Predicting sites of ADAR editing in double-stranded RNA View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2011-09

AUTHORS

Julie M. Eggington, Tom Greene, Brenda L. Bass

ABSTRACT

ADAR (adenosine deaminase that acts on RNA) editing enzymes target coding and noncoding double-stranded RNA (dsRNA) and are essential for neuronal function. Early studies showed that ADARs preferentially target adenosines with certain 5' and 3' neighbours. Here we use current Sanger sequencing protocols to perform a more accurate and quantitative analysis. We quantified editing sites in an ∼800-bp dsRNA after reaction with human ADAR1 or ADAR2, or their catalytic domains alone. These large data sets revealed that neighbour preferences are mostly dictated by the catalytic domain, but ADAR2's dsRNA-binding motifs contribute to 3' neighbour preferences. For all proteins, the 5' nearest neighbour was most influential, but adjacent bases also affected editing site choice. We developed algorithms to predict editing sites in dsRNA of any sequence, and provide a web-based application. The predictive power of the algorithm on fully base-paired dsRNA, compared with biological substrates containing mismatches, bulges and loops, elucidates structural contributions to editing specificity. More... »

PAGES

319

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ncomms1324

DOI

http://dx.doi.org/10.1038/ncomms1324

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1002794403

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/21587236


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