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在一轮接合转移终止时对用于DNA加工的oriT的识别。

Recognition of oriT for DNA processing at termination of a round of conjugal transfer.

作者信息

Becker E C, Meyer R J

机构信息

Section of Molecular Genetics and Microbiology School of Biology and Institute for Cellular and Molecular Biology, Austin, TX 78712, USA.

出版信息

J Mol Biol. 2000 Jul 28;300(5):1067-77. doi: 10.1006/jmbi.2000.3902.

Abstract

Conjugal transfer of plasmid DNA is terminated when the transferred strand, linearized at the 38 base-pair origin of transfer (oriT), is recircularized. For the plasmid R1162, it is the protein MobA, covalently linked to the linear strand, that rejoins the ends by a reversible transesterification reaction. We have identified from those oligonucleotides with a partially degenerate oriT base sequence, subpopulations bound by MobA that undergo transesterification, and support efficient termination of conjugal transfer. Two domains of oriT, a ten base-pair inverted repeat and an adjacent TAA, are required for tight binding by the protein, whereas the location of the dinucleotide YG determines the site of strand cleavage. The results indicate that capture of MobA by oriT, and subsequent processing of the DNA for termination, are determined by different sequence motifs within this locus.

摘要

当在38个碱基对的转移起点(oriT)处线性化的转移链重新环化时,质粒DNA的接合转移就会终止。对于质粒R1162而言,是与线性链共价连接的MobA蛋白通过可逆的转酯反应使末端重新连接。我们从那些具有部分简并oriT碱基序列的寡核苷酸中鉴定出了被MobA结合并发生转酯反应的亚群,这些亚群支持接合转移的有效终止。oriT的两个结构域,一个10个碱基对的反向重复序列和一个相邻的TAA,是蛋白质紧密结合所必需的,而二核苷酸YG的位置决定了链切割的位点。结果表明,oriT对MobA的捕获以及随后用于终止的DNA加工,是由该位点内不同的序列基序决定的。

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