Literature DB >> 10454627

Identification of differentially expressed 5'-end mRNA variants by an improved RACE technique (PEETA).

G Flouriot1, H Brand, F Gannon.   

Abstract

A rapid and efficient procedure is described for mapping and cloning the 5'-ends of mRNAs, including those generated from a unique gene by alternative splicing and promoter usage. This method involves reverse transcription of the targeted mRNAs from a long, highly labeled specific primer, resolution of the extension products on a DNA sequencing gel, elution and poly(dC) tailing of the single-stranded cDNAs of interest, amplification of these cDNAs by PCR using an oligo(dG) adapter-primer and a gene-specific primer and finally DNA sequencing of the subcloned PCR fragments. The overall method is called PEETA (primer extension, electrophoresis, elution, tailing and amplification).

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Year:  1999        PMID: 10454627      PMCID: PMC148519          DOI: 10.1093/nar/27.15.e8

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  8 in total

1.  cDNA cloning of 5' terminal regions.

Authors:  P Towner; W Gärtner
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

2.  Ligation-anchored PCR: a simple amplification technique with single-sided specificity.

Authors:  A B Troutt; M G McHeyzer-Williams; B Pulendran; G J Nossal
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

3.  Differentially expressed messenger RNA isoforms of the human estrogen receptor-alpha gene are generated by alternative splicing and promoter usage.

Authors:  G Flouriot; C Griffin; M Kenealy; V Sonntag-Buck; F Gannon
Journal:  Mol Endocrinol       Date:  1998-12

4.  Improved efficiency for primer extension by using a long, highly-labeled primer generated from immobilized single-stranded DNA templates.

Authors:  G Flouriot; C Pope; M R Kenealy; F Gannon
Journal:  Nucleic Acids Res       Date:  1997-04-15       Impact factor: 16.971

5.  Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer.

Authors:  M A Frohman; M K Dush; G R Martin
Journal:  Proc Natl Acad Sci U S A       Date:  1988-12       Impact factor: 11.205

6.  Polymerase chain reaction with single-sided specificity: analysis of T cell receptor delta chain.

Authors:  E Y Loh; J F Elliott; S Cwirla; L L Lanier; M M Davis
Journal:  Science       Date:  1989-01-13       Impact factor: 47.728

7.  One-sided polymerase chain reaction: the amplification of cDNA.

Authors:  O Ohara; R L Dorit; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

8.  Mapping the 5' and 3' ends of Tetrahymena thermophila mRNAs using RNA ligase mediated amplification of cDNA ends (RLM-RACE).

Authors:  X Liu; M A Gorovsky
Journal:  Nucleic Acids Res       Date:  1993-10-25       Impact factor: 16.971

  8 in total

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