The Landscape of Novel Expressed Chimeric RNAs in Rheumatoid Arthritis

• Published in: Cells (Basel, Switzerland) Vol. 11; no. 7; p. 1092
• Main Authors: Detroja, Rajesh, Mukherjee, Sumit, Frenkel-Morgenstern, Milana
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 24.03.2022; MDPI
• Subjects: Adaptive immunity; Arthritis, Rheumatoid; autoimmunity; Biopsy; Cancer therapies; Cell activation; chimeric RNA; Classification; fusion gene; Gene expression; Humans; Immune response; Inflammation; Inflammation - metabolism; Lymphocytes B; Pathogenesis; Patients; Proteins; Quality control; Rheumatoid arthritis; RNA - metabolism; Synovial Membrane - metabolism; Synovium; autoimmunity; fusion gene; rheumatoid arthritis; chimeric RNA
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells11071092

In cancers and other complex diseases, the fusion of two genes can lead to the production of chimeric RNAs, which are associated with disease development. Several recurrent chimeric RNAs are expressed in different cancers and are thus used for clinical cancer diagnosis. Rheumatoid arthritis (RA) is an immune-mediated joint disorder resulting in synovial inflammation and joint destruction. Despite advances in therapy, many patients do not respond to treatment and present persistent inflammation. Understanding the landscape of chimeric RNA expression in RA patients could provide a better insight into RA pathogenesis, which might provide better treatment strategies and tailored therapies. Accordingly, we analyzed the publicly available RNA-seq data of synovium tissue from 151 RA patients and 28 healthy controls and were able to identify 37 recurrent chimeric RNAs found to be expressed in at least 3 RA samples. Furthermore, the parental genes of these 37 recurrent chimeric RNAs were found to be differentially expressed and enriched in immune-related processes, such as adaptive immune response and the positive regulation of B-cell activation. Interestingly, the appearance of 5 coding and 23 non-coding chimeric RNAs might be associated with regulating their parental gene expression, leading to the generation of dysfunctional immune responses, such as inflammation and bone destruction. Therefore, in this paper, we present the first study to demonstrate the novel chimeric RNAs that are highly expressed and functional in RA.