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膜蛋白 Bqt3 和 -4 将端粒锚定在核膜上,以确保染色体花束的形成。

Membrane proteins Bqt3 and -4 anchor telomeres to the nuclear envelope to ensure chromosomal bouquet formation.

机构信息

Kobe Advanced ICT Research Center, National Institute of Information and Communications Technology, Nishi-ku, Kobe 651-2492, Japan.

出版信息

J Cell Biol. 2009 Nov 2;187(3):413-27. doi: 10.1083/jcb.200902122.

DOI:10.1083/jcb.200902122
PMID:19948484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2779253/
Abstract

In many organisms, telomeres cluster to form a bouquet arrangement of chromosomes during meiotic prophase. Previously, we reported that two meiotic proteins, Bqt1 and -2, are required for tethering telomeres to the spindle pole body (SPB) during meiotic prophase in fission yeast. This study has further identified two novel, ubiquitously expressed inner nuclear membrane (INM) proteins, Bqt3 and -4, which are required for bouquet formation. We found that in the absence of Bqt4, telomeres failed to associate with the nuclear membranes in vegetative cells and consequently failed to cluster to the SPB in meiotic prophase. In the absence of Bqt3, Bqt4 protein was degraded during meiosis, leading to a phenotype similar to that of the bqt4-null mutant. Collectively, these results show that Bqt4 anchors telomeres to the INM and that Bqt3 protects Bqt4 from protein degradation. Interestingly, the functional integrity of telomeres is maintained even when they are separated from the nuclear envelope in vegetative cells.

摘要

在许多生物中,端粒在减数分裂前期聚集形成染色体的花束排列。之前,我们报道了两个减数分裂蛋白,Bqt1 和 -2,在有丝分裂前期将端粒与纺锤体极体(SPB)连接在一起是必需的。本研究进一步鉴定了两种新型的、普遍表达的核内膜(INM)蛋白,Bqt3 和 -4,它们是花束形成所必需的。我们发现,在 bqt4 缺失的情况下,端粒在营养细胞中无法与核膜结合,因此在减数分裂前期无法聚集到 SPB。在 bqt3 缺失的情况下,Bqt4 蛋白在减数分裂过程中被降解,导致与 bqt4 缺失突变体相似的表型。总之,这些结果表明 Bqt4 将端粒锚定在 INM 上,而 Bqt3 保护 Bqt4 免受蛋白降解。有趣的是,即使在营养细胞中端粒与核膜分离,端粒的功能完整性仍能得到维持。

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本文引用的文献

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2
Csm4-dependent telomere movement on nuclear envelope promotes meiotic recombination.Csm4 依赖的端粒在核膜上的移动促进减数分裂重组。
PLoS Genet. 2008 Sep 26;4(9):e1000196. doi: 10.1371/journal.pgen.1000196.
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Csm4, in collaboration with Ndj1, mediates telomere-led chromosome dynamics and recombination during yeast meiosis.Csm4与Ndj1协同作用,在酵母减数分裂过程中介导端粒引导的染色体动态变化和重组。
着丝粒定位协调端粒花束形成和减数分裂分化的起始。
Nat Commun. 2025 Jan 20;16(1):837. doi: 10.1038/s41467-025-56049-9.
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The Greatwall-Endosulfine-PP2A/B55 pathway regulates entry into quiescence by enhancing translation of Elongator-tunable transcripts.长城-内硫磷蛋白-PP2A/B55通路通过增强延伸因子可调节转录本的翻译来调控进入静止期。
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Structural basis for C. elegans pairing center DNA binding specificity by the ZIM/HIM-8 family proteins.ZIM/HIM-8 家族蛋白介导的秀丽隐杆线虫配对中心 DNA 结合特异性的结构基础。
Nat Commun. 2024 Nov 28;15(1):10355. doi: 10.1038/s41467-024-54548-9.
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Structural duality enables a single protein to act as a toxin-antidote pair for meiotic drive.结构双重性使单个蛋白质能够充当减数分裂驱动的毒素-解毒剂对。
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The SUN-family protein Sad1 mediates heterochromatin spatial organization through interaction with histone H2A-H2B.SUN 家族蛋白 Sad1 通过与组蛋白 H2A-H2B 的相互作用介导异染色质的空间组织。
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Non-random spatial organization of telomeres varies during the cell cycle and requires LAP2 and BAF.端粒的非随机空间组织在细胞周期中会发生变化,且需要LAP2和BAF。
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Dev Cell. 2007 Jun;12(6):873-85. doi: 10.1016/j.devcel.2007.05.004.