The plant early recombinosome: a high security complex to break DNA during meiosis.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-12-01 Epub Date: 2024-09-27 DOI:10.1007/s00497-024-00509-7
Nahid Rafiei, Arnaud Ronceret
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Abstract

Key message: The formacion of numerous unpredictable DNA Double Strand Breaks (DSBs) on chromosomes iniciates meiotic recombination. In this perspective, we propose a 'multi-key lock' model to secure the risky but necesary breaks as well as a 'one per pair of cromatids' model for the topoisomerase-like early recombinosome. During meiosis, homologous chromosomes recombine at few sites of crossing-overs (COs) to ensure correct segregation. The initiation of meiotic recombination involves the formation of DNA double strand breaks (DSBs) during prophase I. Too many DSBs are dangerous for genome integrity: if these DSBs are not properly repaired, it could potentially lead to chromosomal fragmentation. Too few DSBs are also problematic: if the obligate CO cannot form between bivalents, catastrophic unequal segregation of univalents lead to the formation of sterile aneuploid spores. Research on the regulation of the formation of these necessary but risky DSBs has recently advanced in yeast, mammals and plants. DNA DSBs are created by the enzymatic activity of the early recombinosome, a topoisomerase-like complex containing SPO11. This opinion paper reviews recent insights on the regulation of the SPO11 cofactors necessary for the introduction of temporally and spatially controlled DSBs. We propose that a 'multi-key-lock' model for each subunit of the early recombinosome complex is required to secure the formation of DSBs. We also discuss the hypothetical implications that the established topoisomerase-like nature of the SPO11 core-complex can have in creating DSB in only one of the two replicated chromatids of early prophase I meiotic chromosomes. This hypothetical 'one per pair of chromatids' DSB formation model could optimize the faithful repair of the self-inflicted DSBs. Each DSB could use three potential intact homologous DNA sequences as repair template: one from the sister chromatid and the two others from the homologous chromosomes.

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植物早期重组体:减数分裂过程中断裂 DNA 的高度安全复合体。
关键信息:染色体上无数不可预测的DNA双链断裂(DSB)的形成是减数分裂重组的诱因。从这一角度出发,我们提出了一种 "多键锁 "模型,以确保有风险但必要的断裂,以及一种类似拓扑异构酶的早期重组体的 "每对色素体一个 "模型。在减数分裂过程中,同源染色体在少数交叉点(CO)上进行重组,以确保正确的分离。减数分裂重组的启动涉及原核I期DNA双链断裂(DSB)的形成。过多的DSB会危害基因组的完整性:如果这些DSB不能得到适当修复,就有可能导致染色体破碎。DSB太少也有问题:如果二价体之间不能形成强制性CO,那么单价体的灾难性不等分离就会导致形成不育的非整倍体孢子。最近,在酵母、哺乳动物和植物中,对这些必要但有风险的 DSB 的形成调控的研究取得了进展。DNA DSB 是由早期重组体的酶活性产生的,早期重组体是一种含有 SPO11 的拓扑异构酶样复合物。这篇观点性论文回顾了对引入时间和空间受控的 DSB 所必需的 SPO11 辅助因子的调控的最新见解。我们提出,早期重组体复合物的每个亚基都需要一个 "多键锁定 "模型来确保 DSB 的形成。我们还讨论了 SPO11 核心复合体已确定的拓扑异构酶样性质在减数分裂前期 I 染色体的两条复制染色体中仅在其中一条染色体上形成 DSB 的假设意义。这种假定的 "每对染色单体一个 "DSB 形成模式可以优化自我造成的 DSB 的忠实修复。每个DSB可使用三个潜在的完整同源DNA序列作为修复模板:一个来自姐妹染色单体,另外两个来自同源染色体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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