MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation

DNA double-strand breaks (DSBs) trigger the recruitment of repair protein and promote signal transduction through posttranslational modifications such as phosphorylation. After DSB induction, ataxia telangiectasia mutated (ATM) phosphorylates H2AX on chromatin surrounds the mega-base pairs proximal...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:DNA repair 2025-01, Vol.145, p.103790, Article 103790
Hauptverfasser: Okumura, Hikaru, Hayashi, Ryota, Unami, Daiki, Isono, Mayu, Yamauchi, Motohiro, Otsuka, Kensuke, Kato, Yu, Oike, Takahiro, Uchihara, Yuki, Shibata, Atsushi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page 103790
container_title DNA repair
container_volume 145
creator Okumura, Hikaru
Hayashi, Ryota
Unami, Daiki
Isono, Mayu
Yamauchi, Motohiro
Otsuka, Kensuke
Kato, Yu
Oike, Takahiro
Uchihara, Yuki
Shibata, Atsushi
description DNA double-strand breaks (DSBs) trigger the recruitment of repair protein and promote signal transduction through posttranslational modifications such as phosphorylation. After DSB induction, ataxia telangiectasia mutated (ATM) phosphorylates H2AX on chromatin surrounds the mega-base pairs proximal to the DSBs. Advanced super-resolution microscopic technology has demonstrated the formation of γH2AX nano foci as a unit of nano domain comprised of multiple nucleosomes. The formation of γH2AX nano foci could be potentially affected by pre-existing chromatin structure prior to DSB induction; however, it remains unclear whether chromatin status around DSBs influences the formation of γH2AX nano foci. In this study, to investigate γH2AX nano foci formation in the context of chromatin relaxation, γH2AX nano foci were examined following the depletion of MeCP2, which is a factor promoting chromatin condensation. Remarkably, by using super-resolution imaging analysis, we found that the volume of γH2AX nano foci cluster in MeCP2-depleted cells was significantly greater than that in control cells, both 5 and 30 min after ionizing radiation (IR). Corresponding to the increased volume size, the number of γH2AX nano foci per cluster was greater than that in control cells, while the distance of each nano focus within foci clusters remained unchanged. These findings suggest that relaxed chromatin condition by MeCP2 depletion facilitates faster and more extensive γH2AX nano foci formation after IR. Collectively, our super-resolution analysis suggests that the chromatin status surrounding DSBs influences the expansion of γH2AX nano foci formation, thus, potentially influencing the DSB repair and signaling. •MeCP2 depletion promotes the speed of γH2AX foci formation in human cells.•MeCP2 depletion enhances the volume of γH2AX nano foci cluster.•MeCP2 depletion enhances the number of γH2AX nano foci per cluster.•Pre-existing chromatin prior to DSB may influence γH2AX nano foci formation.
doi_str_mv 10.1016/j.dnarep.2024.103790
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3146580160</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1568786424001666</els_id><sourcerecordid>3146580160</sourcerecordid><originalsourceid>FETCH-LOGICAL-c241t-4742c3332e976b7bde9aab3dae1a1acadd2f8892c4a3ffe2575f8a8681bebbe03</originalsourceid><addsrcrecordid>eNp9kEFOwzAQRS0EoqVwA4S8ZJMS24mTbJCqCihSESCBxM6a2GNw1SbFThHlWtyDM5GSwpLV_Bn9ma95hByzeMhiJs9mQ1OBx-WQxzxpRyIr4h3SZ6nMoyxP5e6flkmPHIQwi2OWZlLuk54oZJIlvOiT-xsc33Fq0DrtsNJrOkcwgTY1bV6Qfn1O-OiJVlDV1NbaUXxfQhVcXVGwDXraKvfhqmfqwTho2vaQ7FmYBzza1gF5vLx4GE-i6e3V9Xg0jTRPWBNt8rUQgmORyTIrDRYApTCADBhoMIbbPC-4TkBYizzNUptDLnNWYlliLAbktLu79PXrCkOjFi5onM-hwnoVlGCJTPOW1MaadFbt6xA8WrX0bgF-rVisNjDVTHUw1Qam6mC2ayfbhFW5QPO39EuvNZx3Bmz_fHPoVfiBiMZ51I0ytfs_4RuSJYhd</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3146580160</pqid></control><display><type>article</type><title>MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Okumura, Hikaru ; Hayashi, Ryota ; Unami, Daiki ; Isono, Mayu ; Yamauchi, Motohiro ; Otsuka, Kensuke ; Kato, Yu ; Oike, Takahiro ; Uchihara, Yuki ; Shibata, Atsushi</creator><creatorcontrib>Okumura, Hikaru ; Hayashi, Ryota ; Unami, Daiki ; Isono, Mayu ; Yamauchi, Motohiro ; Otsuka, Kensuke ; Kato, Yu ; Oike, Takahiro ; Uchihara, Yuki ; Shibata, Atsushi</creatorcontrib><description>DNA double-strand breaks (DSBs) trigger the recruitment