Skip to main content
Top
Published in: Acta Diabetologica 4/2015

01-08-2015 | Original Article

Data interpretation: deciphering the biological function of Type 2 diabetes associated risk loci

Authors: Asima Zia, Attya Bhatti, Peter John, Aysha Karim Kiani

Published in: Acta Diabetologica | Issue 4/2015

Login to get access

Abstract

Aims

Type 2 diabetes (T2D) is a complex multifactorial disorder with more than 40 loci associated with disease susceptibility. Most of these genome-wide significant loci reside in noncoding regions, it is important to decipher the potential regulatory function of these variants and to differentiate between true and tag signals. Nowadays, databases are being developed to study and predict the function of these associated variants, and RegulomeDB is one such database.

Methods

We used RegulomeDB to analyze the potential function of the associated variants reported in five genome-wide association studies (GWAS) of T2D.

Results

We investigated the 1,567 single nucleotide polymorphisms (SNPs) with 989 SNPs with a score of 1–6. Of those 989 SNPs, only 64 returned with RegulomeDB score <3 (evidence of regulatory function), and only four of these were GWAS significant SNPs (THADA/rs10203174, score = 1b; UBE2E2/rs7612463, score = 2a; ARAP1/rs1552224 and TP53INP1/rs8996852, score = 2b). But only 63 % of the annotated SNPs showed regulatory function that is an important limitation of the RegulomeDB as this database only provides information of few regulatory elements.

