دورية أكاديمية

Allele-specific methylation of type 1 diabetes susceptibility genes.

التفاصيل البيبلوغرافية
العنوان: Allele-specific methylation of type 1 diabetes susceptibility genes.
المؤلفون: Kindt, A., Fuerst, R.W., Knoop, J., Laimighofer, M., Telieps, T., Hippich, M., Woerheide, M.A., Wahl, S., Wilson, R., Sedlmeier, E.-M., Hommel, A., Todd, J.A., Krumsiek, J., Ziegler, A.-G., Bonifacio, E.
المصدر: J. Autoimmun. 89, 63-74 (2018)
سنة النشر: 2018
المجموعة: PuSH - Publikationsserver des Helmholtz Zentrums München
مصطلحات موضوعية: Autoimmunity, Epigenetics, Hla, Insulin Autoantibodies, Insulin Gene, Lactate Dehydrogenase C
الوصف: The susceptibility to autoimmune diseases is influenced by genes encoding major histocompatibility complex (MHC) proteins. By examining the epigenetic methylation maps of cord blood samples, we found marked differences in the methylation status of CpG sites within the MHC genes (cis-metQTLs) between carriers of the type 1 diabetes risk haplotypes HLA-DRB1*03-DQA1*0501-DQB1*0201 (DR3-DQ2) and HLA-DRB1*04-DQA1*0301-DQB1*0302 (DR4-DQ8). These differences were found in children and adults, and were accompanied by reduced HLA-DR protein expression in immune cells with the HLA-DR3-DQ2 haplotype. Extensive cis-metQTLs were identified in all 45 immune and non-immune type 1 diabetes susceptibility genes analyzed in this study. We observed and validated a novel association between the methylation status of CpG sites within the LDHC gene and the development of insulin autoantibodies in early childhood in children who are carriers of the highest type 1 diabetes risk genotype. Functionally relevant epigenetic changes in susceptibility genes may represent therapeutic targets for type 1 diabetes.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: German
تدمد: 0896-8411
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29224923; info:eu-repo/semantics/altIdentifier/wos/WOS:000431158100007; info:eu-repo/semantics/altIdentifier/isbn/0896-8411; info:eu-repo/semantics; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52522Test; urn:isbn:0896-8411; urn:issn:0896-8411
DOI: 10.1016/j.jaut.2017.11.008
الإتاحة: https://doi.org/10.1016/j.jaut.2017.11.008Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52522Test
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.43B7B08D
قاعدة البيانات: BASE
الوصف
تدمد:08968411
DOI:10.1016/j.jaut.2017.11.008