Suppr超能文献

人类ε-珠蛋白基因的分子克隆

Molecular cloning of human epsilon-globin gene.

作者信息

Proudfoot N J, Baralle F E

出版信息

Proc Natl Acad Sci U S A. 1979 Nov;76(11):5435-9. doi: 10.1073/pnas.76.11.5435.

Abstract

Human beta-like globin genes were investigated by use of rabbit beta-globin cDNA plasmid as a cross-species hybridization probe. Normal and beta 0/delta beta 0 thalassemic DNA were compared by filter hybridization procedures. It proved possible to demonstrate that the rabbit probe detected G gamma, A gamma, delta, beta, beta 0, and delta beta 0 human globin genes as well as an additional unidentified beta-like globin gene. By use of an agarose gel elution procedure, fractions of HindIII-digested DNA enriched for beta-like globin genes were purified. One of these fractions, 8.0 kilobases in size, was clonedinto lambda 788, and EK2 lambda HindIII vector. A positive clone was obtained and characterized by restriction mapping and sequence analysis. The sequence data obtained predicted an amino acid sequence that exactly matches a part of human epsilon-globin. The human non-alpha-globin locus is now nearly complete. delta, beta, and gamma human globin genes have already been cloned and analyzed. We describe here the cloning of the remaining non-alpha-globin gene, epsilon.

摘要

利用兔β-珠蛋白cDNA质粒作为种间杂交探针,对人β样珠蛋白基因进行了研究。通过滤膜杂交程序比较了正常和β0/δβ0地中海贫血DNA。结果表明,兔探针可检测到Gγ、Aγ、δ、β、β0和δβ0人珠蛋白基因以及另一个未鉴定的β样珠蛋白基因。通过琼脂糖凝胶洗脱程序,纯化了富含β样珠蛋白基因的HindIII消化DNA片段。其中一个大小为8.0千碱基的片段被克隆到λ788和EK2λHindIII载体中。获得了一个阳性克隆,并通过限制性图谱分析和序列分析对其进行了表征。所获得的序列数据预测的氨基酸序列与人类ε-珠蛋白的一部分完全匹配。人类非α-珠蛋白基因座现已基本完整。δ、β和γ人珠蛋白基因已经被克隆和分析。我们在此描述剩余非α-珠蛋白基因ε的克隆。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3850/411663/367fe314a01e/pnas00011-0030-a.jpg

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