STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS
Glioblastoma stem cells (GSCs) they may be one reason for inevitable recurrence of GBM. We previously discovered that Zinc Finger Homeobox 4 (ZFHX4), a 450kD transcription factor, is required to maintain the GSC state. ZFHX4 interacts with CHD4, a core member of the nucleosome remodeling and deacety...
Gespeichert in:
Veröffentlicht in: | Neuro-oncology (Charlottesville, Va.) Va.), 2020-11, Vol.22 (Supplement_2), p.ii199-ii199 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | ii199 |
---|---|
container_issue | Supplement_2 |
container_start_page | ii199 |
container_title | Neuro-oncology (Charlottesville, Va.) |
container_volume | 22 |
creator | Galdieri, Luciano Grinwald, Mitchell Gugala, Zibi Oates, Edward Chheda, Milan |
description | Glioblastoma stem cells (GSCs) they may be one reason for inevitable recurrence of GBM. We previously discovered that Zinc Finger Homeobox 4 (ZFHX4), a 450kD transcription factor, is required to maintain the GSC state. ZFHX4 interacts with CHD4, a core member of the nucleosome remodeling and deacetylase (NuRD) complex, which activates or represses gene expression via two distinct functions - histone deacetylation and ATP-dependent chromatin remodeling. CHD4 suppression phenocopies ZFHX4 suppression. The precise nature and function of the ZFHX4 interaction with CHD4 is not understood. Here we report that the ZFHX4-CHD4 interaction requires a single zinc-finger domain. An incremental truncation screen revealed that ZFHX4 amino acids 1838 to 2387, which contains zinc fingers 14 and 15, are required to bind CHD4. Disrupting the zinc coordination of zinc finger 14 impaired the ZFHX4-CHD4 interaction. Moreover, by overexpressing ZFHX4 amino acids 1838 to 2487, we decreased CHD4 recruitment to transcription regulatory regions of the stem cell genes SOX2 and SOX9, decreased transcription, and reduced clonogenic self-renewal. These results may provide the structural basis for new treatments to target GSCs and prevent recurrence in this devastating disease. |
doi_str_mv | 10.1093/neuonc/noaa215.830 |
format | Article |
fullrecord | <record><control><sourceid>pubmedcentral_cross</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7651283</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>pubmedcentral_primary_oai_pubmedcentral_nih_gov_7651283</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1420-cac16bdf87767c6e70380255da13f328d4d27c8a9305fbb82eef62586e8927653</originalsourceid><addsrcrecordid>eNpVkF9LwzAUxYMoOKdfwKd8gc78adLsRYixXQtdC1sHspeQpqlOtna0TvDb2_1B8Oke7rnnwP0B8IjRBKMpfWrcoW3sU9MaQzCbCIquwAgzQj0mOL8-aeIJhoNbcNf3nwgNZxyPQLUswrmH6QRGq0wVSZ7JFKpYLqQqwkWylscVzCNYxCFcR_Gb76n41YdJNtjyFBg0nKVJ_pLKZZHPJVQyU-ECHpuhCtN0eQ9uarPt3cNljsEqCgsVe2k-S5RMPYt9gjxrLOZlVYsg4IHlLkBUIMJYZTCtKRGVX5HACjOliNVlKYhzNSfDg05MScAZHYPnc-_-UO5cZV3z1Zmt3nebnel-dGs2-r_TbD70e_uthzAmgg4F5Fxgu7bvO1f_ZTHSR9D6DFpfQOsBNP0FEeRspA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Galdieri, Luciano ; Grinwald, Mitchell ; Gugala, Zibi ; Oates, Edward ; Chheda, Milan</creator><creatorcontrib>Galdieri, Luciano ; Grinwald, Mitchell ; Gugala, Zibi ; Oates, Edward ; Chheda, Milan</creatorcontrib><description>Glioblastoma stem cells (GSCs) they may be one reason for inevitable recurrence of GBM. We previously discovered that Zinc Finger Homeobox 4 (ZFHX4), a 450kD transcription factor, is required to maintain the GSC state. ZFHX4 interacts with CHD4, a core member of the nucleosome remodeling and deacetylase (NuRD) complex, which activates or represses gene expression via two distinct functions - histone deacetylation and ATP-dependent chromatin remodeling. CHD4 suppression phenocopies ZFHX4 