Jeffs B, Negrin C D, Graham D, Clark J S, Anderson N H, Gauguier D, Dominiczak A F
Department of Medicine and Therapeutics, University of Glasgow, Western Infirmary, Glasgow, UK.
Hypertension. 2000 Jan;35(1 Pt 2):179-87. doi: 10.1161/01.hyp.35.1.179.
The identification of any quantitative trait locus (QTL) via a genome scan is only the first step toward the ultimate goal of gene identification. The next step is the production of congenic strains by which the existence of a QTL may be verified and the implicated chromosomal region be reduced to a size applicable to positional cloning of the causal gene. We used a speed congenic breeding protocol previously verified in mice for 2 blood pressure QTLs on rat chromosome 2. Four congenic strains were produced through introgression of various segments of chromosome 2 from Wistar-Kyoto rats from Glasgow colonies [WKY((Gla)) rats] into the recipient stroke-prone spontaneously hypertensive rats from Glasgow colonies [SHRSP((Gla))], and vice versa. The number of backcross generations required for each strain to achieve complete homozygosity at 83 background genetic markers in a "best" male varied between 3 and 4. Transfer of the region of rat chromosome 2 containing both QTLs from WKY((Gla)) into an SHRSP((Gla)) genetic background lowered both baseline and salt-loaded systolic blood pressure by approximately 20 and approximately 40 mm Hg in male congenic rats compared with the SHRSP parental strain (F=53.4, P<0.005; F=28.0, P< 0.0005, respectively). In contrast, control animals for stowaway heterozygosity presented no deviation from the blood pressure values recorded for the SHRSP((Gla)), indicating that if such heterozygosity exists, its effect on blood pressure is negligible. A reciprocal strategy in which 1 or both QTLs on rat chromosome 2 were transferred from SHRSP((Gla)) into a WKY((Gla)) genetic background resulted in statistically significant but smaller blood pressure increases for 1 of these QTLs. These results confirm the existence of blood pressure QTLs on rat chromosome 2 and demonstrate the applicability of a speed congenic strategy in the rat and emphasize the important role of the genetic background.
通过基因组扫描鉴定任何数量性状基因座(QTL)仅仅是朝着基因鉴定这一最终目标迈出的第一步。下一步是培育近交系,通过它可以验证QTL的存在,并将涉及的染色体区域缩小到适用于因果基因定位克隆的大小。我们使用了一种先前在小鼠中验证过的快速近交育种方案,用于大鼠2号染色体上的2个血压QTL。通过将来自格拉斯哥殖民地的Wistar-Kyoto大鼠[WKY((Gla))大鼠]2号染色体的各个片段导入来自格拉斯哥殖民地的易中风自发性高血压大鼠[SHRSP((Gla))],反之亦然,培育出了4个近交系。每个品系在一只“最佳”雄性大鼠中83个背景遗传标记处达到完全纯合所需的回交代数在3到4代之间。将含有两个QTL的大鼠2号染色体区域从WKY((Gla))转移到SHRSP((Gla))遗传背景中,与SHRSP亲本品系相比,雄性近交系大鼠的基线收缩压和盐负荷收缩压分别降低了约20和约40 mmHg(F = 53.4,P < 0.005;F = 28.0,P < 0.0005)。相比之下,携带隐匿杂合性的对照动物的血压值与SHRSP((Gla))记录的血压值没有偏差,这表明如果存在这种杂合性,其对血压的影响可以忽略不计。一种反向策略,即将大鼠2号染色体上的1个或2个QTL从SHRSP((Gla))转移到WKY((Gla))遗传背景中,其中1个QTL导致血压有统计学意义但较小的升高。这些结果证实了大鼠2号染色体上存在血压QTL,并证明了快速近交策略在大鼠中的适用性,强调了遗传背景的重要作用。