Suppr超能文献

酵母中两种线粒体核糖体蛋白的核基因克隆与分析

Cloning and analysis of the nuclear genes for two mitochondrial ribosomal proteins in yeast.

作者信息

Matsushita Y, Kitakawa M, Isono K

机构信息

Department of Biology, Faculty of Science, Kobe University, Japan.

出版信息

Mol Gen Genet. 1989 Oct;219(1-2):119-24. doi: 10.1007/BF00261166.

Abstract

Two mitochondrial ribosomal proteins of yeast (Saccharomyces cerevisiae) were purified and their N-terminal amino acid sequences determined. The sequence data were used for the synthesis of oligonucleotide probes to clone the corresponding genes. Thus, the genes for two proteins, termed YMR-31 and YMR-44, were cloned and their nucleotide sequences determined. From the nucleotide sequence data, the coding region of the gene for protein YMR-31 was found to be composed of 369 nucleotide pairs. Comparison of the amino acid sequence of protein YMR-31 and the one deduced from the nucleotide sequence of its gene suggests that it contains an octapeptide leader sequence. The calculated molecular weight of protein YMR-31 without the leader sequence is 12,792 dalton. The gene for protein YMR-44 was found to contain a 147 bp intron which contains two sequences conserved among yeast introns. The length of the two exons flanking the intron totals 294 nucleotide pairs which can encode a protein with a calculated molecular weight of 11,476 dalton. The gene for protein YMR-31 is located on chromosome VI, while the gene for protein YMR-44 is located on either chromosome XIII or XVI.

摘要

纯化了酵母(酿酒酵母)的两种线粒体核糖体蛋白,并测定了它们的N端氨基酸序列。序列数据用于合成寡核苷酸探针以克隆相应基因。因此,克隆了两种名为YMR - 31和YMR - 44的蛋白质的基因,并测定了它们的核苷酸序列。从核苷酸序列数据中发现,蛋白质YMR - 31的基因编码区由369个核苷酸对组成。蛋白质YMR - 31的氨基酸序列与其基因核苷酸序列推导的氨基酸序列的比较表明,它含有一个八肽前导序列。不含前导序列的蛋白质YMR - 31的计算分子量为12,792道尔顿。发现蛋白质YMR - 44的基因含有一个147 bp的内含子,该内含子包含酵母内含子中保守的两个序列。内含子两侧的两个外显子的长度总计294个核苷酸对,可编码一种计算分子量为11,476道尔顿的蛋白质。蛋白质YMR - 31的基因位于第六条染色体上,而蛋白质YMR - 44的基因位于第十三条或第十六条染色体上。

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