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钠/氢逆向转运蛋白:一种“熔解”多态性可实现对1号染色体短臂的区域定位。

The Na+/H+ antiporter: a "melt" polymorphism allows regional mapping to the short arm of chromosome 1.

作者信息

Dudley C R, Giuffra L A, Tippett P, Kidd K K, Reeders S T

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06510.

出版信息

Hum Genet. 1990 Nov;86(1):79-83. doi: 10.1007/BF00205179.

Abstract

The Na+/H+ antiporter is a ubiquitous membrane-associated protein that plays an important role in the regulation of intracellular pH. APNH, a gene encoding the antiporter, has been cloned and mapped to the short arm of chromosome 1 by in situ hybridization. Using the polymerase chain reaction, we have amplified a 376 base pair fragment corresponding to the 5' end of APNH. We have detected a polymorphism within this fragment by denaturing gradient gel electrophoresis. Using polymorphisms at other 1p loci (ALPL, the gene for alkaline phosphatase, RH and D1S57), we have been able to map APNH telomeric to D1S57 and close to RH and ALPL by genetic linkage. APNH is a plausible candidate gene for human essential hypertension; the APNH polymorphism combined with a knowledge of its genetic map location allow this candidate to be tested in hypertensive kindreds and sib-pairs.

摘要

钠氢交换体是一种普遍存在的膜相关蛋白,在细胞内pH调节中起重要作用。APNH是编码该交换体的一个基因,已通过原位杂交克隆并定位到1号染色体短臂上。利用聚合酶链反应,我们扩增出了一个与APNH 5'端相对应的376个碱基对的片段。我们通过变性梯度凝胶电泳在该片段内检测到了一种多态性。利用1p其他位点(碱性磷酸酶基因ALPL、RH和D1S57)的多态性,我们通过遗传连锁将APNH定位到D1S57的端粒侧,且靠近RH和ALPL。APNH是人类原发性高血压一个合理的候选基因;APNH多态性及其遗传图谱位置信息使得该候选基因能够在高血压家系和同胞对中进行检测。

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