Dhanda A, et al: C. elegans EGL-9 and mammalian homologs define a family of dioxygenases that regulate HIF by prolyl hydroxylation. Cell. 2001, 107 (1): 43-54. 10.1016/S0092-8674(01)00507-4.View ArticlePubMedGoogle Scholar
- Silander K, Scott LJ, Valle TT, Mohlke KL, Stringham HM, Wiles KR, Duren WL, Doheny KF, Pugh EW, Chines P, et al: A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14. Diabetes. 2004, 53 (3): 821-829. 10.2337/diabetes.53.3.821.View ArticlePubMedGoogle Scholar
- Yamada N, Horikawa Y, Oda N, Iizuka K, Shihara N, Kishi S, Takeda J: Genetic variation in the hypoxia-inducible factor-1alpha gene is associated with type 2 diabetes in Japanese. The Journal of clinical endocrinology and metabolism. 2005, 90 (10): 5841-5847. 10.1210/jc.2005-0991.View ArticlePubMedGoogle Scholar
- Boor K, Ronai Z, Nemoda Z, Gaszner P, Sasvari-Szekely M, Guttman A, Kalasz H: Noninvasive genotyping of dopamine receptor D4 (DRD4) using nanograms of DNA from substance-dependent patients. Curr Med Chem. 2002, 9 (8): 793-797. 10.2174/0929867024606821.View ArticlePubMedGoogle Scholar
- Percy MJ, Mooney SM, McMullin MF, Flores A, Lappin TR, Lee FS: A common polymorphism in the oxygen-dependent degradation (ODD) domain of hypoxia inducible factor-1alpha (HIF-1alpha) does not impair Pro-564 hydroxylation. Molecular cancer. 2003, 2: 31-10.1186/1476-4598-2-31.View ArticlePubMedPubMed CentralGoogle Scholar
- Faul F, Erdfelder E, Lang AG, Buchner A: G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences. Behav Res Methods. 2007, 39 (2): 175-191.View ArticlePubMedGoogle Scholar
- Cohen J: Statistical power analysis for the behavioral sciences. 1988, Hillsdale, NJ.: Erlbaum, 2Google Scholar
- Blaak E: Sex differences in the control of glucose homeostasis. Curr Opin Clin Nutr Metab Care. 2008, 11 (4): 500-504. 10.1097/MCO.0b013e32830467d3.View ArticlePubMedGoogle Scholar
- Gale EA, Gillespie KM: Diabetes and gender. Diabetologia. 2001, 44 (1): 3-15. 10.1007/s001250051573.View ArticlePubMedGoogle Scholar
- Hlatky MA, Quertermous T, Boothroyd DB, Priest JR, Glassford AJ, Myers RM, Fortmann SP, Iribarren C, Tabor HK, Assimes TL, et al: Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease. Am Heart J. 2007, 154 (6): 1035-1042. 10.1016/j.ahj.2007.07.042.View ArticlePubMedGoogle Scholar
- Field SF, Howson JM, Smyth DJ, Walker NM, Dunger DB, Todd JA: Analysis of the type 2 diabetes gene, TCF7L2, in 13,795 type 1 diabetes cases and control subjects. Diabetologia. 2007, 50 (1): 212-213. 10.1007/s00125-006-0506-y.View ArticlePubMedGoogle Scholar
- Field SF, Howson JM, Walker NM, Dunger DB, Todd JA: Analysis of the obesity gene FTO in 14,803 type 1 diabetes cases and controls. Diabetologia. 2007, 50 (10): 2218-2220. 10.1007/s00125-007-0767-0.View ArticlePubMedPubMed CentralGoogle Scholar
- Wilkin TJ: The accelerator hypothesis: weight gain as the missing link between Type I and Type II diabetes. Diabetologia. 2001, 44 (7): 914-922. 10.1007/s001250100548.View ArticlePubMedGoogle Scholar
- Dahlquist G, Blom L, Tuvemo T, Nystrom L, Sandstrom A, Wall S: The Swedish childhood diabetes study – results from a nine year case register and a one year case-referent study indicating that type 1 (insulin-dependent) diabetes mellitus is associated with both type 2 (non-insulin-dependent) diabetes mellitus and autoimmune disorders. Diabetologia. 1989, 32 (1): 2-6. 10.1007/BF00265396.View ArticlePubMedGoogle Scholar
- Li H, Lindholm E, Almgren P, Gustafsson A, Forsblom C, Groop L, Tuomi T: Possible human leukocyte antigen-mediated genetic interaction between type 1 and type 2 Diabetes. The Journal of clinical endocrinology and metabolism. 2001, 86 (2): 574-582. 10.1210/jc.86.2.574.PubMedGoogle Scholar
