Author/Authors :
Ron Korstanje، نويسنده , , Per Eriksson، نويسنده , , Ann Samneg?rd، نويسنده , , Per G. Olsson، نويسنده , , Kristina Forsman-Semb، نويسنده , , Saunak Sen، نويسنده , , Gary A. Churchill، نويسنده , , Jarod Rollins، نويسنده , , STEPHEN HARRIS، نويسنده , , Anders Hamsten، نويسنده , , Beverly Paigen، نويسنده ,
Abstract :
A previous study revealed that the difference in susceptibility to atherosclerotic lesions between inbred mouse strains SM/J and NZB/BlNJ was determined by one major locus (Ath8). In this study a (SM/J × NZB/BlNJ) F1 × SM/J backcross localized Ath8 by quantitative trait locus mapping to chromosome 4 with a suggestive LOD score of 2.7. This quantitative trait locus (QTL) was confirmed using an (SM/J × NZB/BlNJ) intercross; Ath8 mapped to a 23 cM region with a significant LOD score of 3.6. The genes for toll-like receptor 4 (T1r4), arachidonic acid epoxygenase (Cyp2j5), and angiopoietin-like protein 3 (Angptl3) map to this region. These candidate genes were analyzed for expression and sequence differences in the mouse and for associations with cardiovascular traits in human. Sequence analysis of Angptl3 shows a base pair substitution in SM, the susceptible strain, giving rise to an amino acid change in the fibrinogen homology domain of the protein. We found a significant association between ANGPTL3 and atherosclerotic lesions (P< 0.05) in human. These results suggest that Angptl3 is involved in atherosclerosis susceptibility in both mouse and human.
Keywords :
mouse , QTL , atherosclerosis , ANGPTL3