Genetics, Vol 122, 153-161, Copyright © 1989


INVESTIGATIONS

A Comprehensive Genetic Map of Murine Chromosome 11 Reveals Extensive Linkage Conservation Between Mouse and Human

A. M. Buchberg, E. Brownell, S. Nagata, N. A. Jenkins and N. G. Copeland
Mammalian Genetics Laboratory, BRI-Basic Research Program, NCI-Frederick Cancer Research Facility, Frederick, Maryland 21701

Interspecific backcross animals from a cross between C57BL/6J and Mus spretus mice were used to generate a comprehensive linkage map of mouse chromosome 11. The relative map positions of genes previously assigned to mouse chromosome 11 by somatic cell hybrid or genetic backcross analysis were determined (Erbb, Rel, Il-3, Csfgm, Trp53-1, Evi-2, Erba, Erbb-2, Csfg, Myhs, Cola-1, Myla, Hox-2 and Pkca). We also analyzed genes that we suspected would map to chromosome 11 by virtue of their location in human chromosomes and the known linkage homologies that exist between murine chromosome 11 and human chromosomes (Mpo, Ngfr, Pdgfr and Fms). Two of the latter genes, Mpo and Ngfr, mapped to mouse chromosome 11. Both genes also mapped to human chromosome 17, extending the degree of linkage conservation observed between human chromosome 17 and mouse chromosome 11. Pdgfr and Fms, which are closely linked to Il-3 and Csfgm in humans on chromosome 5, mapped to mouse chromosome 18 rather than mouse chromosome 11, thereby defining yet another conserved linkage group between human and mouse chromosomes. The mouse chromosome 11 linkage map generated in these studies substantially extends the framework for identifying homologous genes in the mouse that are involved in human disease, for elucidating the genes responsible for several mouse mutations, and for gaining insights into chromosome evolution and genome organization.


This article has been cited by other articles:


Home page
MutagenesisHome page
L.S. Clark, K. Harrington-Brock, J. Wang, L. Sargent, D. Lowry, S. H. Reynolds, and M. M. Moore
Loss of P53 heterozygosity is not responsible for the small colony thymidine kinase mutant phenotype in L5178Y mouse lymphoma cells
Mutagenesis, July 1, 2004; 19(4): 263 - 268.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
N. W. Shworak, J. Liu, L. M. Petros, L. Zhang, M. Kobayashi, N. G. Copeland, N. A. Jenkins, and R. D. Rosenberg
Multiple Isoforms of Heparan Sulfate D-Glucosaminyl 3-O-Sulfotransferase. ISOLATION, CHARACTERIZATION, AND EXPRESSION OF HUMAN cDNAs AND IDENTIFICATION OF DISTINCT GENOMIC LOCI
J. Biol. Chem., February 19, 1999; 274(8): 5170 - 5184.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
F. J. Tavner, R. Simpson, S. Tashiro, D. Favier, N. A. Jenkins, D. J. Gilbert, N. G. Copeland, E. M. Macmillan, J. Lutwyche, R. A. Keough, et al.
Molecular Cloning Reveals that the p160 Myb-Binding Protein Is a Novel, Predominantly Nucleolar Protein Which May Play a Role in Transactivation by Myb
Mol. Cell. Biol., February 1, 1998; 18(2): 989 - 1002.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
Y. Wang, J. P. Macke, B. S. Abella, K. Andreasson, P. Worley, D. J. Gilbert, N. G. Copeland, N. A. Jenkins, and J. Nathans
A Large Family of Putative Transmembrane Receptors Homologous to the Product of the Drosophila Tissue Polarity Gene frizzled
J. Biol. Chem., February 23, 1996; 271(8): 4468 - 4476.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
Y Ai, N A Jenkins, N G Copeland, D H Gilbert, D J Bergsma, and D Stambolian
Mouse galactokinase: isolation, characterization, and location on chromosome 11.
Genome Res., August 1, 1995; 5(1): 53 - 59.
[Abstract] [PDF]


Home page
DevelopmentHome page
J. Cross, M. Flannery, M. Blanar, E Steingrimsson, N. Jenkins, N. Copeland, W. Rutter, and Z Werb
Hxt encodes a basic helix-loop-helix transcription factor that regulates trophoblast cell development
Development, January 8, 1995; 121(8): 2513 - 2523.
[Abstract] [PDF]