A straightforward approach to isolate DNA sequences with potential linkage to the retinoblastoma locus |
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Authors: | Scheffer H. van der Lelie D. Aanstoot G. H. Goor Nicole Nienhaus Anneke J. van der Hout Annemieke H. Pearson P. L. Buys C. H. C. M. |
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Affiliation: | (1) Department of Human Genetics, State University of Groningen, Antonius Deusinglaan 4, NL-9713 AW Groningen, The Netherlands;(2) Department of Human Genetics, State University of Leiden, Leiden, The Netherlands |
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Abstract: | ![]() Summary From a human-Chinese hamster somatic cell hybrid a clone was derived containing chromosome 13 in duplicate as its only human material. This clone was used to construct a human chromosome 13-specific recombinant DNA-library. Overlapping Sau3AI DNA sequences (11.9–17.2 kb) from the cell hybrid were inserted into the lambda phage vector EMBL4. From eleven recombinants having a human insert thirteen putative unique DNA sequences were isolated and cloned into the plasmid vector pBR329. A human-mouse hybrid containing a human chromosome 13 with a deletion of 13q14 and lacking its undeleted homologue was constructed to be used in a selection procedure for DNA sequences belonging to band q14. Three probes originating from two different phages were assigned to 13q14 because they did not hybridise to DNA from this cell hybrid. One of these 13q14 probes detects a low frequency (2/44) Msp I restriction fragment length polymorphism. The probes are now being used for screening a cosmid library to find adjacent polymorphic sequences with a RFLP information content suitable for application in the diagnosis of hereditary retinoblastoma.Preliminary reports of these experiments were presented at the 8th International Workshop on Human Gene Mapping, Helsinki, August 4–10, 1985, and the 13th International Congress of Biochemistry, Amsterdam, August 25–30, 1985 (Scheffer et al. 1985a,b) |
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