- Atkinson MA, Eisenbarth GS: Type 1 diabetes: new perspectives on disease pathogenesis and treatment. Lancet. 2001, 358 (9277): 221-229. 10.1016/S0140-6736(01)05415-0.View ArticlePubMedGoogle Scholar
- Johansen A, Jensen DP, Bergholdt R, Mortensen HB, Pociot F, Nerup J, Hansen T, Pedersen O: IRS1, KCNJ11, PPARgamma2 and HNF-1alpha: do amino acid polymorphisms in these candidate genes support a shared aetiology between type 1 and type 2 diabetes?. Diabetes Obes Metab. 2006, 8 (1): 75-82. 10.1111/j.1463-1326.2005.00471.x.View ArticlePubMedGoogle Scholar
- Galanakis E, Kofteridis D, Stratigi K, Petraki E, Vazgiourakis V, Fragouli E, Mamoulakis D, Boumpas DT, Goulielmos GN: Intron 4 a/b polymorphism of the endothelial nitric oxide synthase gene is associated with both type 1 and type 2 diabetes in a genetically homogeneous population. Hum Immunol. 2008, 69 (4–5): 279-283. 10.1016/j.humimm.2008.03.001.View ArticlePubMedGoogle Scholar
- Clifford SC, Astuti D, Hooper L, Maxwell PH, Ratcliffe PJ, Maher ER: The pVHL-associated SCF ubiquitin ligase complex: molecular genetic analysis of elongin B and C, Rbx1 and HIF-1alpha in renal cell carcinoma. Oncogene. 2001, 20 (36): 5067-5074. 10.1038/sj.onc.1204602.View ArticlePubMedGoogle Scholar
- Tanimoto K, Yoshiga K, Eguchi H, Kaneyasu M, Ukon K, Kumazaki T, Oue N, Yasui W, Imai K, Nakachi K, et al: Hypoxia-inducible factor-1alpha polymorphisms associated with enhanced transactivation capacity, implying clinical significance. Carcinogenesis. 2003, 24 (11): 1779-1783. 10.1093/carcin/bgg132.View ArticlePubMedGoogle Scholar
- Fu XS, Choi E, Bubley GJ, Balk SP: Identification of hypoxia-inducible factor-1alpha (HIF-1alpha) polymorphism as a mutation in prostate cancer that prevents normoxia-induced degradation. Prostate. 2005, 63 (3): 215-221. 10.1002/pros.20190.View ArticlePubMedGoogle Scholar
- Liu Y, Cox SR, Morita T, Kourembanas S: Hypoxia regulates vascular endothelial growth factor gene expression in endothelial cells. Identification of a 5' enhancer. Circulation research. 1995, 77 (3): 638-643.View ArticlePubMedGoogle Scholar
- Forsythe JA, Jiang BH, Iyer NV, Agani F, Leung SW, Koos RD, Semenza GL: Activation of vascular endothelial growth factor gene transcription by hypoxia-inducible factor 1. Molecular and cellular biology. 1996, 16 (9): 4604-4613.View ArticlePubMedPubMed CentralGoogle Scholar
- Pages G, Pouyssegur J: Transcriptional regulation of the Vascular Endothelial Growth Factor gene – a concert of activating factors. Cardiovasc Res. 2005, 65 (3): 564-573. 10.1016/j.cardiores.2004.09.032.View ArticlePubMedGoogle Scholar
- Stagner J, Mokshagundam S, Wyler K, Samols E, Rilo H, Stagner M, Parthasarathy L, Parthasarathy R: Beta-cell sparing in transplanted islets by vascular endothelial growth factor. Transplantation proceedings. 2004, 36 (4): 1178-1180. 10.1016/j.transproceed.2004.04.036.View ArticlePubMedGoogle Scholar
- Zhang N, Richter A, Suriawinata J, Harbaran S, Altomonte J, Cong L, Zhang H, Song K, Meseck M, Bromberg J, et al: Elevated vascular endothelial growth factor production in islets improves islet graft vascularization. Diabetes. 2004, 53 (4): 963-970. 10.2337/diabetes.53.4.963.View ArticlePubMedGoogle Scholar
- Lammert E, Cleaver O, Melton D: Induction of pancreatic differentiation by signals from blood vessels. Science (New York, NY). 2001, 294 (5542): 564-567.View ArticleGoogle Scholar
- Del Bo R, Scarlato M, Ghezzi S, Maestroni A, Sjolind L, Forsblom C, Wessman M, Groop PH, Comi GP, Bresolin N, et al: VEGF gene variability and type 1 diabetes: evidence for a protective role. Immunogenetics. 2006, 58 (2–3): 107-112.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2350/10/79/prepub
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