首页> 外文OA文献 >Expansion of the alpha 2-adrenergic receptor family: cloning and characterization of a human alpha 2-adrenergic receptor subtype, the gene for which is located on chromosome 2.
【2h】

Expansion of the alpha 2-adrenergic receptor family: cloning and characterization of a human alpha 2-adrenergic receptor subtype, the gene for which is located on chromosome 2.

机译:扩展α2-肾上腺素受体家族:克隆和表征人类α2-肾上腺素受体亚型,该基因的基因位于2号染色体上。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pharmacologic, biochemical, and genetic analyses have demonstrated the existence of multiple alpha 2-adrenergic receptor (alpha 2AR) subtypes. We have cloned a human alpha 2AR by using the polymerase chain reaction with oligonucleotide primers homologous to conserved regions of the previously cloned alpha 2ARs, the genes for which are located on human chromosomes 4 (C4) and 10 (C10). The deduced amino acid sequence encodes a protein of 450 amino acids whose putative topology is similar to that of the family of guanine nucleotide-binding protein-coupled receptors, but whose structure most closely resembles that of the alpha 2ARs. Competition curve analysis of the binding properties of the receptor expressed in COS-7 cells with a variety of adrenergic ligands demonstrates a unique alpha 2AR pharmacology. Hybridization with somatic cell hybrids shows that the gene for this receptor is located on chromosome 2. Northern blot analysis of various rat tissues shows expression in liver and kidney. The unique pharmacology and tissue localization of this receptor suggest that this is an alpha 2AR subtype not previously identified by classical pharmacological or ligand binding approaches.
机译:药理,生化和遗传分析已证明存在多种α2-肾上腺素受体(α2AR)亚型。我们已经通过使用与先前克隆的alpha 2ARs保守区同源的寡核苷酸引物的聚合酶链反应,克隆了人alpha 2AR,其基因位于人4号染色体(C4)和10号染色体(C10)上。推导的氨基酸序列编码一个450个氨基酸的蛋白质,其推定的拓扑结构与鸟嘌呤核苷酸结合蛋白偶联受体家族相似,但其结构与α2AR最相似。在COS-7细胞中表达的受体与各种肾上腺素配体的结合特性的竞争曲线分析表明,其独特的α2AR药理作用。与体细胞杂种的杂交表明该受体的基因位于2号染色体上。对各种大鼠组织的Northern印迹分析表明它们在肝脏和肾脏中均有表达。该受体的独特药理作用和组织定位表明,这是先前未通过经典药理或配体结合方法鉴定的α2AR亚型。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号