Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response
The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activat...
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creator | Hu, Chen Zhang, Shengping Gao, Xuan Gao, Xiaojing Xu, Xiaohong Lv, Ya Zhang, Yan Zhu, Zhenhong Zhang, Changqing Li, Qiao Wong, Jiemin Cui, Yongping Zhang, Wen Ma, Lin Wang, Chuangui |
description | The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress.
KAP1 is important for epigenetic modifications and the DNA damage response.
Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis.
KAP1 S473p is required for efficient DNA repair and cell survival under stress.
Our studies reveal functions for KAP1 S473p under stress. |
doi_str_mv | 10.1074/jbc.M111.313262 |
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KAP1 is important for epigenetic modifications and the DNA damage response.
Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis.
KAP1 S473p is required for efficient DNA repair and cell survival under stress.
Our studies reveal functions for KAP1 S473p under stress.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M111.313262</identifier><identifier>PMID: 22496453</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Apoptosis ; Apoptosis - physiology ; Ataxia Telangiectasia Mutated Proteins ; Cell Cycle Proteins - genetics ; Cell Cycle Proteins - metabolism ; Checkpoint Kinase 1 ; Checkpoint Kinase 2 ; Chk2 ; Chromatin Assembly and Disassembly ; Co-repressor Transcription ; DNA Damage ; DNA Damage Response ; DNA-Binding Proteins - genetics ; DNA-Binding Proteins - metabolism ; E2F Transcription Factor ; E2F1 ; E2F1 Transcription Factor - genetics ; E2F1 Transcription Factor - metabolism ; HEK293 Cells ; HeLa Cells ; HP1 ; Humans ; KAP1 ; KRAB-ZNFs ; Phosphorylation - genetics ; Protein Kinases - genetics ; Protein Kinases - metabolism ; Protein Phosphorylation ; Protein-Serine-Threonine Kinases - genetics ; Protein-Serine-Threonine Kinases - metabolism ; Repressor Proteins - genetics ; Repressor Proteins - metabolism ; Serine - genetics ; Serine - metabolism ; Signal Transduction ; Tripartite Motif-Containing Protein 28 ; Tumor Suppressor Proteins - genetics ; Tumor Suppressor Proteins - metabolism</subject><ispartof>The Journal of biological chemistry, 2012-06, Vol.287 (23), p.18937-18952</ispartof><rights>2012 © 2012 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2012 by The American Society for Biochemistry and Molecular Biology, Inc. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-e44c49f62aa88814092ab908bfbd5e0e508e61fb7017e7bd32790e2cd477933</citedby><cites>FETCH-LOGICAL-c509t-e44c49f62aa88814092ab908bfbd5e0e508e61fb7017e7bd32790e2cd477933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365928/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3365928/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22496453$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Chen</creatorcontrib><creatorcontrib>Zhang, Shengping</creatorcontrib><creatorcontrib>Gao, Xuan</creatorcontrib><creatorcontrib>Gao, Xiaojing</creatorcontrib><creatorcontrib>Xu, Xiaohong</creatorcontrib><creatorcontrib>Lv, Ya</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Zhu, Zhenhong</creatorcontrib><creatorcontrib>Zhang, Changqing</creatorcontrib><creatorcontrib>Li, Qiao</creatorcontrib><creatorcontrib>Wong, Jiemin</creatorcontrib><creatorcontrib>Cui, Yongping</creatorcontrib><creatorcontrib>Zhang, Wen</creatorcontrib><creatorcontrib>Ma, Lin</creatorcontrib><creatorcontrib>Wang, Chuangui</creatorcontrib><title>Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress.
KAP1 is important for epigenetic modifications and the DNA damage response.
Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis.
KAP1 S473p is required for efficient DNA repair and cell survival under stress.
