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接合性DNA合成:R1162与滚环复制问题

Conjugative DNA synthesis: R1162 and the question of rolling-circle replication.

作者信息

Parker Christopher, Zhang Xiao-lin, Henderson Dorian, Becker Eric, Meyer Richard

机构信息

Section of Molecular Genetics and Microbiology, School of Biology, University of Texas at Austin, Austin, TX 78712, USA.

出版信息

Plasmid. 2002 Nov;48(3):186-92. doi: 10.1016/s0147-619x(02)00105-1.

Abstract

Strand-replacement synthesis during conjugative mating has been characterized by introducing into donor cells R1162 plasmid DNA containing a base-pair mismatch. Conjugative synthesis in donors occurs in the absence of vegetative plasmid replication, but with a lag between rounds of transfer, and with most strands being initiated at the normal site within the replicative origin. These characteristics argue against the idea that multiple plasmid copies are generated for successive rounds of transfer by rolling-circle replication. However, the R1162 relaxase protein can process molecules containing multiple transfer origins in the manner expected for the conversion of single-strand multimers, generated by rolling-circle replication, to unit-length molecules. This capability appears to be the result of a secondary cleavage reaction carried out by the protein. The possibility is raised that the processing of molecules with more than one origin of transfer might be a repair mechanism directed against adventitious DNA synthesis during transfer.

摘要

在接合交配过程中的链置换合成已通过将含有碱基对错配的R1162质粒DNA导入供体细胞来进行表征。供体中的接合合成在没有营养性质粒复制的情况下发生,但两轮转移之间存在延迟,并且大多数链在复制起点内的正常位点起始。这些特征与通过滚环复制为连续轮次的转移产生多个质粒拷贝的观点相悖。然而,R1162松弛酶蛋白能够以预期的方式处理含有多个转移起点的分子,即将滚环复制产生的单链多聚体转化为单位长度的分子。这种能力似乎是该蛋白进行二级切割反应的结果。由此提出一种可能性,即对具有多个转移起点的分子进行处理可能是一种针对转移过程中偶然DNA合成的修复机制。

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