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Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination
During meiotic prophase, chromosomes display rapid movement, and their telomeres attach to the nuclear envelope and cluster to form a “chromosomal bouquet.” Little is known about the roles of the chromosome movement and telomere clustering in this phase. In budding yeast, telomere clustering is prom...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533704/ https://www.ncbi.nlm.nih.gov/pubmed/18818742 http://dx.doi.org/10.1371/journal.pgen.1000196 |
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author | Kosaka, Hiromichi Shinohara, Miki Shinohara, Akira |
author_facet | Kosaka, Hiromichi Shinohara, Miki Shinohara, Akira |
author_sort | Kosaka, Hiromichi |
collection | PubMed |
description | During meiotic prophase, chromosomes display rapid movement, and their telomeres attach to the nuclear envelope and cluster to form a “chromosomal bouquet.” Little is known about the roles of the chromosome movement and telomere clustering in this phase. In budding yeast, telomere clustering is promoted by a meiosis-specific, telomere-binding protein, Ndj1. Here, we show that a meiosis-specific protein, Csm4, which forms a complex with Ndj1, facilitates bouquet formation. In the absence of Csm4, Ndj1-bound telomeres tether to nuclear envelopes but do not cluster, suggesting that telomere clustering in the meiotic prophase consists of at least two distinct steps: Ndj1-dependent tethering to the nuclear envelope and Csm4-dependent clustering/movement. Similar to Ndj1, Csm4 is required for several distinct steps during meiotic recombination. Our results suggest that Csm4 promotes efficient second-end capture of a double-strand break following a homology search, as well as resolution of the double-Holliday junction during crossover formation. We propose that chromosome movement and associated telomere dynamics at the nuclear envelope promotes the completion of key biochemical steps during meiotic recombination. |
format | Text |
id | pubmed-2533704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25337042008-09-26 Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination Kosaka, Hiromichi Shinohara, Miki Shinohara, Akira PLoS Genet Research Article During meiotic prophase, chromosomes display rapid movement, and their telomeres attach to the nuclear envelope and cluster to form a “chromosomal bouquet.” Little is known about the roles of the chromosome movement and telomere clustering in this phase. In budding yeast, telomere clustering is promoted by a meiosis-specific, telomere-binding protein, Ndj1. Here, we show that a meiosis-specific protein, Csm4, which forms a complex with Ndj1, facilitates bouquet formation. In the absence of Csm4, Ndj1-bound telomeres tether to nuclear envelopes but do not cluster, suggesting that telomere clustering in the meiotic prophase consists of at least two distinct steps: Ndj1-dependent tethering to the nuclear envelope and Csm4-dependent clustering/movement. Similar to Ndj1, Csm4 is required for several distinct steps during meiotic recombination. Our results suggest that Csm4 promotes efficient second-end capture of a double-strand break following a homology search, as well as resolution of the double-Holliday junction during crossover formation. We propose that chromosome movement and associated telomere dynamics at the nuclear envelope promotes the completion of key biochemical steps during meiotic recombination. Public Library of Science 2008-09-26 /pmc/articles/PMC2533704/ /pubmed/18818742 http://dx.doi.org/10.1371/journal.pgen.1000196 Text en Kosaka et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kosaka, Hiromichi Shinohara, Miki Shinohara, Akira Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title | Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title_full | Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title_fullStr | Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title_full_unstemmed | Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title_short | Csm4-Dependent Telomere Movement on Nuclear Envelope Promotes Meiotic Recombination |
title_sort | csm4-dependent telomere movement on nuclear envelope promotes meiotic recombination |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2533704/ https://www.ncbi.nlm.nih.gov/pubmed/18818742 http://dx.doi.org/10.1371/journal.pgen.1000196 |
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