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Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans
The tumor-suppressor proteins BRCA1 and BARD1 function as an E3 ubiquitin ligase to facilitate transcriptional repression and DNA damage repair. This is mediated in-part through its ability to mono-ubiquitylate histone H2A in nucleosomes. Studies in Caenorhabditis elegans have been used to elucidate...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018340/ https://www.ncbi.nlm.nih.gov/pubmed/36250637 http://dx.doi.org/10.1093/nar/gkac877 |
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author | Thapa, Ishor Vahrenkamp, Russell Witus, Samuel R Lightle, Caitlin Falkenberg, Owen Sellin Jeffries, Marlo K Klevit, Rachel E Stewart, Mikaela D |
author_facet | Thapa, Ishor Vahrenkamp, Russell Witus, Samuel R Lightle, Caitlin Falkenberg, Owen Sellin Jeffries, Marlo K Klevit, Rachel E Stewart, Mikaela D |
author_sort | Thapa, Ishor |
collection | PubMed |
description | The tumor-suppressor proteins BRCA1 and BARD1 function as an E3 ubiquitin ligase to facilitate transcriptional repression and DNA damage repair. This is mediated in-part through its ability to mono-ubiquitylate histone H2A in nucleosomes. Studies in Caenorhabditis elegans have been used to elucidate numerous functions of BRCA1 and BARD1; however, it has not been established that the C. elegans orthologs, BRC-1 and BRD-1, retain all the functions of their human counterparts. Here we explore the conservation of enzymatic activity toward nucleosomes which leads to repression of estrogen-metabolizing cytochrome P450 (cyp) genes in humans. Biochemical assays establish that BRC-1 and BRD-1 contribute to ubiquitylation of histone H2A in the nucleosome. Mutational analysis shows that while BRC-1 likely binds the nucleosome using a conserved interface, BRD-1 and BARD1 have evolved different modes of binding, resulting in a difference in the placement of ubiquitin on H2A. Gene expression analysis reveals that in spite of this difference, BRC-1 and BRD-1 also contribute to cyp gene repression in C. elegans. Establishing conservation of these functions in C. elegans allows for use of this powerful model organism to address remaining questions regarding regulation of gene expression by BRCA1 and BARD1. |
format | Online Article Text |
id | pubmed-10018340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-100183402023-03-17 Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans Thapa, Ishor Vahrenkamp, Russell Witus, Samuel R Lightle, Caitlin Falkenberg, Owen Sellin Jeffries, Marlo K Klevit, Rachel E Stewart, Mikaela D Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The tumor-suppressor proteins BRCA1 and BARD1 function as an E3 ubiquitin ligase to facilitate transcriptional repression and DNA damage repair. This is mediated in-part through its ability to mono-ubiquitylate histone H2A in nucleosomes. Studies in Caenorhabditis elegans have been used to elucidate numerous functions of BRCA1 and BARD1; however, it has not been established that the C. elegans orthologs, BRC-1 and BRD-1, retain all the functions of their human counterparts. Here we explore the conservation of enzymatic activity toward nucleosomes which leads to repression of estrogen-metabolizing cytochrome P450 (cyp) genes in humans. Biochemical assays establish that BRC-1 and BRD-1 contribute to ubiquitylation of histone H2A in the nucleosome. Mutational analysis shows that while BRC-1 likely binds the nucleosome using a conserved interface, BRD-1 and BARD1 have evolved different modes of binding, resulting in a difference in the placement of ubiquitin on H2A. Gene expression analysis reveals that in spite of this difference, BRC-1 and BRD-1 also contribute to cyp gene repression in C. elegans. Establishing conservation of these functions in C. elegans allows for use of this powerful model organism to address remaining questions regarding regulation of gene expression by BRCA1 and BARD1. Oxford University Press 2022-10-17 /pmc/articles/PMC10018340/ /pubmed/36250637 http://dx.doi.org/10.1093/nar/gkac877 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Gene regulation, Chromatin and Epigenetics Thapa, Ishor Vahrenkamp, Russell Witus, Samuel R Lightle, Caitlin Falkenberg, Owen Sellin Jeffries, Marlo K Klevit, Rachel E Stewart, Mikaela D Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title | Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title_full | Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title_fullStr | Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title_full_unstemmed | Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title_short | Conservation of transcriptional regulation by BRCA1 and BARD1 in Caenorhabditis elegans |
title_sort | conservation of transcriptional regulation by brca1 and bard1 in caenorhabditis elegans |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018340/ https://www.ncbi.nlm.nih.gov/pubmed/36250637 http://dx.doi.org/10.1093/nar/gkac877 |
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