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质粒ColE1的反式可互补拷贝数突变体

Trans-complementable copy-number mutants of plasmid ColE1.

作者信息

Twigg A J, Sherratt D

出版信息

Nature. 1980 Jan 10;283(5743):216-8. doi: 10.1038/283216a0.

Abstract

Plasmid ColE1, like many other small non-conjugative plasmids, is present in multiple copies (about 15 per chromsome equivalent) in Escherichia coli cells. Because of their high copy number, the replication of such plasmids has been described as 'relaxed', even though there is good evidence that it is strictly controlled: ColE1 derivatives have characteristic but different copy numbers and ColE1 copy-number mutants have been characterised. No plasmid-specified protein is essential for the replication of ColE1 and related plasmids, as extensive replication can occur in chloramphenicol-treated cells, in plasmid-free chloramphenicol-treated cells transfected with a hybrid ColE1/phage replicon and in vitro in extracts derived from plasmid-free cells. Nevertheless, it is possible that a plasmid-specified protein is involved in ColE1 replication control in viable cells. Here we show that deletion of a given non-essential region from ColE1-like plasmids results in a raised copy number. Such plasmids are stably maintained and have their copy number returned to normal when a complementing plasmid is present in the same cell, indicating that a plasmid-specified diffusible gene product regulates the plasmid content of ColE1-containing cells. Deletion of the equivalent region from the cloning vector pBR322 gives a derivative which has a raised copy number and which has also lost its origin for conjugal transfer; unlike pBR322, it cannot be mobilised.

摘要

与许多其他小型非接合性质粒一样,质粒ColE1在大肠杆菌细胞中以多拷贝形式存在(约每染色体当量15个拷贝)。由于它们的拷贝数高,这类质粒的复制被描述为“松弛型”,尽管有充分证据表明其复制受到严格控制:ColE1衍生物具有特征性但不同的拷贝数,并且已经鉴定出ColE1拷贝数突变体。对于ColE1及相关质粒的复制而言,没有质粒编码的蛋白质是必需的,因为在氯霉素处理的细胞、用ColE1/噬菌体杂种复制子转染的无质粒氯霉素处理细胞以及无质粒细胞提取物的体外反应中均可发生大量复制。然而,在活细胞中可能有质粒编码的蛋白质参与ColE1复制的控制。在这里我们表明,从类ColE1质粒中缺失特定的非必需区域会导致拷贝数增加。这类质粒能够稳定维持,并且当同一细胞中存在互补质粒时其拷贝数会恢复正常,这表明质粒编码的可扩散基因产物调节含ColE1细胞的质粒含量。从克隆载体pBR322中缺失等效区域会产生一个衍生物,该衍生物的拷贝数增加,并且也失去了其接合转移的起始点;与pBR322不同,它不能被动员。

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