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拓扑异构酶III而非拓扑异构酶I能够在θ型DNA复制过程中支持新生链的延伸。

Topoisomerase III, but not topoisomerase I, can support nascent chain elongation during theta-type DNA replication.

作者信息

Hiasa H, Marians K J

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.

出版信息

J Biol Chem. 1994 Dec 23;269(51):32655-9.

PMID:7798272
Abstract

Topoisomerase III, but not topoisomerase I, could, in the absence of DNA gyrase, support bidirectional DNA replication in an oriC plasmid DNA replication system reconstituted with purified proteins. The initial rate of DNA synthesis and the efficiency of nascent chain elongation showed that topoisomerase III-stimulated DNA replication was as efficient as gyrase-stimulated DNA replication. In addition, topoisomerase III was also able, in the absence of DNA gyrase, to decatenate the replicating daughter DNA molecules to form monomer product. Thus, of the four topoisomerases in Escherichia coli, three, topoisomerases III and IV and DNA gyrase, can support nascent chain elongation, whereas only two, topoisomerases III and IV, can topologically resolve the daughter molecules.

摘要

在一个用纯化蛋白重构的oriC质粒DNA复制系统中,拓扑异构酶III而非拓扑异构酶I,在没有DNA促旋酶的情况下,能够支持双向DNA复制。DNA合成的初始速率和新生链延伸的效率表明,拓扑异构酶III刺激的DNA复制与促旋酶刺激的DNA复制效率相同。此外,拓扑异构酶III在没有DNA促旋酶的情况下,也能够解开正在复制的子代DNA分子,形成单体产物。因此,在大肠杆菌的四种拓扑异构酶中,三种,即拓扑异构酶III、IV和DNA促旋酶,能够支持新生链延伸,而只有两种,即拓扑异构酶III和IV,能够在拓扑学上解析子代分子。

相似文献

1
Topoisomerase III, but not topoisomerase I, can support nascent chain elongation during theta-type DNA replication.拓扑异构酶III而非拓扑异构酶I能够在θ型DNA复制过程中支持新生链的延伸。
J Biol Chem. 1994 Dec 23;269(51):32655-9.
2
Decatenating activity of Escherichia coli DNA gyrase and topoisomerases I and III during oriC and pBR322 DNA replication in vitro.体外oriC和pBR322 DNA复制过程中大肠杆菌DNA促旋酶以及拓扑异构酶I和III的解连环活性。
J Biol Chem. 1994 Jan 21;269(3):2093-9.
3
Topoisomerase IV can support oriC DNA replication in vitro.拓扑异构酶IV能够在体外支持oriC DNA复制。
J Biol Chem. 1994 Jun 10;269(23):16371-5.
4
Decatenation activity of topoisomerase IV during oriC and pBR322 DNA replication in vitro.体外oriC和pBR322 DNA复制过程中拓扑异构酶IV的解连环活性。
Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8571-5. doi: 10.1073/pnas.90.18.8571.
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[DNA supercoiling and topoisomerases in Escherichia coli].[大肠杆菌中的DNA超螺旋与拓扑异构酶]
Rev Latinoam Microbiol. 1995 Jul-Sep;37(3):291-304.
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DNA gyrase and topoisomerase IV: biochemical activities, physiological roles during chromosome replication, and drug sensitivities.DNA 回旋酶和拓扑异构酶IV:生化活性、染色体复制过程中的生理作用以及药物敏感性。
Biochim Biophys Acta. 1998 Oct 1;1400(1-3):29-43. doi: 10.1016/s0167-4781(98)00126-2.
7
Escherichia coli topoisomerase I can segregate replicating pBR322 daughter DNA molecules in vitro.大肠杆菌拓扑异构酶I能够在体外分离正在复制的pBR322子代DNA分子。
J Biol Chem. 1986 Sep 5;261(25):11906-17.
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A topoisomerase from Escherichia coli related to DNA gyrase.一种来自大肠杆菌的与DNA促旋酶相关的拓扑异构酶。
Proc Natl Acad Sci U S A. 1979 Dec;76(12):6110-4. doi: 10.1073/pnas.76.12.6110.
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Replication of pBR322 DNA in vitro with purified proteins. Requirement for topoisomerase I in the maintenance of template specificity.用纯化蛋白在体外复制pBR322 DNA。拓扑异构酶I在维持模板特异性中的作用。
J Biol Chem. 1985 Aug 5;260(16):9316-25.
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Replication initiated at the origin (oriC) of the E. coli chromosome reconstituted with purified enzymes.复制起始于用纯化酶重建的大肠杆菌染色体的原点(oriC)。
Cell. 1984 Aug;38(1):183-90. doi: 10.1016/0092-8674(84)90539-7.

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