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Identification of novel synaptonemal complex components in C. elegans
The synaptonemal complex (SC) is a tripartite protein scaffold that forms between homologous chromosomes during meiosis. Although the SC is essential for stable homologue pairing and crossover recombination in diverse eukaryotes, it is unknown how individual components assemble into the highly conse...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199856/ https://www.ncbi.nlm.nih.gov/pubmed/32211899 http://dx.doi.org/10.1083/jcb.201910043 |
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author | Hurlock, Matthew E. Čavka, Ivana Kursel, Lisa E. Haversat, Jocelyn Wooten, Matthew Nizami, Zehra Turniansky, Rashi Hoess, Philipp Ries, Jonas Gall, Joseph G. Rog, Ofer Köhler, Simone Kim, Yumi |
author_facet | Hurlock, Matthew E. Čavka, Ivana Kursel, Lisa E. Haversat, Jocelyn Wooten, Matthew Nizami, Zehra Turniansky, Rashi Hoess, Philipp Ries, Jonas Gall, Joseph G. Rog, Ofer Köhler, Simone Kim, Yumi |
author_sort | Hurlock, Matthew E. |
collection | PubMed |
description | The synaptonemal complex (SC) is a tripartite protein scaffold that forms between homologous chromosomes during meiosis. Although the SC is essential for stable homologue pairing and crossover recombination in diverse eukaryotes, it is unknown how individual components assemble into the highly conserved SC structure. Here we report the biochemical identification of two new SC components, SYP-5 and SYP-6, in Caenorhabditis elegans. SYP-5 and SYP-6 are paralogous to each other and play redundant roles in synapsis, providing an explanation for why these genes have evaded previous genetic screens. Superresolution microscopy reveals that they localize between the chromosome axes and span the width of the SC in a head-to-head manner, similar to the orientation of other known transverse filament proteins. Using genetic redundancy and structure–function analyses to truncate C-terminal tails of SYP-5/6, we provide evidence supporting the role of SC in both limiting and promoting crossover formation. |
format | Online Article Text |
id | pubmed-7199856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71998562020-11-04 Identification of novel synaptonemal complex components in C. elegans Hurlock, Matthew E. Čavka, Ivana Kursel, Lisa E. Haversat, Jocelyn Wooten, Matthew Nizami, Zehra Turniansky, Rashi Hoess, Philipp Ries, Jonas Gall, Joseph G. Rog, Ofer Köhler, Simone Kim, Yumi J Cell Biol Article The synaptonemal complex (SC) is a tripartite protein scaffold that forms between homologous chromosomes during meiosis. Although the SC is essential for stable homologue pairing and crossover recombination in diverse eukaryotes, it is unknown how individual components assemble into the highly conserved SC structure. Here we report the biochemical identification of two new SC components, SYP-5 and SYP-6, in Caenorhabditis elegans. SYP-5 and SYP-6 are paralogous to each other and play redundant roles in synapsis, providing an explanation for why these genes have evaded previous genetic screens. Superresolution microscopy reveals that they localize between the chromosome axes and span the width of the SC in a head-to-head manner, similar to the orientation of other known transverse filament proteins. Using genetic redundancy and structure–function analyses to truncate C-terminal tails of SYP-5/6, we provide evidence supporting the role of SC in both limiting and promoting crossover formation. Rockefeller University Press 2020-03-25 /pmc/articles/PMC7199856/ /pubmed/32211899 http://dx.doi.org/10.1083/jcb.201910043 Text en © 2020 Hurlock et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/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 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Hurlock, Matthew E. Čavka, Ivana Kursel, Lisa E. Haversat, Jocelyn Wooten, Matthew Nizami, Zehra Turniansky, Rashi Hoess, Philipp Ries, Jonas Gall, Joseph G. Rog, Ofer Köhler, Simone Kim, Yumi Identification of novel synaptonemal complex components in C. elegans |
title | Identification of novel synaptonemal complex components in C. elegans |
title_full | Identification of novel synaptonemal complex components in C. elegans |
title_fullStr | Identification of novel synaptonemal complex components in C. elegans |
title_full_unstemmed | Identification of novel synaptonemal complex components in C. elegans |
title_short | Identification of novel synaptonemal complex components in C. elegans |
title_sort | identification of novel synaptonemal complex components in c. elegans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199856/ https://www.ncbi.nlm.nih.gov/pubmed/32211899 http://dx.doi.org/10.1083/jcb.201910043 |
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