Conclusion

This study further supports that some of the noncoding GWAS variants are the true associations and not the tag ones. This study also proves the utility and importance of the RegulomeDB and other such databases. Although it is an extensive database of regulatory elements but has certain limitation due to utilization of only few types of regulatory elements and pathways.
Appendix
Available only for authorised users
Literature
1.
2.
go back to reference Hindorff LA, Sethupathy P, Junkins HA et al (2009) Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362–9367PubMedCentralPubMedCrossRef Hindorff LA, Sethupathy P, Junkins HA et al (2009) Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc Natl Acad Sci USA 106:9362–9367PubMedCentralPubMedCrossRef
3.
4.
go back to reference Venter JC, Adams MD, Myers EW et al (2001) The sequence of the human genome. Science 291:1304–1351PubMedCrossRef Venter JC, Adams MD, Myers EW et al (2001) The sequence of the human genome. Science 291:1304–1351PubMedCrossRef
5.
go back to reference Birney E, Stamatoyannopoulos JA, Dutta A et al (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447:799–816PubMedCrossRef Birney E, Stamatoyannopoulos JA, Dutta A et al (2007) Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project. Nature 447:799–816PubMedCrossRef
6.
go back to reference Bernstein BE, Birney E, Dunham I, Green ED, Gunter C, Snyder M (2012) An integrated encyclopedia of DNA elements in the human genome. Nature 489:57–74CrossRef Bernstein BE, Birney E, Dunham I, Green ED, Gunter C, Snyder M (2012) An integrated encyclopedia of DNA elements in the human genome. Nature 489:57–74CrossRef
7.
go back to reference Stumvoll M, Goldstein BJ, van Haeften TW (2005) Type 2 diabetes: principles of pathogenesis and therapy. Lancet 365:1333–1346PubMedCrossRef Stumvoll M, Goldstein BJ, van Haeften TW (2005) Type 2 diabetes: principles of pathogenesis and therapy. Lancet 365:1333–1346PubMedCrossRef
8.
go back to reference Sanghera DK, Blackett PR (2012) Type 2 diabetes genetics: beyond GWAS. J Diabetes Metab 3:2–13CrossRef Sanghera DK, Blackett PR (2012) Type 2 diabetes genetics: beyond GWAS. J Diabetes Metab 3:2–13CrossRef
9.
go back to reference Herder C, Roden M (2011) Genetics of type 2 diabetes: pathophysiologic and clinical relevance. Eur J Clin Invest 41:679–692PubMedCrossRef Herder C, Roden M (2011) Genetics of type 2 diabetes: pathophysiologic and clinical relevance. Eur J Clin Invest 41:679–692PubMedCrossRef
10.
go back to reference Voight BF, Scott LJ, Steinthorsdottir V et al (2010) Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet 42:579–589PubMedCentralPubMedCrossRef Voight BF, Scott LJ, Steinthorsdottir V et al (2010) Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat Genet 42:579–589PubMedCentralPubMedCrossRef
11.
go back to reference Zeggini E, Scott LJ, Saxena R et al (2008) Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 40:638–645PubMedCentralPubMedCrossRef Zeggini E, Scott LJ, Saxena R et al (2008) Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nat Genet 40:638–645PubMedCentralPubMedCrossRef
12.
go back to reference Ip W, Chiang YT, Jin T (2012) The involvement of the wnt signaling pathway and TCF7L2 in diabetes mellitus: the current understanding, dispute, and perspective. Cell Biosci 2:28PubMedCentralPubMedCrossRef Ip W, Chiang YT, Jin T (2012) The involvement of the wnt signaling pathway and TCF7L2 in diabetes mellitus: the current understanding, dispute, and perspective. Cell Biosci 2:28PubMedCentralPubMedCrossRef
13.
go back to reference Rosenthal SL, Barmada MM, Wang X, Demirci FY, Kamboh MI (2014) Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer’s disease GWAS findings. PLoS ONE 9:e95152PubMedCentralPubMedCrossRef Rosenthal SL, Barmada MM, Wang X, Demirci FY, Kamboh MI (2014) Connecting the dots: potential of data integration to identify regulatory SNPs in late-onset Alzheimer’s disease GWAS findings. PLoS ONE 9:e95152PubMedCentralPubMedCrossRef
14.
go back to reference Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O’Donnell CJ, de Bakker PI (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24:2938–2939PubMedCentralPubMedCrossRef Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O’Donnell CJ, de Bakker PI (2008) SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24:2938–2939PubMedCentralPubMedCrossRef
15.
go back to reference Saxena R, Voight BF, Lyssenko V et al (2007) Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 316:1331–1336PubMedCrossRef Saxena R, Voight BF, Lyssenko V et al (2007) Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science 316:1331–1336PubMedCrossRef
16.
go back to reference Saxena R, Saleheen D, Been LF et al (2013) Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi Origin from India. Diabetes Saxena R, Saleheen D, Been LF et al (2013) Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi Origin from India. Diabetes
