Frantz S A, Kaiser M, Gardiner S M, Gauguier D, Vincent M, Thompson J R, Bennett T, Samani N J
Departments of Cardiology and Ophthalmology, University of Leicester, Leicester, UK.
Hypertension. 1998 Oct;32(4):639-46. doi: 10.1161/01.hyp.32.4.639.
Linkage analyses in experimental crosses of hypertensive and normotensive rats have strongly suggested the presence of a quantitative trait locus (QTL) influencing blood pressure on rat chromosome 1, at or near the Sa gene. To confirm the presence of such a locus and move toward identification of the causative gene, we have developed, through targeted breeding over 10 generations using an Sa gene polymorphism to select breeders at each generation, 2 congenic strains, 1 containing a segment of spontaneously hypertensive rat (SHR) chromosome 1 in a Wistar-Kyoto rat (WKY) genetic background (WKY.SHR-Sa), and the other a segment of WKY chromosome 1 in an SHR background (SHR.WKY-Sa). WKY.SHR-Sa contains at least approximately 26 cM of SHR chromosome 1, between markers mD7mit206 and D1Mit2 (and including the SHR allele of the Sa gene), and SHR.WKY-Sa carries at least approximately 15 cM of WKY chromosome 1, between mD7mit206 and D1Wox34 (and including the WKY allele of the Sa gene). Blood pressure of WKY.SHR-Sa rats measured at 16, 20, and 25 weeks of age was significantly higher than that of WKY, whereas blood pressure of SHR.WKY-Sa rats was significantly lower than that of SHR. At 25 weeks, the mean differences in systolic and diastolic blood pressure between WKY.SHR-Sa and WKY were +11.5 mm Hg (P=0.001) and +11.6 mm Hg mm Hg (P<0.001), respectively. The corresponding differences between SHR.WKy-Sa and SHR were -11.3 mm Hg (P=0.002) and -9.1 mm Hg (P=0.005), respectively. The differences represent about one fifth of the blood pressure difference between SHR and WKY. Renal Sa mRNA levels in the congenic strains reflected their Sa allele with a high level in WKY. SHR-Sa and a low level in SHR.WKY-Sa, consistent with previous data suggesting that the level of Sa expression is primarily determined by cis-acting elements in or near the Sa gene. Our results show that we have successfully isolated a major rat chromosome 1 blood pressure QTL located in the vicinity of the Sa gene in reciprocal congenic strains derived from SHR and WKY. The strains can now be used to further define the region containing the QTL and also to characterize intermediary mechanisms through which the QTL influences blood pressure. In addition, comparison of the regions introgressed in our congenic strains with the location of the peak LOD score for chromosome 1 blood pressure QTL in second filial generation progeny derived from our SHRxWKY cross suggests that there may be at least 1 further QTL influencing blood pressure on this rat chromosome.
在高血压大鼠与正常血压大鼠的实验杂交中进行的连锁分析有力地表明,在大鼠1号染色体上,靠近或位于Sa基因处,存在一个影响血压的数量性状基因座(QTL)。为了证实该基因座的存在并朝着鉴定致病基因的方向推进,我们通过连续10代的定向育种,利用Sa基因多态性在每一代选择育种大鼠,培育出了2个近交系,一个是在Wistar - Kyoto大鼠(WKY)遗传背景中含有一段自发性高血压大鼠(SHR)1号染色体的品系(WKY.SHR - Sa),另一个是在SHR背景中含有一段WKY 1号染色体的品系(SHR.WKY - Sa)。WKY.SHR - Sa在标记mD7mit206和D1Mit2之间(包括Sa基因的SHR等位基因)至少含有约26 cM的SHR 1号染色体,而SHR.WKY - Sa在mD7mit206和D1Wox34之间(包括Sa基因的WKY等位基因)至少携带约15 cM的WKY 1号染色体。在16、20和25周龄时测量的WKY.SHR - Sa大鼠的血压显著高于WKY大鼠,而SHR.WKY - Sa大鼠的血压显著低于SHR大鼠。在25周时,WKY.SHR - Sa与WKY之间收缩压和舒张压的平均差异分别为 +11.5 mmHg(P = 0.001)和 +11.6 mmHg(P < 0.001)。SHR.WKy - Sa与SHR之间的相应差异分别为 -11.3 mmHg(P = 0.002)和 -9.1 mmHg(P = 0.005)。这些差异约占SHR与WKY之间血压差异的五分之一。近交系中的肾脏Sa mRNA水平反映了它们的Sa等位基因,WKY.SHR - Sa中水平较高,而SHR.WKY - Sa中水平较低,这与先前的数据一致,表明Sa表达水平主要由Sa基因内或其附近的顺式作用元件决定。我们的结果表明,我们已成功在源自SHR和WKY的相互近交系中分离出位于Sa基因附近的大鼠1号染色体上的一个主要血压QTL。这些品系现在可用于进一步界定包含该QTL的区域,并用于表征该QTL影响血压的中间机制。此外,将我们近交系中渗入的区域与我们的SHRxWKY杂交产生的第二代子代中1号染色体血压QTL的最高LOD得分位置进行比较表明,在这条大鼠染色体上可能至少还有1个影响血压的QTL。