Identification of a BALB/c H-2L^d gene by DNA-mediated gene transfer
Abstract
Gene transfer and immunoselection were used in the identification of a BALB/c genomic clone containing an H-2L^d gene (clone 27.5). Transformation of thymidine kinase-negative C3H mouse L cells with the cloned 27.5 DNA together with the herpes simplex virus tk gene produced transformants expressing L^d molecules detected by radioimmune assay with monoclonal hybridoma antibodies to Ld antigens. The foreign L^d gene products expressed by cloned mouse L cell transformants were shown to be virtually indistinguishable from BALB/c spleen L^d molecules by two-dimensional electrophoretic analysis of H-2L^d immunoprecipitates. These results indicate that the genomic clone 27.5 contains a functional BALB/c H-2L^d gene and demonstrate the usefulness of this approach for identifying the gene products encoded by cloned genes which are members of a multigene family. Furthermore, the ability to place cell-surface recognition molecules on the surfaces of foreign cells provides a powerful opportunity for functional analyses of these molecules.
Additional Information
© 1982 American Association for the Advancement of Science. 5 November 1981; revised 16 December 1981. Supported by NIH grants GM 06965, CA 22662, CA 26199, and CA 25911. R.S.G. is a senior Lievre fellow of the California Division of the American Cancer Society. J .A.F. is the recipient of an American Cancer Society faculty research award. We thank D. Sachs and T. Hansen for supplying the monoclonal hybridoma antibodies used in these studies.Additional details
- Eprint ID
- 54390
- DOI
- 10.1126/science.7058331
- Resolver ID
- CaltechAUTHORS:20150204-152008392
- NIH
- GM 06965
- NIH
- CA 22662
- NIH
- CA 26199
- NIH
- CA 25911
- Created
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2015-02-05Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field