17.
go back to reference Kooner JS, Saleheen D, Sim X et al (2011) Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet 43:984–989PubMedCentralPubMedCrossRef Kooner JS, Saleheen D, Sim X et al (2011) Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet 43:984–989PubMedCentralPubMedCrossRef
18.
go back to reference Rees SD, Hydrie MZ, Shera AS et al (2011) Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia 54:1368–1374PubMedCrossRef Rees SD, Hydrie MZ, Shera AS et al (2011) Replication of 13 genome-wide association (GWA)-validated risk variants for type 2 diabetes in Pakistani populations. Diabetologia 54:1368–1374PubMedCrossRef
19.
go back to reference Morris AP, Voight BF, Teslovich TM et al (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 44:981–990PubMedCentralPubMedCrossRef Morris AP, Voight BF, Teslovich TM et al (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 44:981–990PubMedCentralPubMedCrossRef
20.
go back to reference Cho YS, Chen CH, Hu C et al (2012) Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet 44:67–72CrossRef Cho YS, Chen CH, Hu C et al (2012) Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet 44:67–72CrossRef
21.
go back to reference Liu L, Amy V, Liu G, McKeehan WL (2002) Novel complex integrating mitochondria and the microtubular cytoskeleton with chromosome remodeling and tumor suppressor RASSF1 deduced by in silico homology analysis, interaction cloning in yeast, and colocalization in cultured cells. In Vitro Cell Dev Biol Anim 38:582–594PubMedCentralPubMedCrossRef Liu L, Amy V, Liu G, McKeehan WL (2002) Novel complex integrating mitochondria and the microtubular cytoskeleton with chromosome remodeling and tumor suppressor RASSF1 deduced by in silico homology analysis, interaction cloning in yeast, and colocalization in cultured cells. In Vitro Cell Dev Biol Anim 38:582–594PubMedCentralPubMedCrossRef
22.
go back to reference Liu L, McKeehan WL (2002) Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal organization, vesicular trafficking, nucleocytosolic shuttling, and chromosome activity. Genomics 79:124–136PubMedCentralPubMedCrossRef Liu L, McKeehan WL (2002) Sequence analysis of LRPPRC and its SEC1 domain interaction partners suggests roles in cytoskeletal organization, vesicular trafficking, nucleocytosolic shuttling, and chromosome activity. Genomics 79:124–136PubMedCentralPubMedCrossRef
23.
go back to reference Liu L, Vo A, Liu G, McKeehan WL (2005) Putative tumor suppressor RASSF1 interactive protein and cell death inducer C19ORF5 is a DNA binding protein. Biochem Biophys Res Commun 332:670–676PubMedCentralPubMedCrossRef Liu L, Vo A, Liu G, McKeehan WL (2005) Putative tumor suppressor RASSF1 interactive protein and cell death inducer C19ORF5 is a DNA binding protein. Biochem Biophys Res Commun 332:670–676PubMedCentralPubMedCrossRef
24.
go back to reference Mootha VK, Lepage P, Miller K et al (2003) Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc Natl Acad Sci USA 100:605–610PubMedCentralPubMedCrossRef Mootha VK, Lepage P, Miller K et al (2003) Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc Natl Acad Sci USA 100:605–610PubMedCentralPubMedCrossRef
25.
go back to reference Xu F, Morin C, Mitchell G, Ackerley C, Robinson BH (2004) The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA. Biochem J 382:331–336PubMedCentralPubMedCrossRef Xu F, Morin C, Mitchell G, Ackerley C, Robinson BH (2004) The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA. Biochem J 382:331–336PubMedCentralPubMedCrossRef
26.
go back to reference Vandin F, Clay P, Upfal E, Raphael BJ (2012) Discovery of mutated subnetworks associated with clinical data in cancer. Pac Symp Biocomput 55–66 Vandin F, Clay P, Upfal E, Raphael BJ (2012) Discovery of mutated subnetworks associated with clinical data in cancer. Pac Symp Biocomput 55–66
27.
go back to reference Kayaba H, Hirokawa M, Watanabe A et al (2000) Serum markers of graft-versus-host disease after bone marrow transplantation. J Allergy Clin Immunol 106:S40–S44PubMedCrossRef Kayaba H, Hirokawa M, Watanabe A et al (2000) Serum markers of graft-versus-host disease after bone marrow transplantation. J Allergy Clin Immunol 106:S40–S44PubMedCrossRef
28.
go back to reference Schoenfeld TA, McKerracher L, Obar R, Vallee RB (1989) MAP 1A and MAP 1B are structurally related microtubule associated proteins with distinct developmental patterns in the CNS. J Neurosci 9:1712–1730PubMed Schoenfeld TA, McKerracher L, Obar R, Vallee RB (1989) MAP 1A and MAP 1B are structurally related microtubule associated proteins with distinct developmental patterns in the CNS. J Neurosci 9:1712–1730PubMed
29.
