PeerJ (Mar 2018)

Global analysis of A-to-I RNA editing reveals association with common disease variants

  • Oscar Franzén,
  • Raili Ermel,
  • Katyayani Sukhavasi,
  • Rajeev Jain,
  • Anamika Jain,
  • Christer Betsholtz,
  • Chiara Giannarelli,
  • Jason C. Kovacic,
  • Arno Ruusalepp,
  • Josefin Skogsberg,
  • Ke Hao,
  • Eric E. Schadt,
  • Johan L.M. Björkegren

DOI
https://doi.org/10.7717/peerj.4466
Journal volume & issue
Vol. 6
p. e4466

Abstract

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RNA editing modifies transcripts and may alter their regulation or function. In humans, the most common modification is adenosine to inosine (A-to-I). We examined the global characteristics of RNA editing in 4,301 human tissue samples. More than 1.6 million A-to-I edits were identified in 62% of all protein-coding transcripts. mRNA recoding was extremely rare; only 11 novel recoding sites were uncovered. Thirty single nucleotide polymorphisms from genome-wide association studies were associated with RNA editing; one that influences type 2 diabetes (rs2028299) was associated with editing in ARPIN. Twenty-five genes, including LRP11 and PLIN5, had editing sites that were associated with plasma lipid levels. Our findings provide new insights into the genetic regulation of RNA editing and establish a rich catalogue for further exploration of this process.

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