4.6 Article

The Landscape of Novel Expressed Chimeric RNAs in Rheumatoid Arthritis

Journal

CELLS
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/cells11071092

Keywords

autoimmunity; chimeric RNA; fusion gene; rheumatoid arthritis

Categories

Funding

  1. Israeli Council for Higher Education through the PBC fellowship program for outstanding postdoctoral researchers from China and India
  2. Israel Innovation Authority (Kamin grant) [66824]
  3. COVID-19 Data Science Institute (DSI) grant from Bar-Ilan University [247017]

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This study demonstrates the presence of highly expressed and functional novel chimeric RNAs in rheumatoid arthritis (RA), which is significant for understanding the pathogenesis of RA and providing better treatment strategies and tailored therapies.
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.

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