Suppr超能文献

大肠杆菌染色体的解离酶基因座可被一个33碱基对的序列取代,但功能取决于其位置。

The dif resolvase locus of the Escherichia coli chromosome can be replaced by a 33-bp sequence, but function depends on location.

作者信息

Tecklenburg M, Naumer A, Nagappan O, Kuempel P

机构信息

Molecular, Cellular and Developmental Biology Department, University of Colorado, Boulder 80309.

出版信息

Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1352-6. doi: 10.1073/pnas.92.5.1352.

Abstract

The dif locus (deletion-induced filamentation) of Escherichia coli is a resolvase site, located in the terminus region of the chromosome, that reduces chromosome multimers to monomers. In strains in which this site has been deleted, a fraction of the cells is filamentous, has abnormal nucleoid structure, and exhibits elevated levels of the SOS repair system. We have demonstrated that a 33-bp sequence, which is sufficient for RecA-independent recombination and which shows similarity to the cer site of pColE1, suppresses the Dif phenotype when inserted in the terminus region. Flanking sequences were not required, since suppression occurred in strains in which dif as well as 12 kb or 173 kb of DNA had been deleted. However, location was important, and insertions at a site 118 kb away from the normal site did not suppress the Dif phenotype. These sites were otherwise still functional, and they exhibited wild-type levels of RecA-independent recombination with dif-containing plasmids and recombined with other chromosomal dif sites to cause deletions and inversions. It is proposed that the functions expressed by a dif site depend on chromosome location and structure, and analysis of these functions provides a way to examine the structure of the terminus region.

摘要

大肠杆菌的dif位点(缺失诱导丝化)是一个解离酶位点,位于染色体末端区域,可将染色体多聚体还原为单体。在该位点已被删除的菌株中,一部分细胞呈丝状,具有异常的类核结构,并表现出SOS修复系统水平升高。我们已经证明,一个33 bp的序列,足以进行不依赖RecA的重组,并且与pColE1的cer位点相似,当插入到末端区域时可抑制Dif表型。不需要侧翼序列,因为在dif以及12 kb或173 kb的DNA已被删除的菌株中也发生了抑制作用。然而,位置很重要,在距离正常位点118 kb的位点插入不会抑制Dif表型。这些位点在其他方面仍然具有功能,并且它们与含dif的质粒表现出野生型水平的不依赖RecA的重组,并与其他染色体dif位点重组以导致缺失和倒位。有人提出,dif位点表达的功能取决于染色体的位置和结构,对这些功能的分析提供了一种检查末端区域结构的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed88/42517/f392aa4b0768/pnas01483-0117-a.jpg

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