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Fine mapping of genes within the IDDM8 region in rheumatoid arthritis
The IDDM8 region on chromosome 6q27, first identified as a susceptibility locus for type 1 diabetes, has previously been linked and associated with rheumatoid arthritis (RA). The region contains a number of potential candidate genes, including programmed cell death 2 (PDCD2), the proteosome subunit...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779440/ https://www.ncbi.nlm.nih.gov/pubmed/16945141 http://dx.doi.org/10.1186/ar2037 |
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author | Hinks, Anne Barton, Anne John, Sally Shephard, Neil Worthington, Jane |
author_facet | Hinks, Anne Barton, Anne John, Sally Shephard, Neil Worthington, Jane |
author_sort | Hinks, Anne |
collection | PubMed |
description | The IDDM8 region on chromosome 6q27, first identified as a susceptibility locus for type 1 diabetes, has previously been linked and associated with rheumatoid arthritis (RA). The region contains a number of potential candidate genes, including programmed cell death 2 (PDCD2), the proteosome subunit beta type 1 (PSMB1), delta-like ligand 1 (DLL-1) and TATA box-binding protein (TBP) amongst others. The aim of this study was to fine map the IDDM8 region on chromosome 6q27, focusing on the genes in the region, to identify polymorphisms that may contribute to susceptibility to RA and potentially to other autoimmune diseases. Validated single nucleotide polymorphisms (SNPs; n = 65) were selected from public databases from the 330 kb region of IDDM8. These were genotyped using Sequenom MassArray genotyping technology in two datasets; the test dataset comprised 180 RA cases and 180 controls. We tested 50 SNPs for association with RA and any significant associations were genotyped in a second dataset of 174 RA cases and 192 controls, and the datasets were combined before analysis. Association analysis was performed by chi-square test implemented in Stata software and linkage disequilibrium and haplotype analysis was performed using Helix tree version 4.1. There was initial weak evidence of association, with RA, of a number of SNPs around the loc154449 putative gene and within the KIAA1838 gene; however, these associations were not significant in the combined dataset. Our study has failed to detect evidence of association with any of the known genes mapping to the IDDM8 locus with RA. |
format | Text |
id | pubmed-1779440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-17794402007-01-19 Fine mapping of genes within the IDDM8 region in rheumatoid arthritis Hinks, Anne Barton, Anne John, Sally Shephard, Neil Worthington, Jane Arthritis Res Ther Research Article The IDDM8 region on chromosome 6q27, first identified as a susceptibility locus for type 1 diabetes, has previously been linked and associated with rheumatoid arthritis (RA). The region contains a number of potential candidate genes, including programmed cell death 2 (PDCD2), the proteosome subunit beta type 1 (PSMB1), delta-like ligand 1 (DLL-1) and TATA box-binding protein (TBP) amongst others. The aim of this study was to fine map the IDDM8 region on chromosome 6q27, focusing on the genes in the region, to identify polymorphisms that may contribute to susceptibility to RA and potentially to other autoimmune diseases. Validated single nucleotide polymorphisms (SNPs; n = 65) were selected from public databases from the 330 kb region of IDDM8. These were genotyped using Sequenom MassArray genotyping technology in two datasets; the test dataset comprised 180 RA cases and 180 controls. We tested 50 SNPs for association with RA and any significant associations were genotyped in a second dataset of 174 RA cases and 192 controls, and the datasets were combined before analysis. Association analysis was performed by chi-square test implemented in Stata software and linkage disequilibrium and haplotype analysis was performed using Helix tree version 4.1. There was initial weak evidence of association, with RA, of a number of SNPs around the loc154449 putative gene and within the KIAA1838 gene; however, these associations were not significant in the combined dataset. Our study has failed to detect evidence of association with any of the known genes mapping to the IDDM8 locus with RA. BioMed Central 2006 2006-08-31 /pmc/articles/PMC1779440/ /pubmed/16945141 http://dx.doi.org/10.1186/ar2037 Text en Copyright © 2006 Hinks et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hinks, Anne Barton, Anne John, Sally Shephard, Neil Worthington, Jane Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title | Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title_full | Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title_fullStr | Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title_full_unstemmed | Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title_short | Fine mapping of genes within the IDDM8 region in rheumatoid arthritis |
title_sort | fine mapping of genes within the iddm8 region in rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779440/ https://www.ncbi.nlm.nih.gov/pubmed/16945141 http://dx.doi.org/10.1186/ar2037 |
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