Literature DB >> 10631680

High temperature cDNA synthesis by AMV reverse transcriptase improves the specificity of PCR.

B Fuchs1, K Zhang, M G Rock, M E Bolander, G Sarkar.   

Abstract

The enzyme avian myeloblastosis virus reverse transcriptase (AMV-RT) is routinely used for cDNA synthesis, which is generally carried out at temperatures between 37 degrees C and 42 degrees C. We show that this enzyme can support cDNA synthesis, at temperatures as high as 70 degrees C. We have utilized this property of the AMV-RT to improve the specificity of polymerase chain reaction (PCR). Furthermore, this apparently thermophilic property of the enzyme, which is an important constituent of a mesophilic organism, raises intriguing questions regarding evolution of the enzyme structure.

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Year:  1999        PMID: 10631680     DOI: 10.1385/MB:12:3:237

Source DB:  PubMed          Journal:  Mol Biotechnol        ISSN: 1073-6085            Impact factor:   2.695


  9 in total

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2.  Effect of dimethyl sulfoxide concentration on specificity of primer matching in PCR.

Authors:  S A Filichkin; S B Gelvin
Journal:  Biotechniques       Date:  1992-06       Impact factor: 1.993

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Authors:  A Sanyal; S W O'Driscoll; J S Fitzsimmons; M E Bolander; G Sarkar
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4.  PIG-B: a homemade monophasic cocktail for the extraction of RNA.

Authors:  K Weber; M E Bolander; G Sarkar
Journal:  Mol Biotechnol       Date:  1998-02       Impact factor: 2.695

5.  Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

Authors:  K B Mullis; F A Faloona
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

6.  Two-step "hot" PCR amplification of GC-rich avian c-myc sequences.

Authors:  M Schuchard; G Sarkar; T Ruesink; T C Spelsberg
Journal:  Biotechniques       Date:  1993-03       Impact factor: 1.993

7.  Development and characterization of a conditionally immortalized human fetal osteoblastic cell line.

Authors:  S A Harris; R J Enger; B L Riggs; T C Spelsberg
Journal:  J Bone Miner Res       Date:  1995-02       Impact factor: 6.741

8.  Capacity of nine thermostable DNA polymerases To mediate DNA amplification in the presence of PCR-inhibiting samples.

Authors:  W Abu Al-Soud; P Râdström
Journal:  Appl Environ Microbiol       Date:  1998-10       Impact factor: 4.792

9.  High-temperature, nonradioactive primer extension assay for determination of a transcription-initiation site.

Authors:  M Yamada; H Izu; T Nitta; K Kurihara; T Sakurai
Journal:  Biotechniques       Date:  1998-07       Impact factor: 1.993

  9 in total
  9 in total

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2.  A group II intron-type open reading frame from the thermophile Bacillus (Geobacillus) stearothermophilus encodes a heat-stable reverse transcriptase.

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4.  The role of template-primer in protection of reverse transcriptase from thermal inactivation.

Authors:  Gary F Gerard; R Jason Potter; Michael D Smith; Kim Rosenthal; Gulshan Dhariwal; Jun Lee; Deb K Chatterjee
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5.  Real-time sequence-validated loop-mediated isothermal amplification assays for detection of Middle East respiratory syndrome coronavirus (MERS-CoV).

Authors:  Sanchita Bhadra; Yu Sherry Jiang; Mia R Kumar; Reed F Johnson; Lisa E Hensley; Andrew D Ellington
Journal:  PLoS One       Date:  2015-04-09       Impact factor: 3.240

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Journal:  Sci Rep       Date:  2017-08-21       Impact factor: 4.379

Review 7.  Advances in real-time PCR: application to clinical laboratory diagnostics.

Authors:  Bernhard Kaltenboeck; Chengming Wang
Journal:  Adv Clin Chem       Date:  2005       Impact factor: 5.394

8.  Selective control of primer usage in multiplex one-step reverse transcription PCR.

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Journal:  BMC Mol Biol       Date:  2009-12-30       Impact factor: 2.946

9.  RTL-P: a sensitive approach for detecting sites of 2'-O-methylation in RNA molecules.

Authors:  Zhi-Wei Dong; Peng Shao; Li-Ting Diao; Hui Zhou; Chun-Hong Yu; Liang-Hu Qu
Journal:  Nucleic Acids Res       Date:  2012-07-24       Impact factor: 16.971

  9 in total

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