go back to reference Xie R, Nguyen S, McKeehan K, Wang F, McKeehan WL, Liu L (2011) Microtubule-associated protein 1S (MAP1S) bridges autophagic components with microtubules and mitochondria to affect autophagosomal biogenesis and degradation. J Biol Chem 286:10367–10377PubMedCentralPubMedCrossRef Xie R, Nguyen S, McKeehan K, Wang F, McKeehan WL, Liu L (2011) Microtubule-associated protein 1S (MAP1S) bridges autophagic components with microtubules and mitochondria to affect autophagosomal biogenesis and degradation. J Biol Chem 286:10367–10377PubMedCentralPubMedCrossRef
30.
go back to reference Xie R, Wang F, McKeehan WL, Liu L (2011) Autophagy enhanced by microtubule- and mitochondrion-associated MAP1S suppresses genome instability and hepatocarcinogenesis. Cancer Res 71:7537–7546PubMedCentralPubMedCrossRef Xie R, Wang F, McKeehan WL, Liu L (2011) Autophagy enhanced by microtubule- and mitochondrion-associated MAP1S suppresses genome instability and hepatocarcinogenesis. Cancer Res 71:7537–7546PubMedCentralPubMedCrossRef
32.
go back to reference Jiang X, Li X, Huang H et al (2014) Elevated levels of mitochondrion-associated autophagy inhibitor LRPPRC are associated with poor prognosis in patients with prostate cancer. Cancer 120:1228–1236PubMedCentralPubMedCrossRef Jiang X, Li X, Huang H et al (2014) Elevated levels of mitochondrion-associated autophagy inhibitor LRPPRC are associated with poor prognosis in patients with prostate cancer. Cancer 120:1228–1236PubMedCentralPubMedCrossRef
34.
go back to reference Weedon MN, Owen KR, Shields B et al (2004) Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population. Diabetes 53:3002–3006PubMedCrossRef Weedon MN, Owen KR, Shields B et al (2004) Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. population. Diabetes 53:3002–3006PubMedCrossRef
35.
go back to reference Duncan SA, Navas MA, Dufort D, Rossant J, Stoffel M (1998) Regulation of a transcription factor network required for differentiation and metabolism. Science 281:692–695PubMedCrossRef Duncan SA, Navas MA, Dufort D, Rossant J, Stoffel M (1998) Regulation of a transcription factor network required for differentiation and metabolism. Science 281:692–695PubMedCrossRef
36.
go back to reference Li J, Ning G, Duncan SA (2000) Mammalian hepatocyte differentiation requires the transcription factor HNF-4alpha. Genes Dev 14:464–474PubMedCentralPubMed Li J, Ning G, Duncan SA (2000) Mammalian hepatocyte differentiation requires the transcription factor HNF-4alpha. Genes Dev 14:464–474PubMedCentralPubMed
37.
go back to reference Yu X, Mertz JE (2003) Distinct modes of regulation of transcription of hepatitis B virus by the nuclear receptors HNF4alpha and COUP-TF1. J Virol 77:2489–2499PubMedCentralPubMedCrossRef Yu X, Mertz JE (2003) Distinct modes of regulation of transcription of hepatitis B virus by the nuclear receptors HNF4alpha and COUP-TF1. J Virol 77:2489–2499PubMedCentralPubMedCrossRef
38.
go back to reference Cauchi S, Meyre D, Choquet H et al (2006) TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Diabetes 55:3189–3192PubMedCrossRef Cauchi S, Meyre D, Choquet H et al (2006) TCF7L2 variation predicts hyperglycemia incidence in a French general population: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study. Diabetes 55:3189–3192PubMedCrossRef
39.
go back to reference Damcott CM, Pollin TI, Reinhart LJ et al (2006) Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes 55:2654–2659PubMedCrossRef Damcott CM, Pollin TI, Reinhart LJ et al (2006) Polymorphisms in the transcription factor 7-like 2 (TCF7L2) gene are associated with type 2 diabetes in the Amish: replication and evidence for a role in both insulin secretion and insulin resistance. Diabetes 55:2654–2659PubMedCrossRef
40.
go back to reference Lyssenko V, Lupi R, Marchetti P et al (2007) Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. J Clin Investig 117:2155–2163PubMedCentralPubMedCrossRef Lyssenko V, Lupi R, Marchetti P et al (2007) Mechanisms by which common variants in the TCF7L2 gene increase risk of type 2 diabetes. J Clin Investig 117:2155–2163PubMedCentralPubMedCrossRef
41.
go back to reference Hayashi T, Iwamoto Y, Kaku K, Hirose H, Maeda S (2007) Replication study for the association of TCF7L2 with susceptibility to type 2 diabetes in a Japanese population. Diabetologia 50:980–984PubMedCrossRef Hayashi T, Iwamoto Y, Kaku K, Hirose H, Maeda S (2007) Replication study for the association of TCF7L2 with susceptibility to type 2 diabetes in a Japanese population. Diabetologia 50:980–984PubMedCrossRef
42.
go back to reference Miyake K, Horikawa Y, Hara K et al (2008) Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects. J Hum Genet 53:174–180PubMedCrossRef Miyake K, Horikawa Y, Hara K et al (2008) Association of TCF7L2 polymorphisms with susceptibility to type 2 diabetes in 4,087 Japanese subjects. J Hum Genet 53:174–180PubMedCrossRef
43.
