Suppr超能文献

通过聚合酶链式反应(PCR)克隆从四膜虫中鉴定出一个低分子量GTP结合蛋白同源物的复杂家族。

The identification of a complex family of low-molecular-weight GTP-binding protein homologues from Paramecium tetraurelia by PCR cloning.

作者信息

Fraga D, Hinrichsen R D

机构信息

Fred Hutchinson Cancer Research Center, Seattle, WA 98115.

出版信息

Gene. 1994 Sep 15;147(1):145-8. doi: 10.1016/0378-1119(94)90055-8.

Abstract

We have used the polymerase chain reaction to clone a large number of gene fragments encoding low-molecular-weight GTP-binding proteins (LMW G-proteins) from Paramecium tetraurelia. All clones were subjected to a computer-assisted search of the GenBank databases to assign putative homologues. On the basis of several conserved features, we place these genes in the rab/ypt and rho subfamilies of the LMW G-proteins. Northern blot analyses indicated that all clones were from active genes. One surprising feature of the cloned genomic sequences was the presence of unusually short introns (20-30 nucleotides).

摘要

我们利用聚合酶链反应从四膜虫中克隆了大量编码低分子量GTP结合蛋白(LMW G蛋白)的基因片段。所有克隆均经过计算机辅助搜索GenBank数据库以确定推定的同源物。基于几个保守特征,我们将这些基因归入LMW G蛋白的rab/ypt和rho亚家族。Northern印迹分析表明所有克隆均来自活性基因。克隆的基因组序列的一个惊人特征是存在异常短的内含子(20 - 30个核苷酸)。

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