Literature DB >> 24034325

Circularized RT-PCR (cRT-PCR): analysis of the 5' ends, 3' ends, and poly(A) tails of RNA.

Shimyn Slomovic1, Gadi Schuster.   

Abstract

Many techniques that are used to characterize individual RNA molecules can potentially alter the original transcript sequence or its posttranscriptional modifications, such as polyadenylation. Methods that are designed to define the ends of an RNA molecule, for example, oligonucleotide ligation, avoid altering the transcript sequence but can usually fulfill only one objective per experiment (e.g., define the 5' or the 3' end). In contrast, not only does circularized reverse transcription coupled with PCR (cRT-PCR) preserve the original 5' and 3' ends of the transcript and posttranscriptionally added extensions, but also the material from one experimental procedure can be utilized in order to characterize both the 5' and 3' ends. Furthermore, if suitable oligonucleotide primers are designed, cRT-PCR can be used to isolate truncated, adenylated (and nonadenylated) molecules that are intermediates in RNA decay (Slomovic and Schuster, 2008).
© 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Circularized RT-PCR (cRT-PCR); Electroporate and plate bacteria; Gel purification; Gene-specific reverse primer; PCR products; Plasmid DNA isolation and sequencing; RNA purification

Mesh:

Substances:

Year:  2013        PMID: 24034325     DOI: 10.1016/B978-0-12-420037-1.00013-0

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


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