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The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo
The synaptonemal complex protein SCP3 is part of the lateral element of the synaptonemal complex, a meiosis-specific protein structure essential for synapsis of homologous chromosomes. We have investigated the fiber-forming properties of SCP3 to elucidate its role in the synaptonemal complex. By syn...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1998
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133048/ https://www.ncbi.nlm.nih.gov/pubmed/9679134 |
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author | Yuan, Li Pelttari, Jeanette Brundell, Eva Björkroth, Birgitta Zhao, Jian Liu, Jian-Guo Brismar, Hjalmar Daneholt, Bertil Höög, Christer |
author_facet | Yuan, Li Pelttari, Jeanette Brundell, Eva Björkroth, Birgitta Zhao, Jian Liu, Jian-Guo Brismar, Hjalmar Daneholt, Bertil Höög, Christer |
author_sort | Yuan, Li |
collection | PubMed |
description | The synaptonemal complex protein SCP3 is part of the lateral element of the synaptonemal complex, a meiosis-specific protein structure essential for synapsis of homologous chromosomes. We have investigated the fiber-forming properties of SCP3 to elucidate its role in the synaptonemal complex. By synthesis of SCP3 in cultured somatic cells, it has been shown that SCP3 can self-assemble into thick fibers and that this process requires the COOH-terminal coiled coil domain of SCP3, as well as the NH(2)-terminal nonhelical domain. We have further analyzed the thick SCP3 fibers by transmission electron microscopy and immunoelectron microscopy. We found that the fibers display a transversal striation with a periodicity of ∼20 nm and consist of a large number of closely associated, thin fibers, 5–10 nm in diameter. These features suggest that the SCP3 fibers are structurally related to intermediate filaments. It is known that in some species the lateral elements of the synaptonemal complex show a highly ordered striated structure resembling that of the SCP3 fibers. We propose that SCP3 fibers constitute the core of the lateral elements of the synaptonemal complex and function as a molecular framework to which other proteins attach, regulating DNA binding to the chromatid axis, sister chromatid cohesion, synapsis, and recombination. |
format | Text |
id | pubmed-2133048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1998 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21330482008-05-01 The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo Yuan, Li Pelttari, Jeanette Brundell, Eva Björkroth, Birgitta Zhao, Jian Liu, Jian-Guo Brismar, Hjalmar Daneholt, Bertil Höög, Christer J Cell Biol Articles The synaptonemal complex protein SCP3 is part of the lateral element of the synaptonemal complex, a meiosis-specific protein structure essential for synapsis of homologous chromosomes. We have investigated the fiber-forming properties of SCP3 to elucidate its role in the synaptonemal complex. By synthesis of SCP3 in cultured somatic cells, it has been shown that SCP3 can self-assemble into thick fibers and that this process requires the COOH-terminal coiled coil domain of SCP3, as well as the NH(2)-terminal nonhelical domain. We have further analyzed the thick SCP3 fibers by transmission electron microscopy and immunoelectron microscopy. We found that the fibers display a transversal striation with a periodicity of ∼20 nm and consist of a large number of closely associated, thin fibers, 5–10 nm in diameter. These features suggest that the SCP3 fibers are structurally related to intermediate filaments. It is known that in some species the lateral elements of the synaptonemal complex show a highly ordered striated structure resembling that of the SCP3 fibers. We propose that SCP3 fibers constitute the core of the lateral elements of the synaptonemal complex and function as a molecular framework to which other proteins attach, regulating DNA binding to the chromatid axis, sister chromatid cohesion, synapsis, and recombination. The Rockefeller University Press 1998-07-27 /pmc/articles/PMC2133048/ /pubmed/9679134 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Yuan, Li Pelttari, Jeanette Brundell, Eva Björkroth, Birgitta Zhao, Jian Liu, Jian-Guo Brismar, Hjalmar Daneholt, Bertil Höög, Christer The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title | The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title_full | The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title_fullStr | The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title_full_unstemmed | The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title_short | The Synaptonemal Complex Protein SCP3 Can Form Multistranded, Cross-striated Fibers In Vivo |
title_sort | synaptonemal complex protein scp3 can form multistranded, cross-striated fibers in vivo |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2133048/ https://www.ncbi.nlm.nih.gov/pubmed/9679134 |
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