Literature DB >> 31486704

LOTTE-seq (Long hairpin oligonucleotide based tRNA high-throughput sequencing): specific selection of tRNAs with 3'-CCA end for high-throughput sequencing.

Lieselotte Erber1, Anne Hoffmann2, Jörg Fallmann2, Heike Betat1, Peter F Stadler2,3,4,5,6,7, Mario Mörl1.   

Abstract

Transfer RNAs belong to the most abundant type of ribonucleic acid in the cell, and detailed investigations revealed correlations between alterations in the tRNA pool composition and certain diseases like breast cancer. However, currently available methods do not sample the entire tRNA pool or lack specificity for tRNAs. A specific disadvantage of such methods is that only full-length tRNAs are analysed, while tRNA fragments or incomplete cDNAs due to RT stops at modified nucleosides are lost. Another drawback in certain approaches is that the tRNA fraction has to be isolated and separated from high molecular weight RNA, resulting in considerable labour costs and loss of material. Based on a hairpin-shaped adapter oligonucleotide selective for tRNA transcripts, we developed a highly specific protocol for efficient and comprehensive high-throughput analysis of tRNAs that combines the benefits of existing methods and eliminates their disadvantages. Due to a 3'-TGG overhang, the adapter is specifically ligated to the tRNA 3'-CCA end. Reverse transcription prior to the ligation of a second adapter allows to include prematurely terminated cDNA products, increasing the number of tRNA reads. This strategy renders this approach a powerful and universal tool to analyse the tRNA pool of cells and organisms under different conditions in health and disease.

Entities:  

Keywords:  CCA end; LOTTE-seq; high-throughput sequencing of tRNA; mature tRNA; tRNA adapter ligation; tRNA pool; tRNA-seq

Mesh:

Substances:

Year:  2019        PMID: 31486704      PMCID: PMC6948972          DOI: 10.1080/15476286.2019.1664250

Source DB:  PubMed          Journal:  RNA Biol        ISSN: 1547-6286            Impact factor:   4.652


  81 in total

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Journal:  Annu Rev Genet       Date:  2011-09-06       Impact factor: 16.830

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8.  YAMAT-seq: an efficient method for high-throughput sequencing of mature transfer RNAs.

Authors:  Megumi Shigematsu; Shozo Honda; Phillipe Loher; Aristeidis G Telonis; Isidore Rigoutsos; Yohei Kirino
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Review 9.  Modifications and functional genomics of human transfer RNA.

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Journal:  Cell Res       Date:  2018-02-20       Impact factor: 25.617

10.  Global analysis of tRNA and translation factor expression reveals a dynamic landscape of translational regulation in human cancers.

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Journal:  Commun Biol       Date:  2018-12-21
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4.  Unusual Occurrence of Two Bona-Fide CCA-Adding Enzymes in Dictyostelium discoideum.

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5.  Non-Redundant tRNA Reference Sequences for Deep Sequencing Analysis of tRNA Abundance and Epitranscriptomic RNA Modifications.

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6.  cyPhyRNA-seq: a genome-scale RNA-seq method to detect active self-cleaving ribozymes by capturing RNAs with 2',3' cyclic phosphates and 5' hydroxyl ends.

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7.  Mitochondrial Genomes in Perkinsus Decode Conserved Frameshifts in All Genes.

Authors:  Sebastian G Gornik; Victor Flores; Franziska Reinhardt; Lieselotte Erber; Dayana E Salas-Leiva; Olga Douvropoulou; Imen Lassadi; Elin Einarsson; Mario Mörl; Anna Git; Peter F Stadler; Arnab Pain; Ross F Waller
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8.  Changes of the tRNA Modification Pattern during the Development of Dictyostelium discoideum.

Authors:  Anne Hoffmann; Lieselotte Erber; Heike Betat; Peter F Stadler; Mario Mörl; Jörg Fallmann
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  8 in total

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