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Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules

Telomere movements during meiotic prophase I facilitate synapsis and recombination of homologous chromosomes. Hereby, chromosome movements depend on the dynamic attachment of meiotic telomeres to the nuclear envelope and generation of forces that actively move the telomeres. In most eukaryotes, forc...

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Autores principales: Spindler, Marie-Christin, Redolfi, Josef, Helmprobst, Frederik, Kollmannsberger, Philip, Stigloher, Christian, Benavente, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791847/
https://www.ncbi.nlm.nih.gov/pubmed/31633067
http://dx.doi.org/10.1038/s42003-019-0621-1
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author Spindler, Marie-Christin
Redolfi, Josef
Helmprobst, Frederik
Kollmannsberger, Philip
Stigloher, Christian
Benavente, Ricardo
author_facet Spindler, Marie-Christin
Redolfi, Josef
Helmprobst, Frederik
Kollmannsberger, Philip
Stigloher, Christian
Benavente, Ricardo
author_sort Spindler, Marie-Christin
collection PubMed
description Telomere movements during meiotic prophase I facilitate synapsis and recombination of homologous chromosomes. Hereby, chromosome movements depend on the dynamic attachment of meiotic telomeres to the nuclear envelope and generation of forces that actively move the telomeres. In most eukaryotes, forces that move telomeres are generated in the cytoplasm by microtubule-associated motor proteins and transduced into the nucleus through the LINC complexes of the nuclear envelope. Meiotic LINC complexes, in mouse comprised of SUN1/2 and KASH5, selectively localize to the attachment sites of meiotic telomeres. For a better understanding of meiotic telomere dynamics, here we provide quantitative information of telomere attachment sites that we have generated with the aid of electron microscope tomography (EM tomography). Our data on the number, length, width, distribution and relation with microtubules of the reconstructed structures indicate that an average number of 76 LINC complexes would be required to move a telomere attachment site.
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spelling pubmed-67918472019-10-18 Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules Spindler, Marie-Christin Redolfi, Josef Helmprobst, Frederik Kollmannsberger, Philip Stigloher, Christian Benavente, Ricardo Commun Biol Article Telomere movements during meiotic prophase I facilitate synapsis and recombination of homologous chromosomes. Hereby, chromosome movements depend on the dynamic attachment of meiotic telomeres to the nuclear envelope and generation of forces that actively move the telomeres. In most eukaryotes, forces that move telomeres are generated in the cytoplasm by microtubule-associated motor proteins and transduced into the nucleus through the LINC complexes of the nuclear envelope. Meiotic LINC complexes, in mouse comprised of SUN1/2 and KASH5, selectively localize to the attachment sites of meiotic telomeres. For a better understanding of meiotic telomere dynamics, here we provide quantitative information of telomere attachment sites that we have generated with the aid of electron microscope tomography (EM tomography). Our data on the number, length, width, distribution and relation with microtubules of the reconstructed structures indicate that an average number of 76 LINC complexes would be required to move a telomere attachment site. Nature Publishing Group UK 2019-10-14 /pmc/articles/PMC6791847/ /pubmed/31633067 http://dx.doi.org/10.1038/s42003-019-0621-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Spindler, Marie-Christin
Redolfi, Josef
Helmprobst, Frederik
Kollmannsberger, Philip
Stigloher, Christian
Benavente, Ricardo
Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title_full Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title_fullStr Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title_full_unstemmed Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title_short Electron tomography of mouse LINC complexes at meiotic telomere attachment sites with and without microtubules
title_sort electron tomography of mouse linc complexes at meiotic telomere attachment sites with and without microtubules
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6791847/
https://www.ncbi.nlm.nih.gov/pubmed/31633067
http://dx.doi.org/10.1038/s42003-019-0621-1
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