Woodley-Miller C, Chao J, Chao L
Department of Biochemistry, Medical University of South Carolina, Charleston 29425.
J Hypertens. 1989 Nov;7(11):865-71. doi: 10.1097/00004872-198911000-00003.
We have explored the role of kallikrein-kinin system in essential hypertension using spontaneously hypertensive rats (SHR) as an animal model. A rat tissue kallikrein complementary (c) DNA (RSK 1105) was used as a probe in Southern blot hybridization to detect restriction fragment length polymorphisms (RFLPs) in SHR. Using 23 different restriction endonucleases, we have identified five RFLPs involving alterations in restriction fragment lengths for the restriction enzymes Bgl II, Dra I, Nde I, Sph I, and Bcl I. Three of the enzymes, Nde I, Sph I, and Bgl II, generate multiple polymorphic fragments. We have further mapped these RFLPs with two additional probes, both from the rat renal kallikrein gene RSKG 7. The 5' probe, consisting of sequences approximately 2000 base pair (bp) 5' of the first exon, recognizes RFLPs in DNA digested with Bcl I and Sph I. The 3' probe, approximately 4400 bp away from the fifth exon, recognizes polymorphic fragments in DNA digested with Bcl I, Dra I and Nde I. These findings indicate possible differences in tissue kallikrein genes or their regulatory regions in SHR that could contribute to the pathogenesis of hypertension in this animal model.
我们以自发性高血压大鼠(SHR)作为动物模型,探讨了激肽释放酶-激肽系统在原发性高血压中的作用。用大鼠组织激肽释放酶互补(c)DNA(RSK 1105)作为探针,进行Southern印迹杂交,以检测SHR中的限制性片段长度多态性(RFLP)。使用23种不同的限制性内切酶,我们鉴定出5种RFLP,涉及限制性内切酶Bgl II、Dra I、Nde I、Sph I和Bcl I的限制性片段长度改变。其中三种酶,Nde I、Sph I和Bgl II,产生多个多态性片段。我们用另外两个均来自大鼠肾激肽释放酶基因RSKG 7的探针,进一步对这些RFLP进行了定位。5'探针由第一个外显子上游约2000个碱基对(bp)的序列组成,可识别用Bcl I和Sph I消化的DNA中的RFLP。3'探针距离第五个外显子约4400 bp,可识别用Bcl I、Dra I和Nde I消化的DNA中的多态性片段。这些发现表明,SHR中组织激肽释放酶基因或其调控区域可能存在差异,这可能导致该动物模型中高血压的发病机制。