Refining the mouse chromosomal location of Cdm, the major gene associated with susceptibility to cadmium-induced testicular necrosisDalton, Timothy P.a; Miller, Marian L.a,b; Wu, Xiaominb; Menon, Anilb,c; Cianciolo, Elia; McKinnon, Ross A.a; Smith, Paul W.a; Robinson, Lindsey J.a; Nebert, Daniel W.a,bPharmacogenetics: March 2000 - Volume 10 - Issue 2 - pp 141-151 Original Article Abstract Author Information Cadmium (Cd++) is a widespread environmental pollutant and classifed as an IARC `Category I' human carcinogen. Cd++ can also cause severe renal toxicity and may be involved clinically in cardiovascular disease and osteoporosis. Genetic differences in sensitivity to cadmium toxicity have been noted in humans, whereas, among inbred mouse strains, unequivocal genetic data exist. Resistance to cadmium-induced testicular damage was reported in 1973 to be associated with a single major recessive gene, named Cdm, which has now been localized to mouse chromosome (Chr) 3. Using polymorphic microsatellite markers and semiquantitative histological parameters, we have corroborated the original 1973 data concerning mendelian inheritance and have further refined the region containing the Cdm gene from more than 24 cM to 0.64 cM (estimated 40–80 genes). We phenotyped 26 recombinant inbred lines generated from C57BL/6 J (B6, resistant) and DBA/2 J (D2, sensitive) inbred mice, and determined that the Cdm gene maps between microsatellite markers D3Mit110 and D3Mit255. Although toxicity to numerous heavy metals is well known, virtually no molecular mechanisms have yet been uncovered either in humans or laboratory animals. Identification and characterization of the mouse Cdm gene should enhance our understanding of heavy metal toxicity by identifying and characterizing, for the first time, a major mammalian gene responsible for susceptibility to diseases caused by heavy metal toxicity. aDepartment of Environmental Health, bCenter for Environmental Genetics cDepartment of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati Medical Center, Cincinnati, Ohio, USA Received 4 June 1999 accepted 1 August 1999 Correspondence to Daniel W. Nebert, Department of Environmental Health and Center for Environmental Genetics, University of Cincinnati Medical Centre, PO Box 670056, Cincinnati, OH 45267-0056, USA Tel/fax: +1 513 821 4664; e-mail: firstname.lastname@example.org © 2000 Lippincott Williams & Wilkins, Inc.