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枯草芽孢杆菌中质粒pUB110前导链复制起点的功能分析。

Functional analysis of the leading strand replication origin of plasmid pUB110 in Bacillus subtilis.

作者信息

Alonso J C, Leonhardt H, Stiege C A

机构信息

Max-Planck-Institut für Molekulare Genetik, Berlin, FRG.

出版信息

Nucleic Acids Res. 1988 Oct 11;16(19):9127-45. doi: 10.1093/nar/16.19.9127.

Abstract

Supercoiled plasmid DNA is the substrate for initiation of pUB110 replication, and - by inference - for binding of its initiator protein (RepU) to the plasmid replication origin (oriU) in vivo. No hairpin structure is required for RepU-oriU recognition. RepH (the pC194 replication initiation protein) failed to initiate replication in trans at oriU. The nucleotides that determine the specificity of the replication initiation process are located within oriU but termination is unefficient. Therefore the segment that forms the full recognition signal for termination is probably located 3' of the oriU recognition sequence. Two overlapping domains, one for initiation and one required for termination, compose the leading strand replication origin of plasmid pUB110.

摘要

超螺旋质粒DNA是pUB110复制起始的底物,并且据此推断,也是其起始蛋白(RepU)在体内与质粒复制起点(oriU)结合的底物。RepU与oriU的识别不需要发夹结构。RepH(pC194复制起始蛋白)不能在oriU处反式起始复制。决定复制起始过程特异性的核苷酸位于oriU内,但终止效率不高。因此,形成完整终止识别信号的片段可能位于oriU识别序列的3'端。两个重叠结构域,一个用于起始,一个用于终止,构成了质粒pUB110的前导链复制起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60cc/338696/c1434db5aa23/nar00161-0070-a.jpg

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