of repair protein and promote signal transduction through posttranslational modifications such as phosphorylation. After DSB induction, ataxia telangiectasia mutated (ATM) phosphorylates H2AX on chromatin surrounds the mega-base pairs proximal to the DSBs. Advanced super-resolution microscopic technology has demonstrated the formation of γH2AX nano foci as a unit of nano domain comprised of multiple nucleosomes. The formation of γH2AX nano foci could be potentially affected by pre-existing chromatin structure prior to DSB induction; however, it remains unclear whether chromatin status around DSBs influences the formation of γH2AX nano foci. In this study, to investigate γH2AX nano foci formation in the context of chromatin relaxation, γH2AX nano foci were examined following the depletion of MeCP2, which is a factor promoting chromatin condensation. Remarkably, by using super-resolution imaging analysis, we found that the volume of γH2AX nano foci cluster in MeCP2-depleted cells was significantly greater than that in control cells, both 5 and 30 min after ionizing radiation (IR). Corresponding to the increased volume size, the number of γH2AX nano foci per cluster was greater than that in control cells, while the distance of each nano focus within foci clusters remained unchanged. These findings suggest that relaxed chromatin condition by MeCP2 depletion facilitates faster and more extensive γH2AX nano foci formation after IR. Collectively, our super-resolution analysis suggests that the chromatin status surrounding DSBs influences the expansion of γH2AX nano foci formation, thus, potentially influencing the DSB repair and signaling. •MeCP2 depletion promotes the speed of γH2AX foci formation in human cells.•MeCP2 depletion enhances the volume of γH2AX nano foci cluster.•MeCP2 depletion enhances the number of γH2AX nano foci per cluster.•Pre-existing chromatin prior to DSB may influence γH2AX nano foci formation.</description><identifier>ISSN: 1568-7864</identifier><identifier>ISSN: 1568-7856</identifier><identifier>EISSN: 1568-7856</identifier><identifier>DOI: 10.1016/j.dnarep.2024.103790</identifier><identifier>PMID: 39647429</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Ataxia Telangiectasia Mutated Proteins - metabolism ; Chromatin - metabolism ; Chromatin relaxation ; DNA Breaks, Double-Stranded ; DNA Repair ; DSB repair ; Histones - metabolism ; Humans ; MeCP2 ; Methyl-CpG-Binding Protein 2 - genetics ; Methyl-CpG-Binding Protein 2 - metabolism ; Mice ; Phosphorylation ; Radiation, Ionizing ; Super-resolution imaging ; γH2AX nano foci</subject><ispartof>DNA repair, 2025-01, Vol.145, p.103790, Article 103790</ispartof><rights>2024 Elsevier B.V.</rights><rights>Copyright © 2024 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-4742c3332e976b7bde9aab3dae1a1acadd2f8892c4a3ffe2575f8a8681bebbe03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1568786424001666$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39647429$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okumura, Hikaru</creatorcontrib><creatorcontrib>Hayashi, Ryota</creatorcontrib><creatorcontrib>Unami, Daiki</creatorcontrib><creatorcontrib>Isono, Mayu</creatorcontrib><creatorcontrib>Yamauchi, Motohiro</creatorcontrib><creatorcontrib>Otsuka, Kensuke</creatorcontrib><creatorcontrib>Kato, Yu</creatorcontrib><creatorcontrib>Oike, Takahiro</creatorcontrib><creatorcontrib>Uchihara, Yuki</creatorcontrib><creatorcontrib>Shibata, Atsushi</creatorcontrib><title>MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation</title><title>DNA repair</title><addtitle>DNA Repair (Amst)</addtitle><description>DNA double-strand breaks (DSBs) trigger the recruitment of repair protein and promote signal transduction through posttranslational modifications such as phosphorylation. After DSB induction, ataxia telangiectasia mutated (ATM) phosphorylates H2AX on chromatin surrounds the mega-base pairs proximal to the DSBs. Advanced super-resolution microscopic technology has demonstrated the formation of γH2AX nano foci as a unit of nano domain comprised of multiple nucleosomes. The formation of γH2AX nano foci could be potentially affected by pre-existing chromatin structure prior to DSB induction; however, it remains unclear whether chromatin status around DSBs influences the formation of γH2AX