Suppr超能文献

γ-氨基丁酸A受体β3亚基基因:来自15q11q13染色体的人类cDNA的特征及在小鼠7号染色体上保守同线区域的定位。

The GABAA receptor beta 3 subunit gene: characterization of a human cDNA from chromosome 15q11q13 and mapping to a region of conserved synteny on mouse chromosome 7.

作者信息

Wagstaff J, Chaillet J R, Lalande M

机构信息

Division of Genetics, Children's Hospital, Boston, Massachusetts.

出版信息

Genomics. 1991 Dec;11(4):1071-8. doi: 10.1016/0888-7543(91)90034-c.

Abstract

A cDNA encoding the human GABAA receptor beta 3 subunit has been isolated from a brain cDNA library and its nucleotide sequence has been determined. This gene, GABRB3, has recently been mapped to human chromosome 15q11q13, the region deleted in Angelman and Prader-Willi syndromes. The association of distinct phenotypes with maternal versus paternal deletions of this region suggests that one or more genes in this region show parental-origin-dependent expression (genetic imprinting). Comparison of the inferred human beta 3 subunit amino acid sequence with beta 3 subunit sequences from rat, cow, and chicken shows a very high degree of evolutionary conservation. We have used this cDNA to map the mouse beta 3 subunit gene, Gabrb-3, in recombinant inbred strains. The gene is located on mouse chromosome 7, very closely linked to Xmv-33 between Tam-1 and Mtv-1, where two other genes from human 15q11q13 have also been mapped. This provides further evidence for a region of conserved synteny between human chromosome 15q11q13 and mouse chromosome 7. Proximal and distal regions of mouse chromosome 7 show genetic imprinting effects; however, the region of homology with human chromosome 15q11q13 has not yet been associated with these effects.

摘要

已从人脑cDNA文库中分离出编码人γ-氨基丁酸A型(GABAA)受体β3亚基的cDNA,并测定了其核苷酸序列。该基因GABRB3最近被定位于人类染色体15q11q13,这一区域在天使综合征和普拉德-威利综合征中发生缺失。该区域母源与父源缺失所导致的不同表型关联表明,该区域中的一个或多个基因呈现亲本来源依赖性表达(基因印记)。将推导的人β3亚基氨基酸序列与大鼠、牛和鸡的β3亚基序列进行比较,结果显示出高度的进化保守性。我们利用此cDNA在重组近交系中对小鼠β3亚基基因Gabrb-3进行定位。该基因位于小鼠的7号染色体上,与Tam-1和Mtv-1之间的Xmv-33紧密连锁,人类15q11q13的另外两个基因也定位于此。这为人类染色体15q11q13与小鼠染色体7之间的保守同线性区域提供了进一步的证据。小鼠7号染色体的近端和远端区域呈现基因印记效应;然而,与人类染色体15q11q13的同源区域尚未发现与这些效应有关联。

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