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达成目标:了解 AAA+ ATP 酶 Pch2/TRIP13 在减数分裂过程中对染色体的募集。

Getting there: understanding the chromosomal recruitment of the AAA+ ATPase Pch2/TRIP13 during meiosis.

机构信息

Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Otto-Hahn-Strasse 11, 44227, Dortmund, Germany.

Department of Molecular Mechanisms of Disease, University of Zürich, Winterthurerstrasse 190, 8057, Zürich, Switzerland.

出版信息

Curr Genet. 2021 Aug;67(4):553-565. doi: 10.1007/s00294-021-01166-3. Epub 2021 Mar 12.

Abstract

The generally conserved AAA+ ATPase Pch2/TRIP13 is involved in diverse aspects of meiosis, such as prophase checkpoint function, DNA break regulation, and meiotic recombination. The controlled recruitment of Pch2 to meiotic chromosomes allows it to use its ATPase activity to influence HORMA protein-dependent signaling. Because of the connection between Pch2 chromosomal recruitment and its functional roles in meiosis, it is important to reveal the molecular details that govern Pch2 localization. Here, we review the current understanding of the different factors that control the recruitment of Pch2 to meiotic chromosomes, with a focus on research performed in budding yeast. During meiosis in this organism, Pch2 is enriched within the nucleolus, where it likely associates with the specialized chromatin of the ribosomal (r)DNA. Pch2 is also found on non-rDNA euchromatin, where its recruitment is contingent on Zip1, a component of the synaptonemal complex (SC) that assembles between homologous chromosomes. We discuss recent findings connecting the recruitment of Pch2 with its association with the Origin Recognition Complex (ORC) and reliance on RNA Polymerase II-dependent transcription. In total, we provide a comprehensive overview of the pathways that control the chromosomal association of an important meiotic regulator.

摘要

普遍保守的 AAA+ ATP 酶 Pch2/TRIP13 参与减数分裂的多个方面,如前期检查点功能、DNA 断裂调节和减数分裂重组。Pch2 被受控招募到减数分裂染色体上,使其能够利用其 ATP 酶活性影响 HORMA 蛋白依赖性信号转导。由于 Pch2 染色体募集与其在减数分裂中的功能作用之间的联系,揭示控制 Pch2 定位的分子细节非常重要。在这里,我们回顾了控制 Pch2 招募到减数分裂染色体的不同因素的现有理解,重点介绍了在芽殖酵母中进行的研究。在该生物体的减数分裂过程中,Pch2 在核仁中富集,在那里它可能与核糖体 (r)DNA 的特殊染色质相关联。Pch2 也存在于非 rDNA 常染色质上,其招募取决于 Zip1,Zip1 是在同源染色体之间组装的联会复合体 (SC) 的一个组成部分。我们讨论了最近的发现,这些发现将 Pch2 的募集与其与起始识别复合物 (ORC) 的关联以及对 RNA 聚合酶 II 依赖性转录的依赖联系起来。总的来说,我们提供了对控制重要减数分裂调节剂染色体关联的途径的全面概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33f9/8254700/8f76abeefa7e/294_2021_1166_Fig1_HTML.jpg

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