Segregation of human hypoxanthine phosphoribosyltransferase activity from somatic cell hybrids isolated after fusion of mouse gene transfer cells with Chinese hamster cells

1977 ◽  
Vol 154 (2) ◽  
pp. 191-197 ◽  
Author(s):  
Peter J. Davies ◽  
Klaus Willecke
Keyword(s):  
Gene Transfer ◽  
Somatic Cell ◽  
Chinese Hamster ◽  
Transfer Cells ◽  
Mouse Gene ◽  
Hypoxanthine Phosphoribosyltransferase ◽  
Somatic Cell Hybrids ◽  
Chinese Hamster Cells ◽  
Cell Hybrids

scholarly journals c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemia.

1983 ◽  
Vol 158 (1) ◽  
pp. 9-15 ◽  
Author(s):  
J Groffen ◽  
N Heisterkamp ◽  
J R Stephenson ◽  
A G van Kessel ◽  
A de Klein ◽  
...  
Keyword(s):  
Somatic Cell ◽  
Chinese Hamster ◽  
Chromosome 9 ◽  
Chromosome 22 ◽  
Chronic Myelocytic Leukemia ◽  
Somatic Cell Hybrids ◽  
Chinese Hamster Cells ◽  
Cell Hybrids ◽  
Myelocytic Leukemia

By analysis of a series of somatic cell hybrids derived by fusion of either mouse or Chinese hamster cells with leukocytes from different chronic myelocytic leukemia (CML) patients or from normal donors, we have localized the human oncogene, c-sis, on the q11 to qter segment of chromosome 22 and demonstrated its translocation from chromosome 22 to chromosome 9 (q34) in CML.

Amplification of the provirus region in Rous sarcoma virus-transformed Chinese hamster cells and segregation of the amplified copies in somatic cell hybrids

Virology ◽  
1983 ◽  
Vol 128 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Jana Hillova ◽  
Miroslav Hill ◽  
Jean Belehradek ◽  
Régine Mariage-Samson ◽  
Maria Marx
Keyword(s):  
Somatic Cell ◽  
Rous Sarcoma Virus ◽  
Chinese Hamster ◽  
Somatic Cell Hybrids ◽  
Chinese Hamster Cells ◽  
Cell Hybrids ◽  
Rous Sarcoma ◽  
Sarcoma Virus

Segregation of recessive phenotypes in somatic cell hybrids: role of mitotic recombination, gene inactivation, and chromosome nondisjunction

1981 ◽  
Vol 1 (4) ◽  
pp. 336-346
Author(s):  
C E Campbell ◽  
R G Worton
Keyword(s):  
Somatic Cell ◽  
Chinese Hamster ◽  
Mitotic Recombination ◽  
Chinese Hamster Cell ◽  
Gene Inactivation ◽  
Chromosome Loss ◽  
Resistance Locus ◽  
Chromosome 2 ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids

Somatic cell hybrids heterozygous at the emetine resistance locus (emtr/emt+) or the chromate resistance locus (chrr/chr+) are known to segregate the recessive drug resistance phenotype at high frequency. We have examined mechanisms of segregation in Chinese hamster cell hybrids heterozygous at these two loci, both of which map to the long arm of Chinese hamster chromosome 2. To follow the fate of chromosomal arms through the segregation process, our hybrids were also heterozygous at the mtx (methotrexate resistance) locus on the short arm of chromosome 2 and carried cytogenetically marked chromosomes with either a short-arm deletion (2p-) or a long-arm addition (2q+). Karyotype and phenotype analysis of emetine- or chromate-resistant segregants from such hybrids allowed us to distinguish four potential segregation mechanisms: (i) loss of the emt+- or chr+-bearing chromosome; (ii) mitotic recombination between the centromere and the emt or chr loci, giving rise to homozygous resistant segregants; (iii) inactivation of the emt+ or chr+ alleles; and (iv) loss of the emt+- or chr+-bearing chromosome with duplication of the homologous chromosome carrying the emtr or chrr allele. Of 48 independent segregants examined, only 9 (20%) arose by simple chromosome loss. Two segregants (4%) were consistent with a gene inactivation mechanism, but because of their rarity, other mechanisms such as mutation or submicroscopic deletion could not be excluded. Twenty-one segregants (44%) arose by either mitotic recombination or chromosome loss and duplication; the two mechanisms were not distinguishable in that experiment. Finally, in hybrids allowing these two mechanisms to be distinguished, 15 segregants (31%) arose by chromosome loss and duplication, and none arose by mitotic recombination.

Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids

1973 ◽  
Vol 20 (3) ◽  
pp. 195-202 ◽  
Author(s):  
Ans Jongsma ◽  
Harry Someren ◽  
Andries Westerveld ◽  
Ann Hagemeijer ◽  
Peter Pearson
Keyword(s):  
Somatic Cell ◽  
Chinese Hamster ◽  
Human Chromosomes ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids

Retention of both parental mitochondrial DNA species in mouse-Chinese hamster somatic cell hybrids

1984 ◽  
Vol 10 (1) ◽  
pp. 85-91 ◽  
Author(s):  
Steven H. Zuckerman ◽  
Joseph F. Solus ◽  
Frances P. Gillespie ◽  
Jerome M. Eisenstadt
Keyword(s):  
Mitochondrial Dna ◽  
Somatic Cell ◽  
Chinese Hamster ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids

Genetical Studies on the Multiple Forms of Human Guanylate Kinase in Man-Chinese Hamster Somatic Cell Hybrids

1974 ◽  
Vol 24 (5-6) ◽  
pp. 415-423 ◽  
Author(s):  
Meera Khan ◽  
W.R.T. Los ◽  
P.L. Pearson ◽  
A. Westerveld ◽  
D. Bootsma
Keyword(s):  
Somatic Cell ◽  
Chinese Hamster ◽  
Somatic Cell Hybrids ◽  
Multiple Forms ◽  
Guanylate Kinase ◽  
Cell Hybrids

5 Persistence of fragmented mouse HSR chromatin in mouse-chinese hamster somatic cell hybrids resistant to actinomycin D

1987 ◽  
Vol 28 (1) ◽  
pp. 29
Author(s):  
G. Levan ◽  
A.-H. Jakobsson ◽  
U. Arnason ◽  
A. Levan ◽  
T. Martinsson
Keyword(s):  
Somatic Cell ◽  
Actinomycin D ◽  
Chinese Hamster ◽  
Somatic Cell Hybrids ◽  
Cell Hybrids
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