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Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines

Epigenetic deregulation is a critical theme which needs further investigation in bladder cancer research. One of the most highly mutated genes in bladder cancer is KDM6A, which functions as an H3K27 demethylase and is one of the MLL3/4 complexes. To decipher the role of KDM6A in normal versus tumor...

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Autores principales: Özden-Yılmaz, Gülden, Savas, Busra, Bursalı, Ahmet, Eray, Aleyna, Arıbaş, Alirıza, Senturk, Serif, Karaca, Ezgi, Karakülah, Gökhan, Erkek-Ozhan, Serap
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047809/
https://www.ncbi.nlm.nih.gov/pubmed/36980177
http://dx.doi.org/10.3390/cells12060836
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author Özden-Yılmaz, Gülden
Savas, Busra
Bursalı, Ahmet
Eray, Aleyna
Arıbaş, Alirıza
Senturk, Serif
Karaca, Ezgi
Karakülah, Gökhan
Erkek-Ozhan, Serap
author_facet Özden-Yılmaz, Gülden
Savas, Busra
Bursalı, Ahmet
Eray, Aleyna
Arıbaş, Alirıza
Senturk, Serif
Karaca, Ezgi
Karakülah, Gökhan
Erkek-Ozhan, Serap
author_sort Özden-Yılmaz, Gülden
collection PubMed
description Epigenetic deregulation is a critical theme which needs further investigation in bladder cancer research. One of the most highly mutated genes in bladder cancer is KDM6A, which functions as an H3K27 demethylase and is one of the MLL3/4 complexes. To decipher the role of KDM6A in normal versus tumor settings, we identified the genomic landscape of KDM6A in normal, immortalized, and cancerous bladder cells. Our results showed differential KDM6A occupancy in the genes involved in cell differentiation, chromatin organization, and Notch signaling depending on the cell type and the mutation status of KDM6A. Transcription factor motif analysis revealed HES1 to be enriched at KDM6A peaks identified in the T24 bladder cancer cell line; moreover, it has a truncating mutation in KDM6A and lacks a demethylase domain. Our co-immunoprecipitation experiments revealed TLE co-repressors and HES1 as potential truncated and wild-type KDM6A interactors. With the aid of structural modeling, we explored how truncated KDM6A could interact with TLE and HES1, as well as RUNX and HHEX transcription factors. These structures provide a solid means of studying the functions of KDM6A independently of its demethylase activity. Collectively, our work provides important contributions to the understanding of KDM6A malfunction in bladder cancer.
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spelling pubmed-100478092023-03-29 Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines Özden-Yılmaz, Gülden Savas, Busra Bursalı, Ahmet Eray, Aleyna Arıbaş, Alirıza Senturk, Serif Karaca, Ezgi Karakülah, Gökhan Erkek-Ozhan, Serap Cells Article Epigenetic deregulation is a critical theme which needs further investigation in bladder cancer research. One of the most highly mutated genes in bladder cancer is KDM6A, which functions as an H3K27 demethylase and is one of the MLL3/4 complexes. To decipher the role of KDM6A in normal versus tumor settings, we identified the genomic landscape of KDM6A in normal, immortalized, and cancerous bladder cells. Our results showed differential KDM6A occupancy in the genes involved in cell differentiation, chromatin organization, and Notch signaling depending on the cell type and the mutation status of KDM6A. Transcription factor motif analysis revealed HES1 to be enriched at KDM6A peaks identified in the T24 bladder cancer cell line; moreover, it has a truncating mutation in KDM6A and lacks a demethylase domain. Our co-immunoprecipitation experiments revealed TLE co-repressors and HES1 as potential truncated and wild-type KDM6A interactors. With the aid of structural modeling, we explored how truncated KDM6A could interact with TLE and HES1, as well as RUNX and HHEX transcription factors. These structures provide a solid means of studying the functions of KDM6A independently of its demethylase activity. Collectively, our work provides important contributions to the understanding of KDM6A malfunction in bladder cancer. MDPI 2023-03-08 /pmc/articles/PMC10047809/ /pubmed/36980177 http://dx.doi.org/10.3390/cells12060836 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Özden-Yılmaz, Gülden
Savas, Busra
Bursalı, Ahmet
Eray, Aleyna
Arıbaş, Alirıza
Senturk, Serif
Karaca, Ezgi
Karakülah, Gökhan
Erkek-Ozhan, Serap
Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title_full Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title_fullStr Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title_full_unstemmed Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title_short Differential Occupancy and Regulatory Interactions of KDM6A in Bladder Cell Lines
title_sort differential occupancy and regulatory interactions of kdm6a in bladder cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047809/
https://www.ncbi.nlm.nih.gov/pubmed/36980177
http://dx.doi.org/10.3390/cells12060836
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