Radiation hybrid map of the mouse genome

Radiation hybrid (RH) maps are a useful tool for genome analysis, providing a direct method for localizing genes and anchoring physical maps and genomic sequence along chromosomes. The construction of a comprehensive RH map for the human genome 1 has resulted in gene maps reflecting the location of...

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Veröffentlicht in:Nature genetics 1999-08, Vol.22 (4), p.384-387
Hauptverfasser: Van Etten, William J., Steen, Robert G., Nguyen, Huy, Castle, Andrew B., Slonim, Donna K., Ge, Bing, Nusbaum, Chad, Schuler, Greg D., Lander, Eric S., Hudson, Thomas J.
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Sprache:eng
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Zusammenfassung:Radiation hybrid (RH) maps are a useful tool for genome analysis, providing a direct method for localizing genes and anchoring physical maps and genomic sequence along chromosomes. The construction of a comprehensive RH map for the human genome 1 has resulted in gene maps reflecting the location of more than 30,000 human genes 2 , 3 . Here we report the first comprehensive RH map of the mouse genome. The map contains 2,486 loci screened against an RH panel of 93 cell lines 4 . Most loci (93%) are simple sequence length polymorphisms (SSLPs) taken from the mouse genetic map, thereby providing direct integration between these two key maps. We performed RH mapping by a new and efficient approach in which we replaced traditional gel- or hybridization-based assays by a homogeneous 5´-nuclease assay 5 involving a single common probe for all genetic markers. The map provides essentially complete connectivity and coverage across the genome, and good resolution for ordering loci, with 1 centiRay (cR) corresponding to an average of approximately 100 kb. The RH map, together with an accompanying World-Wide Web server, makes it possible for any investigator to rapidly localize sequences in the mouse genome. Together with the previously constructed genetic map 6 and a YAC-based physical map reported in a companion paper 7 , the fundamental maps required for mouse genomics are now available.
ISSN:1061-4036
1546-1718
DOI:10.1038/11962