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The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins
During the last stages of oogenesis, oocyte chromosomes condense and come close together, forming the so-called karyosphere. Karyosphere formation is accompanied by an essential decrease in transcriptional activity. In the grass frog Rana temporaria, the karyosphere is surrounded by an extrachromoso...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244735/ https://www.ncbi.nlm.nih.gov/pubmed/30272509 http://dx.doi.org/10.1080/19491034.2018.1530935 |
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author | Ilicheva, Nadya Podgornaya, Olga Bogolyubov, Dmitry Pochukalina, Galina |
author_facet | Ilicheva, Nadya Podgornaya, Olga Bogolyubov, Dmitry Pochukalina, Galina |
author_sort | Ilicheva, Nadya |
collection | PubMed |
description | During the last stages of oogenesis, oocyte chromosomes condense and come close together, forming the so-called karyosphere. Karyosphere formation is accompanied by an essential decrease in transcriptional activity. In the grass frog Rana temporaria, the karyosphere is surrounded by an extrachromosomal capsule that separates the chromosomes from the rest of the nucleoplasm. The karyosphere capsule (KC) of R. temporaria has been investigated in detail at the ultrastructural level, but its protein composition remained largely unknown. We demonstrate here that nuclear actin, especially F-actin, as well as lamins A/C and B are the most abundant proteins of the KC. Key proteins of nuclear pore complexes, such as Nup93 and Nup35, are also detectable in the KC. New antibodies recognizing the telomere-binding protein TRF2 allowed us to localize TRF2 in nuclear speckles. We also found that the R. temporaria KC contains some proteins involved in chromatin remodeling, including topoisomerase II and ATRX. Thus, we believe that KC isolates the chromosomes from the rest of the nucleoplasm during the final period of oocyte growth (late diplotene) and represents a specialized oocyte nuclear compartment to store a variety of factors involved in nuclear metabolism that can be used in future early development. Abbreviations: BrUTP: 5-bromouridine 5’-triphosphate; CytD: cytochalasin D; IGCs: interchromatin granule clasters; IgG: immunoglobulin G; KC: karyosphere capsule; Mw: molecular weight; NE: nuclear envelope; PBS: phosphate buffered saline; SDS-PAGE: sodium dodecyl sulfate polyacrylamide gel electrophoresis; Topo II: topoisomerase II |
format | Online Article Text |
id | pubmed-6244735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-62447352018-11-26 The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins Ilicheva, Nadya Podgornaya, Olga Bogolyubov, Dmitry Pochukalina, Galina Nucleus Research Article During the last stages of oogenesis, oocyte chromosomes condense and come close together, forming the so-called karyosphere. Karyosphere formation is accompanied by an essential decrease in transcriptional activity. In the grass frog Rana temporaria, the karyosphere is surrounded by an extrachromosomal capsule that separates the chromosomes from the rest of the nucleoplasm. The karyosphere capsule (KC) of R. temporaria has been investigated in detail at the ultrastructural level, but its protein composition remained largely unknown. We demonstrate here that nuclear actin, especially F-actin, as well as lamins A/C and B are the most abundant proteins of the KC. Key proteins of nuclear pore complexes, such as Nup93 and Nup35, are also detectable in the KC. New antibodies recognizing the telomere-binding protein TRF2 allowed us to localize TRF2 in nuclear speckles. We also found that the R. temporaria KC contains some proteins involved in chromatin remodeling, including topoisomerase II and ATRX. Thus, we believe that KC isolates the chromosomes from the rest of the nucleoplasm during the final period of oocyte growth (late diplotene) and represents a specialized oocyte nuclear compartment to store a variety of factors involved in nuclear metabolism that can be used in future early development. Abbreviations: BrUTP: 5-bromouridine 5’-triphosphate; CytD: cytochalasin D; IGCs: interchromatin granule clasters; IgG: immunoglobulin G; KC: karyosphere capsule; Mw: molecular weight; NE: nuclear envelope; PBS: phosphate buffered saline; SDS-PAGE: sodium dodecyl sulfate polyacrylamide gel electrophoresis; Topo II: topoisomerase II Taylor & Francis 2018-10-01 /pmc/articles/PMC6244735/ /pubmed/30272509 http://dx.doi.org/10.1080/19491034.2018.1530935 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ilicheva, Nadya Podgornaya, Olga Bogolyubov, Dmitry Pochukalina, Galina The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title_full | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title_fullStr | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title_full_unstemmed | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title_short | The karyosphere capsule in Rana temporaria oocytes contains structural and DNA-binding proteins |
title_sort | karyosphere capsule in rana temporaria oocytes contains structural and dna-binding proteins |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244735/ https://www.ncbi.nlm.nih.gov/pubmed/30272509 http://dx.doi.org/10.1080/19491034.2018.1530935 |
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