• 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

一种来自多头绒泡菌的可移动I组内含子能够插入酿酒酵母的核糖体DNA并诱发点突变。

A mobile group I intron from Physarum polycephalum can insert itself and induce point mutations in the nuclear ribosomal DNA of saccharomyces cerevisiae.

作者信息

Muscarella D E, Vogt V M

机构信息

Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853.

出版信息

Mol Cell Biol. 1993 Feb;13(2):1023-33. doi: 10.1128/mcb.13.2.1023-1033.1993.

DOI:10.1128/mcb.13.2.1023-1033.1993
PMID:8380887
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358987/
Abstract

Pp LSU3 is a mobile group I intron in the extrachromosomal nuclear ribosomal DNA (rDNA) of Physarum polycephalum. As found for other mobile introns, Pp LSU3 encodes a site-specific endonuclease, I-Ppo, which mediates "homing" to unoccupied target sites in Physarum rDNA. The recognition sequence for this enzyme is conserved in all eucaryotic nuclear rDNAs. We have introduced this intron into a heterologous species, Saccharomyces cerevisiae, in which nuclear group I introns have not been detected. The expression of Pp LSU3, under control of the inducible GAL10 promoter, was found to be lethal as a consequence of double-strand breaks in the rDNA. However, surviving colonies that are resistant to the lethal effects of I-Ppo because of alterations in the rDNA at the cleavage site were recovered readily. These survivors are of two classes. The first comprises cells that acquired one of three types of point mutations. The second comprises cells in which Pp LSU3 became inserted into the rDNA. In both cases, each resistant survivor appears to carry the same alterations in all approximately 150 rDNA repeats. When it is embedded in yeast rDNA, Pp LSU3 leads to the synthesis of I-Ppo and appears to be mobile in appropriate genetic crosses. The existence of yeast cells carrying a mobile intron should allow dissection of the steps that allow expression of the highly unusual I-Ppo gene.

摘要

多头绒泡菌的线粒体外核核糖体DNA(rDNA)中的Pp LSU3是一种I类移动内含子。正如在其他移动内含子中所发现的那样,Pp LSU3编码一种位点特异性内切核酸酶I-Ppo,它介导“归巢”到多头绒泡菌rDNA中未被占据的靶位点。这种酶的识别序列在所有真核细胞核rDNA中都是保守的。我们已将此内含子导入一个未检测到核I类内含子的异源物种酿酒酵母中。发现在可诱导的GAL10启动子控制下,Pp LSU3的表达因rDNA中的双链断裂而具有致死性。然而,由于切割位点处rDNA的改变而对I-Ppo的致死效应具有抗性的存活菌落很容易被回收。这些存活者有两类。第一类包括获得三种点突变类型之一的细胞。第二类包括Pp LSU3插入到rDNA中的细胞。在这两种情况下,每个抗性存活者似乎在所有大约150个rDNA重复序列中都携带相同的改变。当Pp LSU3嵌入酵母rDNA中时,它会导致I-Ppo的合成,并且在适当的遗传杂交中似乎是可移动的。携带移动内含子的酵母细胞的存在应该有助于剖析允许高度异常的I-Ppo基因表达的步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/74c246a05d59/molcellb00014-0313-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/f40b624cfbf1/molcellb00014-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/e9c2a8b41dd2/molcellb00014-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/00260d6b5b74/molcellb00014-0312-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/a8a942e28beb/molcellb00014-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/74c246a05d59/molcellb00014-0313-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/f40b624cfbf1/molcellb00014-0310-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/e9c2a8b41dd2/molcellb00014-0311-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/00260d6b5b74/molcellb00014-0312-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/a8a942e28beb/molcellb00014-0313-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd62/358987/74c246a05d59/molcellb00014-0313-b.jpg

