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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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