Title
Genetic structure and origin of t haplotypes of mice, analyzed with H-2 cDNA probes
UMMS Affiliation
Department of Molecular Genetics and Microbiology
Publication Date
1982-7
Document Type
Article
Subjects
Animals; Chromosome Mapping; Cloning, Molecular; DNA; DNA Restriction Enzymes; H-2 Antigens; Mice; Mice, Mutant Strains; Nucleic Acid Hybridization; Polymorphism, Genetic; Recombination, Genetic
Disciplines
Life Sciences | Medicine and Health Sciences | Women's Studies
Abstract
We investigated the genetic organization and evolutionary origin of t chromosomes of mice by examining the restriction fragment patterns of DNA from t haplotypes and normal chromosomes with cDNA probes to H-2 class I genes. On genomic DNA blots, the restriction fragments containing H-2-related sequences were highly variable among different inbred strains of mice, whereas they were very similar among different t haplotypes even when the t haplotypes carried serologically different H-2 haplotypes. These observations suggest that all t haplotypes have a common origin and are not products of independent mutational events. We also mapped the position of several restriction fragments characteristic of t DNA by using a battery of recombinant t haplotypes, defined with respect to their t-lethal factors and H-2 haplotypes. We thus show that restriction fragments containing H-2-related sequences map to the left of the H-2 class I genes in t chromosomes, a region in which the tw32 b-lethal factor also maps. The cloning of these fragments can be expected to provide an entry for the structural analysis of t DNA.
DOI of Published Version
10.1016/0092-8674(82)90460-3
Source
Cell. 1982 Jul;29(3):969-76.
Journal/Book/Conference Title
Cell
Related Resources
PubMed ID
6295638
Repository Citation
Shin HS, Stavnezer J, Artzt K, Bennett DA. (1982). Genetic structure and origin of t haplotypes of mice, analyzed with H-2 cDNA probes. Women’s Health Research Faculty Publications. https://doi.org/10.1016/0092-8674(82)90460-3. Retrieved from https://escholarship.umassmed.edu/wfc_pp/244