suppression. The precise nature and function of the ZFHX4 interaction with CHD4 is not understood. Here we report that the ZFHX4-CHD4 interaction requires a single zinc-finger domain. An incremental truncation screen revealed that ZFHX4 amino acids 1838 to 2387, which contains zinc fingers 14 and 15, are required to bind CHD4. Disrupting the zinc coordination of zinc finger 14 impaired the ZFHX4-CHD4 interaction. Moreover, by overexpressing ZFHX4 amino acids 1838 to 2487, we decreased CHD4 recruitment to transcription regulatory regions of the stem cell genes SOX2 and SOX9, decreased transcription, and reduced clonogenic self-renewal. These results may provide the structural basis for new treatments to target GSCs and prevent recurrence in this devastating disease.</description><identifier>ISSN: 1522-8517</identifier><identifier>EISSN: 1523-5866</identifier><identifier>DOI: 10.1093/neuonc/noaa215.830</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Cancer Stem Cells</subject><ispartof>Neuro-oncology (Charlottesville, Va.), 2020-11, Vol.22 (Supplement_2), p.ii199-ii199</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7651283/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7651283/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids></links><search><creatorcontrib>Galdieri, Luciano</creatorcontrib><creatorcontrib>Grinwald, Mitchell</creatorcontrib><creatorcontrib>Gugala, Zibi</creatorcontrib><creatorcontrib>Oates, Edward</creatorcontrib><creatorcontrib>Chheda, Milan</creatorcontrib><title>STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS</title><title>Neuro-oncology (Charlottesville, Va.)</title><description>Glioblastoma stem cells (GSCs) they may be one reason for inevitable recurrence of GBM. We previously discovered that Zinc Finger Homeobox 4 (ZFHX4), a 450kD transcription factor, is required to maintain the GSC state. ZFHX4 interacts with CHD4, a core member of the nucleosome remodeling and deacetylase (NuRD) complex, which activates or represses gene expression via two distinct functions - histone deacetylation and ATP-dependent chromatin remodeling. CHD4 suppression phenocopies ZFHX4 suppression. The precise nature and function of the ZFHX4 interaction with CHD4 is not understood. Here we report that the ZFHX4-CHD4 interaction requires a single zinc-finger domain. An incremental truncation screen revealed that ZFHX4 amino acids 1838 to 2387, which contains zinc fingers 14 and 15, are required to bind CHD4. Disrupting the zinc coordination of zinc finger 14 impaired the ZFHX4-CHD4 interaction. Moreover, by overexpressing ZFHX4 amino acids 1838 to 2487, we decreased CHD4 recruitment to transcription regulatory regions of the stem cell genes SOX2 and SOX9, decreased transcription, and reduced clonogenic self-renewal. These results may provide the structural basis for new treatments to target GSCs and prevent recurrence in this devastating disease.</description><subject>Cancer Stem Cells</subject><issn>1522-8517</issn><issn>1523-5866</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpVkF9LwzAUxYMoOKdfwKd8gc78adLsRYixXQtdC1sHspeQpqlOtna0TvDb2_1B8Oke7rnnwP0B8IjRBKMpfWrcoW3sU9MaQzCbCIquwAgzQj0mOL8-aeIJhoNbcNf3nwgNZxyPQLUswrmH6QRGq0wVSZ7JFKpYLqQqwkWylscVzCNYxCFcR_Gb76n41YdJNtjyFBg0nKVJ_pLKZZHPJVQyU-ECHpuhCtN0eQ9uarPt3cNljsEqCgsVe2k-S5RMPYt9gjxrLOZlVYsg4IHlLkBUIMJYZTCtKRGVX5HACjOliNVlKYhzNSfDg05MScAZHYPnc-_-UO5cZV3z1Zmt3nebnel-dGs2-r_TbD70e_uthzAmgg4F5Fxgu7bvO1f_ZTHSR9D6DFpfQOsBNP0FEeRspA</recordid><startdate>20201109</startdate><enddate>20201109</enddate><creator>Galdieri, Luciano</creator><creator>Grinwald, Mitchell</creator><creator>Gugala, Zibi</creator><creator>Oates, Edward</creator><creator>Chheda, Milan</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20201109</creationdate><title>STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS</title><author>Galdieri, Luciano ; Grinwald, Mitchell ; Gugala, Zibi ; Oates, Edward ; Chheda, Milan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1420-cac16bdf87767c6e70380255da13f328d4d27c8a9305fbb82eef62586e8927653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cancer Stem Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Galdieri, Luciano</creatorcontrib><creatorcontrib>Grinwald, Mitchell</creatorcontrib><creatorcontrib>Gugala, Zibi</creatorcontrib><creatorcontrib>Oates, Edward</creatorcontrib><creatorcontrib>Chheda, Milan</creatorcontrib><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Galdieri, Luciano</au><au>Grinwald, Mitchell</au><au>Gugala, Zibi</au><au>Oates, Edward</au><au>Chheda, Milan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS</atitle><jtitle>Neuro-oncology (Charlottesville, Va.)</jtitle><date>2020-11-09</date><risdate>2020</risdate><volume>22</volume><issue>Supplement_2</issue><spage>ii199</spage><epage>ii199</epage><pages>ii199-ii199</pages><issn>1522-8517</issn><eissn>1523-5866</eissn><abstract>Glioblastoma stem cells (GSCs) they may be one reason for inevitable recurrence of GBM. We previously discovered that Zinc Finger Homeobox 4 (ZFHX4), a 450kD transcription factor, is required to maintain the GSC state. ZFHX4 interacts with CHD4, a core member of the nucleosome remodeling and deacetylase (NuRD) complex, which activates or represses gene expression via two distinct functions - histone deacetylation and ATP-dependent chromatin remodeling. CHD4 suppression phenocopies ZFHX4 suppression. The precise nature and function of the ZFHX4 interaction with CHD4 is not understood. Here we report that the ZFHX4-CHD4 interaction requires a single zinc-finger domain. An incremental truncation screen revealed that ZFHX4 amino acids 1838 to 2387, which contains zinc fingers 14 and 15, are required to bind CHD4. Disrupting the zinc coordination of zinc finger 14 impaired the ZFHX4-CHD4 interaction. Moreover, by overexpressing ZFHX4 amino acids 1838 to 2487, we decreased CHD4 recruitment to transcription regulatory regions of the stem cell genes SOX2 and SOX9, decreased transcription, and reduced clonogenic self-renewal. These results may provide the structural basis for new treatments to target GSCs and prevent recurrence in this devastating disease.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/neuonc/noaa215.830</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1522-8517 |
ispartof | Neuro-oncology (Charlottesville, Va.), 2020-11, Vol.22 (Supplement_2), p.ii199-ii199 |
issn | 1522-8517 1523-5866 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7651283 |
source | Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Cancer Stem Cells |
title | STEM-13. FUNCTIONAL CHARACTERIZATION OF THE ZFHX4-CHD4 INTERACTION IN GLIOBLASTOMA CANCER STEM CELLS |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T13%3A35%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmedcentral_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=STEM-13.%20FUNCTIONAL%20CHARACTERIZATION%20OF%20THE%20ZFHX4-CHD4%20INTERACTION%20IN%20GLIOBLASTOMA%20CANCER%20STEM%20CELLS&rft.jtitle=Neuro-oncology%20(Charlottesville,%20Va.)&rft.au=Galdieri,%20Luciano&rft.date=2020-11-09&rft.volume=22&rft.issue=Supplement_2&rft.spage=ii199&rft.epage=ii199&rft.pages=ii199-ii199&rft.issn=1522-8517&rft.eissn=1523-5866&rft_id=info:doi/10.1093/neuonc/noaa215.830&rft_dat=%3Cpubmedcentral_cross%3Epubmedcentral_primary_oai_pubmedcentral_nih_gov_7651283%3C/pubmedcentral_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |