Lyons Malcolm A, Wittenburg Henning, Li Renhua, Walsh Kenneth A, Korstanje Ron, Churchill Gary A, Carey Martin C, Paigen Beverly
The Jackson Laboratory, Bar Harbor, Maine 04609, USA.
Physiol Genomics. 2004 Mar 12;17(1):60-8. doi: 10.1152/physiolgenomics.00142.2003.
To identify genetic determinants of lipoprotein levels, we are performing quantitative trait locus (QTL) analysis on a series of mouse intercrosses in a "daisy chain" experimental design, to increase the power of detecting QTL and to identify common variants that should segregate in multiple intercrosses. In this study, we intercrossed strains CAST/Ei and 129S1/SvImJ, determined HDL, total, and non-HDL cholesterol levels, and performed QTL mapping using Pseudomarker software. For HDL cholesterol, we identified two significant QTL on chromosome (Chr) 1 (Hdlq5, 82 cM, 60-100 cM) and Chr 4 (Hdlq10, 20 cM, 10-30 cM). For total cholesterol, we identified three significant QTL on Chr 1 (Chol7, 74 cM, 65-80 cM), Chr 4 (Chol8, 12 cM, 0-30 cM), and Chr 17 (Chol9, 54 cM, 20-60 cM). For non-HDL cholesterol, we identified significant QTL on Chr 8 (Nhdlq1, 34 cM, 20-60 cM) and Chr X (Nhdlq2, 6 cM, 0-18 cM). Hdlq10 was the only QTL detected in two intercrosses involving strain CAST/Ei. Hdlq5, Hdlq10, Nhdlq1, and two suggestive QTL at D7Mit246 and D15Mit115 coincided with orthologous human lipoprotein QTL. Our analysis furthers the knowledge of the genetic control of lipoprotein levels and points to the importance of Hdlq10, which was detected repeatedly in multiple studies.
为了确定脂蛋白水平的遗传决定因素,我们正在采用“雏菊链”实验设计,对一系列小鼠杂交系进行数量性状基因座(QTL)分析,以提高检测QTL的能力,并识别应在多个杂交系中分离的常见变异。在本研究中,我们将CAST/Ei和129S1/SvImJ品系进行杂交,测定高密度脂蛋白(HDL)、总胆固醇和非HDL胆固醇水平,并使用伪标记软件进行QTL定位。对于HDL胆固醇,我们在染色体(Chr)1(Hdlq5,82 cM,60 - 100 cM)和Chr 4(Hdlq10,20 cM,10 - 30 cM)上鉴定出两个显著的QTL。对于总胆固醇,我们在Chr 1(Chol7,74 cM,65 - 80 cM)、Chr 4(Chol8,1 cM,0 - 30 cM)和Chr 17(Chol9,54 cM,20 - 60 cM)上鉴定出三个显著的QTL。对于非HDL胆固醇,我们在Chr 8(Nhdlq1,34 cM,20 - 60 cM)和Chr X(Nhdlq2,6 cM,0 - 18 cM)上鉴定出显著的QTL。Hdlq10是在涉及CAST/Ei品系的两个杂交系中检测到的唯一QTL。Hdlq5、Hdlq10、Nhdlq1以及在D7Mit246和D15Mit115处的两个提示性QTL与直系同源的人类脂蛋白QTL一致。我们的分析进一步加深了对脂蛋白水平遗传控制的认识,并指出了Hdlq10的重要性,该基因座在多项研究中被反复检测到。