• 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

使用荷马系列载体构建真核生物DNA的黏粒文库。

The construction of cosmid libraries of eukaryotic DNA using the Homer series of vectors.

作者信息

Chia W, Scott M R, Rigby P W

出版信息

Nucleic Acids Res. 1982 Apr 24;10(8):2503-20. doi: 10.1093/nar/10.8.2503.

DOI:10.1093/nar/10.8.2503
PMID:6281732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC320630/
Abstract

We have constructed and characterised a series of approved, disabled cosmid vectors which we call Homer cosmids and have examined the optimal conditions for the construction of libraries of eukaryotic DNA segments using these vectors. Analysis of these libraries shows that most of the sequences we have tested for are present at the expected frequency and that the libraries can be stably propagated. We have also directly tested the stability of cosmid clones carrying tandemly repeated inserts. This work shows that it should be possible to clone most eukaryotic genes using cosmid vectors and that such cloning systems have considerable advantages over those more commonly used.

摘要

我们构建并鉴定了一系列经过改造的黏粒载体,我们将其称为霍默黏粒,并研究了使用这些载体构建真核DNA片段文库的最佳条件。对这些文库的分析表明,我们所检测的大多数序列都以预期的频率存在,并且这些文库能够稳定地扩增。我们还直接测试了携带串联重复插入片段的黏粒克隆的稳定性。这项工作表明,使用黏粒载体克隆大多数真核基因应该是可行的,并且这种克隆系统比那些更常用的系统具有相当大的优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe20/320630/1f639f78ad00/nar00377-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe20/320630/eae428be41a5/nar00377-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe20/320630/1f639f78ad00/nar00377-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe20/320630/eae428be41a5/nar00377-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe20/320630/1f639f78ad00/nar00377-0034-a.jpg

相似文献

1
The construction of cosmid libraries of eukaryotic DNA using the Homer series of vectors.使用荷马系列载体构建真核生物DNA的黏粒文库。
Nucleic Acids Res. 1982 Apr 24;10(8):2503-20. doi: 10.1093/nar/10.8.2503.
2
A new high-capacity cosmid vector and its use.一种新型高容量黏粒载体及其应用。
Gene. 1980 Nov;11(3-4):271-82. doi: 10.1016/0378-1119(80)90067-0.
3
Versatile cosmid vectors for the isolation, expression, and rescue of gene sequences: studies with the human alpha-globin gene cluster.用于基因序列分离、表达和拯救的多功能黏粒载体:对人α-珠蛋白基因簇的研究
Proc Natl Acad Sci U S A. 1983 Sep;80(17):5225-9. doi: 10.1073/pnas.80.17.5225.
4
The construction of cosmid libraries which can be used to transform eukaryotic cells.可用于转化真核细胞的黏粒文库的构建。
Nucleic Acids Res. 1982 Nov 11;10(21):6715-32. doi: 10.1093/nar/10.21.6715.
5
Cloning and stable maintenance of DNA fragments over 300 kb in Escherichia coli with conventional plasmid-based vectors.利用传统的基于质粒的载体在大肠杆菌中克隆和稳定保存超过300 kb的DNA片段。
Nucleic Acids Res. 1998 Nov 1;26(21):4901-9. doi: 10.1093/nar/26.21.4901.
6
Construction of an Actinobacillus pleuropneumoniae-Escherichia coli cosmid cloning vector [Gene 160 (1995) 81-86].胸膜肺炎放线杆菌-大肠杆菌黏粒克隆载体的构建[《基因》160(1995)81 - 86]
Gene. 1995 Jul 4;160(1):87-8. doi: 10.1016/0378-1119(95)00225-u.
7
Selective isolation of cosmid clones by homologous recombination in Escherichia coli.通过大肠杆菌中的同源重组进行黏粒克隆的选择性分离。
Proc Natl Acad Sci U S A. 1984 Jul;81(13):4129-33. doi: 10.1073/pnas.81.13.4129.
8
[The selective isolation of cosmid clones by homologous recombination in Escherichia coli--a cosmid clone containing t complex linkage DNA sequence of mouse was isolated].[通过大肠杆菌中的同源重组进行黏粒克隆的选择性分离——分离出一个含有小鼠t复合体位点连锁DNA序列的黏粒克隆]
Yi Chuan Xue Bao. 1990;17(1):38-45.
9
Double cos site vectors: simplified cosmid cloning.双cos位点载体:简化的黏粒克隆
Gene. 1983 Dec;26(2-3):137-46. doi: 10.1016/0378-1119(83)90183-x.
10
Cloning of DNA fragments carrying hydrogenase genes of Rhodopseudomonas capsulata.携带荚膜红假单胞菌氢化酶基因的DNA片段的克隆
Biochimie. 1986 Jan;68(1):147-55. doi: 10.1016/s0300-9084(86)81079-3.

引用本文的文献

1
Efficient cloning of genes of Neurospora crassa.高效克隆粗糙脉孢菌基因。
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4869-73. doi: 10.1073/pnas.83.13.4869.
2
Widely differing degrees of sequence conservation of the two types of rDNA insertion within the melanogaster species sub-group of Drosophila.在果蝇的黑腹果蝇种亚组内,两种 rDNA 插入的序列保守性程度有很大差异。
EMBO J. 1983;2(5):721-6. doi: 10.1002/j.1460-2075.1983.tb01491.x.
3
A Bkm-associated human y-chromosomal DNA is conserved and transcribed in the testis of mouse.

