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该突变体为端粒Cdc13-Stn1-Ten1功能障碍对细胞周期进程的影响提供了新见解。

The - Mutant Provides New Insight into the Impacts of Telomeric Cdc13-Stn1-Ten1 Dysfunction on Cell Cycle Progression.

作者信息

Grandin Nathalie, Charbonneau Michel

机构信息

GReD Institute, CNRS UMR6293, INSERM U1103, Faculty of Medicine, University Clermont-Auvergne, 28 Place Henri Dunant, BP 38, 63001 Clermont-Ferrand Cedex, France.

出版信息

Cells. 2025 May 26;14(11):784. doi: 10.3390/cells14110784.

DOI:10.3390/cells14110784
PMID:40497960
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12153855/
Abstract

The conserved and essential Cdc13/CTC1-Stn1-Ten1 telomeric complex (CST) ensures chromosome stability by protecting telomere ends and regulating telomerase accessibility. In a recent study, we uncovered mutants of the . CST, in which damage was sensed by the two major G2/M spindle checkpoints (one is Bub2-dependent and the other one Mad2-dependent), as well as the major G2/M DNA damage checkpoint (Mec1-dependent). In this study, we found, by fluorescence microscopy, that the stability of the mitotic tubulin spindle was profoundly affected in the best-studied of these mutants, -. Additional data from genetic analyses suggested the potential involvement of Stu1 and Stu2, as well as Slk19, in these defects. Throughout this study, we compared the phenotypes of - with those of -, the best-studied CST mutant, which also serves as a prototype of telomere-damage-characterized CST mutants. We propose that - represents the prototype of mutants characterized by tubulin spindle damage. These newly described phenotypes potentially represent the basis for identifying new functions of the CST telomeric complex. These functions might consist of ensuring correct chromosome segregation through the stabilization of the mitotic spindle.

摘要

保守且必需的Cdc13/CTC1-Stn1-Ten1端粒复合体(CST)通过保护端粒末端和调节端粒酶可及性来确保染色体稳定性。在最近的一项研究中,我们发现了CST的突变体,其中损伤由两个主要的G2/M纺锤体检查点(一个是依赖Bub2的,另一个是依赖Mad2的)以及主要的G2/M DNA损伤检查点(依赖Mec1的)感知。在本研究中,我们通过荧光显微镜发现,在这些突变体中研究得最深入的突变体中,有丝分裂微管纺锤体的稳定性受到了深远影响。来自遗传分析的其他数据表明,Stu1和Stu2以及Slk19可能参与了这些缺陷。在整个研究过程中,我们将该突变体的表型与研究得最深入的CST突变体的表型进行了比较,该突变体也作为端粒损伤特征化的CST突变体的原型。我们提出,该突变体代表了以微管纺锤体损伤为特征的突变体的原型。这些新描述的表型可能代表了识别CST端粒复合体新功能的基础。这些功能可能包括通过稳定有丝分裂纺锤体来确保正确的染色体分离。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/b0af147c20e9/cells-14-00784-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/88c96e589c23/cells-14-00784-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/3b6d4172ab72/cells-14-00784-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/6d9fac100fba/cells-14-00784-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/c6f4e3f951ed/cells-14-00784-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/b09a8e895dd1/cells-14-00784-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/b0af147c20e9/cells-14-00784-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/88c96e589c23/cells-14-00784-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/3b6d4172ab72/cells-14-00784-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/6d9fac100fba/cells-14-00784-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/c6f4e3f951ed/cells-14-00784-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/b09a8e895dd1/cells-14-00784-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af43/12153855/b0af147c20e9/cells-14-00784-g006a.jpg

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本文引用的文献

1
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Cells. 2024 Sep 25;13(19):1605. doi: 10.3390/cells13191605.
2
POT1 recruits and regulates CST-Polα/primase at human telomeres.POT1 在人类端粒处招募并调节 CST-Polα/引发酶。
Cell. 2024 Jul 11;187(14):3638-3651.e18. doi: 10.1016/j.cell.2024.05.002. Epub 2024 Jun 4.
3
CST-Polα/Primase: the second telomere maintenance machine.CST-Polα/Primase:第二 telomere 维持机器。
Genes Dev. 2023 Jul 1;37(13-14):555-569. doi: 10.1101/gad.350479.123. Epub 2023 Jul 26.
4
Deficiency in mammalian STN1 promotes colon cancer development via inhibiting DNA repair.哺乳动物 STN1 缺乏通过抑制 DNA 修复促进结肠癌的发展。
Sci Adv. 2023 May 10;9(19):eadd8023. doi: 10.1126/sciadv.add8023.
5
To Fix or Not to Fix: Maintenance of Chromosome Ends Versus Repair of DNA Double-Strand Breaks.修复还是不修复:染色体末端的维持与 DNA 双链断裂的修复。
Cells. 2022 Oct 14;11(20):3224. doi: 10.3390/cells11203224.
6
Tubulin isotypes - functional insights from model organisms.微管蛋白同工型 - 模式生物的功能见解。
J Cell Sci. 2022 May 1;135(9). doi: 10.1242/jcs.259539. Epub 2022 May 6.
7
Pan-Cancer Analyses Identify the CTC1-STN1-TEN1 Complex as a Protective Factor and Predictive Biomarker for Immune Checkpoint Blockade in Cancer.泛癌分析确定CTC1-STN1-TEN1复合物为癌症免疫检查点阻断的保护因子和预测生物标志物。
Front Genet. 2022 Mar 16;13:859617. doi: 10.3389/fgene.2022.859617. eCollection 2022.
8
Slk19 enhances cross-linking of microtubules by Ase1 and Stu1.Slk19 增强了 Ase1 和 Stu1 对微管的交联。
Mol Biol Cell. 2021 Nov 1;32(21):ar22. doi: 10.1091/mbc.E21-05-0279. Epub 2021 Sep 8.
9
Telomere Replication: Solving Multiple End Replication Problems.端粒复制:解决多个末端复制问题。
Front Cell Dev Biol. 2021 Apr 1;9:668171. doi: 10.3389/fcell.2021.668171. eCollection 2021.
10
CST in maintaining genome stability: Beyond telomeres.CST 在维持基因组稳定性方面的作用:超越端粒。
DNA Repair (Amst). 2021 Jun;102:103104. doi: 10.1016/j.dnarep.2021.103104. Epub 2021 Mar 22.