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RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis
Replication Protein A (RPA) is a critical complex that acts in replication and promotes homologous recombination by allowing recombinase recruitment to processed DSB ends. Most organisms possess three RPA subunits (RPA1, RPA2, RPA3) that form a trimeric complex critical for viability. The Caenorhabd...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913698/ https://www.ncbi.nlm.nih.gov/pubmed/33476370 http://dx.doi.org/10.1093/nar/gkaa1293 |
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author | Hefel, Adam Honda, Masayoshi Cronin, Nicholas Harrell, Kailey Patel, Pooja Spies, Maria Smolikove, Sarit |
author_facet | Hefel, Adam Honda, Masayoshi Cronin, Nicholas Harrell, Kailey Patel, Pooja Spies, Maria Smolikove, Sarit |
author_sort | Hefel, Adam |
collection | PubMed |
description | Replication Protein A (RPA) is a critical complex that acts in replication and promotes homologous recombination by allowing recombinase recruitment to processed DSB ends. Most organisms possess three RPA subunits (RPA1, RPA2, RPA3) that form a trimeric complex critical for viability. The Caenorhabditis elegans genome encodes RPA-1, RPA-2 and an RPA-2 paralog RPA-4. In our analysis, we determined that RPA-2 is critical for germline replication and normal repair of meiotic DSBs. Interestingly, RPA-1 but not RPA-2 is essential for somatic replication, in contrast to other organisms that require both subunits. Six different hetero- and homodimeric complexes containing permutations of RPA-1, RPA-2 and RPA-4 can be detected in whole animal extracts. Our in vivo studies indicate that RPA-1/4 dimer is less abundant in the nucleus and its formation is inhibited by RPA-2. While RPA-4 does not participate in replication or recombination, we find that RPA-4 inhibits RAD-51 filament formation and promotes apoptosis of a subset of damaged nuclei. Altogether these findings point to sub-functionalization and antagonistic roles of RPA complexes in C. elegans. |
format | Online Article Text |
id | pubmed-7913698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-79136982021-03-03 RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis Hefel, Adam Honda, Masayoshi Cronin, Nicholas Harrell, Kailey Patel, Pooja Spies, Maria Smolikove, Sarit Nucleic Acids Res Genome Integrity, Repair and Replication Replication Protein A (RPA) is a critical complex that acts in replication and promotes homologous recombination by allowing recombinase recruitment to processed DSB ends. Most organisms possess three RPA subunits (RPA1, RPA2, RPA3) that form a trimeric complex critical for viability. The Caenorhabditis elegans genome encodes RPA-1, RPA-2 and an RPA-2 paralog RPA-4. In our analysis, we determined that RPA-2 is critical for germline replication and normal repair of meiotic DSBs. Interestingly, RPA-1 but not RPA-2 is essential for somatic replication, in contrast to other organisms that require both subunits. Six different hetero- and homodimeric complexes containing permutations of RPA-1, RPA-2 and RPA-4 can be detected in whole animal extracts. Our in vivo studies indicate that RPA-1/4 dimer is less abundant in the nucleus and its formation is inhibited by RPA-2. While RPA-4 does not participate in replication or recombination, we find that RPA-4 inhibits RAD-51 filament formation and promotes apoptosis of a subset of damaged nuclei. Altogether these findings point to sub-functionalization and antagonistic roles of RPA complexes in C. elegans. Oxford University Press 2021-01-21 /pmc/articles/PMC7913698/ /pubmed/33476370 http://dx.doi.org/10.1093/nar/gkaa1293 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genome Integrity, Repair and Replication Hefel, Adam Honda, Masayoshi Cronin, Nicholas Harrell, Kailey Patel, Pooja Spies, Maria Smolikove, Sarit RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title | RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title_full | RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title_fullStr | RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title_full_unstemmed | RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title_short | RPA complexes in Caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
title_sort | rpa complexes in caenorhabditis elegans meiosis; unique roles in replication, meiotic recombination and apoptosis |
topic | Genome Integrity, Repair and Replication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913698/ https://www.ncbi.nlm.nih.gov/pubmed/33476370 http://dx.doi.org/10.1093/nar/gkaa1293 |
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