本文引用的文献

1
Trans-complementable copy-number mutants of plasmid ColE1.质粒ColE1的反式可互补拷贝数突变体
Nature. 1980 Jan 10;283(5743):216-8. doi: 10.1038/283216a0.
2
Plasmid screening at high colony density.高菌落密度下的质粒筛选
Gene. 1980 Jun;10(1):63-7. doi: 10.1016/0378-1119(80)90144-4.
3
Beta + thalassemia: aberrant splicing results from a single point mutation in an intron.β+地中海贫血:异常剪接由内含子中的单个点突变引起。
一种与Bkm相关的人类Y染色体DNA在小鼠睾丸中保守且转录。
Chromosoma. 1995 Dec;104(4):274-81. doi: 10.1007/BF00352258.
4
The organization of the tadpole and adult alpha globin genes of Xenopus laevis.非洲爪蟾蝌蚪和成体α珠蛋白基因的组织情况。
Nucleic Acids Res. 1982 Dec 20;10(24):7935-45. doi: 10.1093/nar/10.24.7935.
5
Functional analysis of a simian virus 40 super T-antigen.猿猴病毒40大T抗原的功能分析
J Virol. 1982 Dec;44(3):974-82. doi: 10.1128/JVI.44.3.974-982.1982.
6
The physical map and organisation of the mitochondrial genome from the fertile cytoplasm of maize.来自玉米可育细胞质的线粒体基因组的物理图谱及组织结构。
Nucleic Acids Res. 1984 Dec 21;12(24):9249-61. doi: 10.1093/nar/12.24.9249.
7
Cosmid clones derived from both euchromatic and heterochromatic regions of the human Y chromosome.来自人类Y染色体常染色质区和异染色质区的黏粒克隆。
EMBO J. 1984 Sep;3(9):1997-2003. doi: 10.1002/j.1460-2075.1984.tb02081.x.
8
Transcription of a cloned rainbow trout protamine gene is accurately initiated following transfection into HeLa cells but the majority of the transcripts fail to polyadenylate at the correct site.克隆的虹鳟鱼鱼精蛋白基因转染到HeLa细胞后转录能准确起始,但大多数转录本未能在正确位点进行多聚腺苷酸化。
Nucleic Acids Res. 1985 Dec 20;13(24):8715-27. doi: 10.1093/nar/13.24.8715.
9
Two-level factorial screening for influence of temperature, pH, and aeration on production of Serratia marcescens nuclease.温度、pH值和通气量对粘质沙雷氏菌核酸酶产量影响的两水平析因筛选
Appl Environ Microbiol. 1987 Oct;53(10):2593-6. doi: 10.1128/aem.53.10.2593-2596.1987.
10
Cosmid vectors for rapid genomic walking, restriction mapping, and gene transfer.用于快速基因组步移、限制性图谱绘制和基因转移的黏粒载体。
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2160-4. doi: 10.1073/pnas.84.8.2160.
Cell. 1981 Dec;27(2 Pt 1):289-98. doi: 10.1016/0092-8674(81)90412-8.
4
The chromosomal arrangement of human alpha-like globin genes: sequence homology and alpha-globin gene deletions.人类α-珠蛋白基因的染色体排列:序列同源性与α-珠蛋白基因缺失
Cell. 1980 May;20(1):119-30. doi: 10.1016/0092-8674(80)90240-8.
5
Expression of a beta-globin gene is enhanced by remote SV40 DNA sequences.β-珠蛋白基因的表达受到远距离SV40 DNA序列的增强。
Cell. 1981 Dec;27(2 Pt 1):299-308. doi: 10.1016/0092-8674(81)90413-x.
6
Identification of DNA sequences required for transcription of the human alpha 1-globin gene in a new SV40 host-vector system.在一种新的SV40宿主-载体系统中鉴定人α1-珠蛋白基因转录所需的DNA序列。
Cell. 1981 Dec;27(2 Pt 1):279-88. doi: 10.1016/0092-8674(81)90411-6.
7
DNA sequences necessary for transcription of the rabbit beta-globin gene in vivo.兔β-珠蛋白基因在体内转录所需的DNA序列。
Nature. 1982 Jan 14;295(5845):120-6. doi: 10.1038/295120a0.
8
Fate of viral DNA in nonpermissive cells infected with simian virus 40.被猴病毒40感染的非允许细胞中病毒DNA的命运
Proc Natl Acad Sci U S A. 1981 Nov;78(11):6638-42. doi: 10.1073/pnas.78.11.6638.
9
Structure of the pro alpha 2 (I) collagen gene.原α2(I)型胶原蛋白基因的结构
Nature. 1981 Nov 12;294(5837):129-35. doi: 10.1038/294129a0.
10
Cloning and characterization of the integrated viral DNA from three lines of SV40-transformed mouse cells.来自三株SV40转化小鼠细胞系的整合病毒DNA的克隆与特性分析
Cell. 1981 Aug;25(2):547-59. doi: 10.1016/0092-8674(81)90073-8.