Alvi Farrakh M, Hasnain Shahida
Department of Microbiology and Molecular Genetics, Quaid-e-Azam Campus, University of Punjab, Lahore 54590, Pakistan.
J Renin Angiotensin Aldosterone Syst. 2008 Mar;9(1):27-31. doi: 10.3317/jraas.2008.006.
The renin-angiotensin-aldosterone system (RAAS) plays a key role in blood pressure (BP) regulation. Among the components of the RAAS, the gene for the angiotensinogen (AGT) has been extensively studied. Several studies in different populations link Threonine instead of methionine at position 235 (M235T) and Methinine instead of threonine at position 174 (T174M) polymorphisms with essential hypertension. We were unable to study these polymorphisms in the Punjab population of Pakistan through routine Restriction Fragment Length Polymorphism (RFLP) method. Considering the importance of this region we decided to further investigate the 300 bp region harbouring these two single nucleotide polymorphisms.
Samples were derived from a larger study group. Polymerase chain reaction amplified fragments were subjected to either RFLP or Single Strand Conformation Polymorphism. Single stranded DNA showing mobility shift on denaturing gel were sequenced.
Sequencing confirmed the presence of M235T and T174M polymorphisms in the local population. In addition to these polymorphisms one additional base was found at an identical position in two of the samples. We found a substitution of G with C just adjacent to T174M polymorphism in all seven of our samples studied.
We report two additional bases and one substitution in the angiotensinogen gene of Punjab population. We also suggest that SsmI can be used for the investigation of T174M polymorphism.
肾素 - 血管紧张素 - 醛固酮系统(RAAS)在血压(BP)调节中起关键作用。在RAAS的组成成分中,血管紧张素原(AGT)基因已得到广泛研究。不同人群的多项研究将235位苏氨酸替代甲硫氨酸(M235T)和174位甲硫氨酸替代苏氨酸(T174M)多态性与原发性高血压联系起来。我们无法通过常规限制性片段长度多态性(RFLP)方法在巴基斯坦旁遮普人群中研究这些多态性。鉴于该区域的重要性,我们决定进一步研究包含这两个单核苷酸多态性的300 bp区域。
样本取自一个更大的研究组。聚合酶链反应扩增片段进行RFLP或单链构象多态性分析。在变性凝胶上显示迁移率变化的单链DNA进行测序。
测序证实当地人群中存在M235T和T174M多态性。除了这些多态性外,在两个样本的相同位置发现了一个额外的碱基。在我们研究的所有七个样本中,发现紧邻T174M多态性处有一个G被C替代。
我们报告了旁遮普人群血管紧张素原基因中的两个额外碱基和一个替代。我们还建议SsmI可用于研究T174M多态性。