Our studies reveal functions for KAP1 S473p under stress.</description><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Ataxia Telangiectasia Mutated Proteins</subject><subject>Cell Cycle Proteins - genetics</subject><subject>Cell Cycle Proteins - metabolism</subject><subject>Checkpoint Kinase 1</subject><subject>Checkpoint Kinase 2</subject><subject>Chk2</subject><subject>Chromatin Assembly and Disassembly</subject><subject>Co-repressor Transcription</subject><subject>DNA Damage</subject><subject>DNA Damage Response</subject><subject>DNA-Binding Proteins - genetics</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>E2F Transcription Factor</subject><subject>E2F1</subject><subject>E2F1 Transcription Factor - genetics</subject><subject>E2F1 Transcription Factor - metabolism</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>HP1</subject><subject>Humans</subject><subject>KAP1</subject><subject>KRAB-ZNFs</subject><subject>Phosphorylation - genetics</subject><subject>Protein Kinases - genetics</subject><subject>Protein Kinases - metabolism</subject><subject>Protein Phosphorylation</subject><subject>Protein-Serine-Threonine Kinases - genetics</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Repressor Proteins - genetics</subject><subject>Repressor Proteins - metabolism</subject><subject>Serine - genetics</subject><subject>Serine - metabolism</subject><subject>Signal Transduction</subject><subject>Tripartite Motif-Containing Protein 28</subject><subject>Tumor Suppressor Proteins - genetics</subject><subject>Tumor Suppressor Proteins - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFP3DAQRq2qVVko594qH-khi8d2EvtSaVlKixYKWnrozXKcCWuUjYOdRfDvCVpA9IAvI42fv7HmEfIV2BRYKQ9vKjc9B4CpAMEL_oFMgCmRiRz-fSQTxjhkmudqh-ymdMPGIzV8JjucS13IXExIXIYWEw0NXcRN32Ob2ZSC83bAmh6Fe3qwWM6Ovr_tzkMWsY84diJdzC6BXmHMZCno5SqkfhXiQ2sHHzrqO3r8Z0aP7dpeI11i6kOX8Av51Ng24f5z3SNXJz__zn9nZxe_Tuezs8zlTA8ZSumkbgpurVIKJNPcVpqpqqnqHBnmTGEBTVUyKLGsasFLzZC7WpalFmKP_Nim9ptqjbXDboi2NX30axsfTLDe_H_T-ZW5DndGiCLXXI0BB88BMdxuMA1m7ZPDtrUdhk0ywEAVomCCj-jhFnUxpBSxeR0DzDx5MqMn8-TJbD2NL769_d0r_yJmBPQWwHFDdx6jSc5j57D2Ed1g6uDfDX8EUB2hnw</recordid><startdate>20120601</startdate><enddate>20120601</enddate><creator>Hu, Chen</creator><creator>Zhang, Shengping</creator><creator>Gao, Xuan</creator><creator>Gao, Xiaojing</creator><creator>Xu, Xiaohong</creator><creator>Lv, Ya</creator><creator>Zhang, Yan</creator><creator>Zhu, Zhenhong</creator><creator>Zhang, Changqing</creator><creator>Li, Qiao</creator><creator>Wong, Jiemin</creator><creator>Cui, Yongping</creator><creator>Zhang, Wen</creator><creator>Ma, Lin</creator><creator>Wang, Chuangui</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</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><scope>5PM</scope></search><sort><creationdate>20120601</creationdate><title>Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response</title><author>Hu, Chen ; Zhang, Shengping ; Gao, Xuan ; Gao, Xiaojing ; Xu, Xiaohong ; Lv, Ya ; Zhang, Yan ; Zhu, Zhenhong ; Zhang, Changqing ; Li, Qiao ; Wong, Jiemin ; Cui, Yongping ; Zhang, Wen ; Ma, Lin ; Wang, Chuangui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-e44c49f62aa88814092ab908bfbd5e0e508e61fb7017e7bd32790e2cd477933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Ataxia Telangiectasia Mutated Proteins</topic><topic>Cell Cycle Proteins - genetics</topic><topic>Cell Cycle Proteins - metabolism</topic><topic>Checkpoint Kinase 1</topic><topic>Checkpoint Kinase 2</topic><topic>Chk2</topic><topic>Chromatin Assembly and Disassembly</topic><topic>Co-repressor Transcription</topic><topic>DNA Damage</topic><topic>DNA Damage Response</topic><topic>DNA-Binding Proteins - genetics</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>E2F Transcription Factor</topic><topic>E2F1</topic><topic>E2F1 Transcription Factor - genetics</topic><topic>E2F1 Transcription Factor - metabolism</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>HP1</topic><topic>Humans</topic><topic>KAP1</topic><topic>KRAB-ZNFs</topic><topic>Phosphorylation - genetics</topic><topic>Protein Kinases - genetics</topic><topic>Protein Kinases - metabolism</topic><topic>Protein Phosphorylation</topic><topic>Protein-Serine-Threonine Kinases - genetics</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Repressor Proteins - genetics</topic><topic>Repressor Proteins - metabolism</topic><topic>Serine - genetics</topic><topic>Serine - metabolism</topic><topic>Signal Transduction</topic><topic>Tripartite Motif-Containing Protein 