• 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

编码酵母线粒体DNA聚合酶催化亚基的核基因MIP1的克隆与测序

Cloning and sequencing of the nuclear gene MIP1 encoding the catalytic subunit of the yeast mitochondrial DNA polymerase.

作者信息

Foury F

机构信息

Laboratoire d'Enzymologie, Université de Louvain, Belgium.

出版信息

J Biol Chem. 1989 Dec 5;264(34):20552-60.

PMID:2684980
Abstract

The nuclear gene MIP1 is strictly required for mitochondrial DNA replication and mitochondrial DNA polymerase activity (Genga, A., Bianchi, L., and Foury, F. (1986) J. Biol. Chem. 261, 9328-9332). The MIP1 gene was cloned by genetic complementation of the mip1-1 allele after cell transformation with a yeast genomic library and was mapped to the right arm of chromosome XV about 20 centimorgans distal to the cpa1 gene by Southern blot hybridization and tetrad analysis. The mapping of the 5' ends of the MIP1 transcript and the nucleotide sequence analysis of a 4.7-kilobase DNA fragment complementing the mip1-1 allele allowed the determination of an open reading frame of 3762 nucleotides encoding a basic protein of 143.5 kDa. The following data show that the MIP1 gene encodes the catalytic subunit of the replicative mitochondrial DNA polymerase. 1) The mutant ts71 exhibits both a thermosensitive mitochondrial DNA replication in vivo and a thermosensitive mitochondrial DNA polymerase activity is observed, when compared to that of the wild type strain. 3) Chromosomal disruption of the MIP1 gene by an 80% deletion of the gene and its replacement by URA3 gene is not lethal to the cell but elicits total loss of mitochondrial DNA and mitochondrial DNA polymerase activity. 4) The MIP1 protein exhibits sequence similarities with both eukaryotic nuclear DNA polymerases and reverse transcriptases. There is no significant resemblance with prokaryotic DNA polymerases.

摘要

核基因MIP1对于线粒体DNA复制和线粒体DNA聚合酶活性是严格必需的(根加,A.,比安基,L.,和富里,F.(1986年)《生物化学杂志》261,9328 - 9332)。在用酵母基因组文库对细胞进行转化后,通过mip1 - 1等位基因的遗传互补克隆了MIP1基因,并通过Southern印迹杂交和四分体分析将其定位到第十五号染色体右臂上,位于cpa1基因远端约20厘摩处。对MIP1转录本5′端的定位以及对与mip1 - 1等位基因互补的4.7千碱基DNA片段的核苷酸序列分析,使得能够确定一个3762个核苷酸的开放阅读框,其编码一个143.5 kDa的碱性蛋白。以下数据表明MIP1基因编码复制性线粒体DNA聚合酶的催化亚基。1)与野生型菌株相比,突变体ts71在体内表现出温度敏感的线粒体DNA复制,并且观察到温度敏感的线粒体DNA聚合酶活性。3)通过对MIP1基因进行80%的缺失并将其替换为URA3基因来对该基因进行染色体破坏,对细胞并非致死,但会导致线粒体DNA和线粒体DNA聚合酶活性完全丧失。4)MIP1蛋白与真核细胞核DNA聚合酶和逆转录酶都表现出序列相似性。与原核DNA聚合酶没有显著相似性。

相似文献

1
Cloning and sequencing of the nuclear gene MIP1 encoding the catalytic subunit of the yeast mitochondrial DNA polymerase.编码酵母线粒体DNA聚合酶催化亚基的核基因MIP1的克隆与测序
J Biol Chem. 1989 Dec 5;264(34):20552-60.
2
A nuclear mutant of Saccharomyces cerevisiae deficient in mitochondrial DNA replication and polymerase activity.一种酿酒酵母的核突变体,其线粒体DNA复制和聚合酶活性存在缺陷。
J Biol Chem. 1986 Jul 15;261(20):9328-32.
3
Yeast mitochondrial DNA polymerase is a highly processive single-subunit enzyme.酵母线粒体 DNA 聚合酶是一种高度连续的单亚基酶。
Mitochondrion. 2011 Jan;11(1):119-26. doi: 10.1016/j.mito.2010.08.007. Epub 2010 Aug 31.
4
Characterization of a new DNA polymerase from Schizosaccharomyces pombe: a probable homologue of the Saccharomyces cerevisiae DNA polymerase gamma.
Gene. 1995 Nov 7;165(1):103-7. doi: 10.1016/0378-1119(95)00412-y.
5
Isolation and characterization of ten mutator alleles of the mitochondrial DNA polymerase-encoding MIP1 gene from Saccharomyces cerevisiae.从酿酒酵母中分离并鉴定线粒体DNA聚合酶编码基因MIP1的十个突变等位基因。
Gene. 1995 Jul 4;160(1):105-10. doi: 10.1016/0378-1119(95)00215-r.
6
MIP1, a new yeast gene homologous to the rat mitochondrial intermediate peptidase gene, is required for oxidative metabolism in Saccharomyces cerevisiae.MIP1是一种与大鼠线粒体中间肽酶基因同源的新酵母基因,是酿酒酵母氧化代谢所必需的。
Mol Cell Biol. 1994 Aug;14(8):5603-16. doi: 10.1128/mcb.14.8.5603-5616.1994.
7
REV3, a Saccharomyces cerevisiae gene whose function is required for induced mutagenesis, is predicted to encode a nonessential DNA polymerase.REV3是酿酒酵母中的一个基因,诱导诱变需要其发挥功能,预计它编码一种非必需的DNA聚合酶。
J Bacteriol. 1989 Oct;171(10):5659-67. doi: 10.1128/jb.171.10.5659-5667.1989.
8
Mitochondrial DNA defects in Saccharomyces cerevisiae caused by functional interactions between DNA polymerase gamma mutations associated with disease in human.人类疾病相关的DNA聚合酶γ突变之间的功能相互作用导致酿酒酵母中的线粒体DNA缺陷。
Biochim Biophys Acta. 2007 Dec;1772(11-12):1225-35. doi: 10.1016/j.bbadis.2007.10.002. Epub 2007 Oct 14.
9
A nuclear gene essential for mitochondrial replication suppresses a defect of mitochondrial transcription in Saccharomyces cerevisiae.线粒体复制所必需的一个核基因抑制酿酒酵母中的线粒体转录缺陷。
Mol Gen Genet. 1988 Oct;214(2):218-23. doi: 10.1007/BF00337714.
10
Structure and function of the Saccharomyces cerevisiae CDC2 gene encoding the large subunit of DNA polymerase III.编码DNA聚合酶III大亚基的酿酒酵母CDC2基因的结构与功能。
EMBO J. 1989 Jun;8(6):1849-54. doi: 10.1002/j.1460-2075.1989.tb03580.x.

