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

Genome Biol. 2016 Oct 24;17(1):219. doi: 10.1186/s13059-016-1079-9.

Abstract

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.

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

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing / genetics
  • Alternative Splicing / immunology
  • Animals
  • Autoantigens / genetics
  • Autoantigens / immunology
  • Cell Differentiation / immunology
  • Epithelial Cells / immunology*
  • Gene Expression Regulation / immunology
  • Humans
  • Mice
  • RNA Editing / genetics*
  • RNA Editing / immunology
  • Self Tolerance / immunology
  • T-Lymphocytes / immunology
  • Thymus Gland / immunology*
  • Transcription Factors / genetics

Substances

  • Autoantigens
  • Transcription Factors