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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...

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Autores principales: Kosaka, Hiromichi, Shinohara, Miki, Shinohara, Akira
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
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.
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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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