2003Humana Press eBooksRequires access

The LoxP/CRE System and Genome Modification

Trevor J. Wilson, Ismail Kola

Open publisher page 25 citations

Abstract

Conventional gene knockout technology by homologous recombination can provide important information toward elucidating the function of some genes; however, the role of many genes cannot be investigated due to early embryonic lethality. Alternatively, the role of a particular gene in adult tissues may be masked by developmental abnormalities in any knockout animals generated. The implementation of site specific recombinases, such as the bacteriophage P1 LoxP /CRE system, enables the development of conditional knockouts that lack a particular gene only in a specific tissue or after a specific stage of development. This system can also be used to facilitate transgene activation/inactivation in vivo, deletions of large stretches of genomic DNA, chromosomal translocation and subtle alterations to genes and/or their regulatory sequences in vivo. 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.

About this research paper

What this paper is about

Conventional gene knockout technology by homologous recombination can provide important information toward elucidating the function of some genes; however, the role of many genes cannot be investigated due to early embryonic lethality. Alternatively, the role of a particular gene in adult tissues may be masked by developmental abnormalities in any knockout animals generated. The implementation of site specific recombinases, such as the bacteriophage P1 LoxP /CRE system, enables the development of conditional knockouts that lack a particular gene only in a specific tissue or after a specific stage of development. This system can also be used to facilitate transgene activation/inactivation in vivo, deletions of large stretches of genomic DNA, chromosomal translocation and subtle alterations to genes and/or their regulatory sequences in vivo. 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.

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Available abstract

Conventional gene knockout technology by homologous recombination can provide important information toward elucidating the function of some genes; however, the role of many genes cannot be investigated due to early embryonic lethality. Alternatively, the role of a particular gene in adult tissues may be masked by developmental abnormalities in any knockout animals generated. The implementation of site specific recombinases, such as the bacteriophage P1 LoxP /CRE system, enables the development of conditional knockouts that lack a particular gene only in a specific tissue or after a specific stage of development. This system can also be used to facilitate transgene activation/inactivation in vivo, deletions of large stretches of genomic DNA, chromosomal translocation and subtle alterations to genes and/or their regulatory sequences in vivo. 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.

Key concepts: Cre recombinase, Recombinase, Cre-Lox recombination, Gene knockout, Conditional gene knockout, Biology, Homologous recombination, Gene targeting

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