© 1993 Oxford University Press
RESEARCH-ARTICLE |
Comparative mapping of 9 human chromosome 22q loci in the laboratory mouse
an*Department of Psychiatry, University of Pennsylvania Philadelphia, PA 19104, USA 1Institut Cochin De Genetique Moteculaire, INSERM, U 129, 24 rue du Faubourg Saint-Jacques Pans, 75014, France 2Department of Pediatrics, Temple University School of Medicine, St Christopher' Hospital for Children, Philadelphia, PA 19134 3Jackson Laboratory, Bar Harbor, Maine, ME 04609 and 4The Children' Hospital of Philadelphia Philadelphia, PA 19104, USA 4The Children's Hospital of Philadelphia Philadelphia, PA 19104, USA
* To whom correspondence should be addressed at: University of Pennsylvania, 111A CRB, 422 Curie Blvd., Philadelphia, PA 191046141, USA
Received February 19, 1993; Revised May 18, 1993; Accepted May 18, 1993
We present a comparative map of genes on human chromosome 22q and homologous loci In the mouse genome. Gene order in humans was established using a panel of somatic cell hybrids. Genetic maps spanning homologous segments on three mouse chromosomes were generated using an Interspecific backcross. The conserved linkage between human chromosome 22 and mouse chromosome 16 Includes two closely linked loci, Comt and Igl-1. The second conserved linkage involves human chromosome 22 and mouse chromosome 11 and contains two genetically and physically linked loci, Lif and Nfh. Finally, conserved synteny involving mouse chromosome 15 and human chromosome 22 spans 30 cM and contains five loci (Acr, Bzrp, Dia-1, II2rb and Pdgfb). Loci within this conserved synteny have been sublocalized to different portions of human chromosome 22. The order of genes on mouse chromosome 15 and human chromosome 22 provides further evidence for chromosomal rearrangements within the conserved synteny that have occurred since the divergence of lineages leading to mice and humans.
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