Literature DB >> 25833336

Four-leaf clover qRT-PCR: A convenient method for selective quantification of mature tRNA.

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

Mesh:

Substances:

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


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