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Genetic Engineering Using Homologous Recombination

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Opus teacher head0.022
GPT teacher head0.295
Teacher spread
0.273 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

In the past few years, in vivo technologies have emerged that, due to their efficiency and simplicity, may one day replace standard genetic engineering techniques. Constructs can be made on plasmids or directly on the Escherichia coli chromosome from PCR products or synthetic oligonucleotides by homologous recombination. This is possible because bacteriophage-encoded recombination functions efficiently recombine sequences with homologies as short as 35 to 50 base pairs. This technology, termed recombineering, is providing new ways to modify genes and segments of the chromosome. This review describes not only recombineering and its applications, but also summarizes homologous recombination in E. coli and early uses of homologous recombination to modify the bacterial chromosome. Finally, based on the premise that phage-mediated recombination functions act at replication forks, specific molecular models are proposed.

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The record

Venue
Annual Review of Genetics
Topic
Bacterial Genetics and Biotechnology
Field
Biochemistry, Genetics and Molecular Biology
Canadian institutions
Funders
McGill University
Keywords
RecombineeringHomologous recombinationBiologyFLP-FRT recombinationGeneticsNon-allelic homologous recombinationRecombinationGenetic recombinationPlasmidHomologous chromosomeChromosomeCre-Lox recombinationBacterial artificial chromosomeComputational biologyGeneGenomeTransgene
Has abstract in OpenAlex
yes