go back to reference Palizban A, Nikpour M, Salehi R, Maracy MR (2012) Association of a common variant in TCF7L2 gene with type 2 diabetes mellitus in a Persian population. Clin Exp Med 12:115–119PubMedCrossRef Palizban A, Nikpour M, Salehi R, Maracy MR (2012) Association of a common variant in TCF7L2 gene with type 2 diabetes mellitus in a Persian population. Clin Exp Med 12:115–119PubMedCrossRef
44.
go back to reference Dou H, Ma E, Yin L, Jin Y, Wang H (2013) The association between gene polymorphism of TCF7L2 and type 2 diabetes in Chinese Han population: a meta-analysis. PLoS ONE 8:e59495PubMedCentralPubMedCrossRef Dou H, Ma E, Yin L, Jin Y, Wang H (2013) The association between gene polymorphism of TCF7L2 and type 2 diabetes in Chinese Han population: a meta-analysis. PLoS ONE 8:e59495PubMedCentralPubMedCrossRef
45.
go back to reference Kaur H, Chen S, Xin X, Chiu J, Khan ZA, Chakrabarti S (2006) Diabetes-induced extracellular matrix protein expression is mediated by transcription coactivator p300. Diabetes 55:3104–3111PubMedCrossRef Kaur H, Chen S, Xin X, Chiu J, Khan ZA, Chakrabarti S (2006) Diabetes-induced extracellular matrix protein expression is mediated by transcription coactivator p300. Diabetes 55:3104–3111PubMedCrossRef
46.
go back to reference Raychaudhuri S, Loew C, Korner R et al (2014) Interplay of acetyltransferase EP300 and the proteasome system in regulating heat shock transcription factor 1. Cell 156:975–985PubMedCrossRef Raychaudhuri S, Loew C, Korner R et al (2014) Interplay of acetyltransferase EP300 and the proteasome system in regulating heat shock transcription factor 1. Cell 156:975–985PubMedCrossRef
47.
go back to reference Ben-Zvi A, Miller EA, Morimoto RI (2009) Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging. Proc Natl Acad Sci USA 106:14914–14919PubMedCentralPubMedCrossRef Ben-Zvi A, Miller EA, Morimoto RI (2009) Collapse of proteostasis represents an early molecular event in Caenorhabditis elegans aging. Proc Natl Acad Sci USA 106:14914–14919PubMedCentralPubMedCrossRef
48.
go back to reference Gupta R, Kasturi P, Bracher A et al (2011) Firefly luciferase mutants as sensors of proteome stress. Nat Methods 8:879–884PubMedCrossRef Gupta R, Kasturi P, Bracher A et al (2011) Firefly luciferase mutants as sensors of proteome stress. Nat Methods 8:879–884PubMedCrossRef
49.
go back to reference Powers ET, Morimoto RI, Dillin A, Kelly JW, Balch WE (2009) Biological and chemical approaches to diseases of proteostasis deficiency. Annu Rev Biochem 78:959–991PubMedCrossRef Powers ET, Morimoto RI, Dillin A, Kelly JW, Balch WE (2009) Biological and chemical approaches to diseases of proteostasis deficiency. Annu Rev Biochem 78:959–991PubMedCrossRef
50.
go back to reference Jesmin J, Rashid MS, Jamil H, Hontecillas R, Bassaganya-Riera J (2010) Gene regulatory network reveals oxidative stress as the underlying molecular mechanism of type 2 diabetes and hypertension. BMC Med Genomics 3:45PubMedCentralPubMedCrossRef Jesmin J, Rashid MS, Jamil H, Hontecillas R, Bassaganya-Riera J (2010) Gene regulatory network reveals oxidative stress as the underlying molecular mechanism of type 2 diabetes and hypertension. BMC Med Genomics 3:45PubMedCentralPubMedCrossRef
51.
go back to reference Wintzerith M, Acker J, Vicaire S, Vigneron M, Kedinger C (1992) Complete sequence of the human RNA polymerase II largest subunit. Nucleic Acids Res 20:910PubMedCentralPubMedCrossRef Wintzerith M, Acker J, Vicaire S, Vigneron M, Kedinger C (1992) Complete sequence of the human RNA polymerase II largest subunit. Nucleic Acids Res 20:910PubMedCentralPubMedCrossRef
52.
go back to reference Yamada K, Hayashi M, Madokoro H et al (2013) Nuclear localization of CD26 induced by a humanized monoclonal antibody inhibits tumor cell growth by modulating of POLR2A transcription. PLoS ONE 8:e62304PubMedCentralPubMedCrossRef Yamada K, Hayashi M, Madokoro H et al (2013) Nuclear localization of CD26 induced by a humanized monoclonal antibody inhibits tumor cell growth by modulating of POLR2A transcription. PLoS ONE 8:e62304PubMedCentralPubMedCrossRef
53.
go back to reference Drucker DJ, Nauck MA (2006) The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet 368:1696–1705PubMedCrossRef Drucker DJ, Nauck MA (2006) The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet 368:1696–1705PubMedCrossRef
54.
go back to reference Deacon CF (2011) Dipeptidyl peptidase-4 inhibitors in the treatment of type 2 diabetes: a comparative review. Diabetes Obes Metab 13:7–18PubMedCrossRef Deacon CF (2011) Dipeptidyl peptidase-4 inhibitors in the treatment of type 2 diabetes: a comparative review. Diabetes Obes Metab 13:7–18PubMedCrossRef
55.
go back to reference Ahren B (2008) Novel combination treatment of type 2 diabetes DPP-4 inhibition + metformin. Vasc Health Risk Manag 4:383–394PubMedCentralPubMed Ahren B (2008) Novel combination treatment of type 2 diabetes DPP-4 inhibition + metformin. Vasc Health Risk Manag 4:383–394PubMedCentralPubMed
