Suppr超能文献

[与酿酒酵母rad蛋白同源的一种新人类基因的克隆及结构测定]

[Cloning and determination of the structure of a new human gene, homologous to Saccharomyces cerevisiae rad proteins].

作者信息

Loseva E F, Kalnin V V

机构信息

Institute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.

出版信息

Genetika. 1999 Jun;35(6):744-50.

Abstract

Cloning of a novel Homo sapiens gene from cDNA libraries of human testes using immunoscreening procedure with affinity-purified polyclonal antibodies against E. coli RecA protein was carried out. The nucleotide sequence and chromosomal localization of this gene were determined. Computer modeling of its primary transcript was conducted. The gene investigated is localized on the P arm of chromosome 19 within the 19p13.1 cluster and consists of seven exons and six introns. It has a leader, 3' untranslated, and translated regions. The translated sequence encodes a 33-kD protein that displays 30-40% homology to the Saccharomyces cerevisae Rad proteins. TATA- and CAAT-like sequences are situated at positions -30 and -40 bp as well as -102 and -148, respectively. The absence of CCGCCC- or GGGCGG-like sequences may indicate that this gene is tissue-specific.

摘要

利用针对大肠杆菌RecA蛋白的亲和纯化多克隆抗体,通过免疫筛选程序从人睾丸的cDNA文库中克隆了一个新的智人基因。确定了该基因的核苷酸序列和染色体定位。对其初级转录本进行了计算机建模。所研究的基因定位于19号染色体的短臂上19p13.1簇内,由7个外显子和6个内含子组成。它有一个前导序列、3'非翻译区和翻译区。翻译后的序列编码一种33-kD的蛋白质,与酿酒酵母Rad蛋白具有30-40%的同源性。TATA样和CAAT样序列分别位于-30和-40 bp以及-102和-148位置。不存在CCGCCC样或GGGCGG样序列可能表明该基因是组织特异性的。

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