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PMID: 12115029 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Genetic characterization of the Dyscalc locus.

Colinayo VV, Qiao JH, Demant P, Krass K, Lusis AJ, Drake TA

Abstract

Calcification occurs frequently in the development of atherosclerotic lesions, and studies in mice have indicated a genetic contribution. We now show that one genetic factor contributing to aortic calcification is the Dyscalc locus, previously shown to contribute to myocardial calcification. Thus, the Dyscalc locus, on proximal mouse Chromosome (Chr) 7, segregated with vascular calcification in a large cross between susceptible strain DBA/2J and resistant strain C57BL/6J. Further evidence was observed by analysis of recombinant inbred strains derived from various susceptible and resistant parental strains. Myocardial and vascular calcifications are importantly influenced by multiple modifier loci as well as the Dyscalc gene, making fine mapping of Dyscalc difficult. In order to allow more detailed genetic and biochemical characterization of Dyscalc, we have identified congenic strains containing the Dyscalc locus from resistant strain C57BL/10 on the background of susceptible strain C3H/DiSnA. The congenic strains exhibit little or no myocardial or vascular calcification, unlike the background HcB C3H strain, and the calcification segregated as a Mendelian factor, allowing finer mapping of Dyscalc.

MeSH Terms
Animals Aortic Diseases/genetics,pathology Arteriosclerosis/genetics,pathology Calcinosis/genetics Chromosome Mapping Genetic Markers Mice Mice, Congenic Mice, Inbred C3H Mice, Inbred C57BL Mice, Inbred DBA Mice, Inbred Strains
Chemicals
Genetic Markers
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Colinayo Veronica V
Department of Microbiology, Immunology and Molecular Genetics, University of California Los Angeles, 90095, USA.
Qiao Jian-Hua
Demant Peter
Krass Kelly
Lusis Aldons J
Drake Thomas A
Article Info
Journal
Mammalian genome : official journal of the International Mammalian Genome Society
Abbr.
Mamm Genome
ISSN
0938-8990
Published
2002-06-00
Pages
283-8
Language
English
Region
United States
NLM ID
9100916
Subset
IM
Grants
NHLBI NIH HHS · HL30568 · United States
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