首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Four additional mouse crosses improve the lipid QTL landscape and identify Lipg as a QTL gene
Authors:Zhiguang Su  Naoki Ishimori  Yaoyu Chen  Edward H Leiter  Gary A Churchill  Beverly Paigen  and Ioannis M Stylianou
Institution:*The Jackson Laboratory, Bar Harbor, ME 04609;Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine, Sapporo, Japan;§University of Pennsylvania, School of Medicine, Institute for Translational Medicine and Therapeutics, Philadelphia, PA 19104
Abstract:To identify genes controlling plasma HDL and triglyceride levels, quantitative trait locus (QTL) analysis was performed in one backcross, (NZO/H1Lt × NON/LtJ) × NON/LtJ, and three intercrosses, C57BL/6J × DBA/2J, C57BL/6J × C3H/HeJ, and NZB/B1NJ × NZW/LacJ. HDL concentrations were affected by 25 QTL distributed on most chromosomes (Chrs); those on Chrs 1, 8, 12, and 16 were newly identified, and the remainder were replications of previously identified QTL. Triglyceride concentrations were controlled by nine loci; those on Chrs 1, 2, 3, 7, 16, and 18 were newly identified QTL, and the remainder were replications. Combining mouse crosses with haplotype analysis for the HDL QTL on Chr 18 reduced the list of candidates to six genes. Further expression analysis, sequencing, and quantitative complementation testing of these six genes identified Lipg as the HDL QTL gene on distal Chr 18. The data from these crosses further increase the ability to perform haplotype analyses that can lead to the identification of causal lipid genes.
Keywords:high density lipoprotein  triglyceride  quantitative trait locus
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号