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Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila
The Polycomb group (PcG) proteins are fundamental epigenetic regulators that control the repressive state of target genes in multicellular organisms. One of the open questions is defining the mechanisms of PcG recruitment to chromatin. In Drosophila, the crucial role in PcG recruitment is thought to...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325914/ https://www.ncbi.nlm.nih.gov/pubmed/37140047 http://dx.doi.org/10.1093/nar/gkad336 |
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author | Erokhin, Maksim Brown, J Lesley Lomaev, Dmitry Vorobyeva, Nadezhda E Zhang, Liangliang Fab, Lika V Mazina, Marina Yu Kulakovskiy, Ivan V Ziganshin, Rustam H Schedl, Paul Georgiev, Pavel Sun, Ming-an Kassis, Judith A Chetverina, Darya |
author_facet | Erokhin, Maksim Brown, J Lesley Lomaev, Dmitry Vorobyeva, Nadezhda E Zhang, Liangliang Fab, Lika V Mazina, Marina Yu Kulakovskiy, Ivan V Ziganshin, Rustam H Schedl, Paul Georgiev, Pavel Sun, Ming-an Kassis, Judith A Chetverina, Darya |
author_sort | Erokhin, Maksim |
collection | PubMed |
description | The Polycomb group (PcG) proteins are fundamental epigenetic regulators that control the repressive state of target genes in multicellular organisms. One of the open questions is defining the mechanisms of PcG recruitment to chromatin. In Drosophila, the crucial role in PcG recruitment is thought to belong to DNA-binding proteins associated with Polycomb response elements (PREs). However, current data suggests that not all PRE-binding factors have been identified. Here, we report the identification of the transcription factor Crooked legs (Crol) as a novel PcG recruiter. Crol is a C2H2-type Zinc Finger protein that directly binds to poly(G)-rich DNA sequences. Mutation of Crol binding sites as well as crol CRISPR/Cas9 knockout diminish the repressive activity of PREs in transgenes. Like other PRE-DNA binding proteins, Crol co-localizes with PcG proteins inside and outside of H3K27me3 domains. Crol knockout impairs the recruitment of the PRC1 subunit Polyhomeotic and the PRE-binding protein Combgap at a subset of sites. The decreased binding of PcG proteins is accompanied by dysregulated transcription of target genes. Overall, our study identified Crol as a new important player in PcG recruitment and epigenetic regulation. |
format | Online Article Text |
id | pubmed-10325914 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103259142023-07-08 Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila Erokhin, Maksim Brown, J Lesley Lomaev, Dmitry Vorobyeva, Nadezhda E Zhang, Liangliang Fab, Lika V Mazina, Marina Yu Kulakovskiy, Ivan V Ziganshin, Rustam H Schedl, Paul Georgiev, Pavel Sun, Ming-an Kassis, Judith A Chetverina, Darya Nucleic Acids Res Gene regulation, Chromatin and Epigenetics The Polycomb group (PcG) proteins are fundamental epigenetic regulators that control the repressive state of target genes in multicellular organisms. One of the open questions is defining the mechanisms of PcG recruitment to chromatin. In Drosophila, the crucial role in PcG recruitment is thought to belong to DNA-binding proteins associated with Polycomb response elements (PREs). However, current data suggests that not all PRE-binding factors have been identified. Here, we report the identification of the transcription factor Crooked legs (Crol) as a novel PcG recruiter. Crol is a C2H2-type Zinc Finger protein that directly binds to poly(G)-rich DNA sequences. Mutation of Crol binding sites as well as crol CRISPR/Cas9 knockout diminish the repressive activity of PREs in transgenes. Like other PRE-DNA binding proteins, Crol co-localizes with PcG proteins inside and outside of H3K27me3 domains. Crol knockout impairs the recruitment of the PRC1 subunit Polyhomeotic and the PRE-binding protein Combgap at a subset of sites. The decreased binding of PcG proteins is accompanied by dysregulated transcription of target genes. Overall, our study identified Crol as a new important player in PcG recruitment and epigenetic regulation. Oxford University Press 2023-05-04 /pmc/articles/PMC10325914/ /pubmed/37140047 http://dx.doi.org/10.1093/nar/gkad336 Text en © The Author(s) 2023. 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 (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 | Gene regulation, Chromatin and Epigenetics Erokhin, Maksim Brown, J Lesley Lomaev, Dmitry Vorobyeva, Nadezhda E Zhang, Liangliang Fab, Lika V Mazina, Marina Yu Kulakovskiy, Ivan V Ziganshin, Rustam H Schedl, Paul Georgiev, Pavel Sun, Ming-an Kassis, Judith A Chetverina, Darya Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title | Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title_full | Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title_fullStr | Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title_full_unstemmed | Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title_short | Crol contributes to PRE-mediated repression and Polycomb group proteins recruitment in Drosophila |
title_sort | crol contributes to pre-mediated repression and polycomb group proteins recruitment in drosophila |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325914/ https://www.ncbi.nlm.nih.gov/pubmed/37140047 http://dx.doi.org/10.1093/nar/gkad336 |
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