nano foci. In this study, to investigate γH2AX nano foci formation in the context of chromatin relaxation, γH2AX nano foci were examined following the depletion of MeCP2, which is a factor promoting chromatin condensation. Remarkably, by using super-resolution imaging analysis, we found that the volume of γH2AX nano foci cluster in MeCP2-depleted cells was significantly greater than that in control cells, both 5 and 30 min after ionizing radiation (IR). Corresponding to the increased volume size, the number of γH2AX nano foci per cluster was greater than that in control cells, while the distance of each nano focus within foci clusters remained unchanged. These findings suggest that relaxed chromatin condition by MeCP2 depletion facilitates faster and more extensive γH2AX nano foci formation after IR. Collectively, our super-resolution analysis suggests that the chromatin status surrounding DSBs influences the expansion of γH2AX nano foci formation, thus, potentially influencing the DSB repair and signaling. •MeCP2 depletion promotes the speed of γH2AX foci formation in human cells.•MeCP2 depletion enhances the volume of γH2AX nano foci cluster.•MeCP2 depletion enhances the number of γH2AX nano foci per cluster.•Pre-existing chromatin prior to DSB may influence γH2AX nano foci formation.</description><subject>Animals</subject><subject>Ataxia Telangiectasia Mutated Proteins - metabolism</subject><subject>Chromatin - metabolism</subject><subject>Chromatin relaxation</subject><subject>DNA Breaks, Double-Stranded</subject><subject>DNA Repair</subject><subject>DSB repair</subject><subject>Histones - metabolism</subject><subject>Humans</subject><subject>MeCP2</subject><subject>Methyl-CpG-Binding Protein 2 - genetics</subject><subject>Methyl-CpG-Binding Protein 2 - metabolism</subject><subject>Mice</subject><subject>Phosphorylation</subject><subject>Radiation, Ionizing</subject><subject>Super-resolution imaging</subject><subject>γH2AX nano foci</subject><issn>1568-7864</issn><issn>1568-7856</issn><issn>1568-7856</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2025</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFOwzAQRS0EoqVwA4S8ZJMS24mTbJCqCihSESCBxM6a2GNw1SbFThHlWtyDM5GSwpLV_Bn9ma95hByzeMhiJs9mQ1OBx-WQxzxpRyIr4h3SZ6nMoyxP5e6flkmPHIQwi2OWZlLuk54oZJIlvOiT-xsc33Fq0DrtsNJrOkcwgTY1bV6Qfn1O-OiJVlDV1NbaUXxfQhVcXVGwDXraKvfhqmfqwTho2vaQ7FmYBzza1gF5vLx4GE-i6e3V9Xg0jTRPWBNt8rUQgmORyTIrDRYApTCADBhoMIbbPC-4TkBYizzNUptDLnNWYlliLAbktLu79PXrCkOjFi5onM-hwnoVlGCJTPOW1MaadFbt6xA8WrX0bgF-rVisNjDVTHUw1Qam6mC2ayfbhFW5QPO39EuvNZx3Bmz_fHPoVfiBiMZ51I0ytfs_4RuSJYhd</recordid><startdate>20250101</startdate><enddate>20250101</enddate><creator>Okumura, Hikaru</creator><creator>Hayashi, Ryota</creator><creator>Unami, Daiki</creator><creator>Isono, Mayu</creator><creator>Yamauchi, Motohiro</creator><creator>Otsuka, Kensuke</creator><creator>Kato, Yu</creator><creator>Oike, Takahiro</creator><creator>Uchihara, Yuki</creator><creator>Shibata, Atsushi</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20250101</creationdate><title>MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation</title><author>Okumura, Hikaru ; Hayashi, Ryota ; Unami, Daiki ; Isono, Mayu ; Yamauchi, Motohiro ; Otsuka, Kensuke ; Kato, Yu ; Oike, Takahiro ; Uchihara, Yuki ; Shibata, Atsushi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-4742c3332e976b7bde9aab3dae1a1acadd2f8892c4a3ffe2575f8a8681bebbe03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2025</creationdate><topic>Animals</topic><topic>Ataxia Telangiectasia Mutated Proteins - metabolism</topic><topic>Chromatin - metabolism</topic><topic>Chromatin relaxation</topic><topic>DNA Breaks, Double-Stranded</topic><topic>DNA Repair</topic><topic>DSB repair</topic><topic>Histones - metabolism</topic><topic>Humans</topic><topic>MeCP2</topic><topic>Methyl-CpG-Binding Protein 2 - genetics</topic><topic>Methyl-CpG-Binding Protein 2 - metabolism</topic><topic>Mice</topic><topic>Phosphorylation</topic><topic>Radiation, Ionizing</topic><topic>Super-resolution imaging</topic><topic>γH2AX nano