28</topic><topic>Tumor Suppressor Proteins - genetics</topic><topic>Tumor Suppressor Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Chen</creatorcontrib><creatorcontrib>Zhang, Shengping</creatorcontrib><creatorcontrib>Gao, Xuan</creatorcontrib><creatorcontrib>Gao, Xiaojing</creatorcontrib><creatorcontrib>Xu, Xiaohong</creatorcontrib><creatorcontrib>Lv, Ya</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Zhu, Zhenhong</creatorcontrib><creatorcontrib>Zhang, Changqing</creatorcontrib><creatorcontrib>Li, Qiao</creatorcontrib><creatorcontrib>Wong, Jiemin</creatorcontrib><creatorcontrib>Cui, Yongping</creatorcontrib><creatorcontrib>Zhang, Wen</creatorcontrib><creatorcontrib>Ma, Lin</creatorcontrib><creatorcontrib>Wang, Chuangui</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Chen</au><au>Zhang, Shengping</au><au>Gao, Xuan</au><au>Gao, Xiaojing</au><au>Xu, Xiaohong</au><au>Lv, Ya</au><au>Zhang, Yan</au><au>Zhu, Zhenhong</au><au>Zhang, Changqing</au><au>Li, Qiao</au><au>Wong, Jiemin</au><au>Cui, Yongping</au><au>Zhang, Wen</au><au>Ma, Lin</au><au>Wang, Chuangui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2012-06-01</date><risdate>2012</risdate><volume>287</volume><issue>23</issue><spage>18937</spage><epage>18952</epage><pages>18937-18952</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The Kruppel-associated box (KRAB)-associated co-repressor KAP1 is an essential nuclear co-repressor for the KRAB zinc finger protein superfamily of transcriptional factors. Ataxia telangiectasia mutated (ATM)-Chk2 and ATM- and Rad3-related (ATR)-Chk1 are two primary kinase signaling cascades activated in response to DNA damage. A growing body of evidence suggests that ATM and ATR phosphorylate KAP1 at Ser-824 in response to DNA damage and regulate KAP1-dependent chromatin condensation, DNA repair, and gene expression. Here, we show that, depending on the type of DNA damage that occurs, KAP1 Ser-473 can be phosphorylated by ATM-Chk2 or ATR-Chk1 kinases. Phosphorylation of KAP1 at Ser-473 attenuated its binding to the heterochromatin protein 1 family proteins and inhibited its transcriptional repression of KRAB-zinc finger protein (KRAB-ZFP) target genes. Moreover, KAP1 Ser-473 phosphorylation induced by DNA damage stimulated KAP1-E2F1 binding. Overexpression of heterochromatin protein 1 significantly inhibited E2F1-KAP1 binding. Elimination of KAP1 Ser-473 phosphorylation increased E2F1-targeted proapoptotic gene expression and E2F1-induced apoptosis in response to DNA damage. Furthermore, loss of phosphorylation of KAP1 Ser-473 led to less BRCA1 focus formation and slower kinetics of loss of γH2AX foci after DNA damage. KAP1 Ser-473 phosphorylation was required for efficient DNA repair and cell survival in response to DNA damage. Our studies reveal novel functions of KAP1 Ser-473 phosphorylation under stress.
KAP1 is important for epigenetic modifications and the DNA damage response.
Distinct DNA damage signaling pathways regulate KAP1 Ser-473 phosphorylation (S473p). DNA damage-induced KAP1 S473p regulates KAP1-HP1 and KAP1-E2F1 interactions, gene transcription, DNA repair, and apoptosis.
KAP1 S473p is required for efficient DNA repair and cell survival under stress.
Our studies reveal functions for KAP1 S473p under stress.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22496453</pmid><doi>10.1074/jbc.M111.313262</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Apoptosis - physiology Ataxia Telangiectasia Mutated Proteins Cell Cycle Proteins - genetics Cell Cycle Proteins - metabolism Checkpoint Kinase 1 Checkpoint Kinase 2 Chk2 Chromatin Assembly and Disassembly Co-repressor Transcription DNA Damage DNA Damage Response DNA-Binding Proteins - genetics DNA-Binding Proteins - metabolism E2F Transcription Factor E2F1 E2F1 Transcription Factor - genetics E2F1 Transcription Factor - metabolism HEK293 Cells HeLa Cells HP1 Humans KAP1 KRAB-ZNFs Phosphorylation - genetics Protein Kinases - genetics Protein Kinases - metabolism Protein Phosphorylation Protein-Serine-Threonine Kinases - genetics Protein-Serine-Threonine Kinases - metabolism Repressor Proteins - genetics Repressor Proteins - metabolism Serine - genetics Serine - metabolism Signal Transduction Tripartite Motif-Containing Protein 28 Tumor Suppressor Proteins - genetics Tumor Suppressor Proteins - metabolism |
title | Roles of Kruppel-associated Box (KRAB)-associated Co-repressor KAP1 Ser-473 Phosphorylation in DNA Damage Response |
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