ASSIGNMENT OF TK1 ENCODING THYMIDINE KINASE TO SYRIAN-HAMSTER CHROMOSOME-9 BY MICROCELL-MEDIATED CHROMOSOME TRANSFER

Authors
Citation
K. Islam et Mq. Islam, ASSIGNMENT OF TK1 ENCODING THYMIDINE KINASE TO SYRIAN-HAMSTER CHROMOSOME-9 BY MICROCELL-MEDIATED CHROMOSOME TRANSFER, Cytogenetics and cell genetics, 66(3), 1994, pp. 177-180
Citations number
21
Categorie Soggetti
Cytology & Histology","Genetics & Heredity
ISSN journal
03010171
Volume
66
Issue
3
Year of publication
1994
Pages
177 - 180
Database
ISI
SICI code
0301-0171(1994)66:3<177:AOTETK>2.0.ZU;2-G
Abstract
We report here the assignment of TK1, the gene for thymidine kinase to Syrian hamster (Mesocricetus auratus) chromosome 9 (MAU9) by compleme ntation mapping. Syrian hamster chromosomes derived from a wild type ( TK+) subline of BHK cells were introduced via microcell-mediated chrom osome transfer into B82 mouse cells deficient in thymidine kinase (TK- ), a defect that prevents their growth in HAT culture media. Hybrid cl ones were selected in HAT media. Chromosome analyses of the microcell hybrids showed that the thymidine kinase deficiency of B82 cells was c orrected by MAU9. Therefore, we assigned TK1 to MAU9. Previously, TK1 was assigned to mouse chromosome 11 (MMU11), rat chromosome 10 (RNO10) , Chinese hamster chromosome 7 (CGR7), and human chromosome 17 (HSA17) . The striking banding homology of MAU9 with RNO10, MMU11, CGR7 and HS A17 provides additional support for the assignment of TK1 to MAU9. To our knowledge, this is the first report of gene assignment to a specif ic Syrian hamster chromosome using the somatic cell hybridization tech nique.