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遗传元件e14的附着位点。

Attachment site of the genetic element e14.

作者信息

Brody H, Hill C W

机构信息

Department of Biological Chemistry, Milton S. Hershey Medical Center, Pennsylvania State University 17033.

出版信息

J Bacteriol. 1988 May;170(5):2040-4. doi: 10.1128/jb.170.5.2040-2044.1988.

Abstract

The Escherichia coli K-12 genetic element, e14, contains a 216-base-pair region that is homologous to a portion of the host chromosome. This region serves as the integration site for the element. The 216-base-pair homology is interrupted by 28 mismatches distributed through the sequence. The actual integrative crossover occurs within the first 11 base pairs from one end of the region. To test factors which affect e14 site-specific recombination, we cloned the attachment sites of free e14 and the host chromosome into the same plasmid. The cloned attachment sites recombined intramolecularly in a process that required the presence of a chromosomal copy of e14 in the host cell as well as the induction of SOS. Recombination events that mimicked both integration and excision occurred under the same conditions and to roughly the same extent.

摘要

大肠杆菌K-12遗传元件e14含有一段与宿主染色体部分区域同源的216个碱基对的区域。该区域作为该元件的整合位点。这216个碱基对的同源性被分布在序列中的28个错配所中断。实际的整合交叉发生在该区域一端的前11个碱基对内。为了测试影响e14位点特异性重组的因素,我们将游离e14和宿主染色体的附着位点克隆到同一个质粒中。克隆的附着位点在一个需要宿主细胞中存在e14的染色体拷贝以及诱导SOS的过程中进行分子内重组。模拟整合和切除的重组事件在相同条件下发生,且程度大致相同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/058f/211083/d17105daf9cf/jbacter00183-0048-a.jpg

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