• 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

含有噬菌体λ的redB-ori区域的重组质粒pSC101中的位点特异性缺失。

Site-specific deletions in the recombinant plasmid pSC101 containing the redB-ori region of phage lambda.

作者信息

Bernardi A, Bernardi F

出版信息

Gene. 1981 Jan-Feb;13(1):103-9. doi: 10.1016/0378-1119(81)90047-0.

DOI:10.1016/0378-1119(81)90047-0
PMID:6263749
Abstract

Large deletions occur in the hybrid plasmid formed by pSC101 and the EcoRI fragment f2 of phage lambda (redB-ori region) under well defined growth conditions (Bernardi and Bernardi, 1980). We have sequenced the novel joints of the four deletions so obtained and shown that they have one endpoint in pSC101, identical in all four cases, the other endpoint being located in four different lambda sequences. Furthermore, the nucleotide sequences of the novel joints show homologies between the conserved pSC101 sequence and the lambda sequences both conserved and deleted. The presence of an IS-type element in pSC101 is postulated; however, this element is unrelated to the 200 bp element already described in pSC101 (Ravetch et al., 1976).

摘要

在明确的生长条件下,由pSC101和噬菌体λ的EcoRI片段f2(redB - ori区域)形成的杂种质粒中会出现大片段缺失(贝尔纳迪和贝尔纳迪,1980年)。我们已对如此获得的四个缺失的新连接点进行了测序,并表明它们在pSC101中有一个端点,在所有四种情况下均相同,另一个端点位于四个不同的λ序列中。此外,新连接点的核苷酸序列显示,保守的pSC101序列与λ序列(包括保守和缺失的序列)之间存在同源性。推测pSC101中存在一个IS型元件;然而,该元件与pSC101中已描述的200 bp元件无关(拉韦奇等人,1976年)。

相似文献

1
Site-specific deletions in the recombinant plasmid pSC101 containing the redB-ori region of phage lambda.含有噬菌体λ的redB-ori区域的重组质粒pSC101中的位点特异性缺失。
Gene. 1981 Jan-Feb;13(1):103-9. doi: 10.1016/0378-1119(81)90047-0.
2
DNA rearrangements in a hybrid plasmid carrying the redB imm region of coliphage lambda.携带λ噬菌体redB免疫区域的杂种质粒中的DNA重排。
Gene. 1980 Apr;9(1-2):13-25. doi: 10.1016/0378-1119(80)90164-x.
3
Identification of sequences necessary for packaging DNA into lambda phage heads.鉴定将DNA包装到λ噬菌体头部所需的序列。
Gene. 1982 Dec;20(2):267-79. doi: 10.1016/0378-1119(82)90045-2.
4
Origin and initiation sites of lambda dv DNA replication in vitro.λ dv DNA体外复制的起源和起始位点。
Basic Life Sci. 1985;30:151-72. doi: 10.1007/978-1-4613-2447-8_15.
5
Transcription of the target is required for IS102 mediated deletions.IS102介导的缺失需要靶标的转录。
Mol Gen Genet. 1988 May;212(2):265-70. doi: 10.1007/BF00334695.
6
Packaging of plasmid DNA containing the cohesive ends of coliphage lambda.含有大肠杆菌噬菌体λ粘性末端的质粒DNA的包装
Gene. 1980 Apr;9(1-2):171-4. doi: 10.1016/0378-1119(80)90174-2.
7
The replication origin of pSC101: the nucleotide sequence and replication functions of the ori region.pSC101的复制起点:ori区域的核苷酸序列及复制功能
Gene. 1984 Jul-Aug;29(1-2):211-9. doi: 10.1016/0378-1119(84)90181-1.
8
Initiation of DNA replication in a ColE1-type plasmid: isolation of mutations in the ori region.ColE1型质粒中DNA复制的起始:ori区域突变的分离
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6744-8. doi: 10.1073/pnas.77.11.6744.
9
A pSC101-derived plasmid which shows no sequence homology to other commonly used cloning vectors.一种源自pSC101的质粒,与其他常用克隆载体无序列同源性。
Gene. 1984 Nov;31(1-3):165-71. doi: 10.1016/0378-1119(84)90207-5.
10
Retrovirus-mediated insertional mutagenesis: phagemid rescue of flanking DNA by selecting plasmid ori.
DNA Cell Biol. 1990 Mar;9(2):139-47. doi: 10.1089/dna.1990.9.139.

引用本文的文献

1
IS6110-mediated deletions of wild-type chromosomes of Mycobacterium tuberculosis.IS6110介导的结核分枝杆菌野生型染色体缺失
J Bacteriol. 1999 Feb;181(3):1014-20. doi: 10.1128/JB.181.3.1014-1020.1999.
2
Complete sequence of an IS element present in pSC101.pSC101中存在的一个插入序列的完整序列。
Nucleic Acids Res. 1981 Jun 25;9(12):2905-11. doi: 10.1093/nar/9.12.2905.
3
Atypical deletions generated by mutated IS102 elements.由突变的IS102元件产生的非典型缺失。
Mol Gen Genet. 1984;195(3):452-8. doi: 10.1007/BF00341446.
4
Transcription of the target is required for IS102 mediated deletions.IS102介导的缺失需要靶标的转录。
Mol Gen Genet. 1988 May;212(2):265-70. doi: 10.1007/BF00334695.
5
Inter- and intramolecular transposition of Tn903.Tn903的分子间和分子内转座
Mol Gen Genet. 1991 May;227(1):22-7. doi: 10.1007/BF00260701.