Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
1R01 HG00318
NHGRI NIH HHS - United States
55000306
Howard Hughes Medical Institute - United States
PubMed
18256238
PubMed Central
PMC2259115
DOI
10.1101/gr.7160508
PII: gr.7160508
Knihovny.cz E-resources
- MeSH
- Phenotype MeSH
- Genetic Variation MeSH
- Mice, Inbred Strains genetics MeSH
- Quantitative Trait Loci * MeSH
- DNA, Mitochondrial chemistry MeSH
- Molecular Sequence Data MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Sex Ratio MeSH
- Reproduction MeSH
- Chromosomes, Mammalian MeSH
- Base Sequence MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- DNA, Mitochondrial MeSH
Consomic (chromosome substitution) strains (CSs) represent the most recent addition to the mouse genetic resources aimed to genetically analyze complex trait loci (QTLs). In this study, we report the development of a set of 28 mouse intersubspecific CSs. In each CS, we replaced a single chromosome of the C57BL/6J (B6) inbred strain (mostly Mus m. domesticus) with its homolog from the PWD/Ph inbred strain of the Mus m. musculus subspecies. These two progenitor subspecies diverged less than 1 million years ago and accumulated a large number of genetic differences that constitute a rich resource of genetic variation for QTL analyses. Altogether, the 18 consomic, nine subconsomic, and one conplastic strain covered all 19 autosomes, X and Y sex chromosomes, and mitochondrial DNA. Most CSs had significantly lower reproductive fitness compared with the progenitor strains. CSs homosomic for chromosomes 10 and 11, and the C57BL/6J-Chr X males, failed to reproduce and were substituted by less affected subconsomics carrying either a proximal, central, or distal part of the respective chromosome. A genome-wide scan of 965 DNA markers revealed 99.87% purity of the B6 genetic background. Thirty-three nonsynonymous substitutions were uncovered in the protein-coding regions of the mitochondrial DNA of the B6.PWD-mt conplastic strain. A pilot-phenotyping experiment project revealed a high number of variations among B6.PWD consomics.
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Phenogenomic resources immortalized in a panel of wild-derived strains of five species of house mice
Genic and chromosomal components of Prdm9-driven hybrid male sterility in mice (Mus musculus)
Chromosome-wide characterization of meiotic noncrossovers (gene conversions) in mouse hybrids
Histone methyltransferase PRDM9 is not essential for meiosis in male mice
Modulation of Prdm9-controlled meiotic chromosome asynapsis overrides hybrid sterility in mice
High-Resolution Maps of Mouse Reference Populations
Hybrid Sterility Locus on Chromosome X Controls Meiotic Recombination Rate in Mouse
X chromosome control of meiotic chromosome synapsis in mouse inter-subspecific hybrids
Mechanistic basis of infertility of mouse intersubspecific hybrids
Interallelic and intergenic incompatibilities of the Prdm9 (Hst1) gene in mouse hybrid sterility
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