• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

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.

DOI:10.1007/BF00261166
PMID:2693936
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。

相似文献

1
Cloning and analysis of the nuclear genes for two mitochondrial ribosomal proteins in yeast.酵母中两种线粒体核糖体蛋白的核基因克隆与分析
Mol Gen Genet. 1989 Oct;219(1-2):119-24. doi: 10.1007/BF00261166.
2
Molecular cloning of the nuclear gene for mitochondrial ribosomal protein YmL31 from Saccharomyces cerevisiae.来自酿酒酵母的线粒体核糖体蛋白YmL31核基因的分子克隆。
Eur J Biochem. 1989 Jul 15;183(1):155-60. doi: 10.1111/j.1432-1033.1989.tb14907.x.
3
Cloning and analysis of YMR26, the nuclear gene for a mitochondrial ribosomal protein in Saccharomyces cerevisiae.酿酒酵母中线粒体核糖体蛋白核基因YMR26的克隆与分析
Mol Gen Genet. 1991 Mar;225(3):474-82. doi: 10.1007/BF00261690.
4
Cloning and analysis of the nuclear gene for YmL33, a protein of the large subunit of the mitochondrial ribosome in Saccharomyces cerevisiae.酿酒酵母线粒体核糖体大亚基蛋白YmL33的核基因克隆与分析。
J Bacteriol. 1991 Jul;173(13):4013-20. doi: 10.1128/jb.173.13.4013-4020.1991.
5
Yeast ribosomal proteins: XI. Molecular analysis of two genes encoding YL41, an extremely small and basic ribosomal protein, from Saccharomyces cerevisiae.酵母核糖体蛋白:XI。来自酿酒酵母的编码YL41(一种极小的碱性核糖体蛋白)的两个基因的分子分析。
Curr Genet. 1990 Mar;17(3):185-90. doi: 10.1007/BF00312608.
6
Cloning and characterization of nuclear genes for two mitochondrial ribosomal proteins in Saccharomyces cerevisiae.酿酒酵母中两种线粒体核糖体蛋白的核基因克隆与特性分析
Nucleic Acids Res. 1990 Mar 25;18(6):1521-9. doi: 10.1093/nar/18.6.1521.
7
Yeast ribosomal proteins: XIII. Saccharomyces cerevisiae YL8A gene, interrupted with two introns, encodes a homolog of mammalian L7.酵母核糖体蛋白:十三。酿酒酵母YL8A基因,有两个内含子中断,编码哺乳动物L7的同源物。
Nucleic Acids Res. 1992 Mar 11;20(5):1011-6. doi: 10.1093/nar/20.5.1011.
8
Yeast ribosomal proteins: XIV. Complete nucleotide sequences of the two genes encoding Saccharomyces cerevisiae YL16.酵母核糖体蛋白:十四。编码酿酒酵母YL16的两个基因的完整核苷酸序列。
Biochim Biophys Acta. 1992 Sep 24;1132(2):195-8. doi: 10.1016/0167-4781(92)90011-n.
9
The gene and the primary structure of acidic ribosomal protein A0 from yeast Saccharomyces cerevisiae which shows partial homology to bacterial ribosomal protein L10.来自酿酒酵母的酸性核糖体蛋白A0的基因及其一级结构,该蛋白与细菌核糖体蛋白L10具有部分同源性。
J Biochem. 1989 Aug;106(2):223-7. doi: 10.1093/oxfordjournals.jbchem.a122836.
10
Isolation and nucleotide sequence of the ribosomal protein S16-encoding gene from Aspergillus nidulans.构巢曲霉核糖体蛋白S16编码基因的分离与核苷酸序列分析
Gene. 1991 Dec 1;108(1):157-62. doi: 10.1016/0378-1119(91)90502-3.

引用本文的文献

1
Widespread use of unconventional targeting signals in mitochondrial ribosome proteins.线粒体核糖体蛋白中非常规靶向信号的广泛使用。
EMBO J. 2022 Jan 4;41(1):e109519. doi: 10.15252/embj.2021109519. Epub 2021 Nov 17.
2
The novel component Kgd4 recruits the E3 subunit to the mitochondrial α-ketoglutarate dehydrogenase.新型组分Kgd4将E3亚基招募至线粒体α-酮戊二酸脱氢酶。
Mol Biol Cell. 2014 Nov 1;25(21):3342-9. doi: 10.1091/mbc.E14-07-1178. Epub 2014 Aug 27.
3
Reconstructing the evolution of the mitochondrial ribosomal proteome.

