Genetic Evaluation of Candidate Genes for the Mom1 Modifier of Intestinal Neoplasia in Mice

• Published in: Genetics (Austin) Vol. 144; no. 4; pp. 1777 - 1785
• Main Authors: Gould, K. A, Luongo, C, Moser, A. R, McNeley, M. K, Borenstein, N, Shedlovsky, A, Dove, W. F, Hong, K, Dietrich, W. F, Lander, E. S
• Format: Journal Article
• Language: English
• Published: United States Genetics Soc America 01.12.1996; Genetics Society of America
• Subjects: Adenoma - genetics; Alleles; Animals; Chromosome Mapping; Digestive system; Genes; Genes, APC; Genetics; Intestinal Neoplasms - genetics; Investigations; Mice; Mutation; Rodents
• ISSN: 0016-6731; 1943-2631; 1943-2631
• DOI: 10.1093/genetics/144.4.1777

As genetic mapping of quantitative trait loci (QTL) becomes routine, the challenge is to identify the underlying genes. This paper develops rigorous genetic tests for evaluation of candidate genes for a QTL, involving determination of allelic status in inbred strains and fine-structure genetic mapping. For the Mom1 modifier of intestinal adenomas caused by ApcMin, these tests are used to evaluate two candidate genes: Pla2g2a, a secretory phospholipase, and Rap1GAP, a GTPase activating protein. Rap1GAP passes the first test but is excluded by a single fine-structure recombinant. Pla2g2a passes both tests and is a strong candidate for Mom1. Significantly, we also find that ApcMin-induced adenomas remain heterozygous for the Mom1 region, consistent with Mom1 acting outside the tumor lineage and encoding a secreted product.