<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>24(3)</volume><submitter>Sakurai M</submitter><pubmed_abstract>Inosine is an abundant RNA modification in the human transcriptome and is essential for many biological processes in modulating gene expression at the post-transcriptional level. Adenosine deaminases acting on RNA (ADARs) catalyze the hydrolytic deamination of adenosines to inosines (A-to-I editing) in double-stranded regions. We previously established a biochemical method called "inosine chemical erasing" (ICE) to directly identify inosines on RNA strands with high reliability. Here, we have applied the ICE method combined with deep sequencing (ICE-seq) to conduct an unbiased genome-wide screening of A-to-I editing sites in the transcriptome of human adult brain. Taken together with the sites identified by the conventional ICE method, we mapped 19,791 novel sites and newly found 1258 edit</pubmed_abstract><journal>Genome research</journal><pagination>522-34</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3941116</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A biochemical landscape of A-to-I RNA editing in the human brain transcriptome.</pubmed_title><pmcid>PMC3941116</pmcid><pubmed_authors>Fujiyama A</pubmed_authors><pubmed_authors>Suzuki T</pubmed_authors><pubmed_authors>Yano T</pubmed_authors><pubmed_authors>Toyoda A</pubmed_authors><pubmed_authors>Mitsuyama T</pubmed_authors><pubmed_authors>Kawabata H</pubmed_authors><pubmed_authors>Sakurai M</pubmed_authors><pubmed_authors>Terajima H</pubmed_authors><pubmed_authors>Okada S</pubmed_authors><pubmed_authors>Ueda H</pubmed_authors></additional><is_claimable>false</is_claimable><name>A biochemical landscape of A-to-I RNA editing in the human brain transcriptome.</name><description>Inosine is an abundant RNA modification in the human transcriptome and is essential for many biological processes in modulating gene expression at the post-transcriptional level. Adenosine deaminases acting on RNA (ADARs) catalyze the hydrolytic deamination of adenosines to inosines (A-to-I editing) in double-stranded regions. We previously established a biochemical method called "inosine chemical erasing" (ICE) to directly identify inosines on RNA strands with high reliability. Here, we have applied the ICE method combined with deep sequencing (ICE-seq) to conduct an unbiased genome-wide screening of A-to-I editing sites in the transcriptome of human adult brain. Taken together with the sites identified by the conventional ICE method, we mapped 19,791 novel sites and newly found 1258 edit</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Mar</publication><modification>2026-04-29T21:02:10.499Z</modification><creation>2019-03-27T01:22:42Z</creation></dates><accession>S-EPMC3941116</accession><cross_references><pubmed>24407955</pubmed><doi>10.1101/gr.162537.113</doi></cross_references></HashMap>