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

Franzen, Oscar (author)
Ermel, Raili (author)
Sukhavasi, Katyayani (author)
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Jain, Rajeev (author)
Jain, Anamika (author)
Betsholtz, Christer (author)
Giannarelli, Chiara (author)
Kovacic, Jason C. (author)
Ruusalepp, Arno (author)
Skogsberg, Josefin (author)
Hao, Ke (author)
Schadt, Eric E. (author)
Bjoerkegren, Johan L. M. (author)
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 (publisher)
2018
2018
English.
In: PeerJ. - 2167-8359. ; 6
  • swepub:Mat__t
Abstract Subject headings
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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.

Subject headings

Medical and Health Sciences  (hsv)
Basic Medicine  (hsv)
Cell and Molecular Biology  (hsv)
Medicin och hälsovetenskap  (hsv)
Medicinska och farmaceutiska grundvetenskaper  (hsv)
Cell- och molekylärbiologi  (hsv)

Keyword

RNA editing
Gene expression
Quantitative trait loci
RNA-seq
Bioinformatics
Biostatistics

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