Nishihara Eri, Tsaih Shirng-Wern, Tsukahara Chieko, Langley Sarah, Sheehan Susan, DiPetrillo Keith, Kunita Satoshi, Yagami Ken-ichi, Churchill Gary A, Paigen Beverly, Sugiyama Fumihiro
Laboratory Animal Resource Center, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, 305-8575, Japan.
Mamm Genome. 2007 Aug;18(8):573-83. doi: 10.1007/s00335-007-9033-5. Epub 2007 Jul 20.
In a previous study in 15 inbred mouse strains, we found highest and lowest systolic blood pressures in NZO/HILtJ mice (metabolic syndrome) and C3H/HeJ mice (common lean strain), respectively. To identify the loci involved in hypertension in metabolic syndrome, we performed quantitative trait locus (QTL) analysis for blood pressure with direction of cross as a covariate in segregating F2 males derived from NZO/HILtJ and C3H/HeJ mice. We detected three suggestive main-effect QTLs affecting systolic and diastolic blood pressures (SBP and DBP). We analyzed the first principle component (PC1) generated from SBP and DBP to investigate blood pressure. In addition to all the suggestive QTLs (Chrs 1, 3, and 8) in SBP and DBP, one suggestive QTL on Chr 4 was found in PC1 in the main scan. Simultaneous search identified two significant epistatic locus pairs (Chrs 1 and 4, Chrs 4 and 8) for PC1. Multiple regression analysis revealed three blood pressure QTLs (Bpq10, 100 cM on Chr 1; Bpq11, 6 cM on Chr 4; Bpq12, 29 cM on Chr 8) accounting for 29.4% of blood pressure variance. These were epistatic interaction QTLs constructing a small network centered on Chr 4, suggesting the importance of genetic interaction for development of hypertension. The blood pressure QTLs on Chrs 1, 4, and 8 were detected repeatedly in multiple studies using common inbred nonobese mouse strains, implying substantial QTL independent of development of obesity and insulin resistance. These results enhance our understanding of complicated genetic factors of hypertension in metabolic diseases.
在之前一项针对15种近交系小鼠品系的研究中,我们发现NZO/HILtJ小鼠(代谢综合征)的收缩压最高,而C3H/HeJ小鼠(普通瘦型品系)的收缩压最低。为了确定代谢综合征中与高血压相关的基因座,我们以杂交方向作为协变量,对源自NZO/HILtJ和C3H/HeJ小鼠的F2代雄性分离群体进行了血压的数量性状基因座(QTL)分析。我们检测到了三个影响收缩压和舒张压(SBP和DBP)的提示性主效QTL。我们分析了由SBP和DBP生成的第一主成分(PC1)以研究血压。除了SBP和DBP中的所有提示性QTL(第1、3和8号染色体)外,在主扫描的PC1中还发现了第4号染色体上的一个提示性QTL。同时搜索确定了PC1的两个显著上位基因座对(第1和4号染色体、第4和8号染色体)。多元回归分析揭示了三个血压QTL(Bpq10,位于第1号染色体100 cM处;Bpq11,位于第4号染色体6 cM处;Bpq12,位于第8号染色体29 cM处),它们解释了29.4%的血压变异。这些是构建以第4号染色体为中心的小网络的上位相互作用QTL,表明基因相互作用对高血压发展的重要性。使用常见的近交非肥胖小鼠品系在多项研究中反复检测到第1、4和8号染色体上的血压QTL,这意味着存在大量独立于肥胖和胰岛素抵抗发展的QTL。这些结果增强了我们对代谢疾病中高血压复杂遗传因素的理解。