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A novel protein binds a key origin sequence to block replication of an E. coli minichromosome.

作者信息

Hwang D S, Kornberg A

机构信息

Department of Biochemistry, Stanford University School of Medicine, California 94305-5307.

出版信息

Cell. 1990 Oct 19;63(2):325-31. doi: 10.1016/0092-8674(90)90165-b.

DOI:10.1016/0092-8674(90)90165-b
PMID:2208289
Abstract

A sequence of three tandem repeats of a 13-mer in the replication origin (oriC) of E. coli is the highly conserved site of opening of the duplex for initiation of DNA synthesis. A protein that binds this sequence has been discovered in E. coli and purified to homogeneity. This novel 33 kd polypeptide behaves as a dimer. Binding to the 13-mers is specific and limited to this region. At a ratio of 10-20 monomers per oriC plasmid, the binding blocks initiation by preventing the opening of the 13-mer region by dnaA protein. Once the 13-mers are opened by dnaA protein action, the 33 kd protein is without effect on the subsequent stages of replication. The specificity of binding and profound inhibitory effect suggest a regulatory role for this protein at an early stage of chromosome initiation.

摘要

相似文献

1
A novel protein binds a key origin sequence to block replication of an E. coli minichromosome.
Cell. 1990 Oct 19;63(2):325-31. doi: 10.1016/0092-8674(90)90165-b.
2
Opposed actions of regulatory proteins, DnaA and IciA, in opening the replication origin of Escherichia coli.
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The central lysine in the P-loop motif of the Escherichia coli DnaA protein is essential for initiating DNA replication from the chromosomal origin, oriC, and the F factor origin, oriS, but is dispensable for initiation from the P1 plasmid origin, oriR.大肠杆菌DnaA蛋白P环基序中的中心赖氨酸对于从染色体复制起点oriC和F因子复制起点oriS起始DNA复制至关重要,但对于从P1质粒复制起点oriR起始复制则可有可无。
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Strand separation required for initiation of replication at the chromosomal origin of E.coli is facilitated by a distant RNA--DNA hybrid.大肠杆菌染色体复制起点处起始复制所需的链分离是由一段远距离的RNA-DNA杂交体促进的。
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E. coli oriC and the dnaA gene promoter are sequestered from dam methyltransferase following the passage of the chromosomal replication fork.在染色体复制叉通过后,大肠杆菌oriC和dnaA基因启动子会与DNA腺嘌呤甲基转移酶隔离。
Cell. 1990 Sep 7;62(5):967-79. doi: 10.1016/0092-8674(90)90271-f.
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The dnaA protein complex with the E. coli chromosomal replication origin (oriC) and other DNA sites.DnaA蛋白与大肠杆菌染色体复制起点(oriC)及其他DNA位点结合。
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The FIS protein fails to block the binding of DnaA protein to oriC, the Escherichia coli chromosomal origin.FIS蛋白无法阻止DnaA蛋白与oriC(大肠杆菌染色体复制起点)的结合。
Nucleic Acids Res. 1998 Nov 15;26(22):5170-5. doi: 10.1093/nar/26.22.5170.

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