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...
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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 |
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•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> |
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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 |
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