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拓扑异构酶 3 锌指结构域与 RMI1 支架协同作用,促进 BTR 复合物在秀丽隐杆线虫生殖系中的重组中间体的稳定结合。

The topoisomerase 3 zinc finger domain cooperates with the RMI1 scaffold to promote stable association of the BTR complex to recombination intermediates in the Caenorhabditis elegans germline.

机构信息

Department of Chromosome Biology, Max Perutz Laboratories, University of Vienna, Vienna Biocenter, Austria.

出版信息

Nucleic Acids Res. 2022 Jun 10;50(10):5652-5671. doi: 10.1093/nar/gkac408.

Abstract

Homologous recombination is the predominant DNA repair pathway used in the gonad. Of the excess DNA double-strand breaks formed in meiosis, only a subset matures into crossovers, with the remainder repaired as non-crossovers. The conserved BTR complex (comprising Bloom helicase, topoisomerase 3 and RMI1/2 scaffold proteins) acts at multiple steps during recombination to dismantle joint DNA molecules, thereby mediating the non-crossover outcome and chromosome integrity. Furthermore, the complex displays a role at the crossover site that is less well understood. Besides catalytic and TOPRIM domains, topoisomerase 3 enzymes contain a variable number of carboxy terminal zinc finger (ZnF) domains. Here, we studied the Caenorhabditis elegans mutant, in which the single ZnF domain is deleted. In contrast to the gene disruption allele, the top-3-ZnF mutant is viable, with no replication defects; the allele appears to be a hypomorph. The TOP-3-ZnF protein is recruited into foci but the mutant has increased numbers of crossovers along its chromosomes, with minor defects in repressing heterologous recombination, and a marked delay in the maturation/processing of recombination intermediates after loading of the RAD-51 recombinase. The ZnF domain cooperates with the RMI1 homolog RMH-2 to stabilize association of the BTR complex with recombination intermediates and to prevent recombination between heterologous DNA sequences.

摘要

同源重组是性腺中主要使用的 DNA 修复途径。在减数分裂中形成的多余 DNA 双链断裂中,只有一部分成熟为交叉,其余部分则作为非交叉修复。保守的 BTR 复合物(由 Bloom 解旋酶、拓扑异构酶 3 和 RMI1/2 支架蛋白组成)在重组过程中的多个步骤中发挥作用,以拆解连接 DNA 分子,从而介导非交叉结果和染色体完整性。此外,该复合物在交叉位点发挥作用,但了解较少。除了催化和 TOPRIM 结构域外,拓扑异构酶 3 酶还含有数量可变的羧基末端锌指 (ZnF) 结构域。在这里,我们研究了秀丽隐杆线虫突变体,其中单个 ZnF 结构域缺失。与基因缺失等位基因相比,top-3-ZnF 突变体是有活力的,没有复制缺陷;该等位基因似乎是一个次等位基因。TOP-3-ZnF 蛋白被招募到焦点中,但突变体的染色体上有更多的交叉,对抑制异源重组的缺陷较小,并且在 RAD-51 重组酶加载后,重组中间体的成熟/加工明显延迟。ZnF 结构域与 RMI1 同源物 RMH-2 合作,稳定 BTR 复合物与重组中间体的结合,并防止异源 DNA 序列之间的重组。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5659/9178014/05b2ae1464b4/gkac408fig1.jpg

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