Clarke, DJ, Gimenez-Abian, JF, Tonnies, H, Neitzel, E, Sperling, K, Downes, Stephen and Johnson, RT (1998) Creation of monosomic derivatives of human cultured cell lines. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 95 (1). pp. 167-171. [Journal article]
Full text not available from this repository.
Monosomic mammalian cell lines would be ideal for studying gene dosage effects, including gene imprinting, and for systematic isolation of recessive somatic mutants parallel to the invaluable mutants derived from haploid yeast. But autosomal monosomies are lethal in early development; although monosomies appear in tumors, deriving cell lines from these tumors is difficult and cannot provide several syngenic lines. We have developed a strategy for generating stable monosomic human cells, based on random autosomal integration of the gpt plasmid, partial inhibition of DNA topoisomerase II during mitosis to promote chromatid nondisjunction, and selection against retention of gpt, These are likely to be valuable as a source of otherwise inaccessible mutants. The strategy can also be used to generate partial mammalian monosomies, which are desirable as a source of information on recessive genes and gene imprinting.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Life and Health Sciences|
Faculty of Life and Health Sciences > School of Biomedical Sciences
|Research Institutes and Groups:||Biomedical Sciences Research Institute > Genomic Medicine|
Biomedical Sciences Research Institute
Biomedical Sciences Research Institute > Genomic Medicine > Nano Systems Biology
|Deposited By:||Professor Stephen Downes|
|Deposited On:||15 Dec 2009 13:33|
|Last Modified:||10 Jun 2010 10:39|
Repository Staff Only: item control page