foci</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okumura, Hikaru</creatorcontrib><creatorcontrib>Hayashi, Ryota</creatorcontrib><creatorcontrib>Unami, Daiki</creatorcontrib><creatorcontrib>Isono, Mayu</creatorcontrib><creatorcontrib>Yamauchi, Motohiro</creatorcontrib><creatorcontrib>Otsuka, Kensuke</creatorcontrib><creatorcontrib>Kato, Yu</creatorcontrib><creatorcontrib>Oike, Takahiro</creatorcontrib><creatorcontrib>Uchihara, Yuki</creatorcontrib><creatorcontrib>Shibata, Atsushi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>DNA repair</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okumura, Hikaru</au><au>Hayashi, Ryota</au><au>Unami, Daiki</au><au>Isono, Mayu</au><au>Yamauchi, Motohiro</au><au>Otsuka, Kensuke</au><au>Kato, Yu</au><au>Oike, Takahiro</au><au>Uchihara, Yuki</au><au>Shibata, Atsushi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation</atitle><jtitle>DNA repair</jtitle><addtitle>DNA Repair (Amst)</addtitle><date>2025-01-01</date><risdate>2025</risdate><volume>145</volume><spage>103790</spage><pages>103790-</pages><artnum>103790</artnum><issn>1568-7864</issn><issn>1568-7856</issn><eissn>1568-7856</eissn><abstract>DNA double-strand breaks (DSBs) trigger the recruitment of repair protein and promote signal transduction through posttranslational modifications such as phosphorylation. After DSB induction, ataxia telangiectasia mutated (ATM) phosphorylates H2AX on chromatin surrounds the mega-base pairs proximal to the DSBs. Advanced super-resolution microscopic technology has demonstrated the formation of γH2AX nano foci as a unit of nano domain comprised of multiple nucleosomes. The formation of γH2AX nano foci could be potentially affected by pre-existing chromatin structure prior to DSB induction; however, it remains unclear whether chromatin status around DSBs influences the formation of γH2AX nano foci. In this study, to investigate γH2AX nano foci formation in the context of chromatin relaxation, γH2AX nano foci were examined following the depletion of MeCP2, which is a factor promoting chromatin condensation. Remarkably, by using super-resolution imaging analysis, we found that the volume of γH2AX nano foci cluster in MeCP2-depleted cells was significantly greater than that in control cells, both 5 and 30 min after ionizing radiation (IR). Corresponding to the increased volume size, the number of γH2AX nano foci per cluster was greater than that in control cells, while the distance of each nano focus within foci clusters remained unchanged. These findings suggest that relaxed chromatin condition by MeCP2 depletion facilitates faster and more extensive γH2AX nano foci formation after IR. Collectively, our super-resolution analysis suggests that the chromatin status surrounding DSBs influences the expansion of γH2AX nano foci formation, thus, potentially influencing the DSB repair and signaling. •MeCP2 depletion promotes the speed of γH2AX foci formation in human cells.•MeCP2 depletion enhances the volume of γH2AX nano foci cluster.•MeCP2 depletion enhances the number of γH2AX nano foci per cluster.•Pre-existing chromatin prior to DSB may influence γH2AX nano foci formation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>39647429</pmid><doi>10.1016/j.dnarep.2024.103790</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1568-7864
ispartof DNA repair, 2025-01, Vol.145, p.103790, Article 103790
issn 1568-7864
1568-7856
1568-7856
language eng
recordid cdi_proquest_miscellaneous_3146580160
source MEDLINE; Elsevier ScienceDirect Journals
subjects Animals
Ataxia Telangiectasia Mutated Proteins - metabolism
Chromatin - metabolism
Chromatin relaxation
DNA Breaks, Double-Stranded
DNA Repair
DSB repair
Histones - metabolism
Humans
MeCP2
Methyl-CpG-Binding Protein 2 - genetics
Methyl-CpG-Binding Protein 2 - metabolism
Mice
Phosphorylation
Radiation, Ionizing
Super-resolution imaging
γH2AX nano foci
title MeCP2 deficiency leads to the γH2AX nano foci expansion after ionizing radiation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T12%3A49%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=MeCP2%20deficiency%20leads%20to%20the%20%CE%B3H2AX%20nano%20foci%20expansion%20after%20ionizing%20radiation&rft.jtitle=DNA%20repair&rft.au=Okumura,%20Hikaru&rft.date=2025-01-01&rft.volume=145&rft.spage=103790&rft.pages=103790-&rft.artnum=103790&rft.issn=1568-7864&rft.eissn=1568-7856&rft_id=info:doi/10.1016/j.dnarep.2024.103790&rft_dat=%3Cproquest_cross%3E3146580160%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3146580160&rft_id=info:pmid/39647429&rft_els_id=S1568786424001666&rfr_iscdi=true