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大肠杆菌K-12染色体的复制起点:携带自主复制信息的最小DNA片段的大小和结构

Replication origin of the Escherichia coli K-12 chromosome: the size and structure of the minimum DNA segment carrying the information for autonomous replication.

作者信息

Oka A, Sugimoto K, Takanami M, Hirota Y

出版信息

Mol Gen Genet. 1980 Apr;178(1):9-20. doi: 10.1007/BF00267207.

Abstract

A DNA fragment containing the replication origin of the Eschericia coli K-12 chromosome was inserted in two correlations at either the BamHI or SalI site of pBR322 DNA. All the resulting hybrid plasmids were found to replicate in both polA and polA+ cells, whereas pBR322 replicates only in polA+ cells. This characteristic provided a method for assaying the autonomously replicating ability (Ori function of the E. coli origin. In order to define the minimum DNA region (ori) that determines Ori function, deletions of various sizes were introduced from either side of the ori-containing segment in the hybrid plasmids by in vitro techniques, and the correlation between the Ori phenotype and nucleotide sequence of the deletion derivatives was analyzed. It was found that the left end of ori is between positions 23 and 35, and the right end is either position 266 or 267 in our nucleotide coordinate (Sugimoto et al., 1979). Therefore, ori is present within a region of minimum 232 base pairs and maximum 245 base pairs in length. The Ori+ and Ori- phenotypes were clearly resolved at both sides of these boundaries by the above assay procedure. To obtain information about the effect of mutations in the internal region of the defined ori stretch, short sequences were inserted or deleted in vitro in the vicinity of several restriction sites within ori on the hybrid plasmids. Most of these plasmids carrying modified sequences showed Ori- phenotype, suggesting that most parts of the ori stretch play important roles in Ori function.

摘要

将含有大肠杆菌K-12染色体复制起点的DNA片段以两种方向插入pBR322 DNA的BamHI或SalI位点。结果发现,所有产生的杂种质粒都能在polA和polA+细胞中复制,而pBR322仅在polA+细胞中复制。这一特性提供了一种检测自主复制能力(大肠杆菌起点的ori功能)的方法。为了确定决定ori功能的最小DNA区域(ori),通过体外技术从杂种质粒中含ori片段的两侧引入不同大小的缺失,并分析缺失衍生物的ori表型与核苷酸序列之间的相关性。发现在我们的核苷酸坐标中(杉本等人,1979),ori的左端在23至35位之间,右端在266或267位。因此,ori存在于长度最小为232个碱基对、最大为245个碱基对的区域内。通过上述检测程序,在这些边界的两侧清楚地分辨出了Ori+和Ori-表型。为了获得有关已定义的ori区段内部区域突变影响的信息,在杂种质粒ori内几个限制位点附近体外插入或缺失短序列。大多数携带修饰序列的这些质粒表现出Ori-表型,这表明ori区段的大部分在ori功能中起重要作用。

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