56.
go back to reference Filippova GN, Fagerlie S, Klenova EM et al (1996) An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes. Mol Cell Biol 16:2802–2813PubMedCentralPubMed Filippova GN, Fagerlie S, Klenova EM et al (1996) An exceptionally conserved transcriptional repressor, CTCF, employs different combinations of zinc fingers to bind diverged promoter sequences of avian and mammalian c-myc oncogenes. Mol Cell Biol 16:2802–2813PubMedCentralPubMed
57.
go back to reference Filippova GN, Lindblom A, Meincke LJ et al (1998) A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers. Genes Chromosom Cancer 22:26–36PubMedCrossRef Filippova GN, Lindblom A, Meincke LJ et al (1998) A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers. Genes Chromosom Cancer 22:26–36PubMedCrossRef
58.
go back to reference Awad TA, Bigler J, Ulmer JE et al (1999) Negative transcriptional regulation mediated by thyroid hormone response element 144 requires binding of the multivalent factor CTCF to a novel target DNA sequence. J Biol Chem 274:27092–27098PubMedCrossRef Awad TA, Bigler J, Ulmer JE et al (1999) Negative transcriptional regulation mediated by thyroid hormone response element 144 requires binding of the multivalent factor CTCF to a novel target DNA sequence. J Biol Chem 274:27092–27098PubMedCrossRef
59.
go back to reference Burcin M, Arnold R, Lutz M et al (1997) Negative protein 1, which is required for function of the chicken lysozyme gene silencer in conjunction with hormone receptors, is identical to the multivalent zinc finger repressor CTCF. Mol Cell Biol 17:1281–1288PubMedCentralPubMed Burcin M, Arnold R, Lutz M et al (1997) Negative protein 1, which is required for function of the chicken lysozyme gene silencer in conjunction with hormone receptors, is identical to the multivalent zinc finger repressor CTCF. Mol Cell Biol 17:1281–1288PubMedCentralPubMed
60.
go back to reference Nakagawa H, Chadwick RB, Peltomaki P, Plass C, Nakamura Y, de La Chapelle A (2001) Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer. Proc Natl Acad Sci USA 98:591–596PubMedCentralPubMedCrossRef Nakagawa H, Chadwick RB, Peltomaki P, Plass C, Nakamura Y, de La Chapelle A (2001) Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer. Proc Natl Acad Sci USA 98:591–596PubMedCentralPubMedCrossRef
61.
go back to reference Docquier F, Farrar D, D’Arcy V et al (2005) Heightened expression of CTCF in breast cancer cells is associated with resistance to apoptosis. Cancer Res 65:5112–5122PubMedCrossRef Docquier F, Farrar D, D’Arcy V et al (2005) Heightened expression of CTCF in breast cancer cells is associated with resistance to apoptosis. Cancer Res 65:5112–5122PubMedCrossRef
62.
63.
go back to reference Qi CF, Martensson A, Mattioli M, Dalla-Favera R, Lobanenkov VV, Morse HC 3rd (2003) CTCF functions as a critical regulator of cell-cycle arrest and death after ligation of the B cell receptor on immature B cells. Proc Natl Acad Sci USA 100:633–638PubMedCentralPubMedCrossRef Qi CF, Martensson A, Mattioli M, Dalla-Favera R, Lobanenkov VV, Morse HC 3rd (2003) CTCF functions as a critical regulator of cell-cycle arrest and death after ligation of the B cell receptor on immature B cells. Proc Natl Acad Sci USA 100:633–638PubMedCentralPubMedCrossRef
65.
go back to reference Kulzer JR, Stitzel ML, Morken MA et al (2014) A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cell. Am J Hum Genet 94:186–197PubMedCentralPubMedCrossRef Kulzer JR, Stitzel ML, Morken MA et al (2014) A common functional regulatory variant at a type 2 diabetes locus upregulates ARAP1 expression in the pancreatic beta cell. Am J Hum Genet 94:186–197PubMedCentralPubMedCrossRef
66.
go back to reference Swafford AD, Howson JM, Davison LJ et al (2011) An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes. Diabetes 60:1041–1044PubMedCentralPubMedCrossRef Swafford AD, Howson JM, Davison LJ et al (2011) An allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetes. Diabetes 60:1041–1044PubMedCentralPubMedCrossRef
67.
go back to reference Ait-Lounis A, Bonal C, Seguin-Estevez Q et al (2010) The transcription factor Rfx3 regulates beta-cell differentiation, function, and glucokinase expression. Diabetes 59:1674–1685PubMedCentralPubMedCrossRef Ait-Lounis A, Bonal C, Seguin-Estevez Q et al (2010) The transcription factor Rfx3 regulates beta-cell differentiation, function, and glucokinase expression. Diabetes 59:1674–1685PubMedCentralPubMedCrossRef
Metadata
Title
Data interpretation: deciphering the biological function of Type 2 diabetes associated risk loci
Authors
Asima Zia
Attya Bhatti
Peter John
Aysha Karim Kiani
Publication date
01-08-2015
Publisher
Springer Milan
Published in
Acta Diabetologica / Issue 4/2015
Print ISSN: 0940-5429
Electronic ISSN: 1432-5233
DOI
https://doi.org/10.1007/s00592-014-0700-1

