Cre‐loxP‐Mediated Recombination: General Principles and Experimental Considerations

Micheal A. McLellan1, Nadia A. Rosenthal2, Alexander R. Pinto3

1 Graduate Program in Genetics, Sackler School of Graduate Biomedical Sciences, Tufts University, Boston, Massachusetts, 2 National Heart and Lung Institute, Imperial College London, London, 3 Australian Regenerative Medicine Institute, Monash University, Melbourne, Victoria
Publication Name:  Current Protocols in Mouse Biology
Unit Number:   
DOI:  10.1002/cpmo.22
Online Posting Date:  March, 2017
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Abstract

The cre‐loxP–mediated recombination system (the “cre‐loxP system”) is an integral experimental tool for mammalian genetics and cell biology. Use of the system has greatly expanded our ability to precisely interrogate gene function in the mouse, providing both spatial and temporal control of gene expression. This has been largely due to the simplicity of its use and its adaptability to address diverse biological questions. While the use of the cre‐loxP system is becoming increasingly widespread, in particular because of growing availability of conditional mouse mutants, many considerations need to be taken into account when utilizing the cre‐loxP system. This review provides an overview of the cre‐loxP system and its various permutations. It addresses the limitations of cre‐loxP technology and related considerations for experimental design, and it discusses alternative strategies for site‐specific genetic recombination and integration. © 2017 by John Wiley & Sons, Inc.

Keywords: cre; loxP; cre‐loxP; gene editing; recombination; site directed mutagenesis; conditional genetics

     
 
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Table of Contents

  • Introduction
  • Operation of the cre‐loxP System
  • Inducible cre Models
  • Limitations of the cre‐loxP System
  • Site‐Specific Recombinase and Integrase Alternatives to cre‐loxP Systems
  • Concluding Remarks
  • Acknowledgments
  • Literature Cited
  • Figures
     
 
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  Repository containing Cre‐expressing strains, inducible Cre strains, Cre reporter strains, and loxP‐flanked (floxed) strains.
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