Advances in Recombinases
DNA recombinases are widely used in multicellular organisms to manipulate the structure of genomes, and to control gene expression. These enzymes, derived from bacteria (bacteriophages) and fungi, catalyze directionally sensitive DNA exchange reactions between short (30–40 nucleotides) target site sequences that are specific to each recombinase. These reactions enable four basic functional modules: excision/insertion, inversion, translocation and cassette exchange, which have been used individually or combined in a wide range of configurations to control gene expression.
In the present book, ten typical literatures about recombinases published on international authoritative journals were selected to introduce the worldwide newest progress, which contains reviews or original researches on recombinases. We hope this book can demonstrate advances in recombinases as well as give references to the researchers, students and other related people.
Sample Chapter(s)
Preface (180 KB)
Components of the Book:
  • Chapter 1
    Structure and engineering of the large serine recombinase Bxb1 for gene integration
  • Chapter 2
    Revealing species diversity in Pseudo-nitzschia blooms in Scotland and Aotearoa (New Zealand) by combining recombinase polymerase amplification and nanopore-sequencing
  • Chapter 3
    Temperature-Dependent Recombinase-Based Genetic Circuits
  • Chapter 4
    Phage parasites targeting phage homologous recombinases provide antiviral immunity
  • Chapter 5
    Direct observation of subunit rotation during DNA strand exchange by serine recombinases
  • Chapter 6
    Lack of activity of HIV-1 integrase strand-transfer inhibitors on recombinase activating gene (RAG) activity at clinically relevant concentrations
  • Chapter 7
    Activation of recombinases at specific DNA loci by zinc-finger domain insertions
  • Chapter 8
    Defining spatial nonuniformities of all ipRGC types using an improved Opn4cre recombinase mouse line
  • Chapter 9
    Efficient site-specific integration of large genes in mammalian cells via continuously evolved recombinases and prime editing
  • Chapter 10
    Rapid Forensic DNA Profiling via Real-Time Recombinase Polymerase Amplification of InDel Markers
Readership: Students, academics, teachers and other people attending or interested in integrated recombinases.
Dario Tagliaferri
Department of Medicine, Division of Engineering in Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA; Gene and Cell Therapy Institute, Mass General Brigham, Cambridge, MA 02139, USA; Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA

Marc Gonzalez-Colell
Synthetic Biology for Biomedical Applications Lab, Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Biomedical Research Park, 08003 Barcelona, Spain

Gillian M. Cadden
School of Molecular Biosciences, University of Glasgow, Bower Building, University Avenue, Glasgow, UK; School of Chemistry, University of Glasgow, Joseph Black Building, University Avenue, Glasgow, UK

and more...
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