Suppr超能文献

用tre癌基因探针筛选分离得到的小鼠L19核糖体蛋白cDNA的核苷酸序列。

Nucleotide sequence of mouse L19 ribosomal protein cDNA isolated in screening with tre oncogene probes.

作者信息

Nakamura T, Onno M, Mariage-Samson R, Hillova J, Hill M

机构信息

Laboratory of Cellular and Molecular Biology, Centre National de la Recherche Scientifique, Villejuif, France.

出版信息

DNA Cell Biol. 1990 Dec;9(10):697-703. doi: 10.1089/dna.1990.9.697.

Abstract

A cDNA library was prepared from cytoplasmic poly(A)RNA from mouse NIH-3T3 cells carrying a transfected human tre oncogene. Screening with tre gene probes identified a tre cDNA clone 11-4 and a co-purifying weakly hybridizing cDNA clone 11-5. The 11-5-specific RNA was expressed in both nontransfected and tre-transfected NIH-3T3 cells, showing it is of mouse rather than tre gene origin. Its nucleotide sequence was 717 bp long and contained, starting from the first nucleotide, an open reading frame of 588 bp followed by a 3' noncoding region and 26 A residues at the 3' terminus. Comparison with the GenBank data base revealed 93.7% homology with cDNA encoding the rat L19 ribosomal protein. Furthermore, the 196-amino-acid polypeptide deduced from 11-5 was of the same length and contained only one amino acid difference compared with the rat L19 protein. Comparison with the weakly hybridizing tre gene probe showed stretches of homology that were, however, too short to be taken into consideration. We conclude that the 11-5 sequence encodes the mouse L19 ribosomal protein.

摘要

从携带转染人tre癌基因的小鼠NIH-3T3细胞的细胞质多聚腺苷酸RNA制备了一个cDNA文库。用tre基因探针筛选鉴定出一个tre cDNA克隆11-4和一个共纯化的弱杂交cDNA克隆11-5。11-5特异性RNA在未转染和tre转染的NIH-3T3细胞中均有表达,表明它起源于小鼠而非tre基因。其核苷酸序列长717 bp,从第一个核苷酸开始,有一个588 bp的开放阅读框,后面跟着一个3'非编码区和3'末端的26个A残基。与GenBank数据库比较发现,它与编码大鼠L19核糖体蛋白的cDNA有93.7%的同源性。此外,从11-5推导的196个氨基酸的多肽长度相同,与大鼠L19蛋白相比仅含一个氨基酸差异。与弱杂交的tre基因探针比较显示出同源性片段,但短得无法考虑。我们得出结论,11-5序列编码小鼠L19核糖体蛋白。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验