Abstract
RecA protein-coated probe has been utilized to enrich genomic digests for desired genes in order to facilitate cloning from genomic libraries. Using a previously cloned HLA-B27 gene as the recA-coated enrichment probe, we obtained a mean 108x in crease in the ratio of specific to nonspecific plaques in lambda libraries screened for B27 variant alleles of estimated 99% homology to the probe. Class I genes of lesser homology were less enriched: 6.7x for non-B27 genes of estimated >95% homology and 3.7x for other Class I genes of >80% homology. Loss of genomic DNA during the enrichment procedure can, however, re strict application of this technique whenever starting genomic DNA is very limited. Nevertheless, the impressive reduction in cloning effort and material makes recA enrichment a useful new tool for cloning homologous genes from genomic DNA. © 1988 IRL Press Limited, Oxford, England.
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CITATION STYLE
Taidi-Laskowski, B., Tyan, D., Honigberg, S. M., Radding, C. R., & Grumet, F. C. (1988). Use of recA protein to enrich for homologous genes in a genomic library. Nucleic Acids Research, 16(16), 8157–8169. https://doi.org/10.1093/nar/16.16.8157
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