Suppr超能文献

一种人类神经肽Y受体的分子遗传学分析。小鼠“Y5”受体的人类同源物可能是一个假基因。

Molecular genetic analysis of a human neuropeptide Y receptor. The human homolog of the murine "Y5" receptor may be a pseudogene.

作者信息

Rose P M, Lynch J S, Frazier S T, Fisher S M, Chung W, Battaglino P, Fathi Z, Leibel R, Fernandes P

机构信息

Department of Microbial Molecular Biology, Bristol-Myers Squibb, Princeton, New Jersey 08543, USA.

出版信息

J Biol Chem. 1997 Feb 7;272(6):3622-7. doi: 10.1074/jbc.272.6.3622.

Abstract

Neuropeptide Y is a 36-amino-acid peptide amide with numerous biological activities. These functions are mediated through several pharmacologically distinct receptors. To date five receptor subtypes have been cloned. Here we report the isolation, by low stringency homology cloning from a hypothalamic library, of a cDNA encoding the human homolog of the murine neuropeptide Y receptor subsequently reported (). Translation of the human Y1-like receptor clone suggested that it encoded a receptor which is truncated in the third extracellular loop. Comparison of the human Y1-like sequence to that of the human Y1 receptor suggested that the truncated receptor could have resulted from a frameshift due to a single nucleotide deletion in the sixth transmembrane domain. Southern blot analysis suggested that the gene is single copy in the human genome. The gene is located on chromosome 5q. To test the hypothesis that allelic variation of nucleic acid length within the sixth transmembrane domain of the Y1-like receptor may exist to produce a functional receptor, genomic DNA from 192 individuals of various ages, ethnic backgrounds, and degrees of obesity were analyzed electrophoretically and by direct sequencing. No variation was detected in any of the subjects, indicating that this receptor subtype may be a transcribed pseudogene in humans.

摘要

神经肽Y是一种具有多种生物活性的含36个氨基酸的肽酰胺。这些功能是通过几种药理学上不同的受体介导的。迄今为止,已克隆出五种受体亚型。在此,我们报告通过从下丘脑文库进行低严格度同源克隆,分离出一个编码小鼠神经肽Y受体人类同源物的cDNA(随后报道)。人类Y1样受体克隆的翻译表明,它编码的受体在第三个细胞外环中被截断。将人类Y1样序列与人类Y1受体序列进行比较表明,该截断的受体可能是由于第六个跨膜结构域中的单个核苷酸缺失导致移码所致。Southern印迹分析表明该基因在人类基因组中是单拷贝的。该基因位于5号染色体q臂上。为了检验Y1样受体第六个跨膜结构域内可能存在核酸长度的等位基因变异以产生功能性受体这一假说,对来自192名不同年龄、种族背景和肥胖程度个体的基因组DNA进行了电泳分析和直接测序。在任何受试者中均未检测到变异,表明该受体亚型在人类中可能是一个转录假基因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验