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大肠杆菌中性别因子F对细胞分裂的控制。I. 42.84 - 43.6 F片段将宿主细菌的细胞分裂与质粒DNA的复制联系起来。

Control of cell division by sex factor F in Escherichia coli. I. The 42.84-43.6 F segment couples cell division of the host bacteria with replication of plasmid DNA.

作者信息

Miki T, Yoshioka K, Horiuchi T

出版信息

J Mol Biol. 1984 Apr 25;174(4):605-25. doi: 10.1016/0022-2836(84)90086-x.

Abstract

The F plasmid of Escherichia coli was used to study the genetic background of the control circuit in the bacteria that co-ordinates DNA replication and cell division of the host cells. When DNA replication of the F plasmid was blocked by growing cells carrying an amber-suppressible replication-defective F plasmid mutant under restrictive conditions, the cells continued to divide for about one generation until F plasmid was supposedly diluted to one copy per cell, and then they stopped dividing and formed non-septated filamentous cells. These observations suggest that completion of a round of replication is a necessary and sufficient condition of F DNA synthesis in the cell division of F+ bacteria; i.e. cell division of the F+ bacteria is coupled with DNA replication of the F plasmid. The observation that Giemsa-stainable materials in the filamentous cells were clustered in the center indicates that partitioning of chromosomal DNA (and presumably of F plasmid DNA) is also coupled with plasmid DNA replication. The function necessary for this coupling is carried by the 42.84-43.6 F (BamHI-PstI) segment, which is located outside the region essential for replication of the F plasmid. The nucleotide sequence demonstrates the existence of two open reading frames in this region, which encode polypeptides of 72 and 101 amino acids, respectively. These two reading frames are most likely to be transcribed as a single polycistronic message in the direction from the BamHI site at 42.84 F to the PstI site at 43.6 F. The expression of this "operon" is likely to be controlled by plasmid DNA replication.

摘要

大肠杆菌的F质粒被用于研究细菌中协调宿主细胞DNA复制和细胞分裂的控制回路的遗传背景。当携带琥珀抑制型复制缺陷F质粒突变体的细胞在限制条件下生长时,F质粒的DNA复制被阻断,细胞继续分裂大约一代,直到F质粒被稀释到每个细胞一个拷贝,然后它们停止分裂并形成无隔膜的丝状细胞。这些观察结果表明,一轮复制的完成是F+细菌细胞分裂中F DNA合成的必要和充分条件;即F+细菌的细胞分裂与F质粒的DNA复制相关联。丝状细胞中吉姆萨染色可染物质聚集在中心的观察结果表明,染色体DNA(可能还有F质粒DNA)的分配也与质粒DNA复制相关联。这种关联所需的功能由42.84-43.6 F(BamHI-PstI)片段承担,该片段位于F质粒复制必需区域之外。核苷酸序列表明该区域存在两个开放阅读框,分别编码72和101个氨基酸的多肽。这两个阅读框很可能以单一多顺反子信息的形式从42.84 F处的BamHI位点向43.6 F处的PstI位点方向转录。这个“操纵子”的表达可能受质粒DNA复制控制。

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