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噬菌体μ和D108在质粒pSC101中的右端及靶位点的定位与序列分析

Orientation and sequence analysis of right ends and target sites of bacteriophage mu and D108 insertions in the plasmid pSC101.

作者信息

Szatmari G B, Kahn J S, DuBow M S

出版信息

Gene. 1986;41(2-3):315-9. doi: 10.1016/0378-1119(86)90113-7.

Abstract

We have isolated four independent insertions of the entire 37-kb D108cts 10 genome in the low-copy-number plasmid pSC101 in vivo. They were all formed by replicative transposition during the D108 lytic cycle. The orientation of these four insertions was found to be the same, with the left ends facing towards pSC101 replication, and the right end facing in the direction of all pSC101 transcription, as was previously found for a Mucts62 insertion in pSC101, pMC321. The exact sites of insertion of two of the D108 prophages, as well as the Mu prophage, have been determined by sequence analysis. All three insertions caused a 5-bp duplication of pSC101 sequences at the target site, as has been found for insertions formed by conservative integration upon lysogeny. Moreover, we have determined the nucleotide sequence of the first 75 bp of the right end of D108 and, though this end is interchangeable with the right end of Mu as a substrate for either phage's transposition functions, there are a number of nucleotide differences between them.

摘要

我们在体内低拷贝数质粒pSC101中分离出了整个37-kb D108cts 10基因组的四个独立插入片段。它们都是在D108裂解周期中通过复制性转座形成的。发现这四个插入片段的方向相同,左端朝向pSC101的复制方向,右端朝向所有pSC101转录的方向,这与之前在pSC101、pMC321中发现的Mucts62插入情况相同。通过序列分析确定了两个D108原噬菌体以及Mu原噬菌体的精确插入位点。所有这三个插入片段在靶位点都导致了pSC101序列的5-bp重复,这与溶源时保守整合形成的插入情况相同。此外,我们确定了D108右端前75 bp的核苷酸序列,尽管作为两种噬菌体转座功能的底物,该末端可与Mu的右端互换,但它们之间存在一些核苷酸差异。

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