Identification of RNA editing sites in the SNP database

被引:41
作者
Eisenberg, E
Adamsky, K
Cohen, L
Amariglio, N
Hirshberg, A
Rechavi, G
Levanon, EY [1 ]
机构
[1] Safra Childrens Hosp, Sheba Med Ctr, Dept Pediat Hematooncol, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Raymond & Beverly Sackler Fac Exact Sci, Sch Phys & Astron, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Sackler Sch Med, IL-69978 Tel Aviv, Israel
[4] Tel Aviv Univ, Sch Dent Med, Dept Oral Pathol, IL-69978 Tel Aviv, Israel
[5] Compugen Ltd, IL-69512 Tel Aviv, Israel
关键词
D O I
10.1093/nar/gki771
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relationship between human inherited genomic variations and phenotypic differences has been the focus of much research effort in recent years. These studies benefit from millions of single-nucleotide polymorphism (SNP) records available in public databases, such as dbSNP. The importance of identifying false dbSNP records increases with the growing role played by SNPs in linkage analysis for disease traits. In particular, the emerging understanding of the abundance of DNA and RNA editing calls for a careful distinction between inherited SNPs and somatic DNA and RNA modifications. In order to demonstrate that some of the SNP database records are actually somatic modification, we focus on one type of these modifications, namely A-to-I RNA editing, and present evidence for hundreds of dbSNP records that are actually editing sites. We provide a list of 102 RNA editing sites previously annotated in dbSNP database as SNPs, and experimentally validate seven of these. Interestingly, we show how dbSNP can serve as a starting point to look for new editing sites. Our results, for this particular type of RNA editing, demonstrate the need for a careful analysis of SNP databases in light of the increasing recognition of the significance of somatic sequence modifications.
引用
收藏
页码:4612 / 4617
页数:6
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