引用本文的文献

1
Structural basis for intrinsic strand displacement activity of mitochondrial DNA polymerase.线粒体DNA聚合酶内在链置换活性的结构基础。
Nat Commun. 2025 Mar 11;16(1):2417. doi: 10.1038/s41467-025-57594-z.
2
PCNA and Rnh1 independently participate in the protection of mitochondrial genome against UV-induced mutagenesis in yeast cells.增殖细胞核抗原(PCNA)和核糖核酸酶H1(Rnh1)独立参与酵母细胞中线粒体基因组免受紫外线诱导的诱变作用。
Sci Rep. 2024 Dec 28;14(1):31017. doi: 10.1038/s41598-024-82104-4.
3
The Identification of the Mitochondrial DNA Polymerase γ (Mip1) of the Entomopathogenic Fungus .
昆虫致病真菌线粒体DNA聚合酶γ(Mip1)的鉴定
Microorganisms. 2024 May 23;12(6):1052. doi: 10.3390/microorganisms12061052.
4
Comparative structural analysis on the mitochondrial DNAs from various strains of .来自不同菌株的线粒体DNA的比较结构分析。 (原文句末不完整,推测补充完整后的译文)
Front Microbiol. 2022 Nov 28;13:1034387. doi: 10.3389/fmicb.2022.1034387. eCollection 2022.
5
Tom70-based transcriptional regulation of mitochondrial biogenesis and aging.基于Tom70的线粒体生物发生与衰老的转录调控
Elife. 2022 Mar 2;11:e75658. doi: 10.7554/eLife.75658.
6
A non-radioactive DNA synthesis assay demonstrates that elements of the Sigma 1278b Mip1 mitochondrial DNA polymerase domain and C-terminal extension facilitate robust enzyme activity.一种非放射性的 DNA 合成测定法表明,Sigma 1278b Mip1 线粒体 DNA 聚合酶结构域和 C 末端延伸的元件有助于实现强大的酶活性。
Yeast. 2021 Apr;38(4):262-275. doi: 10.1002/yea.3541. Epub 2021 Jan 26.
7
Systematic analysis of nuclear gene function in respiratory growth and expression of the mitochondrial genome in .对……中呼吸生长过程中核基因功能及线粒体基因组表达的系统分析。 (注:原文句子不完整,缺少关键信息)
Microb Cell. 2020 Jun 30;7(9):234-249. doi: 10.15698/mic2020.09.729.
8
Extension of Cellular Lifespan by Methionine Restriction Involves Alterations in Central Carbon Metabolism and Is Mitophagy-Dependent.通过蛋氨酸限制延长细胞寿命涉及中心碳代谢的改变且依赖于线粒体自噬。
Front Cell Dev Biol. 2019 Nov 28;7:301. doi: 10.3389/fcell.2019.00301. eCollection 2019.
9
Autophagy balances mtDNA synthesis and degradation by DNA polymerase POLG during starvation.自噬通过 DNA 聚合酶 POLG 平衡饥饿时的 mtDNA 合成和降解。
J Cell Biol. 2018 May 7;217(5):1601-1611. doi: 10.1083/jcb.201801168. Epub 2018 Mar 8.
10
Efficient termination of nuclear lncRNA transcription promotes mitochondrial genome maintenance.高效终止核长链非编码 RNA 转录可促进线粒体基因组的维持。
Elife. 2018 Mar 5;7:e31989. doi: 10.7554/eLife.31989.