4.5 Article

Extensive RNA editing and splicing increase immune self-representation diversity in medullary thymic epithelial cells

Journal

GENOME BIOLOGY
Volume 17, Issue -, Pages -

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/s13059-016-1079-9

Keywords

Medullary thymic epithelial cells (mTECs); Thymus; Alternative splicing; RNA editing; RNA sequencing; Self-tolerance

Funding

  1. European Research Council [311257]
  2. I-CORE Program of the Planning and Budgeting Committee in Israel [41/11, 1796/12]
  3. Israel Science Foundation [1380/14, 1825/10]
  4. Sy Syms Foundation
  5. Dr. Celia Zwillenberg-Fridman and Dr. Lutz Fridman Career Development Chair
  6. Agence Nationale de Recherche [2011-CHEX-001-R12004KK]
  7. Azrieli Foundation

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Background: In order to become functionally competent but harmless mediators of the immune system, T cells undergo a strict educational program in the thymus, where they learn to discriminate between self and non-self. This educational program is, to a large extent, mediated by medullary thymic epithelial cells that have a unique capacity to express, and subsequently present, a large fraction of body antigens. While the scope of promiscuously expressed genes by medullary thymic epithelial cells is well-established, relatively little is known about the expression of variants that are generated by co-transcriptional and post-transcriptional processes. Results: Our study reveals that in comparison to other cell types, medullary thymic epithelial cells display significantly higher levels of alternative splicing, as well as A-to-I and C-to-U RNA editing, which thereby further expand the diversity of their self-antigen repertoire. Interestingly, Aire, the key mediator of promiscuous gene expression in these cells, plays a limited role in the regulation of these transcriptional processes. Conclusions: Our results highlight RNA processing as another layer by which the immune system assures a comprehensive self-representation in the thymus which is required for the establishment of self-tolerance and prevention of autoimmunity.

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