Lindpaintner K, Hilbert P, Ganten D, Nadal-Ginard B, Inagami T, Iwai N
Department of Cardiology, Children's Hospital, Boston, Massachusetts 02115.
J Hypertens. 1993 Jan;11(1):19-23. doi: 10.1097/00004872-199301000-00004.
The SA-gene shows markedly higher levels of expression in the kidneys of spontaneously hypertensive rats (SHR) than in their non-hypertensive reference strain, the Wistar-Kyoto (WKY) rat. Based on the important role of the kidney in blood pressure regulation, the possibility has been raised that this gene, the translational product of which remains unknown, may participate in the pathogenesis of primary hypertension. The present study was conducted to test this hypothesis and to ascertain the chromosomal localization of the SA-gene.
A cosegregation study was performed using an F2 intercross between stroke-prone SHR (SHRSP) and WKY rats, and a previously described restriction fragment length polymorphism of the SA-gene for characterization of genotype. Mapping of the SA-gene was accomplished by screening a somatic cell-hybrid panel and by linkage group analysis.
A statistically significant difference in systolic blood pressure was found after sodium loading, but not under basal conditions between groups of rats defined by zygosity at the SA locus, consistent with a hypertensive effect of the SHRSP allele. No effect of SA genotype on diastolic blood pressure was observed. The SA-gene was localized on rat chromosome 1.
This study establishes the SA locus on chromosome 1 as a region in which a gene or genes contributing to blood pressure regulation in this model are localized, and provides further evidence for a possible role of the SA-gene in the pathogenesis of hypertension.
SA基因在自发性高血压大鼠(SHR)肾脏中的表达水平明显高于其非高血压对照品系Wistar-Kyoto(WKY)大鼠。鉴于肾脏在血压调节中的重要作用,有人提出该基因(其翻译产物尚不清楚)可能参与原发性高血压的发病机制。本研究旨在验证这一假设并确定SA基因的染色体定位。
使用易卒中型SHR(SHRSP)和WKY大鼠之间的F2杂交进行共分离研究,并使用先前描述的SA基因限制性片段长度多态性来鉴定基因型。通过筛选体细胞杂交板和连锁群分析完成SA基因的定位。
在钠负荷后,在SA位点按纯合性定义的大鼠组之间发现收缩压有统计学显著差异,但在基础条件下未发现差异,这与SHRSP等位基因的高血压效应一致。未观察到SA基因型对舒张压有影响。SA基因定位于大鼠1号染色体。
本研究确定1号染色体上的SA位点是该模型中一个或多个参与血压调节的基因所在区域,并为SA基因在高血压发病机制中可能发挥的作用提供了进一步证据。