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Publication : Genotyping new BXD recombinant inbred mouse strains and comparison of BXD and consensus maps.

First Author  Taylor BA Year  1999
Journal  Mamm Genome Volume  10
Issue  4 Pages  335-48
PubMed ID  10087289 Mgi Jnum  J:49829
Mgi Id  MGI:1278415 Doi  10.1007/s003359900998
Citation  Taylor BA, et al. (1999) Genotyping new BXD recombinant inbred mouse strains and comparison of BXD and consensus maps. Mamm Genome 10(4):335-48
abstractText  Nine additional BXD recombinant inbred (RI) strains have been developed from the F-2 cross of C57BL/6J and DBA/2J mouse strains. A tenth line stopped breeding in the F-12 generation. F-20 generation breeding pairs from the nine surviving strains and an F-12 pair from the extinct line were genotyped at 319 genetic markers (primarily microsatellites) spanning most of the genome. Where typing data were lacking, the established set of 26 BXD strains also were genotyped at these same loci. The availability of these additional nine strains enhances the value of the BXD RI set for analysis of complex phenotypic traits. The proportion of loci still segregating at the F-20 generation was found to closely approximate expectation, suggesting that selection favoring the retention of heterozygosity is not a strong factor. However, the number of crossovers between adjacent markers was frequently less than predicted from consensus map distances. A significant deficiency of recombinants was observed on Chrs 3, 4, 14, and X. On Chr 14, the estimated cumulative BXD map distance between the most proximal and distal markers was only 30.2 cM, compared with a distance of 60.0 cM in the consensus map. On the X Chr, the estimated and predicted cumulative distances were 38.8 and 69.5 cM, respectively. Over all chromosomes, the BXD RI map is 14.5% shorter than predicted from the consensus map. It is suggested that distances in some of the consensus maps are inflated. Alternatively, recombinant genotypes could be selected against during inbreeding owing to allelic interactions affecting fitness. The latter interpretation implies that relatively strong intrachromosomal epistasis is common.
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