减数分裂前期的检查点控制:独特的需求需要独特的特性

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Current Topics in Developmental Biology Pub Date : 2023-01-01 Epub Date: 2022-06-20 DOI:10.1016/bs.ctdb.2022.04.007
Vivek B Raina, Maud Schoot Uiterkamp, Gerben Vader
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引用次数: 0

摘要

复制、重组和分离等染色体交易由细胞周期检查点级联监控。这些检查点确保正确执行从一个细胞到下一个细胞以及跨代忠实遗传基因组所需的过程。在减数分裂前期,一个专门的检查点监控着减数分裂的决定性事件:程序化的DNA断裂形成,然后通过基于同源染色体间(IH)交叉的重组进行专门修复。这种检查点与体细胞周期中活跃的典型DNA损伤检查点具有相同的分子特征。然而,减数分裂前期的特殊要求为这一信号级联引入了独特的特征。在这篇综述中,我们将讨论减数分裂前期检查点的独特之处。减数分裂前期检查点与典型的DNA损伤检查点级联有关,同时也与保护染色体分离的纺锤体装配检查点(SAC)有相似之处。我们将重点介绍减数分裂前期和染色体分离的检查点信号逻辑中新出现的这些相似之处,以及思考这些相似之处如何帮助我们更好地理解减数分裂前期的控制。我们还讨论了一项研究,该研究表明,当减数分裂前期检查点的成分异常表达时,可能会改变癌细胞中的DNA修复保真度和染色体分离。根据减数分裂前期的特殊性所提出的要求来考虑检查点的功能,有助于我们理解检查点与减数分裂细胞周期机制的整合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Checkpoint control in meiotic prophase: Idiosyncratic demands require unique characteristics.

Chromosomal transactions such as replication, recombination and segregation are monitored by cell cycle checkpoint cascades. These checkpoints ensure the proper execution of processes that are needed for faithful genome inheritance from one cell to the next, and across generations. In meiotic prophase, a specialized checkpoint monitors defining events of meiosis: programmed DNA break formation, followed by dedicated repair through recombination based on interhomolog (IH) crossovers. This checkpoint shares molecular characteristics with canonical DNA damage checkpoints active during somatic cell cycles. However, idiosyncratic requirements of meiotic prophase have introduced unique features in this signaling cascade. In this review, we discuss the unique features of the meiotic prophase checkpoint. While being related to canonical DNA damage checkpoint cascades, the meiotic prophase checkpoint also shows similarities with the spindle assembly checkpoint (SAC) that guards chromosome segregation. We highlight these emerging similarities in the signaling logic of the checkpoints that govern meiotic prophase and chromosome segregation, and how thinking of these similarities can help us better understand meiotic prophase control. We also discuss work showing that, when aberrantly expressed, components of the meiotic prophase checkpoint might alter DNA repair fidelity and chromosome segregation in cancer cells. Considering checkpoint function in light of demands imposed by the special characteristics of meiotic prophase helps us understand checkpoint integration into the meiotic cell cycle machinery.

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CiteScore
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