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Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity

Title: Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity
Authors: Hrdlickova, Barbara; Kumar, Vinod; Kanduri, Kartiek; Zhernakova, Daria V.; Tripathi, Subhash; Karjalainen, Juha; Lund, Riikka J.; Li, Yang; Ullah, Ubaid; Modderman, Rutger; Abdulahad, Wayel; Lahdesmaki, Harri; Franke, Lude; Lahesmaa, Riitta; Wijmenga, Cisca; Withoff, Sebo
Source: Hrdlickova, B, Kumar, V, Kanduri, K, Zhernakova, D V, Tripathi, S, Karjalainen, J, Lund, R J, Li, Y, Ullah, U, Modderman, R, Abdulahad, W, Lahdesmaki, H, Franke, L, Lahesmaa, R, Wijmenga, C & Withoff, S 2014, 'Expression profiles of long non-coding RNAs located in autoimmune disease-associated regions reveal immune cell-type specificity', Genome medicine, vol. 6, no. 10, 88. https://doi.org/10.1186/s13073-014-0088-0
Publication Year: 2014
Collection: University of Groningen research database
Subject Terms: SUSCEPTIBILITY LOCI; RHEUMATOID-ARTHRITIS; GENETIC-VARIATION; SHARED GENETICS; CELIAC-DISEASE; RISK LOCI; TH1 CELLS; TGF-BETA; IDENTIFICATION; CANCER
Description: Background: Although genome-wide association studies (GWAS) have identified hundreds of variants associated with a risk for autoimmune and immune-related disorders (AID), our understanding of the disease mechanisms is still limited. In particular, more than 90% of the risk variants lie in non-coding regions, and almost 10% of these map to long non-coding RNA transcripts (lncRNAs). lncRNAs are known to show more cell-type specificity than protein-coding genes. Methods: We aimed to characterize lncRNAs and protein-coding genes located in loci associated with nine AIDs which have been well-defined by Immunochip analysis and by transcriptome analysis across seven populations of peripheral blood leukocytes (granulocytes, monocytes, natural killer (NK) cells, B cells, memory T cells, naive CD4(+) and naive CD8(+) T cells) and four populations of cord blood-derived T-helper cells (precursor, primary, and polarized (Th1, Th2) T-helper cells). Results: We show that lncRNAs mapping to loci shared between AID are significantly enriched in immune cell types compared to lncRNAs from the whole genome (a
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
ISSN: 1756-994X
Relation: info:eu-repo/semantics/altIdentifier/pmid/25419237; info:eu-repo/semantics/altIdentifier/wos/000345714400001; info:eu-repo/semantics/altIdentifier/hdl/https://hdl.handle.net/11370/ca051e99-5085-4ce1-9b8d-7047850021fe; info:eu-repo/semantics/altIdentifier/pissn/1756-994X
DOI: 10.1186/s13073-014-0088-0
Availability: https://hdl.handle.net/11370/ca051e99-5085-4ce1-9b8d-7047850021fe; https://research.rug.nl/en/publications/ca051e99-5085-4ce1-9b8d-7047850021fe; https://doi.org/10.1186/s13073-014-0088-0; https://pure.rug.nl/ws/files/43846463/Expression_profiles_of_long_non_coding_RNAs_located_in_autoimmune.pdf
Rights: info:eu-repo/semantics/openAccess ; http://creativecommons.org/licenses/by/4.0/
Accession Number: edsbas.948FD15B
Database: BASE