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The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair
Repair of damaged DNA is required for the viability of all organisms. Studies in Drosophila melanogaster, driven by the power of genetic screens, pioneered the discovery and characterization of many genes and pathways involved in DNA repair in animals. However, fewer than half of the alleles identif...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056982/ https://www.ncbi.nlm.nih.gov/pubmed/31900333 http://dx.doi.org/10.1534/g3.119.400903 |
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author | Carvajal-Garcia, Juan Gales, Evan R. Ramsden, Dale A. Sekelsky, Jeff |
author_facet | Carvajal-Garcia, Juan Gales, Evan R. Ramsden, Dale A. Sekelsky, Jeff |
author_sort | Carvajal-Garcia, Juan |
collection | PubMed |
description | Repair of damaged DNA is required for the viability of all organisms. Studies in Drosophila melanogaster, driven by the power of genetic screens, pioneered the discovery and characterization of many genes and pathways involved in DNA repair in animals. However, fewer than half of the alleles identified in these screens have been mapped to a specific gene, leaving a potential for new discoveries in this field. Here we show that the previously uncharacterized mutagen sensitive gene mus302 codes for the Drosophila melanogaster ortholog of the E3 ubiquitin ligase RING finger and WD domain protein 3 (RFWD3). In human cells, RFWD3 promotes ubiquitylation of RPA and RAD51 to facilitate repair of collapsed replication forks and double-strand breaks through homologous recombination. Despite the high similarity in sequence to the human ortholog, our evidence fails to support a role for Mus302 in the repair of these types of damage. Last, we observe that the N-terminal third of RFWD3 is only found in mammals, but not in other vertebrates or invertebrates. We propose that the new N-terminal sequence accounts for the acquisition of a new biological function in mammals that explains the functional differences between the human and the fly orthologs, and that Drosophila Mus302 may retain the ancestral function of the protein. |
format | Online Article Text |
id | pubmed-7056982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-70569822020-03-12 The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair Carvajal-Garcia, Juan Gales, Evan R. Ramsden, Dale A. Sekelsky, Jeff G3 (Bethesda) Investigations Repair of damaged DNA is required for the viability of all organisms. Studies in Drosophila melanogaster, driven by the power of genetic screens, pioneered the discovery and characterization of many genes and pathways involved in DNA repair in animals. However, fewer than half of the alleles identified in these screens have been mapped to a specific gene, leaving a potential for new discoveries in this field. Here we show that the previously uncharacterized mutagen sensitive gene mus302 codes for the Drosophila melanogaster ortholog of the E3 ubiquitin ligase RING finger and WD domain protein 3 (RFWD3). In human cells, RFWD3 promotes ubiquitylation of RPA and RAD51 to facilitate repair of collapsed replication forks and double-strand breaks through homologous recombination. Despite the high similarity in sequence to the human ortholog, our evidence fails to support a role for Mus302 in the repair of these types of damage. Last, we observe that the N-terminal third of RFWD3 is only found in mammals, but not in other vertebrates or invertebrates. We propose that the new N-terminal sequence accounts for the acquisition of a new biological function in mammals that explains the functional differences between the human and the fly orthologs, and that Drosophila Mus302 may retain the ancestral function of the protein. Genetics Society of America 2020-01-03 /pmc/articles/PMC7056982/ /pubmed/31900333 http://dx.doi.org/10.1534/g3.119.400903 Text en Copyright © 2020 Carvajal-Garcia et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International 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 | Investigations Carvajal-Garcia, Juan Gales, Evan R. Ramsden, Dale A. Sekelsky, Jeff The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title | The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title_full | The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title_fullStr | The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title_full_unstemmed | The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title_short | The Drosophila melanogaster Ortholog of RFWD3 Functions Independently of RAD51 During DNA Repair |
title_sort | drosophila melanogaster ortholog of rfwd3 functions independently of rad51 during dna repair |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056982/ https://www.ncbi.nlm.nih.gov/pubmed/31900333 http://dx.doi.org/10.1534/g3.119.400903 |
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