Other articles of this Issue 4/2015

Acta Diabetologica 4/2015 Go to the issue
Live Webinar | 27-06-2024 | 18:00 (CEST)

Keynote webinar | Spotlight on medication adherence

Live: Thursday 27th June 2024, 18:00-19:30 (CEST)

WHO estimates that half of all patients worldwide are non-adherent to their prescribed medication. The consequences of poor adherence can be catastrophic, on both the individual and population level.

Join our expert panel to discover why you need to understand the drivers of non-adherence in your patients, and how you can optimize medication adherence in your clinics to drastically improve patient outcomes.

Prof. Kevin Dolgin
Prof. Florian Limbourg
Prof. Anoop Chauhan
Developed by: Springer Medicine
Obesity Clinical Trial Summary

At a glance: The STEP trials

A round-up of the STEP phase 3 clinical trials evaluating semaglutide for weight loss in people with overweight or obesity.

Developed by: Springer Medicine

Highlights from the ACC 2024 Congress

Year in Review: Pediatric cardiology

Watch Dr. Anne Marie Valente present the last year's highlights in pediatric and congenital heart disease in the official ACC.24 Year in Review session.

Year in Review: Pulmonary vascular disease

The last year's highlights in pulmonary vascular disease are presented by Dr. Jane Leopold in this official video from ACC.24.

Year in Review: Valvular heart disease

Watch Prof. William Zoghbi present the last year's highlights in valvular heart disease from the official ACC.24 Year in Review session.

Year in Review: Heart failure and cardiomyopathies

Watch this official video from ACC.24. Dr. Biykem Bozkurt discusses last year's major advances in heart failure and cardiomyopathies.