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Physiol. Genomics 21: 404-410, 2005. First published March 1, 2005; doi:10.1152/physiolgenomics.00199.2004
1094-8341/05 $8.00
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Received 1 September 2004; accepted in final form 27 February 2005.
Physiological Genomics 21:404-410 (2005)
1094-8341/05 $8.00 © 2005 American Physiological Society

Homocysteine levels in A/J and C57BL/6J mice: genetic, diet, gender, and parental effects

Sheila Ernest1,2, Angela Hosack3, William E. O’Brien4, David S. Rosenblatt3 and Joseph H. Nadeau1,2

1 Department of Genetics, Case Western Reserve University School of Medicine, Cleveland, Ohio
2 Center for Computational Genomics and Systems Biology, Case Western Reserve University, Cleveland, Ohio
3 Departments of Human Genetics, Medicine, Pediatrics, and Biology, McGill University, Montreal, Quebec, Canada
4 Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas

Increased levels of homocysteine in the blood have been associated with various birth defects and adult diseases. However, the extent to which genetic factors control homocysteine levels in healthy individuals is unclear. Laboratory mice are valuable models for dissecting the genetic and environmental controls of total homocysteine (tHcy) levels. We assessed the inheritance of tHcy levels in two inbred strains, A/J and C57BL/6J (B6), under controlled physiological conditions and assessed the relative importance of genetic, diet, gender, and parental effects. Diet affected mean tHcy levels, whereas gender affected both the mean and variance of tHcy levels. Moreover, gender of the parents influenced mean tHcy levels in reciprocal F1 hybrids, suggesting maternal effects. Finally, gene-diet interactions affected heritability of mean tHcy levels. These studies showed that each of these factors contributes to tHcy levels and provided important clues to understanding homocysteine homeostasis in humans.

genetics; folate; gene environment




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