Academic Journal

Identification of functional enhancer variants associated with type I diabetes in CD4+ T cells

التفاصيل البيبلوغرافية
العنوان: Identification of functional enhancer variants associated with type I diabetes in CD4+ T cells
المؤلفون: Mishra, Arpit, Jajodia, Ajay, Weston, Eryn, Jayavelu, Naresh Doni, Garcia, Mariana, Hossack, Daniel, Hawkins, R. David
المساهمون: National Institute of Diabetes and Digestive and Kidney Diseases
المصدر: Frontiers in Immunology ; volume 15 ; ISSN 1664-3224
بيانات النشر: Frontiers Media SA
سنة النشر: 2024
المجموعة: Frontiers (Publisher - via CrossRef)
الوصف: Type I diabetes is an autoimmune disease mediated by T-cell destruction of β cells in pancreatic islets. Currently, there is no known cure, and treatment consists of daily insulin injections. Genome-wide association studies and twin studies have indicated a strong genetic heritability for type I diabetes and implicated several genes. As most strongly associated variants are noncoding, there is still a lack of identification of functional and, therefore, likely causal variants. Given that many of these genetic variants reside in enhancer elements, we have tested 121 CD4+ T-cell enhancer variants associated with T1D. We found four to be functional through massively parallel reporter assays. Three of the enhancer variants weaken activity, while the fourth strengthens activity. We link these to their cognate genes using 3D genome architecture or eQTL data and validate them using CRISPR editing. Validated target genes include CLEC16A and SOCS1. While these genes have been previously implicated in type 1 diabetes and other autoimmune diseases, we show that enhancers controlling their expression harbor functional variants. These variants, therefore, may act as causal type 1 diabetic variants.
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
DOI: 10.3389/fimmu.2024.1387253
DOI: 10.3389/fimmu.2024.1387253/full
الاتاحة: http://dx.doi.org/10.3389/fimmu.2024.1387253
https://www.frontiersin.org/articles/10.3389/fimmu.2024.1387253/full
Rights: https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.9B37D40A
قاعدة البيانات: BASE
الوصف
DOI:10.3389/fimmu.2024.1387253