The landscape of the A-to-I RNA editome from 462 human genomes

Sci Rep. 2018 Aug 13;8(1):12069. doi: 10.1038/s41598-018-30583-7.

Abstract

A-to-I editing, as a post-transcriptional modification process mediated by ADAR, plays a crucial role in many biological processes in metazoans. However, how and to what extent A-to-I editing diversifies and shapes population diversity at the RNA level are largely unknown. Here, we used 462 mRNA-sequencing samples from five populations of the Geuvadis Project and identified 16,518 A-to-I editing sites, with false detection rate of 1.03%. These sites form the landscape of the RNA editome of the human genome. By exploring RNA editing within and between populations, we revealed the geographic restriction of rare editing sites and population-specific patterns of edQTL editing sites. Moreover, we showed that RNA editing can be used to characterize the subtle but substantial diversity between different populations, especially those from different continents. Taken together, our results demonstrated that the nature and structure of populations at the RNA level are illustrated well by RNA editing, which provides insights into the process of how A-to-I editing shapes population diversity at the transcriptomic level. Our work will facilitate the understanding of the landscape of the RNA editome at the population scale and will be helpful for interpreting differences in the distribution and prevalence of disease among individuals and across populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine / metabolism
  • Adenosine Deaminase / metabolism
  • Computational Biology
  • Databases, Genetic
  • Deamination / genetics
  • Genetics, Population*
  • Genome, Human / genetics*
  • Humans
  • Inosine / metabolism
  • Quantitative Trait Loci / genetics
  • RNA Editing / genetics*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / metabolism
  • Transcriptome / genetics*

Substances

  • RNA, Messenger
  • RNA-Binding Proteins
  • Inosine
  • Adenosine Deaminase
  • Adenosine