Lee Soon Jin, Liu Jun, Westcott Allison M, Vieth Joshua A, DeRaedt Sarah J, Yang Siming, Joe Bina, Cicila George T
Department of Physiology, Pharmacology, Metabolism and Cardiovascular Sciences, University of Toledo College of Medicine, Toledo, Ohio 43614, USA.
Genetics. 2006 Dec;174(4):2203-13. doi: 10.1534/genetics.106.061747. Epub 2006 Oct 8.
Substitution mapping was used to refine the localization of blood pressure (BP) quantitative trait loci (QTL) within the congenic region of S.R-Edn3 rats located at the q terminus of rat chromosome 3 (RNO3). An F2(SxS.R-Edn3) population (n=173) was screened to identify rats having crossovers within the congenic region of RNO3 and six congenic substrains were developed that carry shorter segments of R-rat-derived RNO3. Five of the six congenic substrains had significantly lower BP compared to the parental S rat. The lack of BP lowering effect demonstrated by the S.R(ET3x5) substrain and the BP lowering effect retained by the S.R(ET3x2) substrain together define the RNO3 BP QTL-containing region as approximately 4.64 Mb. Two nonoverlapping substrains, S.R(ET3x1) and S.R(ET3x6), had significantly lower BP compared to the S strain, indicating the presence of two distinct BP QTL in the RNO3 q terminus. The RNO3 q terminus was fine mapped with newly developed polymorphic markers to characterize the extent of the congenic regions. The two RNO3 BP QTL regions were thus defined as within intervals of 0.05-1.12 and 0.72-1.25 Mb, respectively. Also important was our difficulty in fine mapping and marker placement in this portion of the rat genome (and thus candidate gene identification) using the available genomic data, including the rat genome sequence.
采用置换作图法对位于大鼠3号染色体(RNO3)q端的S.R-Edn3大鼠同源区域内的血压(BP)数量性状基因座(QTL)进行定位优化。对一个F2(S×S.R-Edn3)群体(n = 173)进行筛选,以鉴定在RNO3同源区域内发生交叉的大鼠,并培育出六个同源亚系,它们携带来自R大鼠的RNO3较短片段。与亲代S大鼠相比,六个同源亚系中的五个具有显著更低的血压。S.R(ET3x5)亚系未表现出血压降低效应,而S.R(ET3x2)亚系保留了血压降低效应,这共同将包含RNO3 BP QTL的区域定义为约4.64 Mb。两个不重叠的亚系S.R(ET3x1)和S.R(ET3x6)与S品系相比具有显著更低的血压,表明在RNO3 q端存在两个不同的BP QTL。利用新开发的多态性标记对RNO3 q端进行精细定位,以表征同源区域的范围。因此,两个RNO3 BP QTL区域分别被定义在0.05 - 1.12 Mb和0.72 - 1.25 Mb的区间内。同样重要的是,我们在利用包括大鼠基因组序列在内的现有基因组数据对大鼠基因组的这一部分进行精细定位和标记放置(从而进行候选基因鉴定)时遇到了困难。