| Literature DB >> 25833336 |
Shozo Honda1, Megumi Shigematsu, Keisuke Morichika, Aristeidis G Telonis, Yohei Kirino.
Abstract
Transfer RNAs (tRNAs) play a central role in translation and also recently appear to have a variety of other functions in biological processes beyond translation. Here we report the development of Four-Leaf clover qRT-PCR (FL-PCR), a convenient PCR-based method, which can specifically quantify individual mature tRNA species. In FL-PCR, T4 RNA ligase 2 specifically ligates a stem-loop adapter to mature tRNAs but not to precursor tRNAs or tRNA fragments. Subsequent TaqMan qRT-PCR amplifies only unmodified regions of the tRNA-adapter ligation products; therefore, FL-PCR quantification is not influenced by tRNA post-transcriptional modifications. FL-PCR has broad applicability for the quantification of various tRNAs in different cell types, and thus provides a much-needed simple method for analyzing tRNA abundance and heterogeneity.Keywords: FL-PCR; RNA; T4 RNA Ligase 2; TaqMan PCR; tRNA; tRNA abundance; tRNA heterogeneity
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Year: 2015 PMID: 25833336 PMCID: PMC4615770 DOI: 10.1080/15476286.2015.1031951
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652