相似文献

1
A mobile group I intron from Physarum polycephalum can insert itself and induce point mutations in the nuclear ribosomal DNA of saccharomyces cerevisiae.一种来自多头绒泡菌的可移动I组内含子能够插入酿酒酵母的核糖体DNA并诱发点突变。
Mol Cell Biol. 1993 Feb;13(2):1023-33. doi: 10.1128/mcb.13.2.1023-1033.1993.
2
Characterization of the self-splicing products of a mobile intron from the nuclear rDNA of Physarum polycephalum.多头绒泡菌核核糖体DNA中一个可移动内含子的自我剪接产物的特性分析
Nucleic Acids Res. 1992 Nov 25;20(22):5899-906. doi: 10.1093/nar/20.22.5899.
3
Characterization of I-Ppo, an intron-encoded endonuclease that mediates homing of a group I intron in the ribosomal DNA of Physarum polycephalum.多头绒泡菌核糖体DNA中I类内含子编码的介导内含子归巢的内切核酸酶I-Ppo的特性分析。
Mol Cell Biol. 1990 Jul;10(7):3386-96. doi: 10.1128/mcb.10.7.3386-3396.1990.
4
A mobile group I intron in the nuclear rDNA of Physarum polycephalum.多头绒泡菌核核糖体DNA中的一个可移动I组内含子。
Cell. 1989 Feb 10;56(3):443-54. doi: 10.1016/0092-8674(89)90247-x.
5
Functional alpha-fragment of beta-galactosidase can be expressed from the mobile group I intron PpLSU3 embedded in yeast pre-ribosomal RNA derived from the chromosomal rDNA locus.β-半乳糖苷酶的功能性α片段可从嵌入源自染色体rDNA位点的酵母前核糖体RNA中的I类移动内含子PpLSU3表达。
Nucleic Acids Res. 2000 Mar 15;28(6):1428-38. doi: 10.1093/nar/28.6.1428.
6
I-PpoI, the endonuclease encoded by the group I intron PpLSU3, is expressed from an RNA polymerase I transcript.I-PpoI是由I组内含子PpLSU3编码的核酸内切酶,由RNA聚合酶I转录本表达。
Mol Cell Biol. 1998 Oct;18(10):5809-17. doi: 10.1128/MCB.18.10.5809.
7
Interaction of the intron-encoded mobility endonuclease I-PpoI with its target site.内含子编码的可移动内切核酸酶I-PpoI与其靶位点的相互作用。
Mol Cell Biol. 1993 Dec;13(12):7531-9. doi: 10.1128/mcb.13.12.7531-7539.1993.
8
Characterization of the self-splicing products of two complex Naegleria LSU rDNA group I introns containing homing endonuclease genes.含有归巢内切酶基因的两个复杂嗜脑阿米巴属大亚基核糖体DNA I组内含子的自我剪接产物的特征分析。
Eur J Biochem. 2002 Mar;269(6):1641-9. doi: 10.1046/j.1432-1327.2002.02802.x.
9
Strain-dependent sequence heterogeneity in the nuclear group I introns and large subunit ribosomal RNA in Physarum polycephalum.
DNA Seq. 1991;2(3):193-6. doi: 10.3109/10425179109039689.
10
Crystallization and preliminary X-ray studies of I-PpoI: a nuclear, intron-encoded homing endonuclease from Physarum polycephalum.多头绒泡菌I-PpoI的结晶及初步X射线研究:一种来自多头绒泡菌的细胞核内、内含子编码的归巢内切酶
Protein Sci. 1997 Dec;6(12):2677-80. doi: 10.1002/pro.5560061226.

引用本文的文献

1
Structural Organization of S516 Group I Introns in Myxomycetes.粘菌 S516 组 I 内含子的结构组织。
Genes (Basel). 2022 May 25;13(6):944. doi: 10.3390/genes13060944.
2
Modeling in yeast how rDNA introns slow growth and increase desiccation tolerance in lichens.在酵母中模拟 rDNA 内含子如何减缓生长速度并提高地衣的干燥耐受性。
G3 (Bethesda). 2021 Oct 19;11(11). doi: 10.1093/g3journal/jkab279.
3
Nucleolar release of rDNA repeats for repair involves SUMO-mediated untethering by the Cdc48/p97 segregase.核仁中 rDNA 重复序列的释放用于修复,涉及 SUMO 介导的 Cdc48/p97 分选酶的去束缚。

