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自发性高血压大鼠中利钠肽基因与血压的共分离分析。

Cosegregation analysis of natriuretic peptide genes and blood pressure in the spontaneously hypertensive rat.

作者信息

Ye Ping, West Malcolm J

机构信息

Department of Medicine, The University of Queensland, Prince Charles Hospital, Brisbane, Queensland, Australia.

出版信息

Clin Exp Pharmacol Physiol. 2003 Dec;30(12):930-6. doi: 10.1111/j.1440-1681.2003.03937.x.

Abstract
  1. The natriuretic peptide precursor A (Nppa) and B (Nppb) genes are candidate genes for hypertension and cardiac hypertrophy in the spontaneously hypertensive rat (SHR). The purpose of the present study was to determine the role of the Nppa and Nppb genes in the development of hypertension in the SHR. 2. A cohort (n = 162) of F2 segregating intercross animals was established between strains of hypertensive SHR and normotensive Wistar-Kyoto rats. Blood pressure and heart weight were measured in each rat at 12-16 weeks of age. Rats were genotyped using 11 informative microsatellite markers, distributed in the vicinity of the Nppa marker on rat chromosome 5 including an Nppb marker. The phenotype values were compared with genotype using the computer package mapmaker 3.0 (Whitehead Institute, Boston, MA, USA) to determine whether there was a link between the genetic variants of the natriuretic peptide family and blood pressure or cardiac hypertrophy. 3. A strong correlation was observed between the Nppa marker and blood pressure. A quantitative trait locus (QTL) for blood pressure on chromosome 5 was identified between the Nppa locus and the D5Mgh15 marker, less than 2 cM from the Nppa locus. The linkage score for the blood pressure QTL on chromosome 5 was 3.8 and the QTL accounted for 43% of the total variance of systolic blood pressure, 54% of diastolic blood pressure and 59% of mean blood pressure. No association was found between the Nppb gene and blood pressure. This is the first report of linkage between the Nppa marker and blood pressure in the rat. There was no correlation between the Nppa or Nppb genes or other markers in this region and either heart weight or left ventricular weight in F2 rats. 4. These findings suggest the existence of a blood pressure-dependent Nppa marker variant or a gene close to Nppa predisposing to spontaneous hypertension in the rat. It provides a strong foundation for further detailed genetic studies in congenic strains, which may help to narrow down the location of this gene and lead to positional cloning.
摘要
  1. 利钠肽前体A(Nppa)基因和B(Nppb)基因是自发性高血压大鼠(SHR)中高血压和心脏肥大的候选基因。本研究的目的是确定Nppa和Nppb基因在SHR高血压发生发展中的作用。2. 在高血压SHR品系和正常血压的Wistar-Kyoto大鼠品系之间建立了一个F2分离杂交动物群体(n = 162)。在12至16周龄时测量每只大鼠的血压和心脏重量。使用11个信息丰富的微卫星标记对大鼠进行基因分型,这些标记分布在大鼠5号染色体上Nppa标记附近,包括一个Nppb标记。使用计算机软件包Mapmaker 3.0(美国马萨诸塞州波士顿怀特黑德研究所)将表型值与基因型进行比较,以确定利钠肽家族的基因变异与血压或心脏肥大之间是否存在联系。3. 观察到Nppa标记与血压之间存在强相关性。在5号染色体上Nppa基因座和D5Mgh15标记之间鉴定出一个血压数量性状基因座(QTL),距离Nppa基因座不到2厘摩。5号染色体上血压QTL的连锁分数为3.8,该QTL占收缩压总方差的43%、舒张压总方差的54%和平均血压总方差的59%。未发现Nppb基因与血压之间存在关联。这是大鼠中Nppa标记与血压之间连锁关系的首次报道。在F2大鼠中,该区域的Nppa或Nppb基因及其他标记与心脏重量或左心室重量之间均无相关性。4. 这些发现表明存在一种依赖血压的Nppa标记变异或一个与Nppa基因相近且易导致大鼠自发性高血压的基因。这为同源近交系中的进一步详细遗传研究提供了坚实基础,这可能有助于缩小该基因的定位范围并实现定位克隆。

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