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Direct cDNA Sequencing Using Sequential Linear/Asymmetric Polymerase Chain Reaction

  • Ivor J. Mason
Protocol
  • 86 Downloads
Part of the Springer Protocols Handbooks book series (SPH)

Abstract

Following the isolation of a clonal recombinant phage or plasmid after screening a cDNA library, the first analyses that are routinely performed are the determination of the insert size and the sequence of the 3′- and 5′-ends of the cloned fragment. Prior to the use of polymerase chain reaction (PCR), this was a laborious process, especially when the cDNA library had been constructed using a vector derivative of bacteriophage λ. I recently described a PCR-based protocol that rapidly generated this information from single-phage plaques and, additionally, produced material suitable for subcloning into plasmid vectors (1). The procedure, which is outlined in Fig. 1, involves an initial PCR reaction using an oligonucleotide primer pair which flank the cDNA insertion site to produce sufficient quantities of double-stranded DNA for sequencing. An aliquot of this reaction is then subjected to further PCR, but with only one of the primers. Any residual second primer is rapidly depleted during this second reaction and large quantities of single-stranded DNA are generated. This material is then used as a template for sequencing using the second oligonucleotide to prime the reaction.

Keywords

Polymerase Chain Reaction Reaction Microfuge Tube Oligonucleotide Prime Pair Asymmetric Polymerase Chain Reaction SeaPlaque Agarose 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. 1.
    Mason, I. J. (1992) Rapid and direct sequencing of DNA from bacteriophage plaques using sequential linear and asymmetric PCR. BioTechniques 12, 60–61.PubMedGoogle Scholar
  2. 2.
    Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.Google Scholar

Copyright information

© Humana Press Inc., Totowa, NJ 2000

Authors and Affiliations

  • Ivor J. Mason
    • 1
  1. 1.Department of Developmental NeurobiologyKing’s College London, Guy’s Hospital CampusLondonUK

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