TY - JOUR
T1 - Systematic identification of abundant A-to-I editing sites in the human transcriptome
AU - Levanon, Erez Y.
AU - Eisenberg, Eli
AU - Yelin, Rodrigo
AU - Nemzer, Sergey
AU - Hallegger, Martina
AU - Shemesh, Ronen
AU - Fligelman, Zipora Y.
AU - Shoshan, Avi
AU - Pollock, Sarah R.
AU - Sztybel, Dan
AU - Olshansky, Moshe
AU - Rechavi, Gideon
AU - Jantsch, Michael F.
N1 - Funding Information:
We thank A. Diber, E. Shuster and S. Zevin for technical help and P. Akiva, A. Amit and R. Sorek for critical reading of the manuscript. The work of E.Y.L. was done in partial fulfillment of the requirements for a PhD degree from the Sackler Faculty of Medicine, Tel Aviv University, Israel. Part of this work was supported by the Austrian Science Foundation grant SFB1706 to M.J.
PY - 2004/8
Y1 - 2004/8
N2 - RNA editing by members of the ADAR (adenosine deaminases acting on RNA) family leads to site-specific conversion of adenosine to inosine (A-to-I) in precursor messenger RNAs. Editing by ADARs is believed to occur in all metazoa, and is essential for mammalian development. Currently, only a limited number of human ADAR substrates are known, whereas indirect evidence suggests a substantial fraction of all pre-mRNAs being affected. Here we describe a computational search for ADAR editing sites in the human transcriptome, using millions of available expressed sequences. We mapped 12,723 A-to-I editing sites in 1,637 different genes, with an estimated accuracy of 95%, raising the number of known editing sites by two orders of magnitude. We experimentally validated our method by verifying the occurrence of editing in 26 novel substrates. A-to-I editing in humans primarily occurs in noncoding regions of the RNA, typically in Alu repeats. Analysis of the large set of editing sites indicates the role of editing in controlling dsRNA stability.
AB - RNA editing by members of the ADAR (adenosine deaminases acting on RNA) family leads to site-specific conversion of adenosine to inosine (A-to-I) in precursor messenger RNAs. Editing by ADARs is believed to occur in all metazoa, and is essential for mammalian development. Currently, only a limited number of human ADAR substrates are known, whereas indirect evidence suggests a substantial fraction of all pre-mRNAs being affected. Here we describe a computational search for ADAR editing sites in the human transcriptome, using millions of available expressed sequences. We mapped 12,723 A-to-I editing sites in 1,637 different genes, with an estimated accuracy of 95%, raising the number of known editing sites by two orders of magnitude. We experimentally validated our method by verifying the occurrence of editing in 26 novel substrates. A-to-I editing in humans primarily occurs in noncoding regions of the RNA, typically in Alu repeats. Analysis of the large set of editing sites indicates the role of editing in controlling dsRNA stability.
UR - http://www.scopus.com/inward/record.url?scp=3543004084&partnerID=8YFLogxK
U2 - 10.1038/nbt996
DO - 10.1038/nbt996
M3 - מאמר
AN - SCOPUS:3543004084
VL - 22
SP - 1001
EP - 1005
JO - Nature Biotechnology
JF - Nature Biotechnology
SN - 1087-0156
IS - 8
ER -