Overview of Post Cohen‐Boyer Methods for Single Segment Cloning and for Multisegment DNA Assembly

Bryan Sands1, Roger Brent1

1 Fred Hutchinson Cancer Research Center, Seattle, Washington
Publication Name:  Current Protocols in Molecular Biology
Unit Number:  Unit 3.26
DOI:  10.1002/0471142727.mb0326s113
Online Posting Date:  January, 2016
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In 1973, Cohen and coworkers published a foundational paper describing the cloning of DNA fragments into plasmid vectors. In it, they used DNA segments made by digestion with restriction enzymes and joined these in vitro with DNA ligase. These methods established working recombinant DNA technology and enabled the immediate start of the biotechnology industry. Since then, “classical” recombinant DNA technology using restriction enzymes and DNA ligase has matured. At the same time, researchers have developed numerous ways to generate large, complex, multisegment DNA constructions that offer advantages over classical techniques. Here, we provide an overview of “post‐Cohen‐Boyer” techniques used for cloning single segments into vectors (T/A, Topo cloning, Gateway and Recombineering) and for multisegment DNA assembly (BioBricks, Golden Gate, Gibson, yeast homologous recombination in vivo, and ligase cycling reaction). We compare and contrast these methods and also discuss issues that researchers should consider before choosing a particular multisegment DNA assembly method. © 2016 by John Wiley & Sons, Inc.

Keywords: DNA cloning; multisegment DNA assembly; biotechnology; molecular biology; plasmid construction

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Table of Contents

  • Introduction
  • Means to Generate Single‐Segment‐into‐Vector Constructions
  • Means to Assemble Complex, Multisegment Constructions
  • Conclusion
  • Future Outlook
  • Literature Cited
  • Figures
  • Tables
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Literature Cited

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