本文引用的文献

1
Discontinuous agarose electrophoretic system for the recovery of stained proteins from polyacrylamide gels.用于从聚丙烯酰胺凝胶中回收染色蛋白质的不连续琼脂糖电泳系统。
Anal Biochem. 1982 Aug;124(2):264-71. doi: 10.1016/0003-2697(82)90037-9.
2
An improved method for two-dimensional gel-electrophoresis: analysis of mutationally altered ribosomal proteins of Escherichia coli.一种改进的二维凝胶电泳方法:大肠杆菌突变核糖体蛋白的分析
Mol Gen Genet. 1981;181(3):309-12. doi: 10.1007/BF00425603.
3
A comparison of yeast ribosomal protein gene DNA sequences.
重建线粒体核糖体蛋白质组的进化
Nucleic Acids Res. 2007;35(14):4686-703. doi: 10.1093/nar/gkm441. Epub 2007 Jun 29.
4
Subunit VII of ubiquinol:cytochrome-c oxidoreductase from Neurospora crassa is functional in yeast and has an N-terminal extension that is not essential for mitochondrial targeting.粗糙脉孢菌泛醇:细胞色素c氧化还原酶的亚基VII在酵母中具有功能,并且有一个N端延伸,该延伸对于线粒体靶向不是必需的。
Biochem J. 1996 Dec 15;320 ( Pt 3)(Pt 3):769-75. doi: 10.1042/bj3200769.
5
Patterns of meiotic double-strand breakage on native and artificial yeast chromosomes.天然和人工酵母染色体上减数分裂双链断裂的模式。
Chromosoma. 1996 Dec;105(5):276-84. doi: 10.1007/BF02524645.
6
Cloning and analysis of the nuclear gene MRP-S9 encoding mitochondrial ribosomal protein S9 of Saccharomyces cerevisiae.酿酒酵母线粒体核糖体蛋白S9编码核基因MRP-S9的克隆与分析。
Curr Genet. 1995 Jun;28(1):26-31. doi: 10.1007/BF00311878.
7
Molecular cloning and analysis of the nuclear gene MRP-L6 coding for a putative mitochondrial ribosomal protein from Saccharomyces cerevisiae.酿酒酵母中编码一种假定线粒体核糖体蛋白的核基因MRP-L6的分子克隆与分析。
Curr Genet. 1993 Jul-Aug;24(1-2):136-40. doi: 10.1007/BF00324677.
8
The yeast nuclear gene MRP-L13 codes for a protein of the large subunit of the mitochondrial ribosome.酵母核基因MRP-L13编码线粒体核糖体大亚基的一种蛋白质。
Curr Genet. 1994 Jul;26(1):8-14. doi: 10.1007/BF00326298.
9
Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae.Mre11与Rad50的相互作用:酿酒酵母中DNA修复和减数分裂特异性双链断裂形成所需的两种蛋白质。
Genetics. 1995 Apr;139(4):1521-32. doi: 10.1093/genetics/139.4.1521.
10
Structural and functional analyses of a yeast mitochondrial ribosomal protein homologous to ribosomal protein S15 of Escherichia coli.与大肠杆菌核糖体蛋白S15同源的酵母线粒体核糖体蛋白的结构与功能分析
Nucleic Acids Res. 1990 Dec 11;18(23):6895-901. doi: 10.1093/nar/18.23.6895.
酵母核糖体蛋白基因DNA序列的比较
Nucleic Acids Res. 1984 Nov 26;12(22):8295-312. doi: 10.1093/nar/12.22.8295.
4
A computer program package for storing and retrieving DNA/RNA and protein sequence data.一个用于存储和检索DNA/RNA及蛋白质序列数据的计算机程序包。
Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):101-12. doi: 10.1093/nar/12.1part1.101.
5
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
6
Electrophoretic separations of large DNA molecules by periodic inversion of the electric field.通过电场的周期性反转对大型DNA分子进行电泳分离。
Science. 1986 Apr 4;232(4746):65-8. doi: 10.1126/science.3952500.
7
A compilation of large subunit RNA sequences presented in a structural format.以结构形式呈现的大亚基RNA序列汇编。
Nucleic Acids Res. 1988;16 Suppl(Suppl):r175-269. doi: 10.1093/nar/16.suppl.r175.
8
The physical map of the whole E. coli chromosome: application of a new strategy for rapid analysis and sorting of a large genomic library.完整大肠杆菌染色体的物理图谱:一种用于大型基因组文库快速分析和分类的新策略的应用
Cell. 1987 Jul 31;50(3):495-508. doi: 10.1016/0092-8674(87)90503-4.
9
Isolation and characterization of the regulatory HEX2 gene necessary for glucose repression in yeast.酵母中葡萄糖阻遏所需的调控基因HEX2的分离与特性分析
Mol Gen Genet. 1987 Mar;206(3):505-9. doi: 10.1007/BF00428892.
10
Assembly of the mitochondrial membrane system. MRP1 and MRP2, two yeast nuclear genes coding for mitochondrial ribosomal proteins.线粒体膜系统的组装。MRP1和MRP2,两个编码线粒体核糖体蛋白的酵母核基因。
J Biol Chem. 1987 Mar 5;262(7):3388-97.