首页> 外文期刊>Journal of Molecular Biology >Protelomerase uses a topoisomerase IB/Y-recombinase type mechanism to generate DNA hairpin ends.
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Protelomerase uses a topoisomerase IB/Y-recombinase type mechanism to generate DNA hairpin ends.

机译:端粒酶使用拓扑异构酶IB / Y重组酶类型的机制来产生DNA发夹末端。

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摘要

Protelomerases are enzymes responsible for the generation of closed hairpin ends in linear DNA. It is proposed that they use a breaking-and-rejoin type mechanism to affect DNA rearrangement on specific DNA sequences. In doing so, one strand turns around and becomes the complementary strand. Using the purified enzyme from the Escherichia coli phage N15 and the Klebsiella phage phiKO2 and synthetic oligonucleotide substrates, we directly demonstrate the location where the cutting/re-ligation occurs. We identified a pair of transient staggered cleavages six base-pairs apart centered around the axis of dyad symmetry of the target site. Two molecules of the protelomerase form a pair of protein-linked DNA intermediates at each 3' end of the cleaved openings leaving a 5'-OH. Then, in a process not yet clearly defined, the partners of the two initial openings are exchanged, and the transient breaks are resealed to generate hairpin ends. The formation of 3'-covalent DNA-protein intermediates is a hallmark of the topoisomerase IB type reaction, and we have thus shown experimentally that protelomerase is a member of the tyrosine-recombinase superfamily. In addition, by introducing single nicks in the substrates as perturbation, we found that the integrity of the nucleotide chain 4 bp away from the cutting site as well as this nucleotide's complementary location on the stem if the strands were to fold into a cruciform structure are required for activity, suggesting that these locations may be important substrate-protein contacts. We determined that N15 and phiKO2 protelomerases are monomers in solution and two molecules are needed to interact with the substrate to form two closed hairpin products. The target sites of protelomerases invariably consist of inverted repeats. Comparative studies using the related target sites of different protelomerases suggest that these proteins may require both sequence-specific and structure (possibly cruciform)-specific recognition for activity.
机译:端粒酶是负责线性DNA中闭合发夹末端生成的酶。提出他们使用断裂-再结合型机制来影响特定DNA序列上的DNA重排。这样一来,一条链就变成了互补链。使用来自大肠杆菌噬菌体N15和克雷伯菌噬菌体phiKO2的纯化酶以及合成的寡核苷酸底物,我们直接证明了发生切割/重新连接的位置。我们确定了一对瞬态交错的分裂,以目标位置的双对称对称轴为中心,相距六个碱基对。两个分子的端粒酶在裂解的开口的每个3'末端形成一对蛋白质连接的DNA中间体,仅留下5'-OH。然后,在一个尚未明确定义的过程中,交换两个初始开口的伙伴,并重新密封瞬时断裂以产生发夹末端。 3'-共价DNA-蛋白质中间体的形成是拓扑异构酶IB型反应的标志,因此我们从实验上证明了端粒酶是酪氨酸重组酶超家族的成员。此外,通过在底物上引入单个缺口作为扰动,我们发现距切割位点4 bp的核苷酸链的完整性以及该核苷酸在茎上的互补位置(如果链要折叠成十字形结构的话)是所需的活性,表明这些位置可能是重要的底物-蛋白质接触。我们确定N15和phiKO2端粒酶是溶液中的单体,需要两个分子与底物相互作用以形成两个闭合的发夹产物。端粒酶的靶位点总是由反向重复组成。使用不同端粒酶相关靶位的比较研究表明,这些蛋白质可能需要序列特异性和结构(可能是十字形)特异性的活性识别。

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