Abstract
We have developed a protocol to isolate a gene from which only limited (amino-acid) sequence information is available. It involves two PCR amplifications using one constant primer and a set of nested primers and subsequent crosswise Southern hybridization. The amplified DNA giving a signal in both lanes is further processed for use in gene bank screening by applying standard procedures. In this way the structural gene for a thiol protease, BLH1, the homologue of the bleomycin A (a cancerostatic drug) resistance gene of rabbit (and man), was isolated from yeast genomic DNA.
References
Chen P, Seeburg P (1985) DNA 4:165–170
Erlich HA, Arnheim N (1992) Annu Rev Genet 26:479–506
Kempter B, Luppa P, Neumeier D (1991) Trends Genet 7:109–110
Knoth K, Roberds S, Poteet C, Tamkun M (1988) Nucleic Acids Res 16:10932
Magdolen U, Müller G, Magdolen V, Bandlow W (1993) Biochim Biophys Acta 1171:299–303
Rothstein RJ (1983) Methods Enzymol 101:202–211
Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
Sherman F, Fink GR, Hicks JB (1986) Methods in yeast genetics: a laboratory manual. Revised edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
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Communicated by F. K. Zimmermann
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Magdolen, U., Magdolen, V., Schmitt, M. et al. Selection of specific gene probes by combined use of low-stringency PCR amplification and Southern-blot hybridization. Curr Genet 27, 390–392 (1995). https://doi.org/10.1007/BF00352110
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DOI: https://doi.org/10.1007/BF00352110