本文引用的文献

1
Unequal meiotic recombination within tandem arrays of yeast ribosomal DNA genes.酵母核糖体DNA基因串联阵列内的不等位减数分裂重组。
Cell. 1980 Mar;19(3):765-74. doi: 10.1016/s0092-8674(80)80052-3.
2
Unequal crossing over in the ribosomal DNA of Saccharomyces cerevisiae.酿酒酵母核糖体DNA中的不等交换
Nature. 1980 Apr 3;284(5755):426-30. doi: 10.1038/284426a0.
3
The structure of the yeast ribosomal RNA genes. 4. Complete sequence of the 25 S rRNA gene from Saccharomyces cerevisae.酵母核糖体RNA基因的结构。4. 酿酒酵母25 S rRNA基因的完整序列。
Nat Commun. 2021 Aug 13;12(1):4918. doi: 10.1038/s41467-021-25205-2.
4
Phenotypic and Genotypic Consequences of CRISPR/Cas9 Editing of the Replication Origins in the rDNA of .CRISPR/Cas9 编辑 rDNA 复制起点的表型和基因型后果。
Genetics. 2019 Sep;213(1):229-249. doi: 10.1534/genetics.119.302351. Epub 2019 Jul 10.
5
Guidelines for DNA recombination and repair studies: Cellular assays of DNA repair pathways.DNA重组与修复研究指南:DNA修复途径的细胞分析
Microb Cell. 2019 Jan 7;6(1):1-64. doi: 10.15698/mic2019.01.664.
6
RNase H eliminates R-loops that disrupt DNA replication but is nonessential for efficient DSB repair.核糖核酸酶 H 可消除破坏 DNA 复制的 R 环,但对于有效修复双链断裂是非必需的。
EMBO Rep. 2018 May;19(5). doi: 10.15252/embr.201745335. Epub 2018 Apr 5.
7
Vector control with driving Y chromosomes: modelling the evolution of resistance.利用驱动Y染色体进行病媒控制:抗药性进化建模
Malar J. 2017 Jul 14;16(1):286. doi: 10.1186/s12936-017-1932-7.
8
Ribosomal DNA status inferred from DNA cloud assays and mass spectrometry identification of agarose-squeezed proteins interacting with chromatin (ASPIC-MS).从DNA云分析以及与染色质相互作用的琼脂糖挤压蛋白的质谱鉴定(ASPIC-MS)推断核糖体DNA状态。
Oncotarget. 2017 Apr 11;8(15):24988-25004. doi: 10.18632/oncotarget.15332.
9
Nuclear group I introns in self-splicing and beyond.核 I 组内含子的自我剪接及其应用。
Mob DNA. 2013 Jun 5;4(1):17. doi: 10.1186/1759-8753-4-17.
10
A new method to efficiently induce a site-specific double-strand break in the fission yeast Schizosaccharomyces pombe.一种在裂殖酵母 Schizosaccharomyces pombe 中高效诱导特定位置双链断裂的新方法。
Yeast. 2012 Jul;29(7):275-91. doi: 10.1002/yea.2908. Epub 2012 Jun 6.
Nucleic Acids Res. 1981 Dec 21;9(24):6953-8. doi: 10.1093/nar/9.24.6953.
4
The double-strand-break repair model for recombination.用于重组的双链断裂修复模型。
Cell. 1983 May;33(1):25-35. doi: 10.1016/0092-8674(83)90331-8.
5
Recombination of plasmids into the Saccharomyces cerevisiae chromosome is reduced by small amounts of sequence heterogeneity.少量的序列异质性会降低质粒与酿酒酵母染色体的重组。
Mol Cell Biol. 1983 Jul;3(7):1204-11. doi: 10.1128/mcb.3.7.1204-1211.1983.
6
An mRNA maturase is encoded by the first intron of the mitochondrial gene for the subunit I of cytochrome oxidase in S. cerevisiae.一种mRNA成熟酶由酿酒酵母细胞色素氧化酶亚基I的线粒体基因的第一个内含子编码。
Cell. 1983 Dec;35(3 Pt 2):733-42. doi: 10.1016/0092-8674(83)90106-x.
7
Genetic applications of yeast transformation with linear and gapped plasmids.使用线性和缺口质粒进行酵母转化的遗传学应用。
Methods Enzymol. 1983;101:228-45. doi: 10.1016/0076-6879(83)01017-4.
8
Yeast recombination: the association between double-strand gap repair and crossing-over.酵母重组:双链缺口修复与交叉互换之间的关联。
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4417-21. doi: 10.1073/pnas.80.14.4417.
9
Homothallic switching of yeast mating type cassettes is initiated by a double-stranded cut in the MAT locus.酵母交配型盒式结构的同宗配合转换由MAT基因座中的双链切割引发。
Cell. 1982 Nov;31(1):183-92. doi: 10.1016/0092-8674(82)90418-4.
10
Critical sequences within mitochondrial introns: pleiotropic mRNA maturase and cis-dominant signals of the box intron controlling reductase and oxidase.线粒体内含子中的关键序列:多效性mRNA成熟酶以及控制还原酶和氧化酶的盒式内含子的顺式显性信号。
Cell. 1982 Apr;28(4):721-32. doi: 10.1016/0092-8674(82)90051-4.