Scambler, Peter J., Wainwright, Brandon, Ramsay, Michele, Farrall, Martin, Bates, Gill, Ho, Meng Fat and Cooper, Colin ORCID: https://orcid.org/0000-0003-2013-8042 (1990) Analysis of the transgenome of MET transfectant cell lines reveals that MET activation is accompanied by an interstitial insertion. Human Genetics, 84 (3). pp. 274-278. ISSN 0340-6717
Full text not available from this repository. (Request a copy)Abstract
The MET oncogene, present in the MNNG-HOS chemically transformed human cell line, is activated by a gene fusion involving sequences from chromosome 1 and chromosome 7. Activated MET can act as a dominant selectable marker for chromosome-mediated gene transfer, and several transfectant cell lines have been established using this technique. Analysis of the transgenomes within these cell lines indicates that MET activation is not simply due to a chromosome translocation, but may involve an interstitial insertion of DNA from chromosome 1, into chromosome 7, probably associated with other rearrangements. Pulse field gel analysis of two transfectants indicates that, despite the presence of complex rearrangements close to MET, chromosome 7 sequences are grossly intact over a 1-Mb region thought to contain the gene defective in cystic fibrosis.
Item Type: | Article |
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Uncontrolled Keywords: | genetics,genetics(clinical) ,/dk/atira/pure/subjectarea/asjc/1300/1311 |
Faculty \ School: | Faculty of Medicine and Health Sciences > Norwich Medical School |
UEA Research Groups: | Faculty of Medicine and Health Sciences > Research Groups > Cancer Studies |
Related URLs: | |
Depositing User: | LivePure Connector |
Date Deposited: | 18 Jul 2022 17:31 |
Last Modified: | 23 Oct 2022 04:02 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/86549 |
DOI: | 10.1007/BF00200574 |
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